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Vitamin D status in children* * See paper by Radonsky et al. in pages 360–366.

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.11 Munns CF, Shaw N, Kiely M, Specker BL, Thacher TD, Ozono K, et al. Global consensus recommendations on prevention and management of nutritional rickets. J Clin Endocrinol Metab. 2016;101:394–415., 22 Bouillon R, Antonio L. Nutritional rickets: historic overview and plan for worldwide eradication. J Steroid Biochem Mol Biol. 2020;198:105563., 33 World Health Organization (WHO). Nutritional Rickets: a Review of Disease Burden, Causes, Diagnosis, Prevention and Treatment. Geneva: WHO; 2019, Licence: CC BY-NC-SA 3.0 IGO. The authors now know that vitamin D is an inactive precursor for 25-hydroxy-vitamin 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.44 Bouillon R, Marcocci C, Carmeliet G, Bikle D, White JH, Dawson-Hughes B, et al. Skeletal and extraskeletal actions of vitamin D: current evidence and outstanding questions. Endocr Rev. 2019; 40:1109–51. 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.44 Bouillon R, Marcocci C, Carmeliet G, Bikle D, White JH, Dawson-Hughes B, et al. Skeletal and extraskeletal actions of vitamin D: current evidence and outstanding questions. Endocr Rev. 2019; 40:1109–51.

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.55 Lips P, Cashman KD, Lamberg-Allardt C, Bischoff-Ferrari HA, Obermayer-Pietsch B, Bianchi ML, et al. Current vitamin D status in European and Middle East countries and strategies to prevent vitamin D deficiency: a position statement of the European Calcified Tissue Society. Eur J Endocrinol. 2019;180:P23–54. 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.66 Mogire RM, Mutua A, Kimita W, Kamau A, Bejon P, Pettifor JM, et al. Prevalence of vitamin D deficiency in Africa: a systematic review and meta-analysis. Lancet Glob Health. 2020;8: e134–e42. Erratum in: Lancet Glob Health. 2022;10:e481. 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.77 Luxwolda MF, Kuipers RS, Kema IP, Dijck-Brouwer DA, Muskiet FA. Traditionally living populations in East Africa have a mean serum 25-hydroxyvitamin D concentration of 115nmol/l. Br J Nutr. 2012;108:1557–61. 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.88 Radonsky V, Lazaretti-Castro M, Chiamolera MI, Biscolla RP, Lima Junior JV, Vieira JG, et al. Alert for the high prevalence of vitamin D deficiency in adolescents in a large Brazilian sample. JPediatr(RioJ). 2024;100:360–6. 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 § 9ng/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 %.22 Bouillon R, Antonio L. Nutritional rickets: historic overview and plan for worldwide eradication. J Steroid Biochem Mol Biol. 2020;198:105563. Ideally, for such kind of large studies, it would be wise to recalibrate the results using well-described methodologies.99 Sempos CT, Heijboer AC, Bikle DD, Bollerslev J, Bouillon R, Brannon PM, et al. Vitamin D assays and the definition of hypovitaminosis D: results from the First International Conference on Controversies in Vitamin D. Br J Clin Pharmacol. 2018;84: 2194–207.

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.1010 Bouillon R. Vitamin D status in Africa is worse than in other continents. Lancet Glob Health. 2020;8:e20–e1. 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 1 1111 Gonzalez-Gross M, Valtuena J, Breidenassel C, Moreno LA, Ferrari M, Kersting M, et al. Vitamin D status among adolescents in Europe: the Healthy Lifestyle in Europe by Nutrition in Adolescence study. Br J Nutr. 2012;107:755–64.,1212 Vierucci F, Del Pistoia M, Fanos M, Gori M, Carlone G, Erba P, et al. Vitamin D status and predictors of hypovitaminosis D in Italian children and adolescents: a cross-sectional study. Eur J Pediatr. 2013;172:1607–17.,1313 Kim SH, Oh MK, Namgung R, Park MJ. Prevalence of 25-hydroxy-vitamin D deficiency in Korean adolescents: association with age, season and parental vitamin D status. Public Health Nutr. 2014;17:122–30.,1414 Dong Y, Pollock N, Stallmann-Jorgensen IS, Gutin B, Lan L, Chen TC, et al. Low 25-hydroxyvitamin D levels in adolescents: race, season, adiposity, physical activity, and fitness. Pediatrics. 2010;125:1104–11.,1515 BaiK,DongH,LiuL, SheX,LiuC, YuM, etal.Serum25-hydroxyvitamin D status of a large Chinese population from 30 provinces by LC-MS/MS measurement for consecutive 3 years: differences by age, sex, season and province. EurJ Nutr. 2023;62:1503–16.,1616 Maguire JL, Birken CS, Khovratovich M, Degroot J, Carsley S, Thorpe KE, et al. Modifiable determinants of serum 25-hydroxyvitamin D status in early childhood: opportunities for prevention. JAMA Pediatr. 2013;167:230–5.,1717 Galvao RA, Pavon B, Moran MC, Barbin MV, Martimbianco AL. Colares Neto GP. Dietary calcium intake in Brazilian preschoolers and schoolchildren: review of the literature. Rev Paul Pediatr. 2022;41:e2021253.,1818 Isa H, Almaliki M, Alsabea A, Mohamed A. Vitamin D deficiency in healthy children in Bahrain: do gender and age matter? East Mediterr Health J. 2020;26:260–7.,1919 Santos BR, Mascarenhas LP, Satler F, Boguszewski MC, Spritzer PM. Vitamin D deficiency in girls from South Brazil: a cross-sectional study on prevalence and association with vitamin D receptor gene variants. BMC Pediatr. 2012;12:62.,2020 Lourenco BH, Silva LL, Fawzi WW, Cardoso MA, Working Group ENFAC. Vitamin D sufficiency in young Brazilian children: associated factors and relationship with vitamin A corrected for inflammatory status. Public Health Nutr. 2020;23:1226–35.,2121 Yang C, Mao M, Ping L, Yu D. Prevalence of vitamin D deficiency and insufficiency among 460,537 children in 825 hospitals from 18 provinces in mainland China. Medicine. 2020;99:e22463.,2222 Li HA, Zou SQ, Li BT, Wang T, Ma ZC, Luo Q, et al. Serum vitamin D status among healthy children in Hainan, South China: a multi-center analysis of 10,262 children. Transl Pediatr. 2022;11:1010–7.,2323 Zhang H, Li Z, Wei Y, Fu J, FengY, Chen D, et al. Status and influential factors of vitamin D among children aged 0 to 6 years in a Chinese population. BMC Public Health. 2020;20:429.,2424 Cashman KD, Dowling KG, Škrabáková Z, Gonzalez-Gross M, Valtueña J, De Henauw S, et al. Vitamin D deficiency in Europe: pandemic? Am J Clin Nutr. 2016;103:1033–44.,2525 Wolters M, Intemann T, Russo P, Moreno LA, Molnár D, Veidebaum T, et al. 25-Hydroxyvitamin D reference percentiles and the role of their determinants among European children and adolescents. Eur J Clin Nutr. 2022;76:564–73.,2626 Lehtonen-Veromaa M, Möttönen T, Irjala K, Kärkkäinen M, Lamberg-Allardt C, Hakola P, et al. Vitamin D intake is low and hypo-vitaminosis D common in healthy 9- to 15-year-old Finnish girls. Eur J Clin Nutr. 1999;53:746–51.,2727 Absoud M, Cummins C, Lim MJ, Wassmer E, Shaw N. Prevalence and predictors of vitamin D insufficiency in children: a Great Britain population based study. PLoS One. 2011;6:e22179.,2828 Marwaha RK, Tandon N, Reddy DR, Aggarwal R, Singh R, Sawhney RC, et al. Vitamin D and bone mineral density status of healthy schoolchildren in northern India. Am J Clin Nutr. 2005;82:477–82.,2929 Chowdhury R, Taneja S, Bhandari N, Strand TA, Bhan MK. Vitamin D deficiency and mild to moderate anemia in young North Indian children: a secondary data analysis. Nutrition. 2019; 57:63–8.,3030 Rabbani A, Alavian SM, Motlagh ME, Ashtiani MT, Ardalan G, Salavati A, et al. Vitamin D insufficiency among children and adolescents living in Tehran, Iran. J Trop Pediatr. 2009;55:189–91.,3131 Carson EL, Pourshahidi LK, Hill TR, Cashman KD, Strain JJ, Boreham CA, et al. Vitamin D, muscle function, and cardiorespiratory fitness in adolescents from the young hearts study. J Clin Endocrinol Metab. 2015;100:4621–8.,3232 Korchia G, Amitai Y, Moshe G, Korchia L, Tenenbaum A, Rosenblum J, et al. Vitamin D deficiency in children in Jerusalem: the need for updating the recommendation for supplementation. IsrMed Assoc J. 2013;15:333–8.,3333 Lippi G, Montagnana M, Targher G. Vitamin D deficiency among Italian children. CMAJ. 2007;177:1529–30. author reply 30.,3434 Marrone G, Rosso I, Moretti R, Valent F, Romanello C. Is vitamin D status known among children living in Northern Italy? Eur J Nutr. 2012;51:143–9.,3535 Mazzoleni S, Toderini D, Boscardin C. The vitamin D grey areas in pediatric primary care. Very low serum 25-hydroxyvitamin D levels in asymptomatic children living in northeastern Italy. Int J Pediatr Endocrinol. 2012;2012:7.,3636 Nichols EK, Khatib IM, Aburto NJ, Serdula MK, Scanlon KS, Wirth JP, et al. Vitamin D status and associated factors of deficiency among Jordanian children of preschool age. Eur J Clin Nutr. 2015;69:90–5.,3737 El-Hajj Fuleihan G, Nabulsi M, Choucair M, Salamoun M, Hajj Shahine C, Kizirian A, et al. Hypovitaminosis D in healthy schoolchildren. Pediatrics. 2001;107:E53.,3838 Flores ME, Rivera-Pasquel M, Valdez-Sanchez A, De la Cruz-Gongora V, Contreras-Manzano A, Shamah-Levy T, et al. Vitamin D status in Mexican children 1 to 11 years of age: an update from the Ensanut 2018-19. Salud Publica Mex. 2021;63:382–93.,3939 Ganmaa D, Uyanga B, Zhou X, Gantsetseg G, Delgerekh B, Enkhmaa D, et al. Vitamin D supplements for prevention of tuberculosis infection and disease. N Engl J Med. 2020;383:359–68.,4040 Holten-Andersen MN, Haugen J, Oma I, Strand TA. Vitamin D status and its determinants in a paediatric population in Norway. Nutrients. 2020;12:1385.,4141 Al Shaikh AM, Abaalkhail B, Soliman A, Kaddam I, Aseri K, Al Saleh Y, et al. Prevalence of vitamin D deficiency and calcium homeostasis in Saudi children. J Clin Res Pediatr Endocrinol. 2016;8:461–7.,4242 Poopedi MA, Norris SA, Pettifor JM. Factors influencing the vitamin D status of 10-year-old urban South African children. Public Health Nutr. 2011;14:334–9.,4343 Karaguüzel G, Dilber B, Can G, Okten A, Deger O, Holick MF. Seasonal vitamin D status of healthy schoolchildren and predictors of low vitamin D status. J Pediatr Gastroenterol Nutr. 2014; 58:654–60.,4444 Das G, Crocombe S, McGrath M, Berry JL, Mughal MZ. Hypovitaminosis D among healthy adolescent girls attending an inner city school. Arch Dis Child. 2006;91:569–72.,4545 Gordon CM, DePeter KC, Feldman HA, Grace E, Emans SJ. Prevalence of vitamin D deficiency among healthy adolescents. Arch Pediatr Adolesc Med. 2004;158:531–7.,4646 Mansbach JM, Ginde AA, Camargo Jr. CA. Serum 25-hydroxyvitamin D levels among US children aged 1 to 11 years: do children need more vitamin D? Pediatrics. 2009;124:1404–10. Erratum in: Pediatrics. 2009;124:1709.,4747 Gordon CM, Feldman HA, Sinclair L, Williams AL, Kleinman PK, Perez-Rossello J, et al. Prevalence of vitamin D deficiency among healthy infants and toddlers. Arch Pediatr Adolesc Med. 2008;162:505–12. summarizes the data obtained in different countries and demonstrates a wide range of situations around the world. There are differentwaystolookatthe resultsofthislarge 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 30nmol/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.

Summary and conclusions

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

  2. 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 hyperparathy-roidism 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.

  3. 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,1111 Gonzalez-Gross M, Valtuena J, Breidenassel C, Moreno LA, Ferrari M, Kersting M, et al. Vitamin D status among adolescents in Europe: the Healthy Lifestyle in Europe by Nutrition in Adolescence study. Br J Nutr. 2012;107:755–64., 1212 Vierucci F, Del Pistoia M, Fanos M, Gori M, Carlone G, Erba P, et al. Vitamin D status and predictors of hypovitaminosis D in Italian children and adolescents: a cross-sectional study. Eur J Pediatr. 2013;172:1607–17. and 13.0 % in Korea.1313 Kim SH, Oh MK, Namgung R, Park MJ. Prevalence of 25-hydroxy-vitamin D deficiency in Korean adolescents: association with age, season and parental vitamin D status. Public Health Nutr. 2014;17:122–30. Similarly, low frequency of severe vitamin D deficiency was also found in Southern USA,1414 Dong Y, Pollock N, Stallmann-Jorgensen IS, Gutin B, Lan L, Chen TC, et al. Low 25-hydroxyvitamin D levels in adolescents: race, season, adiposity, physical activity, and fitness. Pediatrics. 2010;125:1104–11. China,1515 BaiK,DongH,LiuL, SheX,LiuC, YuM, etal.Serum25-hydroxyvitamin D status of a large Chinese population from 30 provinces by LC-MS/MS measurement for consecutive 3 years: differences by age, sex, season and province. EurJ Nutr. 2023;62:1503–16. or Canada.1616 Maguire JL, Birken CS, Khovratovich M, Degroot J, Carsley S, Thorpe KE, et al. Modifiable determinants of serum 25-hydroxyvitamin D status in early childhood: opportunities for prevention. JAMA Pediatr. 2013;167:230–5. The rickets consensus11 Munns CF, Shaw N, Kiely M, Specker BL, Thacher TD, Ozono K, et al. Global consensus recommendations on prevention and management of nutritional rickets. J Clin Endocrinol Metab. 2016;101:394–415. 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.

  4. 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.

  5. 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.

  6. 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.

  7. 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.1717 Galvao RA, Pavon B, Moran MC, Barbin MV, Martimbianco AL. Colares Neto GP. Dietary calcium intake in Brazilian preschoolers and schoolchildren: review of the literature. Rev Paul Pediatr. 2022;41:e2021253.

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

References

  • 1
    Munns CF, Shaw N, Kiely M, Specker BL, Thacher TD, Ozono K, et al. Global consensus recommendations on prevention and management of nutritional rickets. J Clin Endocrinol Metab. 2016;101:394–415.
  • 2
    Bouillon R, Antonio L. Nutritional rickets: historic overview and plan for worldwide eradication. J Steroid Biochem Mol Biol. 2020;198:105563.
  • 3
    World Health Organization (WHO). Nutritional Rickets: a Review of Disease Burden, Causes, Diagnosis, Prevention and Treatment. Geneva: WHO; 2019, Licence: CC BY-NC-SA 3.0 IGO.
  • 4
    Bouillon R, Marcocci C, Carmeliet G, Bikle D, White JH, Dawson-Hughes B, et al. Skeletal and extraskeletal actions of vitamin D: current evidence and outstanding questions. Endocr Rev. 2019; 40:1109–51.
  • 5
    Lips P, Cashman KD, Lamberg-Allardt C, Bischoff-Ferrari HA, Obermayer-Pietsch B, Bianchi ML, et al. Current vitamin D status in European and Middle East countries and strategies to prevent vitamin D deficiency: a position statement of the European Calcified Tissue Society. Eur J Endocrinol. 2019;180:P23–54.
  • 6
    Mogire RM, Mutua A, Kimita W, Kamau A, Bejon P, Pettifor JM, et al. Prevalence of vitamin D deficiency in Africa: a systematic review and meta-analysis. Lancet Glob Health. 2020;8: e134–e42. Erratum in: Lancet Glob Health. 2022;10:e481.
  • 7
    Luxwolda MF, Kuipers RS, Kema IP, Dijck-Brouwer DA, Muskiet FA. Traditionally living populations in East Africa have a mean serum 25-hydroxyvitamin D concentration of 115nmol/l. Br J Nutr. 2012;108:1557–61.
  • 8
    Radonsky V, Lazaretti-Castro M, Chiamolera MI, Biscolla RP, Lima Junior JV, Vieira JG, et al. Alert for the high prevalence of vitamin D deficiency in adolescents in a large Brazilian sample. JPediatr(RioJ). 2024;100:360–6.
  • 9
    Sempos CT, Heijboer AC, Bikle DD, Bollerslev J, Bouillon R, Brannon PM, et al. Vitamin D assays and the definition of hypovitaminosis D: results from the First International Conference on Controversies in Vitamin D. Br J Clin Pharmacol. 2018;84: 2194–207.
  • 10
    Bouillon R. Vitamin D status in Africa is worse than in other continents. Lancet Glob Health. 2020;8:e20–e1.
  • 11
    Gonzalez-Gross M, Valtuena J, Breidenassel C, Moreno LA, Ferrari M, Kersting M, et al. Vitamin D status among adolescents in Europe: the Healthy Lifestyle in Europe by Nutrition in Adolescence study. Br J Nutr. 2012;107:755–64.
  • 12
    Vierucci F, Del Pistoia M, Fanos M, Gori M, Carlone G, Erba P, et al. Vitamin D status and predictors of hypovitaminosis D in Italian children and adolescents: a cross-sectional study. Eur J Pediatr. 2013;172:1607–17.
  • 13
    Kim SH, Oh MK, Namgung R, Park MJ. Prevalence of 25-hydroxy-vitamin D deficiency in Korean adolescents: association with age, season and parental vitamin D status. Public Health Nutr. 2014;17:122–30.
  • 14
    Dong Y, Pollock N, Stallmann-Jorgensen IS, Gutin B, Lan L, Chen TC, et al. Low 25-hydroxyvitamin D levels in adolescents: race, season, adiposity, physical activity, and fitness. Pediatrics. 2010;125:1104–11.
  • 15
    BaiK,DongH,LiuL, SheX,LiuC, YuM, etal.Serum25-hydroxyvitamin D status of a large Chinese population from 30 provinces by LC-MS/MS measurement for consecutive 3 years: differences by age, sex, season and province. EurJ Nutr. 2023;62:1503–16.
  • 16
    Maguire JL, Birken CS, Khovratovich M, Degroot J, Carsley S, Thorpe KE, et al. Modifiable determinants of serum 25-hydroxyvitamin D status in early childhood: opportunities for prevention. JAMA Pediatr. 2013;167:230–5.
  • 17
    Galvao RA, Pavon B, Moran MC, Barbin MV, Martimbianco AL. Colares Neto GP. Dietary calcium intake in Brazilian preschoolers and schoolchildren: review of the literature. Rev Paul Pediatr. 2022;41:e2021253.
  • 18
    Isa H, Almaliki M, Alsabea A, Mohamed A. Vitamin D deficiency in healthy children in Bahrain: do gender and age matter? East Mediterr Health J. 2020;26:260–7.
  • 19
    Santos BR, Mascarenhas LP, Satler F, Boguszewski MC, Spritzer PM. Vitamin D deficiency in girls from South Brazil: a cross-sectional study on prevalence and association with vitamin D receptor gene variants. BMC Pediatr. 2012;12:62.
  • 20
    Lourenco BH, Silva LL, Fawzi WW, Cardoso MA, Working Group ENFAC. Vitamin D sufficiency in young Brazilian children: associated factors and relationship with vitamin A corrected for inflammatory status. Public Health Nutr. 2020;23:1226–35.
  • 21
    Yang C, Mao M, Ping L, Yu D. Prevalence of vitamin D deficiency and insufficiency among 460,537 children in 825 hospitals from 18 provinces in mainland China. Medicine. 2020;99:e22463.
  • 22
    Li HA, Zou SQ, Li BT, Wang T, Ma ZC, Luo Q, et al. Serum vitamin D status among healthy children in Hainan, South China: a multi-center analysis of 10,262 children. Transl Pediatr. 2022;11:1010–7.
  • 23
    Zhang H, Li Z, Wei Y, Fu J, FengY, Chen D, et al. Status and influential factors of vitamin D among children aged 0 to 6 years in a Chinese population. BMC Public Health. 2020;20:429.
  • 24
    Cashman KD, Dowling KG, Škrabáková Z, Gonzalez-Gross M, Valtueña J, De Henauw S, et al. Vitamin D deficiency in Europe: pandemic? Am J Clin Nutr. 2016;103:1033–44.
  • 25
    Wolters M, Intemann T, Russo P, Moreno LA, Molnár D, Veidebaum T, et al. 25-Hydroxyvitamin D reference percentiles and the role of their determinants among European children and adolescents. Eur J Clin Nutr. 2022;76:564–73.
  • 26
    Lehtonen-Veromaa M, Möttönen T, Irjala K, Kärkkäinen M, Lamberg-Allardt C, Hakola P, et al. Vitamin D intake is low and hypo-vitaminosis D common in healthy 9- to 15-year-old Finnish girls. Eur J Clin Nutr. 1999;53:746–51.
  • 27
    Absoud M, Cummins C, Lim MJ, Wassmer E, Shaw N. Prevalence and predictors of vitamin D insufficiency in children: a Great Britain population based study. PLoS One. 2011;6:e22179.
  • 28
    Marwaha RK, Tandon N, Reddy DR, Aggarwal R, Singh R, Sawhney RC, et al. Vitamin D and bone mineral density status of healthy schoolchildren in northern India. Am J Clin Nutr. 2005;82:477–82.
  • 29
    Chowdhury R, Taneja S, Bhandari N, Strand TA, Bhan MK. Vitamin D deficiency and mild to moderate anemia in young North Indian children: a secondary data analysis. Nutrition. 2019; 57:63–8.
  • 30
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Publication Dates

  • Publication in this collection
    15 July 2024
  • Date of issue
    Jul-Aug 2024
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