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          "en" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">DNA fragments on agarose gel electrophoresis after restriction enzyme digestion of exon 1 of the mannose-binding lectin &#40;<span class="elsevierStyleItalic">MBL2</span>&#41; gene codon 54&#46; In all&#44; 349<span class="elsevierStyleHsp" style=""></span>bp PCR product was digested with <span class="elsevierStyleItalic">BanI</span> for codon 54 polymorphism&#46; The normal allele &#40;allele A&#41; is cut into two fragments with <span class="elsevierStyleItalic">BanI</span> &#40;lanes 2 and 5&#41;&#44; 89 and 260<span class="elsevierStyleHsp" style=""></span>bp&#46; The variant allele &#40;allele O&#41; remains uncut &#40;lanes 1 and 6&#41;&#46; Both uncut and digested fragments are seen in AO heterozygote &#40;lanes 3 and 4&#41;&#46; L&#58; 100<span class="elsevierStyleHsp" style=""></span>bp DNA ladder&#46;</p>"
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and mutant <span class="elsevierStyleItalic">MBL2</span> alleles occur as a result of three single-point mutations in this gene &#40;B&#44; C&#44; and D&#41;&#46; Although functional MBL levels are low in heterozygous polymorphisms&#44; MBL levels in homozygous polymorphisms are so low that they may not even be determinable&#46;<a class="elsevierStyleCrossRefs" href="#bib0145"><span class="elsevierStyleSup">4&#44;5</span></a> MBL activates the complement system by binding to mannose or sugar motifs&#44; which are found in many microorganisms&#44; and plays an important role in innate immunity and inflammation&#46;<a class="elsevierStyleCrossRefs" href="#bib0135"><span class="elsevierStyleSup">2&#44;6</span></a> In newborns&#44; an increase in sepsis frequency is observed when MBL levels are low&#46;<a class="elsevierStyleCrossRefs" href="#bib0135"><span class="elsevierStyleSup">2&#44;3&#44;7</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">The mortality and morbidity rates in preterm infants are higher than those in term infants&#46; As gestational week and birth weight decrease&#44; the risk of complications increases&#46; In preterm infants&#44; complications are observed in the early &#40;neonatal period&#41; and late periods &#40;after discharge&#41;&#46; Although the survival rate of most preterm infants has improved because of advances in medical care&#44; the incidence of short-term complications remains relatively stable&#46; Short-term complications increase the risk of long-term sequelae&#46;<a class="elsevierStyleCrossRefs" href="#bib0165"><span class="elsevierStyleSup">8&#44;9</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">In recent years&#44; many studies have been conducted on the importance of MBL during the neonatal period&#44; and most of these are associated with sepsis&#46; In sepsis&#44; proinflammatory and anti-inflammatory cytokine ratio is vital in terms of defense against infectious agents&#46; The imbalance in this ratio is manifested by increased morbidity and mortality during the neonatal period&#46;<a class="elsevierStyleCrossRefs" href="#bib0150"><span class="elsevierStyleSup">5&#44;6</span></a> Increased cytokine levels have a significant role in the pathophysiology of morbidities such as respiratory distress syndrome &#40;RDS&#41;&#44; intraventricular hemorrhage &#40;IVH&#41;&#44; necrotizing enterocolitis &#40;NEC&#41;&#44; bronchopulmonary dysplasia &#40;BPD&#41;&#44; and retinopathy of prematurity &#40;ROP&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0175"><span class="elsevierStyleSup">10</span></a> This prospective study aimed to investigate the association of <span class="elsevierStyleItalic">MBL2</span> polymorphism with short-term outcomes in preterm infants&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0070">Materials and methods</span><p id="par0020" class="elsevierStylePara elsevierViewall">All preterm infants of &#60;37 gestational weeks who were admitted to the neonatal intensive care unit &#40;NICU&#41; of the Uludag University Medical School during a two-year period were enrolled in this prospective study&#46; The neonates were categorized into two groups according to their <span class="elsevierStyleItalic">MBL2</span> genotypes&#46; Normal <span class="elsevierStyleItalic">MBL2</span> genotype was defined as <span class="elsevierStyleItalic">MBL2</span> wild-type &#40;AA genotype&#41;&#44; whereas mutant <span class="elsevierStyleItalic">MBL2</span> genotype was defined as <span class="elsevierStyleItalic">MBL2</span> variant-type &#40;AO or OO genotype&#41;&#46; The exclusion criteria included refusal of parental consent&#44; infants with major congenital abnormalities&#44; and those undergoing a major surgical procedure&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">Gestational age&#44; birth weight&#44; gender&#44; mode of delivery&#44; Apgar score at 1 and 5<span class="elsevierStyleHsp" style=""></span>min&#44; prenatal demographics&#44; antenatal steroid administration&#44; premature rupture of membranes&#44; history of chorioamnionitis and durations of invasive mechanical ventilation&#44; total supplemental oxygen&#44; central catheterization&#44; and total parenteral nutrition were recorded&#46; The presence of neonatal morbidities such as RDS&#44; late-onset sepsis &#40;LOS&#41;&#44; IVH&#44; NEC&#44; BPD&#44; ROP&#44; and the mortality data of the preterm infants were recorded&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">RDS was diagnosed based on clinical findings &#40;tachypnea&#44; retractions&#44; nasal flaring&#44; and cyanosis&#41; or radiological findings &#40;reticular granular pattern or air bronchograms&#41;&#46; All neonates underwent the same management according to the NICU protocols and as recommended by European consensus guidelines on the management of neonatal respiratory distress syndrome in preterm infants&#46;<a class="elsevierStyleCrossRefs" href="#bib0180"><span class="elsevierStyleSup">11&#44;12</span></a> Neonatal sepsis was defined as the presence of clinical signs of sepsis with a positive blood culture&#46; Blood cultures were analyzed using the fully automated BACTEC method in a BACTEC 9240 device &#40;Becton Dickinson&#44; Heidelberg&#44; Germany&#41;&#46; LOS was determined by the time at which sepsis occurred between 4 and 30 days after birth&#46;<a class="elsevierStyleCrossRef" href="#bib0190"><span class="elsevierStyleSup">13</span></a> IVH was evaluated by cranial ultrasound examinations&#44; which were performed by the same pediatric radiologist and diagnosed using the Papile classification system&#46;<a class="elsevierStyleCrossRef" href="#bib0195"><span class="elsevierStyleSup">14</span></a> NEC was diagnosed according to clinical and radiographic findings and classified according to modified Bell&#39;s criteria&#46;<a class="elsevierStyleCrossRef" href="#bib0200"><span class="elsevierStyleSup">15</span></a> BPD was classified into three groups in terms of BPD severity depending on the duration and level of supplemental oxygen and mechanical ventilatory support at 36 weeks postmenstrual age&#46;<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">16</span></a> ROP was classified according to the International Classification of Retinopathy of Prematurity&#46;<a class="elsevierStyleCrossRef" href="#bib0210"><span class="elsevierStyleSup">17</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">The MBL levels and gene polymorphisms were assessed within 3<span class="elsevierStyleHsp" style=""></span>h in most infants and within 24<span class="elsevierStyleHsp" style=""></span>h after birth in all infants&#46; The blood samples for the measurement of MBL levels were collected in a test tube and these blood samples were centrifuged within thirty minutes after obtaining&#46; After the centrifugation process&#44; serum of the samples were immediately stored at &#8722;80<span class="elsevierStyleHsp" style=""></span>&#176;C until analysis&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">Blood samples were analyzed using enzyme-linked immunosorbent assay&#46; PCR and restriction fragment length polymorphism were used for <span class="elsevierStyleItalic">MBL</span>2 genotyping&#46; Serum MBL levels were measured using an immunoassay kit &#40;Oligomer ELISA kit&#59; Antibody Shop&#44; Copenhagen&#44; Denmark&#41; according to the manufacturer instructions&#46; The lowest detectable MBL concentration was 10<span class="elsevierStyleHsp" style=""></span>ng&#47;mL&#46; For the definition of the functional MBL deficiency&#44; this study used two different cut-off values of MBL concentration&#46; An MBL level<span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>700<span class="elsevierStyleHsp" style=""></span>ng&#47;mL was determined as deficiency and &#60;150<span class="elsevierStyleHsp" style=""></span>ng&#47;mL as severe deficiency&#46;<a class="elsevierStyleCrossRefs" href="#bib0130"><span class="elsevierStyleSup">1&#8211;3&#44;18</span></a> DNA was extracted from the blood samples using a commercially available kit &#40;Puregene&#44; Gentra&#44; MN&#44; United States&#41;&#44; and <span class="elsevierStyleItalic">MBL2</span> genotyping was performed using these samples&#46; DNA samples were maintained at &#8722;20<span class="elsevierStyleHsp" style=""></span>&#176;C until use&#46; All genotypes were detected using PCR and restriction enzyme digestion&#46; Exon 1 of <span class="elsevierStyleItalic">MBL2</span> was amplified by PCR&#46; The primer sequences were 5&#8242;-GTA GGA CAG AGG GCA TGC TC-3&#8242; and 5&#8242;-CAG GCA GTT TCC TCT GGA AGG-3&#8242;&#46; In all&#44; a 349-bp PCR product was digested with <span class="elsevierStyleItalic">BanI</span> and <span class="elsevierStyleItalic">MboII</span> for codon 54 and codon 57&#44; respectively&#46; The normal allele &#40;allele A&#41; was cut into two fragments with <span class="elsevierStyleItalic">BanI</span>&#44; 260 and 89<span class="elsevierStyleHsp" style=""></span>bp&#46; The variant allele B &#40;rs1800450&#41; and allele D &#40;rs5030737&#41; remained uncut&#46; <span class="elsevierStyleItalic">MboII</span> cleaved the variant allele C &#40;rs1800451&#41; into 270 and 79<span class="elsevierStyleHsp" style=""></span>bp fragments&#46; The fragments were visualized using electrophoresis on 2&#37; agarose gel&#46; At electrophoresis&#44; the dual band at the restriction site was defined as a heterozygous mutation&#44; whereas the single band was defined as a homozygous mutation&#46; As stated&#44; the normal structural <span class="elsevierStyleItalic">MBL2</span> allele was named A&#44; whereas alleles B&#44; C and D &#40;mutation in codons 54&#44; 57 and 52&#41; were named O&#46; A representative gel electrophoresis of the <span class="elsevierStyleItalic">MBL2</span> exon 1 codon 54 polymorphisms is shown in <a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0045" class="elsevierStylePara elsevierViewall">This study was approved by the Ethics Committee of Uludag University Medical School and conformed to the standards set by the Declaration of Helsinki &#40;15&#46;01&#46;2013-1&#47;20&#41;&#46; All parents provided informed consents prior to the inclusion of their children in the study&#46;</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0075">Statistical analysis</span><p id="par0050" class="elsevierStylePara elsevierViewall">Statistical analysis was performed using SPSS v&#46; 20&#46;0 software &#40;SPSS Inc&#46;&#44; Chicago&#44; IL&#44; United States&#41;&#46; The results are presented as median &#40;interquartile range&#41; for the variables showing non-Gaussian distribution and mean<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>standard deviation for data showing normal distribution&#46; Student&#39;s <span class="elsevierStyleItalic">t</span>-test was used for group comparisons of normal distributions&#44; and the Mann&#8211;Whitney <span class="elsevierStyleItalic">U</span> test was used for group comparisons of non-normal distributions&#46; The chi-squared test and Fisher&#39;s exact test were used for the comparison of categorical variables&#46; Logistic regression analysis was performed to investigate the effect of <span class="elsevierStyleItalic">MBL2</span> genotype on RDS&#46; The analysis included factors that were demonstrated in the literature to have an effect on RDS&#58; gestational age&#44; birth weight&#44; sex&#44; antenatal steroid administration&#44; and <span class="elsevierStyleItalic">MBL2</span> genotype were included in the analysis&#46; A <span class="elsevierStyleItalic">p</span>-value of &#60;0&#46;05 was considered statistically significant&#46;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0080">Results</span><p id="par0055" class="elsevierStylePara elsevierViewall">Overall&#44; 131 preterm infants were included in this study&#46; Ten were excluded because of blood sample insufficiency&#44; four because of major congenital abnormalities&#44; and one because of major surgery&#46; In the final analysis&#44; a total of 116 preterm infants were included&#58; 69 with <span class="elsevierStyleItalic">MBL2</span> wild-type &#40;AA genotype&#41; and 47 with <span class="elsevierStyleItalic">MBL2</span> variant-type &#40;AO&#47;OO genotype&#41;&#46; Overall&#44; the rate of <span class="elsevierStyleItalic">MBL2</span> variant-type in preterm infants was 41&#37;&#46; MBL levels were significantly lower and MBL deficiency and severe deficiency were higher in <span class="elsevierStyleItalic">MBL2</span> variant-type than in <span class="elsevierStyleItalic">MBL2</span> wild-type &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#46;001&#41;&#46; <a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a> shows the demographic features of the study population&#46; Codon 57 and 52 polymorphisms were not detected in any of the 116 preterm infants during the genetic evaluation&#46; <span class="elsevierStyleItalic">MBL2</span> codon 54 genotype and allele frequencies were 59&#37; for <span class="elsevierStyleItalic">MBL2</span> wild-type &#40;AA genotype&#41; and 41&#37; for <span class="elsevierStyleItalic">MBL2</span> variant-type &#40;AO and OO genotype&#41;&#46;</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0060" class="elsevierStylePara elsevierViewall">Evaluation of short-term morbidity based on <span class="elsevierStyleItalic">MBL2</span> genotype revealed that RDS and mortality rates were significantly higher in the <span class="elsevierStyleItalic">MBL2</span> variant-type group &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#46;001&#44; <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#46;03&#59; respectively&#41;&#46; NEC was found to be more prevalent in the <span class="elsevierStyleItalic">MBL2</span> wild-type group &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#46;01&#41;&#46; There was no difference between the <span class="elsevierStyleItalic">MBL2</span> wild-type and variant-type groups in terms of IVH&#44; BPD&#44; ROP&#44; and LOS &#40;<a class="elsevierStyleCrossRef" href="#tbl0010">Table 2</a>&#41;&#46; Consideration of short-term morbidity based on MBL levels revealed that RDS was significantly higher in both the MBL deficient and severely deficient groups &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#46;001&#41;&#46; NEC was found to be more common with normal levels of MBL &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#46;002&#41;&#46; There was no significant difference in infants with or without MBL deficiency with respect to IVH&#44; BPD&#44; ROP&#44; LOS&#44; and mortality &#40;<a class="elsevierStyleCrossRef" href="#tbl0015">Table 3</a>&#41;&#46; Further&#44; because univariate analyses revealed that RDS development was more common in the <span class="elsevierStyleItalic">MBL2</span> variant-type&#44; the effect of gestational age&#44; birth weight&#44; gender&#44; antenatal steroid use&#44; and <span class="elsevierStyleItalic">MBL2</span> genetics&#44; which are factors that may affect RDS development&#44; was investigated by logistic regression analysis&#46; <span class="elsevierStyleItalic">MBL2</span> variant-type was found to be an independent factor for the development of RDS &#40;OR&#58; 5&#46;1&#44; 95&#37; CI&#58; 2&#46;2&#8211;11&#46;9&#44; <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#46;001&#41;&#46;</p><elsevierMultimedia ident="tbl0010"></elsevierMultimedia><elsevierMultimedia ident="tbl0015"></elsevierMultimedia></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0085">Discussion</span><p id="par0065" class="elsevierStylePara elsevierViewall">It was observed that MBL levels were lower in preterm infants with <span class="elsevierStyleItalic">MBL2</span> variant-type than in those with <span class="elsevierStyleItalic">MBL2</span> wild-type&#46; RDS was significantly more common in the <span class="elsevierStyleItalic">MBL2</span> variant-type group and also in the MBL deficient group&#46; Additionally&#44; the mortality rates were higher in preterm infants with <span class="elsevierStyleItalic">MBL2</span> variant-type&#46; In the study model&#44; <span class="elsevierStyleItalic">MBL2</span> variant-type was a significant independent factor for RDS after adjusting for the effects of other factors&#46; Besides&#44; the prevalence of NEC was higher in the <span class="elsevierStyleItalic">MBL2</span> wild-type group and with normal MBL levels&#46; It is believed that these findings will contribute toward accumulating evidence on the effect of MBL in preterm morbidities&#46;</p><p id="par0070" class="elsevierStylePara elsevierViewall">The collectin family and MBL play an important role in the primary immune elimination of invasive microorganisms in the innate immune response as well as in the regulation of ongoing immune responses against microbial invasion&#46; Studies have reported an association between MBL deficiency or variant genotype as well as infection and pulmonary pathologies&#46;<a class="elsevierStyleCrossRef" href="#bib0220"><span class="elsevierStyleSup">19</span></a> Pulmonary function impairment has been reported in patients with MBL deficiency and cystic fibrosis&#46; Patients with bronchiectasis with MBL deficiency or variant-type have a higher rate of chronic microbial colonization and frequent recurrence of pulmonary problems&#46;<a class="elsevierStyleCrossRefs" href="#bib0220"><span class="elsevierStyleSup">19&#44;20</span></a> In some studies&#44; similar to the results obtained in the present study&#44; it has been shown that MBL deficiency or variant-type cause respiratory morbidity independent of infection&#46;<a class="elsevierStyleCrossRefs" href="#bib0130"><span class="elsevierStyleSup">1&#44;21</span></a> There is high sequence homology between MBL and SP-A and SP-D&#46; The genes encoding these proteins are located on the long arm of chromosome 10 and belong to a similar lineage&#46;<a class="elsevierStyleCrossRef" href="#bib0235"><span class="elsevierStyleSup">22</span></a> SP-A and SP-D are involved in the removal of many pathogens in the lungs&#44; and although SP-A is particularly known for its immune functions&#44; RDS is associated with decreased SP-A levels&#46;<a class="elsevierStyleCrossRef" href="#bib0240"><span class="elsevierStyleSup">23</span></a> Mutant <span class="elsevierStyleItalic">MBL2</span> genetics are associated with insufficient surfactant protein-A production&#44; which may facilitate the development of RDS&#46; Similarly&#44; the present study also found a significant increase in RDS prevalence and mortality in patients with mutant <span class="elsevierStyleItalic">MBL2</span> genetics&#46; Early selective surfactant therapy in RDS has been reported to reduce pulmonary injury and mortality&#46;<a class="elsevierStyleCrossRef" href="#bib0245"><span class="elsevierStyleSup">24</span></a> It is believed that during the evaluation of <span class="elsevierStyleItalic">MBL2</span> genotype at the time of delivery in premature infants with high RDS risk and &#8804;32 gestational weeks and in borderline cases with an indication for surfactant&#44; the early administration of surfactants to patients with mutant <span class="elsevierStyleItalic">MBL2</span> genetics will reduce mortality and pulmonary morbidities&#46;</p><p id="par0075" class="elsevierStylePara elsevierViewall">In recent years&#44; there has been an increased interest in the association between MBL and inflammatory morbidities&#46; It has been reported that MBL activates the lectin pathway of complement&#44; resulting in ischemia-perfusion damage&#46; In patients with <span class="elsevierStyleItalic">MBL2</span> wild-type&#44; higher MBL levels have been reported and associated with NEC&#44; resulting in reperfusion injury after intestinal ischemia&#46;<a class="elsevierStyleCrossRef" href="#bib0175"><span class="elsevierStyleSup">10</span></a> In agreement with these findings&#44; in the present study the prevalence of NEC was higher in preterm infants with <span class="elsevierStyleItalic">MBL2</span> wild-type and normal MBL levels&#46; However&#44; some studies have reported that there is no association between <span class="elsevierStyleItalic">MBL2</span> genotype and NEC&#46;<a class="elsevierStyleCrossRefs" href="#bib0150"><span class="elsevierStyleSup">5&#44;25</span></a> In the present work&#44; the development of NEC may have been relatively more common because of significantly higher mortality rates in patients with <span class="elsevierStyleItalic">MBL2</span> wild-type&#46; Because there are debatable opinions in the literature on <span class="elsevierStyleItalic">MBL2</span> genotype and NEC development&#44; additional studies are needed to clarify this issue&#46;</p><p id="par0080" class="elsevierStylePara elsevierViewall">In this study&#44; in agreement with previous data&#44; no correlation was found between <span class="elsevierStyleItalic">MBL2</span> genotype and MBL levels with inflammation-associated pathologies&#44; BPD&#44; IVH&#44; and ROP&#46;<a class="elsevierStyleCrossRefs" href="#bib0150"><span class="elsevierStyleSup">5&#44;25</span></a> The evaluation of the association between <span class="elsevierStyleItalic">MBL2</span> genotype and morbidity was the common aspect of these studies&#46; It would be misleading to evaluate the association of <span class="elsevierStyleItalic">MBL2</span> genotype and MBL value obtained at the time of delivery with morbidities alone&#46; Because MBL levels increases as the gestational week increases in the <span class="elsevierStyleItalic">MBL2</span> wild-type group&#44; the evaluation of morbidity development with MBL levels obtained at different postnatal weeks may provide more accurate results to demonstrate the association between lectin pathway and inflammatory morbidities&#46;<a class="elsevierStyleCrossRef" href="#bib0135"><span class="elsevierStyleSup">2</span></a> There is a clear need for extensive studies to investigate the association between MBL and inflammatory morbidities in premature infants&#46;</p><p id="par0085" class="elsevierStylePara elsevierViewall">Although the association of <span class="elsevierStyleItalic">MBL2</span> genotype with culture-proven sepsis has not been reported in the literature&#44; the association between <span class="elsevierStyleItalic">MBL2</span> genotype and early clinical sepsis has been reported&#46;<a class="elsevierStyleCrossRefs" href="#bib0145"><span class="elsevierStyleSup">4&#44;5&#44;25</span></a> In contrast&#44; the association between MBL deficiency and sepsis has been reported in many studies&#46;<a class="elsevierStyleCrossRefs" href="#bib0140"><span class="elsevierStyleSup">3&#44;18</span></a> In the present study&#44; no association was found between <span class="elsevierStyleItalic">MBL2</span> genotype and MBL levels with LOS&#46; The authors believe that inadequate immune response to infection is observed because of low MBL levels in the early postnatal weeks in preterm infants even if the <span class="elsevierStyleItalic">MBL2</span> genotype is wild-type&#46; Therefore&#44; future studies should evaluate MBL values at the time of sepsis together with genotype&#46;</p><p id="par0090" class="elsevierStylePara elsevierViewall">This study had some limitations&#46; Morbidity was evaluated based on only <span class="elsevierStyleItalic">MBL2</span> genotype and with the levels of MBL within 24<span class="elsevierStyleHsp" style=""></span>h after birth because the MBL levels of the infants were not reassessed during the subsequent postnatal days&#46; Additionally&#44; the results obtained with a limited number of cases may not reflect the overall results&#46; The strength of this study was that it evaluated the association of <span class="elsevierStyleItalic">MBL2</span> genotype with MBL level and morbidities in preterm infants and simultaneously examined the MBL level in the first 24<span class="elsevierStyleHsp" style=""></span>h of life&#46;</p><p id="par0095" class="elsevierStylePara elsevierViewall">In conclusion&#44; the presence of <span class="elsevierStyleItalic">MBL2</span> variant-type and low MBL levels are important risk factors for RDS development in preterm infants&#46; Additionally&#44; there is an association between <span class="elsevierStyleItalic">MBL2</span> wild-type and NEC&#46; Considering the importance of showing that <span class="elsevierStyleItalic">MBL2</span> variant-type is an independent predictor of RDS&#44; further prospective randomized studies on this topic are clearly required&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0090">Conflicts of interest</span><p id="par0100" class="elsevierStylePara elsevierViewall">The authors declare no conflicts of interest&#46;</p></span></span>"
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    "fechaRecibido" => "2019-01-03"
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            0 => "Mannose-binding lectin"
            1 => "Preterm"
            2 => "Respiratory distress syndrome"
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          "titulo" => "Palavras-chave"
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          "palabras" => array:3 [
            0 => "Lectina ligante de manose"
            1 => "Prematuro"
            2 => "S&#237;ndrome do desconforto respirat&#243;rio"
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        "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Objective</span><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Mannose-binding lectin&#44; which belongs to the collectin family&#44; is an acute-phase reactant that activates the complement system&#46; This study aimed to investigate the effect of <span class="elsevierStyleItalic">MBL2</span> gene polymorphism on short-term outcomes in preterm infants&#46;</p></span> <span id="abst0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Method</span><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Infants of &#60;37 gestational weeks who were admitted to the neonatal intensive care unit during a two-year period were enrolled in this prospective study&#46; The neonates were categorized into two groups according to their <span class="elsevierStyleItalic">MBL2</span> genotypes&#46; Normal <span class="elsevierStyleItalic">MBL2</span> genotype was defined as <span class="elsevierStyleItalic">MBL2</span> wild-type &#40;AA genotype&#41;&#44; whereas mutant <span class="elsevierStyleItalic">MBL2</span> genotype was defined as <span class="elsevierStyleItalic">MBL2</span> variant-type &#40;AO&#47;OO genotype&#41;&#46; The relationship between <span class="elsevierStyleItalic">MBL2</span> genotype and short-term morbidity and mortality was evaluated&#46;</p></span> <span id="abst0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Results</span><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">During the two-year study period&#44; 116 preterm infants were enrolled in this study&#46; In <span class="elsevierStyleItalic">MBL2</span> variant-type&#44; mannose-binding lectin levels were significantly lower and incidences of mannose-binding lectin deficiency &#40;MBL level<span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>700<span class="elsevierStyleHsp" style=""></span>ng&#47;mL&#41; were higher &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#46;001&#41;&#46; In this group&#44; the prevalence of respiratory distress syndrome and mortality was significantly higher &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#46;001&#44; <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#46;03 respectively&#41;&#46; In the <span class="elsevierStyleItalic">MBL2</span> wild-type group&#44; the prevalence of necrotizing enterocolitis &#40;NEC&#41; was higher &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#46;01&#41;&#46; Logistic regression analyses revealed that <span class="elsevierStyleItalic">MBL2</span> variant-type had a significant effect on respiratory distress syndrome development &#40;odds ratio&#44; 5&#46;1&#59; 95&#37; confidence interval&#44; 2&#46;2&#8211;11&#46;9&#59; <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#46;001&#41;&#46;</p></span> <span id="abst0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Conclusions</span><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleItalic">MBL2</span> variant-type and mannose-binding lectin deficiency are important risk factors for respiratory distress syndrome development in preterm infants&#46; Additionally&#44; there is an association between <span class="elsevierStyleItalic">MBL2</span> wild-type and NEC&#46; Further studies on this subject are needed&#46;</p></span>"
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      "pt" => array:3 [
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        "resumen" => "<span id="abst0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Objetivo</span><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">A lectina ligante de manose &#40;MBL&#44; do ingl&#234;s <span class="elsevierStyleItalic">mannose-binding lectin</span>&#41;&#44; que pertence &#224; fam&#237;lia das colectinas&#44; &#233; um reagente de fase aguda que ativa o sistema complemento&#46; Este estudo teve como objetivo investigar o efeito do polimorfismo do gene <span class="elsevierStyleItalic">MBL2</span> em desfechos de curto prazo em prematuros&#46;</p></span> <span id="abst0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">M&#233;todo</span><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Este estudo prospectivo incluiu crian&#231;as com menos de 37 semanas de gesta&#231;&#227;o admitidas na unidade de terapia intensiva neonatal durante dois anos&#46; Os neonatos foram categorizados em dois grupos de acordo com os gen&#243;tipos do <span class="elsevierStyleItalic">MBL2</span>&#46; O gen&#243;tipo normal do gene <span class="elsevierStyleItalic">MBL2</span> foi definido como <span class="elsevierStyleItalic">MBL2</span> do tipo selvagem &#40;gen&#243;tipo AA&#41;&#44; enquanto o gen&#243;tipo mutante do gene <span class="elsevierStyleItalic">MBL2</span> foi definido como o gene variante &#40;gen&#243;tipo AO&#47;OO&#41;&#46; Foi avaliada a rela&#231;&#227;o entre o gen&#243;tipo <span class="elsevierStyleItalic">MBL2</span> e a morbidade e mortalidade em curto prazo&#46;</p></span> <span id="abst0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Resultados</span><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Durante o per&#237;odo de dois anos&#44; 116 beb&#234;s prematuros foram inclu&#237;dos neste estudo&#46; Os n&#237;veis de lectina ligante de manose foram significativamente menores nos variantes do <span class="elsevierStyleItalic">MBL2</span> e as incid&#234;ncias de defici&#234;ncia de lectina ligante de manose &#40;n&#237;vel de MBL &#60; 700 ng&#47;mL&#41; foram maiores &#40;p &#60; 0&#44;001&#41;&#46; Nesse grupo&#44; a preval&#234;ncia de s&#237;ndrome do desconforto respirat&#243;rio &#40;SDR&#41; e a mortalidade foram significativamente maiores &#40;p &#60; 0&#44;001&#44; p &#61; 0&#44;03&#44; respectivamente&#41;&#46; No grupo <span class="elsevierStyleItalic">MBL2</span> do tipo selvagem&#44; a preval&#234;ncia de enterocolite necrosante foi maior &#40;p &#61; 0&#44;01&#41;&#46; An&#225;lises de regress&#227;o log&#237;stica revelaram que os genes variantes do <span class="elsevierStyleItalic">MBL2</span> apresentaram um efeito significativo no desenvolvimento da s&#237;ndrome do desconforto respirat&#243;rio &#40;<span class="elsevierStyleItalic">odds ratio</span>&#44; 5&#44;1&#59; intervalo de confian&#231;a de 95&#37;&#44; 2&#44;2&#8211;11&#44;9&#59; p &#60; 0&#44;001&#41;&#46;</p></span> <span id="abst0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Conclus&#245;es</span><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">As variantes do <span class="elsevierStyleItalic">MBL2</span> e a defici&#234;ncia de lectina ligante de manose s&#227;o importantes fatores de risco para o desenvolvimento da s&#237;ndrome do desconforto respirat&#243;rio em neonatos prematuros&#46; Al&#233;m disso&#44; existe uma associa&#231;&#227;o entre <span class="elsevierStyleItalic">MBL2</span> do tipo selvagem e a enterocolite necrosante&#46; Mais estudos s&#227;o necess&#225;rios sobre esse assunto&#46;</p></span>"
        "secciones" => array:4 [
          0 => array:2 [
            "identificador" => "abst0025"
            "titulo" => "Objetivo"
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          1 => array:2 [
            "identificador" => "abst0030"
            "titulo" => "M&#233;todo"
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          2 => array:2 [
            "identificador" => "abst0035"
            "titulo" => "Resultados"
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          3 => array:2 [
            "identificador" => "abst0040"
            "titulo" => "Conclus&#245;es"
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    "NotaPie" => array:1 [
      0 => array:2 [
        "etiqueta" => "&#9734;"
        "nota" => "<p class="elsevierStyleNotepara" id="npar0040">Please cite this article as&#58; Dogan P&#44; Ozkan H&#44; Koksal N&#44; Oral HB&#44; Bagci O&#44; Guney Varal I&#46; Mannose-binding lectin gene polymorphism and its effect on short term outcomes in preterm infants&#46; J Pediatr &#40;Rio J&#41;&#46; 2020&#59;96&#58;520&#8211;6&#46;</p>"
      ]
    ]
    "multimedia" => array:4 [
      0 => array:7 [
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        "etiqueta" => "Figure 1"
        "tipo" => "MULTIMEDIAFIGURA"
        "mostrarFloat" => true
        "mostrarDisplay" => false
        "figura" => array:1 [
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        "descripcion" => array:1 [
          "en" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">DNA fragments on agarose gel electrophoresis after restriction enzyme digestion of exon 1 of the mannose-binding lectin &#40;<span class="elsevierStyleItalic">MBL2</span>&#41; gene codon 54&#46; In all&#44; 349<span class="elsevierStyleHsp" style=""></span>bp PCR product was digested with <span class="elsevierStyleItalic">BanI</span> for codon 54 polymorphism&#46; The normal allele &#40;allele A&#41; is cut into two fragments with <span class="elsevierStyleItalic">BanI</span> &#40;lanes 2 and 5&#41;&#44; 89 and 260<span class="elsevierStyleHsp" style=""></span>bp&#46; The variant allele &#40;allele O&#41; remains uncut &#40;lanes 1 and 6&#41;&#46; Both uncut and digested fragments are seen in AO heterozygote &#40;lanes 3 and 4&#41;&#46; L&#58; 100<span class="elsevierStyleHsp" style=""></span>bp DNA ladder&#46;</p>"
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      1 => array:8 [
        "identificador" => "tbl0005"
        "etiqueta" => "Table 1"
        "tipo" => "MULTIMEDIATABLA"
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        "detalles" => array:1 [
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        "tabla" => array:3 [
          "leyenda" => "<p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">Values with significance are presented in bold&#46;</p><p id="spar0060" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleItalic">MBL2</span>&#44; mannose-binding lectin&#59; GA&#44; gestational age&#59; SGA&#44; small for gestational age&#59; PPROM&#44; preterm premature rupture of membranes&#46;</p>"
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                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Male&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t\ttable-entry\n
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                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Minute 5&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t">8 &#40;7&#8211;9&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
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                  \t\t\t\t</td><td class="td" title="\n
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                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t">0&#46;4<a class="elsevierStyleCrossRef" href="#tblfn0015"><span class="elsevierStyleSup">c</span></a>&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
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                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t">0&#46;4<a class="elsevierStyleCrossRef" href="#tblfn0015"><span class="elsevierStyleSup">c</span></a>&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
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                  \t\t\t\t\ttable-entry\n
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                  \t\t\t\t">0&#46;4<a class="elsevierStyleCrossRef" href="#tblfn0015"><span class="elsevierStyleSup">c</span></a>&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t">0&#46;7<a class="elsevierStyleCrossRef" href="#tblfn0015"><span class="elsevierStyleSup">c</span></a>&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
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                  \t\t\t\t"><span class="elsevierStyleItalic">MBL levels&#44; &#40;ng&#47;mL&#41; median &#40;range&#41;</span>&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t">993 &#40;257&#8211;1812&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t</td><td class="td" title="\n
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                  \t\t\t\t"><span class="elsevierStyleBold">&#60;0&#46;001</span><a class="elsevierStyleCrossRef" href="#tblfn0005"><span class="elsevierStyleSup">a</span></a>&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t"><span class="elsevierStyleBold">&#60;0&#46;001</span><a class="elsevierStyleCrossRef" href="#tblfn0015"><span class="elsevierStyleSup">c</span></a>&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t">3 &#40;6&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
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                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t">0&#46;2&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
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                  \t\t\t\t">LOS&#44; <span class="elsevierStyleItalic">n</span> &#40;&#37;&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t">18 &#40;26&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
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                  \t\t\t\t">Mortality&#44; <span class="elsevierStyleItalic">n</span> &#40;&#37;&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t">6 &#40;9&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t"><span class="elsevierStyleBold">0&#46;03</span>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr></tbody></table>
                  """
              ]
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                0 => "xTab2367358.png"
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            0 => array:3 [
              "identificador" => "tblfn0020"
              "etiqueta" => "a"
              "nota" => "<p class="elsevierStyleNotepara" id="npar0020">Chi-squared test&#46;</p> <p class="elsevierStyleNotepara" id="npar0025">Values with significance are presented in bold&#46;</p> <p class="elsevierStyleNotepara" id="npar0030"><span class="elsevierStyleItalic">MBL2</span>&#44; mannose-binding lectin&#59; RDS&#44; respiratory distress syndrome&#59; LOS&#44; late onset sepsis&#59; IVH&#44; intraventricular hemorrhage&#59; NEC&#44; necrotizing enterocolitis&#59; BPD&#44; bronchopulmonary dysplasia&#59; ROP&#44; retinopathy of prematurity&#46;</p>"
            ]
          ]
        ]
        "descripcion" => array:1 [
          "en" => "<p id="spar0065" class="elsevierStyleSimplePara elsevierViewall">Frequency of early neonatal outcomes according to mannose binding lectin genotypes&#46;</p>"
        ]
      ]
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        "identificador" => "tbl0015"
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        "tipo" => "MULTIMEDIATABLA"
        "mostrarFloat" => true
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          "leyenda" => "<p id="spar0085" class="elsevierStyleSimplePara elsevierViewall">Values with significance are presented in bold&#46;</p><p id="spar0090" class="elsevierStyleSimplePara elsevierViewall">MBL&#44; mannose-binding lectin&#59; RDS&#44; respiratory distress syndrome&#59; LOS&#44; late onset sepsis&#59; IVH&#44; intraventricular hemorrhage&#59; NEC&#44; necrotizing enterocolitis&#59; BPD&#44; bronchopulmonary dysplasia&#59; ROP&#44; retinopathy of prematurity&#46;</p>"
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                  \t\t\t\t  " align="" valign="\n
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                  \t\t\t\t" scope="col">&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">&#60;150<span class="elsevierStyleHsp" style=""></span>ng&#47;mL&#40;<span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>36&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">150&#8211;700<span class="elsevierStyleHsp" style=""></span>ng&#47;mL&#40;<span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>36&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t  " align="" valign="\n
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                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
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                  \t\t\t\t">RDS&#44; <span class="elsevierStyleItalic">n</span> &#40;&#37;&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t">23 &#40;64&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
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                  \t\t\t\t">1 &#40;3&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
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                  \t\t\t\t">IVH&#44; &#40;Papile grade 3&#8211;4&#41;&#44; <span class="elsevierStyleItalic">n</span> &#40;&#37;&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">1 &#40;3&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
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                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t">2 &#40;5&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t">0&#46;7&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">NEC&#44; &#40;&#62;grade 1&#41;&#44; <span class="elsevierStyleItalic">n</span> &#40;&#37;&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">0 &#40;0&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t">1 &#40;3&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t">8 &#40;20&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t"><span class="elsevierStyleBold">0&#46;002</span>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">BPD&#44; &#40;grade 2&#8211;3&#41;&#44; <span class="elsevierStyleItalic">n</span> &#40;&#37;&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
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                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t">5 &#40;13&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="char" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">5 &#40;14&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="char" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">12 &#40;29&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="char" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">0&#46;1&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">ROP&#44; &#40;&#62;stage 2&#41;&#44; <span class="elsevierStyleItalic">n</span> &#40;&#37;&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
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                  \t\t\t\t">3 &#40;8&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t">6 &#40;15&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t">0&#46;06&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">LOS&#44; <span class="elsevierStyleItalic">n</span> &#40;&#37;&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
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                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t">14 &#40;36&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="char" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">10 &#40;28&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="char" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">10 &#40;24&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t">0&#46;5&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Mortality&#44; <span class="elsevierStyleItalic">n</span> &#40;&#37;&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
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                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t">7 &#40;18&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
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                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t">7 &#40;19&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
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                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t">3 &#40;7&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="char" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">0&#46;3&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr></tbody></table>
                  """
              ]
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                0 => "xTab2367360.png"
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        ]
        "descripcion" => array:1 [
          "en" => "<p id="spar0080" class="elsevierStyleSimplePara elsevierViewall">Mannose binding lectin levels in relation to early neonatal outcomes&#46;</p>"
        ]
      ]
    ]
    "bibliografia" => array:2 [
      "titulo" => "References"
      "seccion" => array:1 [
        0 => array:2 [
          "identificador" => "bibs0015"
          "bibliografiaReferencia" => array:25 [
            0 => array:3 [
              "identificador" => "bib0130"
              "etiqueta" => "1"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "MBL2 genotypes and their associations with MBL levels and NICU morbidity in a cohort of Greek neonates"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => true
                          "autores" => array:6 [
                            0 => "M&#46; Speletas"
                            1 => "A&#46; Gounaris"
                            2 => "E&#46; Sevdali"
                            3 => "M&#46; Kompoti"
                            4 => "K&#46; Konstantinidi"
                            5 => "R&#46; Sokou"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:2 [
                      "doi" => "10.1155/2015/478412"
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Original article
Mannose-binding lectin gene polymorphism and its effect on short term outcomes in preterm infants
Polimorfismo do gene da lectina ligante de manose e seu efeito em desfechos de curto prazo em bebês prematuros
Pelin Dogana,
Corresponding author
pelin_akbas@yahoo.com

Corresponding author.
, Hilal Ozkana, Nilgun Koksala, Haluk Barbaros Oralb, Onur Bagcia, Ipek Guney Varala
a Uludag University, Faculty of Medicine, Department of Pediatrics, Bursa, Turkey
b Uludag University, Faculty of Medicine, Department of Immunology, Bursa, Turkey
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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0065">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Mannose-binding lectin &#40;MBL&#41; is an acute-phase reactant that activates the complement system&#46; It belongs to the collectin family of proteins&#44; which includes lung surfactant protein A &#40;SP-A&#41; and SP-D&#46;<a class="elsevierStyleCrossRef" href="#bib0130"><span class="elsevierStyleSup">1</span></a> MBL plays a key role in first-line immune responses as a component of innate immunity&#46;<a class="elsevierStyleCrossRef" href="#bib0135"><span class="elsevierStyleSup">2</span></a> Because adaptive immunity is underdeveloped in preterm infants&#44; innate immunity gains higher importance&#46;<a class="elsevierStyleCrossRefs" href="#bib0135"><span class="elsevierStyleSup">2&#44;3</span></a> The <span class="elsevierStyleItalic">MBL2</span> gene is located on the long arm of chromosome 10&#44; and mutant <span class="elsevierStyleItalic">MBL2</span> alleles occur as a result of three single-point mutations in this gene &#40;B&#44; C&#44; and D&#41;&#46; Although functional MBL levels are low in heterozygous polymorphisms&#44; MBL levels in homozygous polymorphisms are so low that they may not even be determinable&#46;<a class="elsevierStyleCrossRefs" href="#bib0145"><span class="elsevierStyleSup">4&#44;5</span></a> MBL activates the complement system by binding to mannose or sugar motifs&#44; which are found in many microorganisms&#44; and plays an important role in innate immunity and inflammation&#46;<a class="elsevierStyleCrossRefs" href="#bib0135"><span class="elsevierStyleSup">2&#44;6</span></a> In newborns&#44; an increase in sepsis frequency is observed when MBL levels are low&#46;<a class="elsevierStyleCrossRefs" href="#bib0135"><span class="elsevierStyleSup">2&#44;3&#44;7</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">The mortality and morbidity rates in preterm infants are higher than those in term infants&#46; As gestational week and birth weight decrease&#44; the risk of complications increases&#46; In preterm infants&#44; complications are observed in the early &#40;neonatal period&#41; and late periods &#40;after discharge&#41;&#46; Although the survival rate of most preterm infants has improved because of advances in medical care&#44; the incidence of short-term complications remains relatively stable&#46; Short-term complications increase the risk of long-term sequelae&#46;<a class="elsevierStyleCrossRefs" href="#bib0165"><span class="elsevierStyleSup">8&#44;9</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">In recent years&#44; many studies have been conducted on the importance of MBL during the neonatal period&#44; and most of these are associated with sepsis&#46; In sepsis&#44; proinflammatory and anti-inflammatory cytokine ratio is vital in terms of defense against infectious agents&#46; The imbalance in this ratio is manifested by increased morbidity and mortality during the neonatal period&#46;<a class="elsevierStyleCrossRefs" href="#bib0150"><span class="elsevierStyleSup">5&#44;6</span></a> Increased cytokine levels have a significant role in the pathophysiology of morbidities such as respiratory distress syndrome &#40;RDS&#41;&#44; intraventricular hemorrhage &#40;IVH&#41;&#44; necrotizing enterocolitis &#40;NEC&#41;&#44; bronchopulmonary dysplasia &#40;BPD&#41;&#44; and retinopathy of prematurity &#40;ROP&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0175"><span class="elsevierStyleSup">10</span></a> This prospective study aimed to investigate the association of <span class="elsevierStyleItalic">MBL2</span> polymorphism with short-term outcomes in preterm infants&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0070">Materials and methods</span><p id="par0020" class="elsevierStylePara elsevierViewall">All preterm infants of &#60;37 gestational weeks who were admitted to the neonatal intensive care unit &#40;NICU&#41; of the Uludag University Medical School during a two-year period were enrolled in this prospective study&#46; The neonates were categorized into two groups according to their <span class="elsevierStyleItalic">MBL2</span> genotypes&#46; Normal <span class="elsevierStyleItalic">MBL2</span> genotype was defined as <span class="elsevierStyleItalic">MBL2</span> wild-type &#40;AA genotype&#41;&#44; whereas mutant <span class="elsevierStyleItalic">MBL2</span> genotype was defined as <span class="elsevierStyleItalic">MBL2</span> variant-type &#40;AO or OO genotype&#41;&#46; The exclusion criteria included refusal of parental consent&#44; infants with major congenital abnormalities&#44; and those undergoing a major surgical procedure&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">Gestational age&#44; birth weight&#44; gender&#44; mode of delivery&#44; Apgar score at 1 and 5<span class="elsevierStyleHsp" style=""></span>min&#44; prenatal demographics&#44; antenatal steroid administration&#44; premature rupture of membranes&#44; history of chorioamnionitis and durations of invasive mechanical ventilation&#44; total supplemental oxygen&#44; central catheterization&#44; and total parenteral nutrition were recorded&#46; The presence of neonatal morbidities such as RDS&#44; late-onset sepsis &#40;LOS&#41;&#44; IVH&#44; NEC&#44; BPD&#44; ROP&#44; and the mortality data of the preterm infants were recorded&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">RDS was diagnosed based on clinical findings &#40;tachypnea&#44; retractions&#44; nasal flaring&#44; and cyanosis&#41; or radiological findings &#40;reticular granular pattern or air bronchograms&#41;&#46; All neonates underwent the same management according to the NICU protocols and as recommended by European consensus guidelines on the management of neonatal respiratory distress syndrome in preterm infants&#46;<a class="elsevierStyleCrossRefs" href="#bib0180"><span class="elsevierStyleSup">11&#44;12</span></a> Neonatal sepsis was defined as the presence of clinical signs of sepsis with a positive blood culture&#46; Blood cultures were analyzed using the fully automated BACTEC method in a BACTEC 9240 device &#40;Becton Dickinson&#44; Heidelberg&#44; Germany&#41;&#46; LOS was determined by the time at which sepsis occurred between 4 and 30 days after birth&#46;<a class="elsevierStyleCrossRef" href="#bib0190"><span class="elsevierStyleSup">13</span></a> IVH was evaluated by cranial ultrasound examinations&#44; which were performed by the same pediatric radiologist and diagnosed using the Papile classification system&#46;<a class="elsevierStyleCrossRef" href="#bib0195"><span class="elsevierStyleSup">14</span></a> NEC was diagnosed according to clinical and radiographic findings and classified according to modified Bell&#39;s criteria&#46;<a class="elsevierStyleCrossRef" href="#bib0200"><span class="elsevierStyleSup">15</span></a> BPD was classified into three groups in terms of BPD severity depending on the duration and level of supplemental oxygen and mechanical ventilatory support at 36 weeks postmenstrual age&#46;<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">16</span></a> ROP was classified according to the International Classification of Retinopathy of Prematurity&#46;<a class="elsevierStyleCrossRef" href="#bib0210"><span class="elsevierStyleSup">17</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">The MBL levels and gene polymorphisms were assessed within 3<span class="elsevierStyleHsp" style=""></span>h in most infants and within 24<span class="elsevierStyleHsp" style=""></span>h after birth in all infants&#46; The blood samples for the measurement of MBL levels were collected in a test tube and these blood samples were centrifuged within thirty minutes after obtaining&#46; After the centrifugation process&#44; serum of the samples were immediately stored at &#8722;80<span class="elsevierStyleHsp" style=""></span>&#176;C until analysis&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">Blood samples were analyzed using enzyme-linked immunosorbent assay&#46; PCR and restriction fragment length polymorphism were used for <span class="elsevierStyleItalic">MBL</span>2 genotyping&#46; Serum MBL levels were measured using an immunoassay kit &#40;Oligomer ELISA kit&#59; Antibody Shop&#44; Copenhagen&#44; Denmark&#41; according to the manufacturer instructions&#46; The lowest detectable MBL concentration was 10<span class="elsevierStyleHsp" style=""></span>ng&#47;mL&#46; For the definition of the functional MBL deficiency&#44; this study used two different cut-off values of MBL concentration&#46; An MBL level<span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>700<span class="elsevierStyleHsp" style=""></span>ng&#47;mL was determined as deficiency and &#60;150<span class="elsevierStyleHsp" style=""></span>ng&#47;mL as severe deficiency&#46;<a class="elsevierStyleCrossRefs" href="#bib0130"><span class="elsevierStyleSup">1&#8211;3&#44;18</span></a> DNA was extracted from the blood samples using a commercially available kit &#40;Puregene&#44; Gentra&#44; MN&#44; United States&#41;&#44; and <span class="elsevierStyleItalic">MBL2</span> genotyping was performed using these samples&#46; DNA samples were maintained at &#8722;20<span class="elsevierStyleHsp" style=""></span>&#176;C until use&#46; All genotypes were detected using PCR and restriction enzyme digestion&#46; Exon 1 of <span class="elsevierStyleItalic">MBL2</span> was amplified by PCR&#46; The primer sequences were 5&#8242;-GTA GGA CAG AGG GCA TGC TC-3&#8242; and 5&#8242;-CAG GCA GTT TCC TCT GGA AGG-3&#8242;&#46; In all&#44; a 349-bp PCR product was digested with <span class="elsevierStyleItalic">BanI</span> and <span class="elsevierStyleItalic">MboII</span> for codon 54 and codon 57&#44; respectively&#46; The normal allele &#40;allele A&#41; was cut into two fragments with <span class="elsevierStyleItalic">BanI</span>&#44; 260 and 89<span class="elsevierStyleHsp" style=""></span>bp&#46; The variant allele B &#40;rs1800450&#41; and allele D &#40;rs5030737&#41; remained uncut&#46; <span class="elsevierStyleItalic">MboII</span> cleaved the variant allele C &#40;rs1800451&#41; into 270 and 79<span class="elsevierStyleHsp" style=""></span>bp fragments&#46; The fragments were visualized using electrophoresis on 2&#37; agarose gel&#46; At electrophoresis&#44; the dual band at the restriction site was defined as a heterozygous mutation&#44; whereas the single band was defined as a homozygous mutation&#46; As stated&#44; the normal structural <span class="elsevierStyleItalic">MBL2</span> allele was named A&#44; whereas alleles B&#44; C and D &#40;mutation in codons 54&#44; 57 and 52&#41; were named O&#46; A representative gel electrophoresis of the <span class="elsevierStyleItalic">MBL2</span> exon 1 codon 54 polymorphisms is shown in <a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0045" class="elsevierStylePara elsevierViewall">This study was approved by the Ethics Committee of Uludag University Medical School and conformed to the standards set by the Declaration of Helsinki &#40;15&#46;01&#46;2013-1&#47;20&#41;&#46; All parents provided informed consents prior to the inclusion of their children in the study&#46;</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0075">Statistical analysis</span><p id="par0050" class="elsevierStylePara elsevierViewall">Statistical analysis was performed using SPSS v&#46; 20&#46;0 software &#40;SPSS Inc&#46;&#44; Chicago&#44; IL&#44; United States&#41;&#46; The results are presented as median &#40;interquartile range&#41; for the variables showing non-Gaussian distribution and mean<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>standard deviation for data showing normal distribution&#46; Student&#39;s <span class="elsevierStyleItalic">t</span>-test was used for group comparisons of normal distributions&#44; and the Mann&#8211;Whitney <span class="elsevierStyleItalic">U</span> test was used for group comparisons of non-normal distributions&#46; The chi-squared test and Fisher&#39;s exact test were used for the comparison of categorical variables&#46; Logistic regression analysis was performed to investigate the effect of <span class="elsevierStyleItalic">MBL2</span> genotype on RDS&#46; The analysis included factors that were demonstrated in the literature to have an effect on RDS&#58; gestational age&#44; birth weight&#44; sex&#44; antenatal steroid administration&#44; and <span class="elsevierStyleItalic">MBL2</span> genotype were included in the analysis&#46; A <span class="elsevierStyleItalic">p</span>-value of &#60;0&#46;05 was considered statistically significant&#46;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0080">Results</span><p id="par0055" class="elsevierStylePara elsevierViewall">Overall&#44; 131 preterm infants were included in this study&#46; Ten were excluded because of blood sample insufficiency&#44; four because of major congenital abnormalities&#44; and one because of major surgery&#46; In the final analysis&#44; a total of 116 preterm infants were included&#58; 69 with <span class="elsevierStyleItalic">MBL2</span> wild-type &#40;AA genotype&#41; and 47 with <span class="elsevierStyleItalic">MBL2</span> variant-type &#40;AO&#47;OO genotype&#41;&#46; Overall&#44; the rate of <span class="elsevierStyleItalic">MBL2</span> variant-type in preterm infants was 41&#37;&#46; MBL levels were significantly lower and MBL deficiency and severe deficiency were higher in <span class="elsevierStyleItalic">MBL2</span> variant-type than in <span class="elsevierStyleItalic">MBL2</span> wild-type &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#46;001&#41;&#46; <a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a> shows the demographic features of the study population&#46; Codon 57 and 52 polymorphisms were not detected in any of the 116 preterm infants during the genetic evaluation&#46; <span class="elsevierStyleItalic">MBL2</span> codon 54 genotype and allele frequencies were 59&#37; for <span class="elsevierStyleItalic">MBL2</span> wild-type &#40;AA genotype&#41; and 41&#37; for <span class="elsevierStyleItalic">MBL2</span> variant-type &#40;AO and OO genotype&#41;&#46;</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0060" class="elsevierStylePara elsevierViewall">Evaluation of short-term morbidity based on <span class="elsevierStyleItalic">MBL2</span> genotype revealed that RDS and mortality rates were significantly higher in the <span class="elsevierStyleItalic">MBL2</span> variant-type group &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#46;001&#44; <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#46;03&#59; respectively&#41;&#46; NEC was found to be more prevalent in the <span class="elsevierStyleItalic">MBL2</span> wild-type group &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#46;01&#41;&#46; There was no difference between the <span class="elsevierStyleItalic">MBL2</span> wild-type and variant-type groups in terms of IVH&#44; BPD&#44; ROP&#44; and LOS &#40;<a class="elsevierStyleCrossRef" href="#tbl0010">Table 2</a>&#41;&#46; Consideration of short-term morbidity based on MBL levels revealed that RDS was significantly higher in both the MBL deficient and severely deficient groups &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#46;001&#41;&#46; NEC was found to be more common with normal levels of MBL &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#46;002&#41;&#46; There was no significant difference in infants with or without MBL deficiency with respect to IVH&#44; BPD&#44; ROP&#44; LOS&#44; and mortality &#40;<a class="elsevierStyleCrossRef" href="#tbl0015">Table 3</a>&#41;&#46; Further&#44; because univariate analyses revealed that RDS development was more common in the <span class="elsevierStyleItalic">MBL2</span> variant-type&#44; the effect of gestational age&#44; birth weight&#44; gender&#44; antenatal steroid use&#44; and <span class="elsevierStyleItalic">MBL2</span> genetics&#44; which are factors that may affect RDS development&#44; was investigated by logistic regression analysis&#46; <span class="elsevierStyleItalic">MBL2</span> variant-type was found to be an independent factor for the development of RDS &#40;OR&#58; 5&#46;1&#44; 95&#37; CI&#58; 2&#46;2&#8211;11&#46;9&#44; <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#46;001&#41;&#46;</p><elsevierMultimedia ident="tbl0010"></elsevierMultimedia><elsevierMultimedia ident="tbl0015"></elsevierMultimedia></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0085">Discussion</span><p id="par0065" class="elsevierStylePara elsevierViewall">It was observed that MBL levels were lower in preterm infants with <span class="elsevierStyleItalic">MBL2</span> variant-type than in those with <span class="elsevierStyleItalic">MBL2</span> wild-type&#46; RDS was significantly more common in the <span class="elsevierStyleItalic">MBL2</span> variant-type group and also in the MBL deficient group&#46; Additionally&#44; the mortality rates were higher in preterm infants with <span class="elsevierStyleItalic">MBL2</span> variant-type&#46; In the study model&#44; <span class="elsevierStyleItalic">MBL2</span> variant-type was a significant independent factor for RDS after adjusting for the effects of other factors&#46; Besides&#44; the prevalence of NEC was higher in the <span class="elsevierStyleItalic">MBL2</span> wild-type group and with normal MBL levels&#46; It is believed that these findings will contribute toward accumulating evidence on the effect of MBL in preterm morbidities&#46;</p><p id="par0070" class="elsevierStylePara elsevierViewall">The collectin family and MBL play an important role in the primary immune elimination of invasive microorganisms in the innate immune response as well as in the regulation of ongoing immune responses against microbial invasion&#46; Studies have reported an association between MBL deficiency or variant genotype as well as infection and pulmonary pathologies&#46;<a class="elsevierStyleCrossRef" href="#bib0220"><span class="elsevierStyleSup">19</span></a> Pulmonary function impairment has been reported in patients with MBL deficiency and cystic fibrosis&#46; Patients with bronchiectasis with MBL deficiency or variant-type have a higher rate of chronic microbial colonization and frequent recurrence of pulmonary problems&#46;<a class="elsevierStyleCrossRefs" href="#bib0220"><span class="elsevierStyleSup">19&#44;20</span></a> In some studies&#44; similar to the results obtained in the present study&#44; it has been shown that MBL deficiency or variant-type cause respiratory morbidity independent of infection&#46;<a class="elsevierStyleCrossRefs" href="#bib0130"><span class="elsevierStyleSup">1&#44;21</span></a> There is high sequence homology between MBL and SP-A and SP-D&#46; The genes encoding these proteins are located on the long arm of chromosome 10 and belong to a similar lineage&#46;<a class="elsevierStyleCrossRef" href="#bib0235"><span class="elsevierStyleSup">22</span></a> SP-A and SP-D are involved in the removal of many pathogens in the lungs&#44; and although SP-A is particularly known for its immune functions&#44; RDS is associated with decreased SP-A levels&#46;<a class="elsevierStyleCrossRef" href="#bib0240"><span class="elsevierStyleSup">23</span></a> Mutant <span class="elsevierStyleItalic">MBL2</span> genetics are associated with insufficient surfactant protein-A production&#44; which may facilitate the development of RDS&#46; Similarly&#44; the present study also found a significant increase in RDS prevalence and mortality in patients with mutant <span class="elsevierStyleItalic">MBL2</span> genetics&#46; Early selective surfactant therapy in RDS has been reported to reduce pulmonary injury and mortality&#46;<a class="elsevierStyleCrossRef" href="#bib0245"><span class="elsevierStyleSup">24</span></a> It is believed that during the evaluation of <span class="elsevierStyleItalic">MBL2</span> genotype at the time of delivery in premature infants with high RDS risk and &#8804;32 gestational weeks and in borderline cases with an indication for surfactant&#44; the early administration of surfactants to patients with mutant <span class="elsevierStyleItalic">MBL2</span> genetics will reduce mortality and pulmonary morbidities&#46;</p><p id="par0075" class="elsevierStylePara elsevierViewall">In recent years&#44; there has been an increased interest in the association between MBL and inflammatory morbidities&#46; It has been reported that MBL activates the lectin pathway of complement&#44; resulting in ischemia-perfusion damage&#46; In patients with <span class="elsevierStyleItalic">MBL2</span> wild-type&#44; higher MBL levels have been reported and associated with NEC&#44; resulting in reperfusion injury after intestinal ischemia&#46;<a class="elsevierStyleCrossRef" href="#bib0175"><span class="elsevierStyleSup">10</span></a> In agreement with these findings&#44; in the present study the prevalence of NEC was higher in preterm infants with <span class="elsevierStyleItalic">MBL2</span> wild-type and normal MBL levels&#46; However&#44; some studies have reported that there is no association between <span class="elsevierStyleItalic">MBL2</span> genotype and NEC&#46;<a class="elsevierStyleCrossRefs" href="#bib0150"><span class="elsevierStyleSup">5&#44;25</span></a> In the present work&#44; the development of NEC may have been relatively more common because of significantly higher mortality rates in patients with <span class="elsevierStyleItalic">MBL2</span> wild-type&#46; Because there are debatable opinions in the literature on <span class="elsevierStyleItalic">MBL2</span> genotype and NEC development&#44; additional studies are needed to clarify this issue&#46;</p><p id="par0080" class="elsevierStylePara elsevierViewall">In this study&#44; in agreement with previous data&#44; no correlation was found between <span class="elsevierStyleItalic">MBL2</span> genotype and MBL levels with inflammation-associated pathologies&#44; BPD&#44; IVH&#44; and ROP&#46;<a class="elsevierStyleCrossRefs" href="#bib0150"><span class="elsevierStyleSup">5&#44;25</span></a> The evaluation of the association between <span class="elsevierStyleItalic">MBL2</span> genotype and morbidity was the common aspect of these studies&#46; It would be misleading to evaluate the association of <span class="elsevierStyleItalic">MBL2</span> genotype and MBL value obtained at the time of delivery with morbidities alone&#46; Because MBL levels increases as the gestational week increases in the <span class="elsevierStyleItalic">MBL2</span> wild-type group&#44; the evaluation of morbidity development with MBL levels obtained at different postnatal weeks may provide more accurate results to demonstrate the association between lectin pathway and inflammatory morbidities&#46;<a class="elsevierStyleCrossRef" href="#bib0135"><span class="elsevierStyleSup">2</span></a> There is a clear need for extensive studies to investigate the association between MBL and inflammatory morbidities in premature infants&#46;</p><p id="par0085" class="elsevierStylePara elsevierViewall">Although the association of <span class="elsevierStyleItalic">MBL2</span> genotype with culture-proven sepsis has not been reported in the literature&#44; the association between <span class="elsevierStyleItalic">MBL2</span> genotype and early clinical sepsis has been reported&#46;<a class="elsevierStyleCrossRefs" href="#bib0145"><span class="elsevierStyleSup">4&#44;5&#44;25</span></a> In contrast&#44; the association between MBL deficiency and sepsis has been reported in many studies&#46;<a class="elsevierStyleCrossRefs" href="#bib0140"><span class="elsevierStyleSup">3&#44;18</span></a> In the present study&#44; no association was found between <span class="elsevierStyleItalic">MBL2</span> genotype and MBL levels with LOS&#46; The authors believe that inadequate immune response to infection is observed because of low MBL levels in the early postnatal weeks in preterm infants even if the <span class="elsevierStyleItalic">MBL2</span> genotype is wild-type&#46; Therefore&#44; future studies should evaluate MBL values at the time of sepsis together with genotype&#46;</p><p id="par0090" class="elsevierStylePara elsevierViewall">This study had some limitations&#46; Morbidity was evaluated based on only <span class="elsevierStyleItalic">MBL2</span> genotype and with the levels of MBL within 24<span class="elsevierStyleHsp" style=""></span>h after birth because the MBL levels of the infants were not reassessed during the subsequent postnatal days&#46; Additionally&#44; the results obtained with a limited number of cases may not reflect the overall results&#46; The strength of this study was that it evaluated the association of <span class="elsevierStyleItalic">MBL2</span> genotype with MBL level and morbidities in preterm infants and simultaneously examined the MBL level in the first 24<span class="elsevierStyleHsp" style=""></span>h of life&#46;</p><p id="par0095" class="elsevierStylePara elsevierViewall">In conclusion&#44; the presence of <span class="elsevierStyleItalic">MBL2</span> variant-type and low MBL levels are important risk factors for RDS development in preterm infants&#46; Additionally&#44; there is an association between <span class="elsevierStyleItalic">MBL2</span> wild-type and NEC&#46; Considering the importance of showing that <span class="elsevierStyleItalic">MBL2</span> variant-type is an independent predictor of RDS&#44; further prospective randomized studies on this topic are clearly required&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0090">Conflicts of interest</span><p id="par0100" class="elsevierStylePara elsevierViewall">The authors declare no conflicts of interest&#46;</p></span></span>"
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          "identificador" => "xpalclavsec1266425"
          "palabras" => array:3 [
            0 => "Mannose-binding lectin"
            1 => "Preterm"
            2 => "Respiratory distress syndrome"
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        ]
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          "identificador" => "xpalclavsec1266424"
          "palabras" => array:3 [
            0 => "Lectina ligante de manose"
            1 => "Prematuro"
            2 => "S&#237;ndrome do desconforto respirat&#243;rio"
          ]
        ]
      ]
    ]
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    "resumen" => array:2 [
      "en" => array:3 [
        "titulo" => "Abstract"
        "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Objective</span><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Mannose-binding lectin&#44; which belongs to the collectin family&#44; is an acute-phase reactant that activates the complement system&#46; This study aimed to investigate the effect of <span class="elsevierStyleItalic">MBL2</span> gene polymorphism on short-term outcomes in preterm infants&#46;</p></span> <span id="abst0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Method</span><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Infants of &#60;37 gestational weeks who were admitted to the neonatal intensive care unit during a two-year period were enrolled in this prospective study&#46; The neonates were categorized into two groups according to their <span class="elsevierStyleItalic">MBL2</span> genotypes&#46; Normal <span class="elsevierStyleItalic">MBL2</span> genotype was defined as <span class="elsevierStyleItalic">MBL2</span> wild-type &#40;AA genotype&#41;&#44; whereas mutant <span class="elsevierStyleItalic">MBL2</span> genotype was defined as <span class="elsevierStyleItalic">MBL2</span> variant-type &#40;AO&#47;OO genotype&#41;&#46; The relationship between <span class="elsevierStyleItalic">MBL2</span> genotype and short-term morbidity and mortality was evaluated&#46;</p></span> <span id="abst0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Results</span><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">During the two-year study period&#44; 116 preterm infants were enrolled in this study&#46; In <span class="elsevierStyleItalic">MBL2</span> variant-type&#44; mannose-binding lectin levels were significantly lower and incidences of mannose-binding lectin deficiency &#40;MBL level<span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>700<span class="elsevierStyleHsp" style=""></span>ng&#47;mL&#41; were higher &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#46;001&#41;&#46; In this group&#44; the prevalence of respiratory distress syndrome and mortality was significantly higher &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#46;001&#44; <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#46;03 respectively&#41;&#46; In the <span class="elsevierStyleItalic">MBL2</span> wild-type group&#44; the prevalence of necrotizing enterocolitis &#40;NEC&#41; was higher &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#46;01&#41;&#46; Logistic regression analyses revealed that <span class="elsevierStyleItalic">MBL2</span> variant-type had a significant effect on respiratory distress syndrome development &#40;odds ratio&#44; 5&#46;1&#59; 95&#37; confidence interval&#44; 2&#46;2&#8211;11&#46;9&#59; <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#46;001&#41;&#46;</p></span> <span id="abst0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Conclusions</span><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleItalic">MBL2</span> variant-type and mannose-binding lectin deficiency are important risk factors for respiratory distress syndrome development in preterm infants&#46; Additionally&#44; there is an association between <span class="elsevierStyleItalic">MBL2</span> wild-type and NEC&#46; Further studies on this subject are needed&#46;</p></span>"
        "secciones" => array:4 [
          0 => array:2 [
            "identificador" => "abst0005"
            "titulo" => "Objective"
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            "identificador" => "abst0010"
            "titulo" => "Method"
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            "identificador" => "abst0015"
            "titulo" => "Results"
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            "identificador" => "abst0020"
            "titulo" => "Conclusions"
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      "pt" => array:3 [
        "titulo" => "Resumo"
        "resumen" => "<span id="abst0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Objetivo</span><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">A lectina ligante de manose &#40;MBL&#44; do ingl&#234;s <span class="elsevierStyleItalic">mannose-binding lectin</span>&#41;&#44; que pertence &#224; fam&#237;lia das colectinas&#44; &#233; um reagente de fase aguda que ativa o sistema complemento&#46; Este estudo teve como objetivo investigar o efeito do polimorfismo do gene <span class="elsevierStyleItalic">MBL2</span> em desfechos de curto prazo em prematuros&#46;</p></span> <span id="abst0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">M&#233;todo</span><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Este estudo prospectivo incluiu crian&#231;as com menos de 37 semanas de gesta&#231;&#227;o admitidas na unidade de terapia intensiva neonatal durante dois anos&#46; Os neonatos foram categorizados em dois grupos de acordo com os gen&#243;tipos do <span class="elsevierStyleItalic">MBL2</span>&#46; O gen&#243;tipo normal do gene <span class="elsevierStyleItalic">MBL2</span> foi definido como <span class="elsevierStyleItalic">MBL2</span> do tipo selvagem &#40;gen&#243;tipo AA&#41;&#44; enquanto o gen&#243;tipo mutante do gene <span class="elsevierStyleItalic">MBL2</span> foi definido como o gene variante &#40;gen&#243;tipo AO&#47;OO&#41;&#46; Foi avaliada a rela&#231;&#227;o entre o gen&#243;tipo <span class="elsevierStyleItalic">MBL2</span> e a morbidade e mortalidade em curto prazo&#46;</p></span> <span id="abst0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Resultados</span><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Durante o per&#237;odo de dois anos&#44; 116 beb&#234;s prematuros foram inclu&#237;dos neste estudo&#46; Os n&#237;veis de lectina ligante de manose foram significativamente menores nos variantes do <span class="elsevierStyleItalic">MBL2</span> e as incid&#234;ncias de defici&#234;ncia de lectina ligante de manose &#40;n&#237;vel de MBL &#60; 700 ng&#47;mL&#41; foram maiores &#40;p &#60; 0&#44;001&#41;&#46; Nesse grupo&#44; a preval&#234;ncia de s&#237;ndrome do desconforto respirat&#243;rio &#40;SDR&#41; e a mortalidade foram significativamente maiores &#40;p &#60; 0&#44;001&#44; p &#61; 0&#44;03&#44; respectivamente&#41;&#46; No grupo <span class="elsevierStyleItalic">MBL2</span> do tipo selvagem&#44; a preval&#234;ncia de enterocolite necrosante foi maior &#40;p &#61; 0&#44;01&#41;&#46; An&#225;lises de regress&#227;o log&#237;stica revelaram que os genes variantes do <span class="elsevierStyleItalic">MBL2</span> apresentaram um efeito significativo no desenvolvimento da s&#237;ndrome do desconforto respirat&#243;rio &#40;<span class="elsevierStyleItalic">odds ratio</span>&#44; 5&#44;1&#59; intervalo de confian&#231;a de 95&#37;&#44; 2&#44;2&#8211;11&#44;9&#59; p &#60; 0&#44;001&#41;&#46;</p></span> <span id="abst0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Conclus&#245;es</span><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">As variantes do <span class="elsevierStyleItalic">MBL2</span> e a defici&#234;ncia de lectina ligante de manose s&#227;o importantes fatores de risco para o desenvolvimento da s&#237;ndrome do desconforto respirat&#243;rio em neonatos prematuros&#46; Al&#233;m disso&#44; existe uma associa&#231;&#227;o entre <span class="elsevierStyleItalic">MBL2</span> do tipo selvagem e a enterocolite necrosante&#46; Mais estudos s&#227;o necess&#225;rios sobre esse assunto&#46;</p></span>"
        "secciones" => array:4 [
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            "titulo" => "Objetivo"
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            "identificador" => "abst0030"
            "titulo" => "M&#233;todo"
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          2 => array:2 [
            "identificador" => "abst0035"
            "titulo" => "Resultados"
          ]
          3 => array:2 [
            "identificador" => "abst0040"
            "titulo" => "Conclus&#245;es"
          ]
        ]
      ]
    ]
    "NotaPie" => array:1 [
      0 => array:2 [
        "etiqueta" => "&#9734;"
        "nota" => "<p class="elsevierStyleNotepara" id="npar0040">Please cite this article as&#58; Dogan P&#44; Ozkan H&#44; Koksal N&#44; Oral HB&#44; Bagci O&#44; Guney Varal I&#46; Mannose-binding lectin gene polymorphism and its effect on short term outcomes in preterm infants&#46; J Pediatr &#40;Rio J&#41;&#46; 2020&#59;96&#58;520&#8211;6&#46;</p>"
      ]
    ]
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      0 => array:7 [
        "identificador" => "fig0005"
        "etiqueta" => "Figure 1"
        "tipo" => "MULTIMEDIAFIGURA"
        "mostrarFloat" => true
        "mostrarDisplay" => false
        "figura" => array:1 [
          0 => array:4 [
            "imagen" => "gr1.jpeg"
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        "descripcion" => array:1 [
          "en" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">DNA fragments on agarose gel electrophoresis after restriction enzyme digestion of exon 1 of the mannose-binding lectin &#40;<span class="elsevierStyleItalic">MBL2</span>&#41; gene codon 54&#46; In all&#44; 349<span class="elsevierStyleHsp" style=""></span>bp PCR product was digested with <span class="elsevierStyleItalic">BanI</span> for codon 54 polymorphism&#46; The normal allele &#40;allele A&#41; is cut into two fragments with <span class="elsevierStyleItalic">BanI</span> &#40;lanes 2 and 5&#41;&#44; 89 and 260<span class="elsevierStyleHsp" style=""></span>bp&#46; The variant allele &#40;allele O&#41; remains uncut &#40;lanes 1 and 6&#41;&#46; Both uncut and digested fragments are seen in AO heterozygote &#40;lanes 3 and 4&#41;&#46; L&#58; 100<span class="elsevierStyleHsp" style=""></span>bp DNA ladder&#46;</p>"
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        "identificador" => "tbl0005"
        "etiqueta" => "Table 1"
        "tipo" => "MULTIMEDIATABLA"
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        "detalles" => array:1 [
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        "tabla" => array:3 [
          "leyenda" => "<p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">Values with significance are presented in bold&#46;</p><p id="spar0060" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleItalic">MBL2</span>&#44; mannose-binding lectin&#59; GA&#44; gestational age&#59; SGA&#44; small for gestational age&#59; PPROM&#44; preterm premature rupture of membranes&#46;</p>"
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                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">&#40;<span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>47&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">30 &#40;29&#8211;33&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t"><span class="elsevierStyleItalic">Birth weight&#44; g &#40;mean</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">&#177;</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">SD&#41;</span>&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">1459<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>556&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">0&#46;5<a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">b</span></a>&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Male&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">18 &#40;38&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">14 &#40;30&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">58 &#40;84&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
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                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Minute 5&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t  " colspan="4" align="left" valign="\n
                  \t\t\t\t\ttop\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
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                  \t\t\t\t\ttop\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t"><span class="elsevierStyleItalic">Maternal preeclampsia&#44; n &#40;&#37;&#41;</span>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
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                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t">0&#46;4<a class="elsevierStyleCrossRef" href="#tblfn0015"><span class="elsevierStyleSup">c</span></a>&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t">0&#46;4<a class="elsevierStyleCrossRef" href="#tblfn0015"><span class="elsevierStyleSup">c</span></a>&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
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                  \t\t\t\t"><span class="elsevierStyleItalic">Chorioamnionitis&#44; n &#40;&#37;&#41;</span>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">4 &#40;6&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t">0&#46;7<a class="elsevierStyleCrossRef" href="#tblfn0015"><span class="elsevierStyleSup">c</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t"><span class="elsevierStyleItalic">MBL levels&#44; &#40;ng&#47;mL&#41; median &#40;range&#41;</span>&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t">993 &#40;257&#8211;1812&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t"><span class="elsevierStyleBold">&#60;0&#46;001</span><a class="elsevierStyleCrossRef" href="#tblfn0005"><span class="elsevierStyleSup">a</span></a>&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t"><span class="elsevierStyleBold">&#60;0&#46;001</span><a class="elsevierStyleCrossRef" href="#tblfn0015"><span class="elsevierStyleSup">c</span></a>&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">BPD&#44; &#40;grade 2&#8211;3&#41;&#44; <span class="elsevierStyleItalic">n</span> &#40;&#37;&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
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                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
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                  \t\t\t\t">BPD&#44; &#40;grade 2&#8211;3&#41;&#44; <span class="elsevierStyleItalic">n</span> &#40;&#37;&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">ROP&#44; &#40;&#62;stage 2&#41;&#44; <span class="elsevierStyleItalic">n</span> &#40;&#37;&#41;&nbsp;\t\t\t\t\t\t\n
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Article information
ISSN: 00217557
Original language: English
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