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. 2012 Feb 14;12:126. doi: 10.1186/1471-2458-12-126

High prevalence of vitamin D deficiency among children aged 1 month to 16 years in Hangzhou, China

Zhiwei Zhu 1, Jianying Zhan 1, Jie Shao 1, Weijun Chen 1, Liqin Chen 2, Wenhao Li 1, Chai Ji 1, Zhengyan Zhao 1,
PMCID: PMC3312872  PMID: 22330045

Abstract

Background

Recent studies have suggested that vitamin D deficiency in children is widespread. But the vitamin D status of Chinese children is seldom investigated. The objective of the present study was to survey the serum levels of 25-hydroxyvitamin D [25(OH)D] in more than 6,000 children aged 1 month to 16 years in Hangzhou (latitude: 30°N), the capital of Zhejiang Province, southeast China.

Methods

The children aged 1 month to 16 years who came to the child health care department of our hospital, the children's hospital affiliated to Zhejiang university school of medicine, for health examination were taken blood for 25(OH) D measurement. Serum 25(OH) D levels were determined by direct enzyme-linked immunosorbent assay and categorized as < 25, < 50, and < 75 nmol/L.

Results

A total of 6,008 children aged 1 month to 16 years participated in this cross-sectional study. All the subjects were divided into subgroups according to their age: 0-1y, 2-5y, 6-11y and 12-16y representing infancy, preschool, school age and adolescence stages respectively. The highest mean level of serum 25(OH)D was found in the 0-1y stage (99 nmol/L) and the lowest one was found in 12-16y stage (52 nmol/L). Accordingly, the prevalence of serum 25(OH)D levels of < 75 nmol/L and < 50 nmol/L were at the lowest among infants (33.6% and 5.4% respectively) and rose to the highest among adolescents (89.6% and 46.4% respectively). The mean levels of serum 25(OH)D and the prevalence of vitamin D deficiency changed according to seasons. In winter and spring, more than 50% of school age children and adolescents had a 25(OH)D level at < 50 nmol/L. If the threshold is changed to < 75 nmol/L, all of the adolescents (100%) had low 25(OH)D levels in winter and 93.7% school age children as well.

Conclusions

The prevalence of vitamin D deficiency and insufficiency among children in Hangzhou Zhejiang province is high, especially among children aged 6-16 years. We suggest that the recommendation for vitamin D supplementation in Chinese children should be extended to adolescence.

Background

Vitamin D deficiency causes rickets in infants and young children. However, rickets can be considered only the tip of the vitamin D deficiency iceberg. The vitamin D receptor is present in the small intestine, colon, osteoblasts, activated T and B lymphocytes, β islet cells, mononuclear cells and most organs in the body including the brain, heart, skin, gonads, prostate, and breast [1]. Many studies over the last 2 decades have suggested important role vitamin D plays in decreasing the risk of many chronic diseases, including cancers[2,3], autoimmune diseases[4,5], infectious diseases[6-8], and cardiovascular diseases[9].

Although there is no consensus on optimal levels of 25-hydroxyvitamin D as measured in serum, vitamin D deficiency is defined by most experts as a 25-hydroxyvitamin D level of less than 50 nmol per liter [10]. After reviewed studies on the thresholds for serum 25(OH)D concentrations in relation to bone mineral density (BMD), lower extremity function, dental health, and risk of falls, fractures, and colorectal cancer, Heike A Bischoff-Ferrari found that, the most advantageous serum concentrations of 25(OH)D begin at 75 nmol/L, and the best are between 90 and 100 nmol/L[11]. In children, the optimal level of serum 25(OH)D for general health is unknown and even more controversial than in adults, because there are fewer outcome data[12,13]. It has been proposed that the minimal optimal circulating vitamin D level should be increased from 50 nmol/L to 75 nmol/L[14,15], because there is evidence that biochemical sequelae of vitamin D deficiency may manifest at cutoff levels of 75 nmol/L[11,16]. And the level of 25-hydroxyvitamin D between 50 and 75 nmol/L can be considered as a relative insufficiency of vitamin D in children.

According to such definitions, the prevalence of vitamin D insufficiency was higher among American children aged 6-11 years (73%) compared with children aged 1-5 years (63%); girls (71%) compared with boys (67%); and non-Hispanic black (92%) and Hispanic (80%) children compared with non-Hispanic white children (59%)[17]. In studies in Australia, Turkey, India, and Lebanon, 30-50% of children and adults had 25(OH)D levels under 50 nmol per liter[18-20]. But the vitamin D status of Chinese children is seldom investigated, especially in southeast China. Hangzhou, the capital of Zhejiang province is located in the southeast of China at northern latitude 30°. In the present study, we analyzed serum 25(OH)D levels of more than 6,000 Chinese children aged 1 month to 16 years in Hangzhou. These data would be important in drawing the policy to prevent vitamin D deficiency and improving the vitamin D status in Zhejiang province as well as all over China.

Methods

Survey and sample

Data collection took place between March 2008 and February 2011, throughout the year, during winter (December through February), spring (March through May), summer (June through August), and autumn (September through November). The children aged 1 month to 16 years who came to the child health care department of our hospital, the Children's Hospital affiliated to Zhejiang university school of medicine, for health examination were taken blood for 25(OH)D measurement. Children were excluded if they were diagnosed as rickets or hypocalcemia or had abnormal liver or renal function that might affect hydroxylation of vitamin D, calcium and phosphorus metabolism. Informed consent was obtained from all parents. This study was approved by the Children's Hospital institutional review board.

25-hydroxyvitamin D measurement

Circulating levels of 25-hydroxyvitamin D [25(OH)D] are considered to be the most reliable measure of overall vitamin D status[1]. In the present study, the serum 25(OH)D levels were measured by a direct enzyme-linked immunosorbent assay with the 25-Hydroxy Vitamin D Direct EIA kit purchased from Immunodiagnostic Systems Ltd. (Fountain Hills, Arizona, USA). This assay has been shown to reliably measure both 25-hydroxyvitamin D isoforms (D2 and D3) [21].

Statistical analyses

Mean serum levels of 25(OH)D were computed and campared between groups by using the 2-tailed t test or analysis of variance where appropriate. Differences were considered significant at P < 0.05. For purposes of analyses, the prevalence of vitamin D deficiency was based on the proposed definition of < 50 nmol/L, and cutoff values of < 25 nmol/L and < 75 nmol/L were used to describe overt vitamin D deficiency and insufficiency, respectively. Statistical analyses were performed by using the program package SPSS 13.0.

Results

Participant characteristics

A total of 6,008 children aged 1 month to 16 years participated in this cross-sectional study. All the participants were divided into four stages according to their ages: 0-1y stage, 2-5y stage, 6-11y stage and 12-16y stage representing infancy, preschool, school age and adolescence stages respectively. The characteristics of the participants were shown in Table 1.

Table 1.

Characteristics of study sample and distribution of serum 25 (OH) D

Mean+/-
SD(nmol/L)
Pvalue < 25 nmol/L,% (95%CI) < 50 nmol/L,% (95%CI) < 75 nmol/L,% (95%CI)
0-1y stage (infancy)

Total (n = 2116) 98.7 ± 47.1 0.4 (NC) 5.4 (4.4-6.4) 33.6 (31.6-35.6)

Gender 0.763

Male (n = 1221) 98.5 ± 47.0 0.4 (NC) 5.3 (4.0-6.6) 34.3 (31.6-37.0)

Female (n = 895) 99.1 ± 47.2 0.3 (NC) 5.5 (4.0-7.0) 32.7 (29.6-35.8)

2-5y stage (preschool)

Total (n = 2269) 69.6 ± 30.4 1.1 (NC) 21.9 (20.2-23.6) 68.6 (66.7-70.5)

Gender 0.108

Male (n = 1454) 70.4 ± 31.4 1.2 (NC) 20.8 (18.7-22.9) 67.7 (65.3-70.1)

Female (n = 815) 68.2 ± 28.6 1.1 (NC) 24.0 (21-27) 70.1 (67.0-73.2)

6-11y stage (school age)

Total (n = 1440) 56.1 ± 19.9 2.0 (NC) 40.4 (37.9-42.9) 88.3 (86.6-90.0)

Gender 0.969

Male (n = 1019) 56.1 ± 18.7 1.6 (NC) 39.1 (36.1-42.1) 88.8 (86.9-90.7)

Female (n = 421) 56.1 ± 22.6 3.1 (NC) 43.7 (39.0-48.4) 86.9 (83.7-90.1)

12-16y stage(adolescence)

Total (n = 183) 52.1 ± 17.0 3.3 (NC) 46.4 (39.2-53.6) 89.6 (85.2-94.0)

Gender 0.051

Male (n = 135) 53.5 ± 17.0 2.2 (NC) 44.4 (36-52.8) 88.1 (82.6-93.6)

Female (n = 48) 48.0 ± 16.6 6.3 (NC) 52.1 (38-66.2) 93.8 (87.6-100)

CI indicates confidence intervals and NC indicates not calculable (n < 30 observations).

Serum 25-hydroxyvitamin D levels and prevalence of low vitamin D status

The mean serum 25(OH)D levels of those children aged 1 month to 16 years decreased while their ages increased. The mean serum 25(OH)D level was the highest (98.7 nmol/L) among infancy and decreased sharply among preschoolers (69.6 nmol/L) and school children (56.1 nmol/L), then reached the lowest among adolescents (52.1 nmol/L) (Table 1).

Accordingly the prevalence of 25(OH)D levels at < 75 nmol/L, < 50 nmol/L and < 25 nmol/L increased while the children got older. More than 1 of every 5 preschoolers and over 40% of school children and adolescents (40.4% and 46.4%, respectively) had 25(OH)D levels of < 50 nmol/L. If the threshold is changed to < 75 nmol/L, almost all children aged 6-16 years had low levels (88.3% among school children and 89.6% among adolescents) and most children aged 2-5 years did as well (68.6%) (Table 1).

No significant differences were found between the mean serum 25(OH)D level of boys and that of girls at any stage. But the mean serum 25(OH)D level among adolescent girls was lower than that of boys, P = 0.05 (Table 1).

Serum 25-hydroxyvitamin D levels changed in different seasons

The mean levels of serum 25(OH)D changed according to seasons. Among school age children and adolescents, the levels of 25(OH)D gradually increased in the order of winter, spring, summer and autumn (from 49 nmol/L to 61.1 nmol/L among school age children and from 38.6 nmol/L to 56.9 nmol/L among adolescents) (Figure 1). Accordingly, the prevalence of 25(OH)D levels at < 75 nmol/L and < 50 nmol/L decreased gradually from winter to autumn among those older children. In winter and spring, more than 50% percent of school age children and adolescents had a 25(OH)D level at < 50 nmol/L (Figure 2). If the threshold is changed to < 75 nmol/L, all of the adolescents (100%) had low 25(OH)D levels in winter and 93.7% school age children as well. Even in autumn, there were still more than 80% of older children had a 25(OH)D level at < 75 nmol/L (Figure 3). But among young children, the levels of 25(OH)D in winter were much higher than in spring, and the prevalence of 25(OH)D levels at < 75 nmol/L and < 50 nmol/L in winter were much lower than that in spring (Figures 2 and 3).

Figure 1.

Figure 1

The mean serum 25(OH) D level changed according to seasons at each stage. *, P < 0.001 when compared with all other seasons at the same stage. ●, P < 0.05 when compared with spring and autumn at the same stage, ▲, P < 0.001 when compared with summer and autumn at the same stage.

Figure 2.

Figure 2

Prevalence of 25(OH)D level at < 50 nmol/L according to seasons at each stage.

Figure 3.

Figure 3

Prevalence of 25(OH)D level at < 75 nmol/L according to seasons at each stage.

Discussion

The present study is the first one to investigate vitamin D status among the pediatric population in Hangzhou, Zhejiang province, the southeast China. Our data demonstrate that the serum 25-hydroxyvitamin D levels among pediatric population decreased when the children became older, and the prevalence of vitamin D deficiency increased at the same time. The mean level of 25(OH) D among infants was much higher than that of any other stages. This is mainly because of the recommendation by the Pediatric Branch of Chinese Medical Association that all children receive 400 IU/day of vitamin D from two weeks after born until they are 2 years old[22]. According to this recommendation, many of the children's health care providers will give parents advices about taking vitamin D supplementation in children's first two years of life. And there are many kinds of oral supplementations containing vitamins D and A for infants, made in aqua or oil drops and can be purchased in pharmacies in Hangzhou. So the parents are easy to get these kinds of supplementations for their infants. Furthermore the parents may will provide vitamin D fortified formula to their young children especially younger than 2 years according to the feeding recommendations for infants and toddlers [23].

But as to the children older than 2 years, we don't have any formal recommendations on vitamin D supplementations. Fewer and fewer children take vitamin D supplements when they grow older than 2 years. This may be one of the causes of the finding in the present study that the mean serum 25(OH)D levels of the children aged 2-16 years were much lower than that of infants, and the prevalence of vitamin D deficiency among children older than 2 years was much higher than that of infants.

When compared with American children, our children had much higher prevalence of vitamin D level at < 50 nmol/L in most of stages, 2-5 years (22% vs 14%), 6-11 years (40% vs 20%) [17] and adolescents (46% vs 28.8%)[24], although the prevalence of 25(OH)D < 25 nmol/L among our children was similar to that of American children. If the threshold is changed to < 75 nmol/L, almost all children aged 6-16 years had low levels (88.3% among children aged 6-11 years and 89.6% among adolescents) and most children aged 2-5 years did as well (68.6%).

Hangzhou is located in the southeast of China at northern latitude 30°. The solar exposure in Hangzhou is more ample than in northern areas. It is reported that the prevalence of vitamin D deficiency among adolescent girls in Beijing was 89% [25], much higher than that of our adolescent girls (52%). In Shanxi province, another northern area of China, the prevalence of 25(OH)D level < 50 nmol/L among children aged 12-24 months was 84.3% in spring and 8.1% in autumn[26,27], much higher than that of our infants (7.7% in spring and 3.4% in autumn).

Given the concerns for vitamin D deficiency in older children and adolescents, in November 2008 the American Academy of Pediatrics released a new recommendation that all children receive 400 IU/day of vitamin D from their first days of life through adolescence [28]. So we suggest that the recommendation on vitamin D supplementation for Chinese pediatric population should be revised to include older children and adolescents now that the low 25(OH)D status of Chinese children are more severe than that of American children.

In the present study, we also analyzed the vitamin D status in different seasons. We found that the mean levels of serum 25(OH)D among children aged 6-16 years changed according to seasons. The levels were very low in winter, increased gradually in spring and summer, and reached the peaks in autumn. This tendency was similar to that of American adolescents [24]. But there were strange findings in our study, that the mean serum 25(OH)D levels among children aged 0-5 years in winter were as high as that in summer or autumn and significantly higher than that in spring. The possible reason is that the vitamin D supplementation for young children may be emphasized in winter when the sunlight is weak and the children will be dressed in many layers when they go outdoors. We did not find any significant differences between boys and girls at any stage. But the mean serum 25(OH)D level among adolescent girls was lower than that of boys, P = 0.05. This significant difference might be hidden by some reasons such as the uneven distribution of subjects between genders, now that it was reported that the serum 25(OH)D level was lower among American adolescent girls than that of boys[29]. The reason need to be explored in the future.

Although the subjects were not sampled from the whole pediatric population, they participated in the present study just for health examination with no medical status that might affect study results. Many of them took the examination before entered in kindergarten or school. Furthermore, the number of the sample was so large and the range of ages was also very big. So to some extent, the sample could represent the pediatric population of Hangzhou.

But there are still some limitations in the present study. The subjects were not sampled from the whole pediatric population in Hangzhou, and other possible relating factors of vitamin D status including intake of supplements, children's BMI and the time of physical activities were not collected. A further study based on subjects sampled on a population basis would be carried out and the possible relating factors of vitamin D status should be investigated. Furthermore, the optimal vitamin D level among children should to be certificated by more studies, now that adequate amount of vitamin D in all human populations for sustaining both innate and acquired immunity against infection is very important [8]. While at the same time, some authors warned that the prevalence of vitamin D deficiency was over estimated and the evidence of the role of vitamin D for extraskeletal outcomes was inconsistent and inconclusive and need to be assessed by more randomized clinical trials [30,31].

Conclusions

The prevalence of vitamin D deficiency and insufficiency among children in Hangzhou Zhejiang province is high, especially among children aged 6-16 years. We suggest that the recommendation for vitamin D supplementation in Chinese children should be extended to adolescence.

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

ZwZ (the first author) and ZyZ (the corresponding author) were responsible for the conception and design of the study. LC carried out the 25-hydroxyvitamin D measurement. ZwZ and WC performed the data analysis and drafted the manuscript. All authors participated in interpretation of the findings. ZyZ and JS revised and commented on the draft and all authors read and approved the final manuscript. All authors confirm that none of the content in the paper has been published or is under consideration for publication elsewhere.

Pre-publication history

The pre-publication history for this paper can be accessed here:

http://www.biomedcentral.com/1471-2458/12/126/prepub

Contributor Information

Zhiwei Zhu, Email: zhuzhiwei@zju.edu.cn.

Jianying Zhan, Email: zhanjianying@zju.edu.cn.

Jie Shao, Email: shaojie@zju.edu.cn.

Weijun Chen, Email: chenwj0575@hotmail.cm.

Liqin Chen, Email: chebk@zju.edu.cn.

Wenhao Li, Email: liwenhao_117@163.com.

Chai Ji, Email: jichai735@hotmail.com.

Zhengyan Zhao, Email: zhaozy@zju.edu.cn.

Acknowledgements

The authors thank all participants and the parents who took part in this project. We would like to thank all of the staff at the child health care department where we conducted the research.

References

  1. Misra M, Pacaud D, Petryk A, Collett-Solberg PF, Kappy M. Vitamin D deficiency in children and its management: review of current knowledge and recommendations. Pediatrics. 2008;122:398–417. doi: 10.1542/peds.2007-1894. [DOI] [PubMed] [Google Scholar]
  2. Tangpricha V, Flanagan JN, Whitlatch LW, Tseng CC, Chen TC, Holt PR, Lipkin MS, Holick MF. 25-hydroxyvitamin D-1alpha-hydroxylase in normal and malignant colon tissue. Lancet. 2001;357:1673–1674. doi: 10.1016/S0140-6736(00)04831-5. [DOI] [PubMed] [Google Scholar]
  3. Grant WB. An ecologic study of dietary and solar ultraviolet-B links to breast carcinoma mortality rates. Cancer. 2002;94:272–281. doi: 10.1002/cncr.10196. [DOI] [PubMed] [Google Scholar]
  4. Hypponen E, Laara E, Reunanen A, Jarvelin MR, Virtanen SM. Intake of vitamin D and risk of type 1 diabetes: a birth-cohort study. Lancet. 2001;358:1500–1503. doi: 10.1016/S0140-6736(01)06580-1. [DOI] [PubMed] [Google Scholar]
  5. Munger KL, Levin LI, Hollis BW, Howard NS, Ascherio A. Serum 25-hydroxyvitamin D levels and risk of multiple sclerosis. JAMA. 2006;296:2832–2838. doi: 10.1001/jama.296.23.2832. [DOI] [PubMed] [Google Scholar]
  6. Ginde AA, Mansbach JM, Camargo CA Jr. Association between serum 25-hydroxyvitamin D level and upper respiratory tract infection in the Third National Health and Nutrition Examination Survey. Arch Intern Med. 2009;169:384–390. doi: 10.1001/archinternmed.2008.560. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Grant WB. Vitamin D supplementation could reduce risk of sepsis in infants. World J Pediatr. 2010;6:185. doi: 10.1007/s12519-010-0034-1. [DOI] [PubMed] [Google Scholar]
  8. Fabri M, Stenger S, Shin DM, Yuk JM, Liu PT, Realegeno S, Lee HM, Krutzik SR, Schenk M, Sieling PA, Teles R, Montoya D, Iyer SS, Bruns H, Lewinsohn DM, Hollis BW, Hewison M, Adams JS, Steinmeyer A, Zugel U, Cheng G, Jo EK, Bloom BR, Modlin RL. Vitamin D is required for IFN-{gamma}-mediated antimicrobial activity of human macrophages. Sci Transl Med. 2011;3:104–104. doi: 10.1126/scitranslmed.3003045. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Zittermann A. Vitamin D and disease prevention with special reference to cardiovascular disease. Prog Biophys Mol Biol. 2006;92:39–48. doi: 10.1016/j.pbiomolbio.2006.02.001. [DOI] [PubMed] [Google Scholar]
  10. Holick MF. High prevalence of vitamin D inadequacy and implications for health. Mayo Clin Proc. 2006;81:353–373. doi: 10.4065/81.3.353. [DOI] [PubMed] [Google Scholar]
  11. Bischoff-Ferrari HA, Giovannucci E, Willett WC, Dietrich T, Dawson-Hughes B. Estimation of optimal serum concentrations of 25-hydroxyvitamin D for multiple health outcomes. Am J Clin Nutr. 2006;84:18–28. doi: 10.1093/ajcn/84.1.18. [DOI] [PubMed] [Google Scholar]
  12. Hollis BW. Circulating 25-hydroxyvitamin D levels indicative of vitamin D sufficiency: implications for establishing a new effective dietary intake recommendation for vitamin D. J Nutr. 2005;135:317–322. doi: 10.1093/jn/135.2.317. [DOI] [PubMed] [Google Scholar]
  13. Greer FR. Vitamin D deficiency-it's more than rickets. J Pediatr. 2003;143:422–423. doi: 10.1067/S0022-3476(03)00465-7. [DOI] [PubMed] [Google Scholar]
  14. Holick MF. Vitamin D deficiency. N Engl J Med. 2007;357:266–281. doi: 10.1056/NEJMra070553. [DOI] [PubMed] [Google Scholar]
  15. Yetley EA. Assessing the vitamin D status of the US population. Am J Clin Nutr. 2008;88:558–564. doi: 10.1093/ajcn/88.2.558S. [DOI] [PubMed] [Google Scholar]
  16. Maalouf J, Nabulsi M, Vieth R, Kimball S, El-Rassi R, Mahfoud Z, El-Hajj Fuleihan G. Short- and long-term safety of weekly high-dose vitamin D3 supplementation in school children. J Clin Endocrinol Metab. 2008;93:2693–2701. doi: 10.1210/jc.2007-2530. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Mansbach JM, Ginde AA, Camargo CA Jr. Serum 25-hydroxyvitamin D levels among US children aged 1 to 11 years: do children need more vitamin D. Pediatrics. 2009;124:1404–1410. doi: 10.1542/peds.2008-2041. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Marwaha RK, Tandon N, Reddy DR, Aggarwal R, Singh R, Sawhney RC, Saluja B, Ganie MA, Singh S. Vitamin D and bone mineral density status of healthy schoolchildren in northern India. Am J Clin Nutr. 2005;82:477–482. doi: 10.1093/ajcn.82.2.477. [DOI] [PubMed] [Google Scholar]
  19. El-Hajj FG, Nabulsi M, Choucair M, Salamoun M, Hajj Shahine C, Kizirian A, Tannous R. Hypovitaminosis D in healthy schoolchildren. Pediatrics. 2001;107:53. doi: 10.1542/peds.107.4.e53. [DOI] [PubMed] [Google Scholar]
  20. McGrath JJ, Kimlin MG, Saha S, Eyles DW, Parisi AV. Vitamin D insufficiency in south-east Queensland. Med J Aust. 2001;174:150–151. doi: 10.5694/j.1326-5377.2001.tb143195.x. [DOI] [PubMed] [Google Scholar]
  21. Carter GD, Carter R, Jones J, Berry J. How accurate are assays for 25-hydroxyvitamin D? Data from the international vitamin D external quality assessment scheme. Clin Chem. 2004;50:2195–2197. doi: 10.1373/clinchem.2004.040683. [DOI] [PubMed] [Google Scholar]
  22. Editorial Committee of Zhonghua Er Ke Za Zhi; Child Health Group of Chinese Academy of Pediatrics; National Scientific Group of Prevention and Cure of Rickets. Recommendation for prevention and treatment of rickets of vitamin D deficiency in childhood. Zhonghua Er Ke Za Zhi. 2008;46:190–191. (in Chinese) [PubMed] [Google Scholar]
  23. Editorial Committee of Zhonghua Er Ke Za Zhi; Child Health Group of Chinese Academy of Pediatrics. Feeding recommendations for infants and toddlers. Zhonghua Er Ke Za Zhi. 2009;47:504–507. (in Chinese) [PubMed] [Google Scholar]
  24. Dong Y, Pollock N, Stallmann-Jorgensen IS, Gutin B, Lan L, Chen TC, Keeton D, Petty K, Holick MF, Zhu H. Low 25-hydroxyvitamin D levels in adolescents: race, season, adiposity, physical activity, and fitness. Pediatrics. 2010;125:1104–1111. doi: 10.1542/peds.2009-2055. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Foo LH, Zhang Q, Zhu K, Ma G, Trube A, Greenfield H, Fraser DR. Relationship between vitamin D status, body composition and physical exercise of adolescent girls in Beijing. Osteoporos Int. 2009;20:417–425. doi: 10.1007/s00198-008-0667-2. [DOI] [PubMed] [Google Scholar]
  26. Strand MA, Perry J, Jin M, Tracer DP, Fischer PR, Zhang P, Xi W, Li S. Diagnosis of rickets and reassessment of prevalence among rural children in northern China. Pediatr Int. 2007;49:202–209. doi: 10.1111/j.1442-200X.2007.02343.x. [DOI] [PubMed] [Google Scholar]
  27. Strand MA, Perry J, Zhao J, Fischer PR, Yang J, Li S. Severe vitamin D-deficiency and the health of North China children. Matern Child Health J. 2009;13:144–150. doi: 10.1007/s10995-007-0250-z. [DOI] [PubMed] [Google Scholar]
  28. Wagner CL, Greer FR. Prevention of rickets and vitamin D deficiency in infants, children, and adolescents. Pediatrics. 2008;122:1142–1152. doi: 10.1542/peds.2008-1862. [DOI] [PubMed] [Google Scholar]
  29. Saintonge S, Bang H, Gerber LM. Implications of a new definition of vitamin D deficiency in a multiracial us adolescent population: the National Health and Nutrition Examination Survey III. Pediatrics. 2009;123:797–803. doi: 10.1542/peds.2008-1195. [DOI] [PubMed] [Google Scholar]
  30. Ross AC, Manson JE, Abrams SA, Aloia JF, Brannon PM, Clinton SK, Durazo-Arvizu RA, Gallagher JC, Gallo RL, Jones G, Kovacs CS, Mayne ST, Rosen CJ, Shapses SA. The 2011 report on dietary reference intakes for calcium and vitamin D from the Institute of Medicine: what clinicians need to know. J Clin Endocrinol Metab. 2011;96:53–58. doi: 10.1210/jc.2010-2704. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Chung M, Balk EM, Brendel M, Ip S, Lau J, Lee J, Lichtenstein A, Patel K, Raman G, Tatsioni A, Terasawa T, Trikalinos TA. Vitamin D and calcium: a systematic review of health outcomes. Evid Rep Technol Assess (Full Rep) 2009;183:1–420. [PMC free article] [PubMed] [Google Scholar]

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