Vitamin D status among residents of Molidawa Daur Autonomous Banner, Inner Mongolia, North China ================================================================================================ * Jingwen Hu * Yunmei Liang * Guiping Wen * Dezhong Chen * Yuanjing Liu * Hongmei Zhang * Xiaosong Qin ## Abstract **Objectives:** To retrospectively analyze the vitamin D (VD) status of residents in northeastern Inner Mongolia and its relationship with the average monthly sunshine hours. **Methods:** Serum 25-hydroxyvitamin D[s-25(OH)D] samples from 4982 outpatients (2092 males) in Moli Dawa Daur Autonomous Banner People’s Hospital, Hulunbuir, China from July 2018 to January 2022 were included in this study. **Results:** The overall median s-25(OH)D was 53.3 nmol/L, VD deficiency (<30 nmol/L), deficiency (30-50 nmol/L), sufficient (>50-250 nmol/L) and excess (>250 nmol/L) were 16% (796/4982), 30% (1495/4982), 53.4% (2658/4982) and 0.7% (33/4982). There were statistically significant differences in median s-25(OH)D by month, age-groups and gender (*p*<0.001). Low VD status (LVDS, including VD deficiency and insufficiency) in females was 54.6% and males was 33.9%, and the LVDS composition differed significantly by age-group and month (*p*<0.05). The changing trend of the median s-25(OH)D level was similar to the monthly average sunshine hours, with a slight lag. **Conclusion:** Nearly half of residents live in LVDS. LVDS is affected by month, gender, and age. Keywords: * vitamin D * vitamin D deficiency * age groups * gender * Inner Mongolia **V**itamin D (VD) is a liposoluble essential vitamin that regulates bone metabolism and the homeostasis of calcium and phosphorus in the body. Vitamin D deficiency can lead to osteoporosis in adults and rickets in children.1 Vitamin D is obtained by a combination of dietary pathways (10-20%) and dermal synthesis under the influence of solar ultraviolet B (UVB) sunlight (80–90%).1 The amount and quality of sunlight reaching the terrestrial surface is impacted by season and latitude, particularly in the UVB area of the spectrum.2,3 According to one study, even when exposed to clear sunlight, no pre-vitamin D is created from November through February (in Boston, MA, USA; 42.2°N).4 This ineffectual solar exposure lasts from October to March at higher latitudes, such as 52°N, whereas VD can be generated in the middle of winter at a latitude of 34°N.4 Furthermore, lifestyle, gender, and age may all have a role in VD status. An estimated one billion people worldwide have inadequate VD levels, and poor VD status continues to be a global public health concern.5 China, as a large country, has a wide latitude range, ranging from tropical and subtropical regions in the south to chilly temperate zones in the north. The incidence of low VD status (LVDS, including VD deficiency and insufficiency) varies substantially with differences in geographic location, dietary choice, and economic development between urban and rural areas.6 Owing to the popularization of children’s health education in China, the LVDS risk among young children and infants has been effectively improved.7 However, the issue of excessive VD in children, and LVDS in adolescents, adults, and elders hardly attracted attention. Molidawa Daur Autonomous Banner is an ethnic minority township in Inner Mongolia, north China, located at high latitude (48.48°N). Locally, adolescents with abnormal spinal development and adults with skeletal deformities of lower extremities are common. Serum 25-hydroxy-vitamin D [s-25(OH)D] is the most common circulating form of VD in the blood and is largely considered the greatest biomarker of VD status.8,9 Based on local single-center s-25(OH)D data, this study investigated the effects of age, gender, and month on the status of VD in Molidawa Daur Autonomous Banner. Our results provide a theoretical basis for local prevention and control of LVDS and avoidance of VD overdose. ## Methods We analyzed retrospective cross-sectional data on the local status of VD. In this study, 4982 blood samples (2092 males) were collected from outpatients aged 0–82 years in the Molidawa Daur Autonomous Banner People’s Hospital who voluntarily visited the hospital during the period from July 2018 to January 2022. The s-25(OH)D data were divided into 4 grades (deficiency, insufficiency, adequacy, and excess), 7 groups by age (0-3, 4-6, 7-11, 12-17, 18-30, 31-50, and 51-82 years old), 2 groups by gender (male and female), and 12 groups by month (from January to December). Ages 0-3, 4-6, 7-11, 12-17, 18-30, 31-50, and 51-82 years were early-stage childhood, late-stage childhood, early-stage adolescence, late-stage adolescence, early-stage adulthood, late-stage adulthood, and elders, respectively. Minors were those under the age of 18. Relationships between the levels of s-25(OH)D levels, age group, gender, and month, as well as the relationship between median monthly s-25(OH)D level and monthly sunshine hours (h) were analyzed. Incomplete data (for example, missing a full date of birth or gender) were excluded from the final analysis. Our research was approved by the local Ethics Committee of Molidawa Daur Autonomous Banner People’s Hospital. All participants were calm and fasting when blood samples were taken in the morning. Blood was drawn from the anterior elbow vein into serum tubes and centrifuged at 3000 rpm for 5 minutes (min) at ambient temperature. The s-25(OH)D levels were determined within 8 hours after blood isolation by electrochemiluminescence using a Roche Diagnostics Modular Cobas e411 device (Roche Diagnostics, Mannheim, Germany) at Molidawa Daur Autonomous Banner People’s Hospital, Inner Mongolia, China. There is still no agreement on the cut-off values of s-25(OH)D to set the VD status. We stratified all the participants using the generally accepted thresholds for VD deficiency (s-25(OH)D <30 nmol/L), insufficiency (s-25(OH)D 30-50 nmol/L), adequacy (s-25(OH)D >50–250 nmol/L), and excess (s-25(OH)D >250 nmol/L).10-12 The LVDS is referred to as s-25(OH)D ≤50 nmol/L.10 ### Statistical analysis All data were analyzed with the Statistical Package fot the Social Sicences for windows, version 22.0 (IBM Corporation, Armonk, NY, USA). Data have been split into separate groups according to the various hypothetical predictors for the VD level as mentioned earlier. The normality of the distribution of all continuous variables was verified through the Kolmogorov–Smirnov test. Continuous variables were depicted with the median because they were inconsistent with the normal distribution. Categorical variables were presented in terms of percentages (%). Group rates were compared through a nonparametric assay. If a comparison was made between 2 independent samples were compared, the Mann–Whitney U test was adopted; if the number of independent samples was greater than 2, the Kruskal–Wallis H test was applicable. If the frequency was <5 or the cases were fewer than 40, Fisher’s exact test was properly utilized. Two-sided *p*-values of <0.05 were applied to determine if the difference was statistically significant. ## Results ### S-25(OH)D levels in Molidawa Daur Autonomous Banner The median level of s-25(OH)D in 4982 samples in this study was 53.3 nmol/L; the difference between genders was statistically significant (*p*<0.001). Refer to Table 1 for more information. View this table: [Table 1](http://smj.org.sa/content/44/4/413/T1) Table 1 - Effect of gender on serum vitamin D level of residents in Molidawa Daur Autonomous Banner. Median levels of s-25(OH)D levels among children aged 0-3 years (98.2 nmol/L) and 4-6 years (59 nmol/L) exceeded 50 nmol/L. The median s-25 (OH)D level was less than 50 nmol/L for individuals 7 years and older. Among them, the early-stage adulthood group (aged 18-30 years) had the lowest median level of s-25(OH)D (36.2 nmol/L). A statistically significant difference in the median s-25(OH)D was observed between the various age groups (*p*<0.001). The difference was statistically significant in VD status among minors, adults, and elders (*p*<0.001), being worst for adults and best for minors. See Table 2 for details. View this table: [Table 2](http://smj.org.sa/content/44/4/413/T2) Table 2 - Effect of age on serum vitamin D level of residents in Molidawa Daur Autonomous Banner. The median s-25(OH)D levels of residents did not reach 50 nmol/L from January to May. The median s-25(OH)D level was lowest in February (39.7 nmol/L), began to rise in June, peaked in September (66.3 nmol/L), and then began to decline. There was a statistical difference in the median levels of s-25(OH)D among different months (*p*<0.001). See Table 3 for additional information. View this table: [Table 3](http://smj.org.sa/content/44/4/413/T3) Table 3 - Effect of month on serum vitamin D level of residents in Molidawa Daur Autonomous Banner. According to the government work report of the weather bureau in Molidawa Daur Autonomous Banner, the average monthly sunshine hours from 2018 to 2021 ranged from 174.2 h in November to 273.2 h in April. Trends in median levels of s-25(OH)D were similar across age groups from January to December (Figure 1). ![Figure 1](http://smj.org.sa/https://smj.org.sa/content/smj/44/4/413/F1.medium.gif) [Figure 1](http://smj.org.sa/content/44/4/413/F1) Figure 1 - Relationship between monthly serum vitamin D level median and monthly sunshine hours. ### The status of VD deficiency, insufficiency, adequacy, or excess in Molidawa Daur Autonomous Banner As a whole, LVDS accounted for 46% of local residents, and VD excess accounted for 0.7%. The composition of LVDS varied in different age groups. The proportion of LVDS varied by age group, with the lowest in early childhood, in children aged 0-3 years (9.2%), and the highest in late-stage adolescents aged 12-17 years (78.3%) and early-stage adults aged 18-30 years (78.8%). The proportion of LVDS was 35.1% in minors, 76.2% in adults, and 63% in elders. Vitamin D excess occurred in early-stage childhood, late-stage childhood, early-stage adolescents, and late-stage adults, with proportions of 1.6%, 0.9%, 0.2%, and 0.2%, respectively. The percentages of LVDS in females was 54.6% and males was 33.9%, and the VD excess percentage was 0.8% for female and 0.5% for male. The LVDS composition of different genders significantly differed in different age groups (Table 4). The proportion of LVDS varied by month, with the highest in February (65.9%) and the lowest in August (26.7%) and September (28.3%). Vitamin D excess occurred from January to November, with proportions of 0.5%, 1.1%, 0.7%, 1.4%, 0.9%, 0.2%, 0.6%, 0.5%, 0.8%, 1.2%, and 0.4%, respectively. Except for January and February, the LVDS composition for different genders significantly differed in different months (*p*<0.001) (Table 5). View this table: [Table 4](http://smj.org.sa/content/44/4/413/T4) Table 4 - Serum vitamin D status varies by gender in different age groups. View this table: [Table 5](http://smj.org.sa/content/44/4/413/T5) Table 5 - Serum vitamin D status varies by gender in different months. ## Discussion Low VD status is strongly associated with osteomalacia, bone loss and fractures, including pediatric nutritional rickets, osteoporosis and osteomalacia in adults, and hip fractures in elders, and remains prevalent in both developing and developed countries.9,13,14 Although there is no uniform standard for the optimal level of VD in the human body, it is generally accepted that concentrations of s-25(OH)D levels under 30 nmol/L raise the risk of osteoporosis or rickets, and that in the range of 50 to 250 nmol/L appears to be secure and sufficient in the overall population for the health of the skeletal health.11 This retrospective analysis showed that nearly half of the residents of the Molidawa Daur Autonomous Banner were in LVDS according to the above criteria. The VD status of minors was better than that of adults and elders. Similar to the results of a Korean study, adults were the group at highest risk for LVDS.15 As society ages, bone health issues in adults and elders deserve more attention. The data suggested that median s-25(OH)D levels were best in early-stage childhood, lower in late-stage childhood and early-stage adolescence, lowest in late-stage adolescence and adulthood, and slightly improved in elders. These data confirmed that the median s-25(OH)D levels were closely related to age and similar to previous findings (in the US, UK and Germany).16 The incidence of LVDS was highest among late-stage adolescents and early-stage adulthood in the Molidawa Daur Autonomous Banner, China. This is similar to situation in Europe, the Duhok area in Iraq, and Sichuan, China.16-18 Compared with previous studies in northern China at a similar latitude (44.04-46.40°N), minors in the Molidawa Daur Autonomous Banner had similar levels of s-25(OH)D and age-related patterns among minors in Heilongjiang Province, but a lower percentage of LVDS, which was related to different criteria for diagnosing LVDS.7 Compared with residents in Sichuan Province (26.03–34.19 °N) in China and in Greece (39.07 °N), adults in Molidawa Daur Autonomous Region had lower s-25(OH)D levels.18,19 Why this difference can be related to the hours of sunshine or solar UVB radiation in the three regions. The major source of VD for humans is dermal synthesis. Ultraviolet B-rich sunlight is a critical environmental factor in the dermal transformation of VD.7 The sunlight exposure time (sunshine hours) is a measure of the amount of UVB that varies by season and geographic location (latitude).16 The geographic location (latitude) and season can therefore affect people’s VD status.20 The synthesis of VD in the skin is not considered to be effective in regions above 35°N latitude (including Poland; 49–54°N latitude).21 However, it has been reported that dermal VD can be produced at high latitudes of 70°N.22 Molidawa Daur Autonomous Banner had the most sunshine hours in April (late spring) and the least sunshine hours in November (early winter). The median s-25(OH)D levels were at LVDS levels from January to May (late winter and early summer), lowest in February (early spring), began to climb in June (summer), and peaked in August–September (autumn), slightly decreasing from October–December (winter), to a moderate state. The percentage of residents with LVDS was highest in February and lowest in August–September. These data suggest that the VD status of residents in the Molidawa Daur Autonomous Banner (48.48°N) is influenced by month and solar UVB light exposure. Trends in median s-25(OH)D levels and monthly sunshine hours were similar, but with a lag. This lag was more pronounced than in a European study.23 The reason for this lag is related to 2 factors, one being the local temperature change and the other the physiological process of VD synthesis in the skin.24 Although there are more sunshine hours from March to June each year, the average temperature from January to May was below 15°C, and the area of skin exposed to the solar UVB light was far less than that from June to September. This shows that the month of the year can change people’s lifestyle through temperature fluctuations, which in turn affects the production of VD from solar UVB light. The physiological input of VD comes either from food or from endogenous synthesis of the skin exposed to UVB rays, but the primary source of VD is from its photochemical synthesis in skin through the action of solar UVB rays.21 The intake of VD in food as a natural nutrient is incapable of maintaining a good vitamin D condition. In regions where the solar UVB light is insufficient, supplementing VD has become an important complementary means of correcting LVDS. The accumulation of VD supply through skin exposure to solar UVB light rarely causes hypervitaminosis D, whereas excessive intake of VD is potentially toxic.24,25 Currently, the dose of VD supplementation in LVDS patients varies from region to region.26,27 With the usage of VD supplementation, incidents of VDI (VDI: also called VD toxicity or hypervitaminosis D) are inevitable.28 VDI is uncommon, but early diagnosis is required to avoid severe acute and long-term complications, such as hypercalcemia, hypercalciuria, nephrocalcification, nephrolithiasis and renal dysfunction, and even mortal situations.29,30 Events of VDI can occur in every age group.31-33 However, the VDI criterion for s-25(OH)D is controversial.26,32,34 In this report, the therapeutic dose of VD supplementation in Molidawa Daur Autonomous Banner was 2,000 IU/day (50 µg) for 3 months, and s-25(OH)D > 250nmol/L was identified as VDI.25,35 Our data showed that individuals with s-25(OH)D levels above 250 nmol/L were found among minors below 11 years old and adults aged 31-50. The incidence was higher in minors than in adults (one case), and the highest incidence was in young children. Except for December, there were cases of children with s-25(OH)D levels exceeding 250 nmol/L every month. Although VD excess rates were highest in April, there was no regularity. This result indicated that the s-25(OH)D >250 nmol/L status of local residents was not caused by month (season), but was caused by excessive intake of VD supplementation, and confirmed that the dose of 2000 IU/day of VD supplementation for a 3-month course was relatively excessive for children, especially young children.36 Therefore, in the treatment of LVDS, factors such as month and age should be considered, and s-25(OH)D should be supervised to avoid the occurrence of VDI. Gender is a notable factor affecting VD status.20 The data in this report show that, overall, the median s-25(OH)D in females was considerably lower than that in males, and females had significantly higher percentages of LVDS. This conclusion is consistent with research findings in many regions.9,17 These data also showed that VD status in early childhood was not affected by gender and was similar to that of Greek counterparts.37 Vitamin D status in late-stage children and adolescents was influenced by gender, which differed from the findings of European and Greek counterparts.9,37 These differences in VD status are thought to be related to supplemental VD intake and lifestyle (outdoor activities). When compared with other age groups, the median s-25(OH)D in early-stage childhood was higher, and the seasonal variation was not obvious. This may be caused by the intake of VD supplementation in early-stage childhood under the guidance of local doctors in accordance with the “Practice Guidelines for Clinical Issues Related to Vitamin D Nutrition in Children in China”, which attenuated the effect of gender factors on VD status.38 In addition, outdoor activities in early-stage childhood are rarely influenced by gender. These data also showed that the VD status in early-stage adulthood (aged 18-30) was also not affected by gender, which is consistent with the view of Romanian researchers.39 This may be related to the exuberance of female hormones in early-stage adulthood.40 However, it may also be related to the bias caused by the unbalanced sample size of males and females. At the same time, it was also shown that the VD status of residents was not affected by gender in January-February. This may be related to changes in people’s lifestyles caused by changes in temperature. Given that January–February is the coldest season in north China (the local temperature fluctuates around -30°C), whether male or female, residents of any age group undertake significantly less outdoor activity, and they wear more clothes during outdoor activities. Their skin is barely exposed to UVB light. In conclusion, nearly half of residents live in LVDS. Low VD status is affected by month, gender, and age. median s-25(OH)D levels were best in early-stage childhood, lower in late-stage childhood and early-stage adolescence, lowest in late-stage adolescence and adulthood, and slightly improved in elders. The median s-25(OH)D levels were at LVDS levels from January to May (late winter and early summer), lowest in February (early spring), began to climb in June (summer), and peaked in August–September (autumn), slightly decreasing from October–December (winter), the median s-25(OH)D in females was considerably lower than that in males, and females had significantly higher percentages of LVDS. The disadvantage of this study was that, in addition to age, gender, and month (season), factors such as smoking, genetics, physiological status, obesity, skin color, and the use of cosmetics also affect VD synthesis, but this report did not carried relevant analysis. ## Acknowledgment *The authors gratefully acknowledge International Science Editing Services for the English language editing.* ## Footnotes * **Disclosure.** Authors have no conflict of interests, and the work was not supported or funded by any drug company. * Received November 4, 2022. * Accepted February 16, 2023. * Copyright: © Saudi Medical Journal This is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work. ## References 1. 1.Norman AW. From vitamin D to hormone D: fundamentals of the vitamin D endocrine system essential for good health. Am J Clin Nutr 2008; 88: 491s–499s. 2. 2.Kimlin MG. Geographic location and vitamin D synthesis. Mol Aspects Med 2008; 29: 453–461. [CrossRef](http://smj.org.sa/lookup/external-ref?access_num=10.1016/j.mam.2008.08.005&link_type=DOI) [PubMed](http://smj.org.sa/lookup/external-ref?access_num=18786559&link_type=MED&atom=%2Fsmj%2F44%2F4%2F413.atom) [Web of Science](http://smj.org.sa/lookup/external-ref?access_num=000261915900011&link_type=ISI) 3. 3.Wang LK, Hung KC, Lin YT, Chang YJ, Wu ZF, Ho CH, et al. Age, gender and season are good predictors of vitamin D status independent of body mass index in office workers in a subtropical region. Nutrients 2020; 12; 2719. 4. 4.Webb AR, Kline L, Holick MF. Influence of season and latitude on the cutaneous synthesis of vitamin D3: exposure to winter sunlight in Boston and Edmonton will not promote vitamin D3 synthesis in human skin. J Clin Endocrinol Metab 1988; 67: 373–378. [CrossRef](http://smj.org.sa/lookup/external-ref?access_num=10.1210/jcem-67-2-373&link_type=DOI) [PubMed](http://smj.org.sa/lookup/external-ref?access_num=2839537&link_type=MED&atom=%2Fsmj%2F44%2F4%2F413.atom) [Web of Science](http://smj.org.sa/lookup/external-ref?access_num=A1988P288700024&link_type=ISI) 5. 5.Palacios C, Gonzalez L. Is vitamin D deficiency a major global public health problem? J Steroid Biochem Mol Biol 2014; 144: 138–145. [CrossRef](http://smj.org.sa/lookup/external-ref?access_num=10.1016/j.jsbmb.2013.11.003&link_type=DOI) [PubMed](http://smj.org.sa/lookup/external-ref?access_num=24239505&link_type=MED&atom=%2Fsmj%2F44%2F4%2F413.atom) 6. 6.Liu W, Hu J, Fang Y, Wang P, Lu Y, Shen N. Vitamin D status in Mainland of China: A systematic review and meta-analysis. EClinicalMedicine 2021; 38: 101017. 7. 7.Zhang X, Chen Y, Jin S, Bi X, Chen D, Zhang D, et al. Association of serum 25-Hydroxyvitamin D with Vitamin D intervention and outdoor activity among children in North China: an observational study. BMC Pediatr 2020; 20: 542. 8. 8.Giustina A, Adler RA, Binkley N, Bollerslev J, Bouillon R, Dawson-Hughes B, et al. Consensus statement from 2nd International Conference on Controversies in Vitamin D. Rev Endocr Metab Disord 2020; 21: 89–116. [CrossRef](http://smj.org.sa/lookup/external-ref?access_num=10.1007/s11154-019-09532-w&link_type=DOI) [PubMed](http://smj.org.sa/lookup/external-ref?access_num=http://www.n&link_type=MED&atom=%2Fsmj%2F44%2F4%2F413.atom) 9. 9.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: 564–573. 10. 10.Amrein K, Scherkl M, Hoffmann M, Neuwersch-Sommeregger S, Köstenberger M, Tmava Berisha A, et al. Vitamin D deficiency 2.0: an update on the current status worldwide. Eur J Clin Nutr 2020; 74: 1498–1513. [CrossRef](http://smj.org.sa/lookup/external-ref?access_num=10.1038/s41430-020-0558-y&link_type=DOI) [PubMed](http://smj.org.sa/lookup/external-ref?access_num=http://www.n&link_type=MED&atom=%2Fsmj%2F44%2F4%2F413.atom) 11. 11.Gupta P, Dabas A, Seth A, Bhatia VL, Khadgawat R, Kumar P, et al. Indian Academy of Pediatrics revised (2021) guidelines on prevention and treatment of vitamin D deficiency and rickets. Indian Pediatr 2022; 59: 142–58. 12. 12.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. Endocrine reviews. 2019; 40: 1109–51. [PubMed](http://smj.org.sa/lookup/external-ref?access_num=http://www.n&link_type=MED&atom=%2Fsmj%2F44%2F4%2F413.atom) 13. 13.Bouillon R, Antonio L, Olarte OR. Calcifediol (25OH Vitamin D3) deficiency: a risk factor from early to old age. Nutrients 2022; 14; 1168. 14. 14.Oshiro CE, Hillier TA, Edmonds G, Peterson M, Hill PL, Hampson S. Vitamin D deficiency and insufficiency in Hawaii: Levels and sources of serum vitamin D in older adults. Am J Hum Biol 2022; 34: e23636. 15. 15.Choi R, Cho SE, Lee SG, Lee EH. Recent Information on Vitamin D Deficiency in an Adult Korean Population Visiting Local Clinics and Hospitals. Nutrients 2022; 14; 1978. 16. 16.Cashman KD. Vitamin D deficiency: defining, prevalence, causes, and strategies of addressing. Calcif Tissue Int 2020; 106: 14–29. [CrossRef](http://smj.org.sa/lookup/external-ref?access_num=10.1007/s00223-019-00559-4&link_type=DOI) 17. 17.Abdulrahman MA, Alkass SY, Mohammed NI. Total and free vitamin D status among apparently healthy adults living in Duhok Governorate. Sci Rep 2022; 12: 1778. 18. 18.Li L, Li K, Li J, Luo Y, Cheng Y, Jian M, et al. Ethnic, geographic, and seasonal differences of vitamin D status among adults in south-west China. J Clin Lab Anal 2020; 34: e23532. 19. 19.Bouloukaki I, Markakis M, Pateli R, Lyronis I, Schiza S, Tsiligianni I. Vitamin D levels in primary care patients: correlations with clinical, seasonal, and quality-of-life parameters. Fam Pract 2022; 39: 678–684. 20. 20.Karacan M, Usta A, Biçer S, Baktir G, İpek Gündogan G, Sancakli Usta C, et al. Serum vitamin D levels in healthy urban population at reproductive age: effects of age, gender and season. Cent Eur J Public Health 2020; 28: 306–312. 21. 21.Krzyścin JW, Guzikowski J, Rajewska-Więch B. Optimal vitamin D3 daily intake of 2000IU inferred from modeled solar exposure of ancestral humans in Northern Tanzania. J Photochem Photobiol B 2016; 159: 101–105. 22. 22.Andersen S, Jakobsen A, Laurberg P. Vitamin D status in North Greenland is influenced by diet and season: indicators of dermal 25-hydroxy vitamin D production north of the Arctic Circle. Br J Nutr 2013; 110: 50–57. 23. 23.O’Neill CM, Kazantzidis A, Ryan MJ, Barber N, Sempos CT, Durazo-Arvizu RA, et al. Seasonal changes in vitamin D-effective UVB availability in Europe and associations with population serum 25-Hydroxyvitamin D. Nutrients 2016; 8: 533. [PubMed](http://smj.org.sa/lookup/external-ref?access_num=http://www.n&link_type=MED&atom=%2Fsmj%2F44%2F4%2F413.atom) 24. 24.Fraser DR. Physiological significance of vitamin D produced in skin compared with oral vitamin D. Journal of nutritional science 2022; 11: e13. 25. 25.Vieth R. Vitamin D toxicity, policy, and science. J Bone Miner Res 2007; 22: V64-V68. 26. 26.Bacchetta J, Edouard T, Laverny G, Bernardor J, Bertholet-Thomas A, Castanet M, et al. Vitamin D and calcium intakes in general pediatric populations: A French expert consensus paper. Arch Pediatr 2022; 29: 312–325. 27. 27.Pludowski P, Takacs I, Boyanov M, Belaya Z, Diaconu CC, Mokhort T, et al. Clinical practice in the prevention, diagnosis and treatment of vitamin D deficiency: a central and eastern European expert consensus statement. Nutrients 2022; 14: 1483. 28. 28.Taylor PN, Davies JS. A review of the growing risk of vitamin D toxicity from inappropriate practice. Br J Clin Pharmacol 2018; 84: 1121–1127. [PubMed](http://smj.org.sa/lookup/external-ref?access_num=http://www.n&link_type=MED&atom=%2Fsmj%2F44%2F4%2F413.atom) 29. 29.Barth K, Sedivy M, Lindner G, Schwarz C. Successful treatment with denosumab for 2 cases with hypercalcemia due to vitamin D intoxication and associated acute kidney injury. CEN Case Rep 2022; 11: 141–145. 30. 30.Nauwynck E, Vanbesien J, De Schepper J, Gies I, Van Leynseele A, De Wachter E, et al. Everything in excess is opposed to nature, even vitamin D: a case report. Endocrinol Diabetes Metab Case Rep 2022; 2022; 21–0181. 31. 31.Simon A. [Three-year-old boy with significant hypercalcemia in the context of vitamin D intoxication]. Monatsschr Kinderheilkd 2022: 1–4. 32. 32.Demir K, Döneray H, Kara C, Atay Z, Çetinkaya S, Çayır A, et al. Comparison of treatment regimens in management of severe hypercalcemia due to vitamin D intoxication in children. J Clin Res Pediatr Endocrinol 2019; 11: 140–148. 33. 33.Batman A, Altuntas Y. Risk of hypercalcemia in elderly patients with hypervitaminosis d and intoxication. Acta Endocrinol (Buchar) 2021; 17: 200–206. 34. 34.Marcinowska-Suchowierska E, Kupisz-Urbańska M, Łukaszkiewicz J, Płudowski P, Jones G. Vitamin D toxicity-a clinical perspective. Front Endocrinol (Lausanne) 2018; 9: 550. 35. 35.Rusińska A, Płudowski P, Walczak M, Borszewska-Kornacka MK, Bossowski A, Chlebna-Sokół D, et al. Vitamin D supplementation guidelines for general population and groups at risk of vitamin D deficiency in Poland-recommendations of the Polish Society of Pediatric Endocrinology and Diabetes and the Expert Panel With Participation of National Specialist Consultants and Representatives of Scientific Societies-2018 update. Front Endocrinol (Lausanne) 2018; 9: 246. 36. 36.Valkama S, Holmlund-Suila E, Enlund-Cerullo M, Rosendahl J, Hauta-Alus H, Helve O, et al. No Severe hypercalcemia with daily vitamin D3 supplementation of up to 30 µg during the First Year of Life. Horm Res Paediatr 2017;88: 147–154. 37. 37.Feketea GM, Bocsan IC, Tsiros G, Voila P, Stanciu LA, Zdrenghea M. Vitamin D status in children in Greece and its relationship with sunscreen application. Children (Basel, Switzerland) 2021; 8: 111. 38. 38.Subspecialty Group of Children Health, the Society of Pediatrics, Chinese Medical Association; Editorial Board, Chinese Journal of Pediatrics. [Practical guidelines for clinical issues related to vitamin D nutrition in Chinese children]. Zhonghua Er Ke Za Zhi 2022; 60: 387–394. 39. 39.Gáll Z, Csukor B, Urkon M, Farczádi L, Kolcsár M. Vitamin D status assessment: lack of correlation between serum and hair 25-hydroxycholecalciferol levels in healthy young adults. Diagnostics (Basel, Switzerland). 2022; 12: 1229. 40. 40.Yang C, Liu X, Li J, Yan N, Dang Y, Chang Z, et al. Association of serum vitamin D and estradiol levels with metabolic syndrome in rural women of Northwest China: a cross-sectional study. Metab Syndr Relat Disord 2022; 20: 182–189.