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Vol. 100. Issue 4.
Pages 335-339 (July - August 2024)
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Vol. 100. Issue 4.
Pages 335-339 (July - August 2024)
Editorial
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Vitamin D status in children
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Roger Bouillon
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roger.bouillon@kuleuven.be

Corresponding author.
, Leen Antonio, Nick Narinx
Clinical and Experimental Endocrinology, Department of Chronic Diseases and Metabolism, KU Leuven, Leuven, Belgium
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Table 1. An overview of the major studies on the vitamin D status of children in different areas of the world. The table is not exhaustive but presents a representative overview of the largest studies. NA, not available.
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Vitamin D was identified, about a century ago, as the agent able to cure nutritional rickets that was endemic in many regions around the world. Cod liver oil or pharmaceutical vitamin D(2) were rapidly introduced as curative agents for the prevention of rickets in many countries as a “national” health policy so that nutritional rickets were largely eradicated in countries and regions with such a strategy. Rickets remains a problem in regions or subgroups that for whatever reason do not implement such a strategy.1-3 The authors now know that vitamin D is an inactive precursor for 25-hydroxyvitamin D (25(OH)D), used as the best indicator for vitamin D status, and 1,25-dihydroxyvitamin D (1,25(OH)2D), the active hormone acting on the vitamin D receptor (VDR). The authors now also realize that activation of the VDR regulates a very large number of genes as about 3 % of the mouse or humans, and even about 10 % of the young zebrafish, genome is directly or indirectly under the control of 1,25(OH)2D. These genes are usually clusters of genes involved in a wide variety of functions, such as cell replication, immune function, and cell differentiation.4 These genetic data in combination with a wealth of studies on cellular, tissue, and whole-body functions lead to the hypothesis that vitamin D might well be implicated in many physiologic functions, and that vitamin D deficiency may contribute to a very large number of major health problems such as cancer, immune, metabolic or vascular diseases.4

Evidently, it became important to evaluate the vitamin D status of subjects around the world and to define a threshold below (or above) which the vitamin D status would generate negative health effects. In addition, many observational studies needed to be complemented by large randomized controlled trials to define which diseases may be avoided by vitamin D supplements given to populations with different risk factors and vitamin D status. Hundreds of publications have generated a wealth of data on the vitamin D status of people living around the world. Most of our vitamin D originates from its synthesis in the skin during exposure to ultraviolet (UV) B sunlight. One might thus expect that people living in countries with plenty of sunshine would have much higher serum 25(OH)D concentrations and a low rate of real deficiency. In reality, the situation is more complex. In Europe, vitamin D status is even lower in Mediterranean countries than in the Scandinavian population and the risk of vitamin D deficiency is much greater in North Africa and Middle East or Gulf countries than in many other countries.5 Differences in lifestyle, including clothing habits and avoidance of direct sun exposure, are the main driving factors for these differences. Based on its location and plenty of sunshine, Africa was supposed to be virtually free of vitamin D deficiency. However, an overview of all publications dealing with 25(OH)D concentrations in African countries, revealed surprising results with a higher than predicted rate of deficiencies in South Africa and especially North African countries.6 When compared with other continents or large regions of the world, the vitamin D status of the African population was not better. Very few studies found mean serum 25(OH)D concentrations that were supposed to be historic levels of early humans as identified by mean serum 25OHD levels of about 45 ng/mL in people with a traditional lifestyle such as the Masai and similar tribes.7 In the overviews following these publications, data from South or Latin America were largely missing.

In the present issue of this journal, Radonsky et al. present data obtained from 413,976 children, aged 0 – 18 years, from different regions of Brazil and thereby generate data to fill one of the major missing gaps to complete a worldwide overview of vitamin D status.8 The children were living in 6 major urban areas and children from rural areas were not included. The mean serum 25(OH)D was 29 ± 9 ng/mL, 12.0 % of the children were vitamin D deficient (serum 25(OH)D below 20 ng/mL) and 0.8 % had severe vitamin D deficiency (serum 25(OH)D below 12 ng/mL). They found an expected 20.0 % variation due to season (obviously according to the climate of the Southern Hemisphere) and a small effect of latitude. Overall, adolescent girls had the lowest vitamin D status. The effect of skin pigmentation or sunscreen usage could not be evaluated. The between-person variation was, as usual around the world, great and exceeded by far the seasonal variation. Indeed, with a standard deviation of 9 ng/mL, the range of ± 2SD would be 11 - 57 ng/mL (if a Gaussian distribution would apply). The reasons for this large variation remain unexplained and clarification of this variation might help in identifying the persons most at risk for vitamin D deficiency and the best focus for targeted supplementation. The paper fortunately also included essential quality control samples to evaluate the accuracy of the 25(OH)D assay. Using DEQAS samples with liquid chromatography-tandem mass spectrometry (LC-MS/MS) verified sera samples, the immunoassay used in the study revealed a relatively small bias of about 6.0 %.2 Ideally, for such kind of large studies, it would be wise to recalibrate the results using well-described methodologies.9

Is the vitamin D status of children very different from the vitamin D status in adults around the world? There are thousands of studies reporting the vitamin D status in different areas of the world but the large majority deals with adults and elderly subjects. A recent overview comparing the situation in different continents concluded that about 7.0 % of the world's population lived with serum 25(OH)D concentrations below 12 ng/mL. This was also the frequency of such severe deficiency in the NHANES study (dealing with samples from subjects older than 12 years), whereas higher percentages were found in European countries (14.0 %) and even much higher percentages in the Middle East or Gulf states, North African countries, Mongolia and Northern China. The lowest rate was found in some equatorial countries such as Ghana and the Seychelles.10 There are fewer data dealing with children and adolescents but in general vitamin D status of children is not much different from that of adults living in the same area. Table 111-47 summarizes the data obtained in different countries and demonstrates a wide range of situations around the world. There are different ways to look at the results of this large survey. Evidently, one would prefer that no child should live with vitamin D deficiency. Comparison with other areas around the world can also help to interpret the results. From Table 1 it is obvious that severe vitamin D deficiency (below 30 nmol/L or 12 ng/mL) is rare in Brazil (0.8 %) and therefore no country in the world can really be better than the virtual absence of such a severe form of deficiency. A more modest deficiency was found in 12.5 % of the Brazilian children in the present study by Radonsky et al. Only two countries were better, South Africa and Canada. The Canadian data can probably be explained by the younger age groups reported (0 - 5 years) and the high rate of implementation of vitamin D supplementation in young children in general. Most countries thus perform less well than Brazil and some areas or countries are being confronted by a more than 30.0 – 50.0 % risk of modest deficiency, e.g., Italy (and some other European countries), Lebanon (and probable several North African and Gulf states), Mongolia (and probably upper China and India) and Korea.

Table 1.

An overview of the major studies on the vitamin D status of children in different areas of the world. The table is not exhaustive but presents a representative overview of the largest studies. NA, not available.

  Geographical area  Study population  Study size (n)  Baseline data  Prevalence,%
          Cutoff of < 20 ng/mL (50 nmol/L)  Cutoff of < 8 - 12 ng/mL (20 - 30 nmol/L) 
Isa et al. (2020)18  Bahrain  0 – 16 years  531  2016  78.3 %  – 
Radonsky et al. (2024)8  Brazil  0 – 18 years  413,976  2014 – 2018  12.5 %  0.8 % 
Santos et al. (2012)19  Brazil  7 – 18 years  234  2008 – 2011  36.3 %  – 
Lourenço et al. (2020)20  Brazil  0 – 2 years  468  2012 – 2013  68.2 %  32.9 % 
Maguire et al. (2013)16  Canada  1 – 5 years  1898  2008 – 2011  6.0 %  – 
Yang et al. (2020)21  China  0 – 18 years  460,537  2016 - 2018  22.6 %  6.7 % 
Li et al. (2022)22  China  0 – 18 years  10,262  2012 – 2020  14.0 %  – 
Zhang et al. (2020)23  China  0 – 6 years  6953  2016  22.1 %  – 
Gonzalez-Gross et al. (2012)11  Europe  12.5 – 17.5 years  1006  2006 – 2007  42.0 %  15.0 % 
Cashman et al. (2016)24  Europe  1 – 17 years  10,015  2002 – 2012  44.5 %  6.0 % 
Wolters et al. (2022)25  Europe  3 – 15 years  2171  2007 – 2014  63.0 %  – 
Lehtonen-Veromaa et al. (1999)26  Finland  9 – 15 years  191  1997 – 1998  –  13.4 % 
Absoud et al. (2011)27  Great Britain  4 – 18 years  1102  1997 – 1998  35.1 %  – 
Marwaha et al. (2005)28  India  10 – 18 years  5137  NA  –  35.7 % 
Chowdhury et al. (2019)29  India  0 – 3 years  960  2010 - 2012  –  34.5 % 
Rabbani et al. (2009)30  Iran  7 – 18 years  963  NA  34.9 %  6.7 % 
Carson et al. (2015)31  Ireland  12 – 15 years  1015  1999 – 2000  66.2 %  16.7 % 
Korchia et al. (2013)32  Israel  1 – 6 years  247  2009 – 2010  28.3 %  – 
Vierucci et al. (2013)12  Italy  2 – 21 years  652  2010 – 2012  45.9 %  9.5 % 
Lippi et al. (2007)33  Italy  0 – 18 years  192  2004 – 2007  –  6.2 % 
Marrone et al. (2012)34  Italy  0 – 18 years  93  2009 - 2010  54.8 %  – 
Mazzoleni et al. (2012)35  Italy  1 – 15 years  58  2010 – 2011  50.0 %  12.1 % 
Nichols et al. (2015)36  Jordan  1 – 5 years  1077  2010  56.5 %  19.8 % 
Kim et al. (2014)13  Korea  10 – 18 years  2062  2008 – 2009  68.1 %  13.4 % 
El-Hajj Fuleihan et al. (2001)37  Lebanon  10 – 16 years  169  1999  65.0 %  21.0 % 
Flores et al. (2021)38  Mexico  1 – 4 years  1209  2018 – 2019  27.3 %  – 
Flores et al. (2021)38  Mexico  5 – 11 years  3482  2018 – 2019  17.2 %  – 
Ganmaa et al. (2020)39  Mongolia  6 – 13 years  8851  2015 - 2017  95.6 %  31.8 % 
Holten-Andersen et al. (2020)40  Norway  0 – 18 years  301  2015 – 2017  22.0 %  1.0 % 
Al Shaikh et al. (2016)41  Saudi Arabia  6 – 15 years  2110  2013 – 2014  95.3 %  45.4 % 
Poopedi et al. (2011)42  South Africa  10 years  385  NA  7.0 %  – 
Karagüzel et al. (2014)43  Türkiye  11 – 18 years  746  2010  93.0 %  – 
Das et al. (2006)44  United Kingdom  14 – 17 years  51  2003  –  73.0 % 
Gordon et al. (2004)45  USA  11 – 18 years  307  2001 – 2003  42.0 %  4.6 % 
Dong et al. (2010)14  USA  14 – 18 years  559  2001 – 2005  28.8 %  5.2 % 
Mansbach et al. (2009)46  USA  1 – 11 years  4558  2001 – 2006  18.0 %  1.0 % 
Gordon et al. (2008)47  USA  0 – 2 years  380  2005 - 2007  12.1 %  – 
Summary and conclusions

  • Vitamin D deficiency, however defined, is frequent around the world.

  • There is no unanimity about which serum 25(OH)D is sufficient for global health. An overview of guidelines concluded that there is great unanimity that serum 25(OH)D concentrations below 12 ng/mL should be avoided at all ages. The UK guidelines prudently concluded that there are no convincing randomized controlled trials that higher levels than 12 ng/mL convey additional benefits. However, most other guidelines recommended a minimal threshold of 20 ng/mL to avoid secondary hyperparathyroidism and its long-term consequences. The Endocrine Society and some other scientific organizations, including the Brazilian Endocrine Society, preferred a serum concentration of at least 30 ng/mL especially because of observational studies linking such “insufficiency“ (serum 25(OH)D between 20 - 30 ng/mL) with major health consequences such as cancer, metabolic and cardiovascular diseases. Finally, a few experts believe serum 25(OH)D should be about or above 40 ng/mL as this level is found in a few tribes living as our early ancestors probably did.

  • The vitamin D status of Brazilian children is certainly much better than in most moderate climates. Severe vitamin D deficiency (< 12 ng/ml) is rare at overall levels below 1.0 %, compared with 15.0 % in Europe,11,12 and 13.0 % in Korea.13 Similarly, low frequency of severe vitamin D deficiency was also found in Southern USA,14 China,15 or Canada.16 The rickets consensus1 and most guidelines consider such low serum 25(OH)D to be a risk factor for rickets. Fortunately, not all children with such low serum 25(OH)D develop rickets and it is unclear what other factors, other than very low calcium intake, are involved in causing this severe disease. Rickets is unfortunately still far too frequent in some regions of the world. The WHO should take up a leading role in formulating strategies and implementation policies to eradicate nutritional rickets.

  • Vitamin D deficiency can relatively easily be corrected. A population-based evaluation of serum 25(OH)D is an excellent strategy to determine to what degree such deficiencies exist, and which strategies could be used to correct such deficiencies. The present study used convenient sampling using existing results of measurements of serum 25(OH)D. Due to its very large number of children from different areas of Brazil, it probably represents a good proxy for the real situation.

  • Modest vitamin D deficiency is highly prevalent in many countries. Brazil is rather well off in comparison with other countries, but of course, 12.5 % of the population is modestly deficient, and higher rates in some subjects in wintertime, require specific attention. For some countries where the majority of the population has such a deficiency, food fortification is probably the best strategy as shown by the Finnish example. For Brazil, a more dedicated approach may be more appropriate. One such option could be to recommend a daily or weekly dose of vitamin D (about 600–1000 IU/d) for subjects most at risk such as adolescent girls during wintertime.

  • Whether achieving levels higher than 20 ng/mL would convey additional benefits is yet unclear. The recent large mega-trials in the US, Australia and New Zealand concluded that vitamin D supplementation of adults, considered vitamin D replete on the basis of serum 25(OH)D well above 25 ng/mL, did not generate beneficial effects on cardiovascular or metabolic risks and also did not decrease cancer incidence. Similar studies in children are not available. There are, however, more solid data linking a good vitamin D status with beneficial immune effects, but the available data do not allow us to define which 25(OH)D levels are needed for such effects.

  • Correction of vitamin D deficiency should always be complemented by assuring adequate calcium intake. Overall, there is room for improvement in the calcium intake of children in Brazil as shown by a large population-based study.17

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See paper by Radonsky et al. in pages 360–366.

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Os artigos submetidos a partir de 1º de setembro de 2018, que forem aceitos para publicação no Jornal de Pediatria, estarão sujeitos a uma taxa para que tenham sua publicação garantida. O artigo aceito somente será publicado após a comprovação do pagamento da taxa de publicação. Ao submeterem o manuscrito a este jornal, os autores concordam com esses termos. A submissão dos manuscritos continua gratuita. Para mais informações, contate jped2@sbp.com.br. Articles submitted as of September 1, 2018, which are accepted for publication in the Jornal de Pediatria, will be subject to a fee to have their publication guaranteed. The accepted article will only be published after proof of the publication fee payment. By submitting the manuscript to this journal, the authors agree to these terms. Manuscript submission remains free of charge. For more information, contact jped2@sbp.com.br.
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