Skip to main content

ORIGINAL RESEARCH article

Front. Public Health, 17 May 2021
Sec. Children and Health
This article is part of the Research Topic The role of Vitamin D in gut health and disease in children View all 9 articles

Vitamin D Status and Its Influence on the Health of Preschool Children in Hangzhou

  • 1Department of Child Health Care, Hangzhou Women's Hospital (Hangzhou Maternity and Child Care Hospital), Hangzhou, China
  • 2Department of Teaching Office, Hangzhou First People's Hospital, Hangzhou, China

Objective: Vitamin D deficiency and insufficiency in children are global public health problems. However, few studies have focused on vitamin D status in healthy preschool children, especially in Asia. This study aimed to investigate vitamin D status and host-related factors in healthy preschool children in Hangzhou to analyze the impact of low vitamin D levels (<30 ng/mL) on health outcomes (obesity, early childhood caries, and respiratory tract infections).

Methods: A total of 1,510 healthy children aged 24–72 months from 15 kindergartens in Hangzhou were included. Data on the children's gender, age, body mass index (BMI), caries, and blood samples available for vitamin D analysis were collected from June to August 2018. A total of 325 children aged 36–48 months took part in a survey on the frequency of respiratory tract infections in the last year.

Results: The children's mean 25(OH)D level was 28.01 ± 7.29 ng/mL. A total of 11.4% of the children had vitamin D deficiency, and 52.6% had vitamin D insufficiency. Only 36.0% had vitamin D sufficiency. No significant difference was found by gender or BMI group. However, children in the obesity group had the highest prevalence of vitamin D deficiency and the lowest 25(OH)D levels. A significant negative correlation was found between the 25(OH)D level and child age (r = −0.144, p < 0.001). Regression analysis showed that the children’s 25(OH)D levels decreased by 0.17 ng/mL per month with age. In addition, children with low vitamin D levels might increase the risk of obesity and early childhood caries. Multiple linear regression indicated that the number of caries in children increased by 0.08 per 1-ng/mL decrease in the 25(OH)D level (β = −0.08, p < 0.001).

Conclusion: Vitamin D deficiency/insufficiency is a serious problem among healthy preschool children in Hangzhou. Public health policies or interventions should be implemented to ensure that preschool children have adequate vitamin D to reduce the risk of related diseases.

Introduction

Vitamin D is a vital steroid hormone that is necessary for calcium and phosphorus absorption to maintain skeletal health (1). Vitamin D deficiency during childhood is known to cause growth retardation and nutritional rickets (2). Recently, an increasing number of studies have indicated that low levels of vitamin D may play an important role in the occurrence and development of extraskeletal diseases because of its immunoregulation and anti-inflammatory effects (3, 4), such as allergic diseases (5), respiratory illnesses (6), and obesity in children (7). Although there is no consensus on the association between vitamin D and related health outcomes, most specialists believe that sufficient vitamin D is essential and protective for children’s health.

Vitamin D is mainly synthesized in the skin. Generally, with unconstrained UVB exposure, the skin can generate adequate levels of vitamin D for human needs (8). However, an increasing number of systematic reviews have revealed that vitamin D deficiency/insufficiency in children is a global public health problem. In both high- and low-latitude regions, children show different degrees of vitamin D deficiency. A study in a high-latitude country (Irish, 51°N) found that more than 70% of children aged 2 years had vitamin D insufficiency (9). Another study from Uganda (2°N) also showed that 38.5% of children aged 5 years had low vitamin D levels (<30 ng/mL) and that 2.7% had vitamin D deficiency (10). Researchers have claimed that in addition to UVB exposure, vitamin D is also affected by genetic inheritance, religion, lifestyle, age, environmental pollution, and other risk factors. This may mean that vitamin D levels are more regional and population specific (11). Unfortunately, most studies on vitamin D levels in children have been conducted in high-latitude Western countries or populations with certain diseases, and few studies have focused on the vitamin D statuses of healthy children in Asia, although the number of related studies has gradually increased in recent years.

Hangzhou, the capital of Zhejiang Province, is located in southeastern China at a latitude of 30°33′ N. In recent years, this rapidly growing city has experienced severe air quality issues (12). Under these conditions, the synthesis of vitamin D is likely to be greatly diminished. However, no studies have investigated the vitamin D statuses of healthy children in Hangzhou in the last 5 years. Unlike infants, who were recommended to receive supplements of 400 international units of vitamin D per day from 2 weeks to 2 years by the Chinese Medical Association, and school-age children, who have plenty of outdoor activity time according to school regulations, preschool children often seem to be neglected. Therefore, in this study, our aims were to investigate the vitamin D statuses of healthy preschool children in Hangzhou and evaluate the host-related influential factors of vitamin D deficiency and insufficiency. Additionally, considering that obesity, early childhood caries (ECC), and respiratory tract infections are diseases with high incidence rates in preschool children, we also analyzed the influence of vitamin D deficiency/insufficiency on these health outcomes.

Materials and Methods

Survey and Participants

A total of 1,510 children aged 24–72 months from 15 kindergartens in Hangzhou were scheduled to attend the child health care department of Hangzhou Women’s Hospital for prekindergarten health examinations from June to August 2018. Data including basic information (gender, age), growth development (height, weight, caries), and serum 25(OH)D levels were collected. Children were assessed on the status of caries by children’s health care doctors. Children with no decayed tooth were classified into caries-free group (caries “No” group), and others were classified into caries group (caries “Yes” group). Body mass index (BMI) was calculated as body mass in kilograms divided by height in meters squared (kg/m2). Obesity was defined as BMI in the ≥95th percentile, overweight was defined as BMI between the 85th and 94th percentiles, normal weight was defined as BMI between the 5th and 84th percentiles, and underweight was defined as BMI in less than the fifth percentile. Blood samples were collected on the day of physical examination, and serum 25(OH)D level was detected within 24 h.

Thirty percent of the participants aged 36–48 months took part in a survey. A total of 345 questionnaires were sent out, and 325 (94.2%) were collected. The questionnaire had four items, including on the frequency of upper respiratory tract infection (URTI) in the last year, the frequency of pneumonia in the last year, the frequency of trachea bronchitis in the last year, and whether the child had taken vitamin D in the last 30 days. All the questionnaires were filled in by the guardian of the child. It is suggested that the guardian should refer to the frequency of illness recorded in the child’s medical record last year. Recurrent respiratory infection was defined as the frequency of URTI ≥6 times/year or the frequency of trachea bronchitis ≥2 times/year or the frequency of pneumonia ≥2 times/year in the past year.

In this cross-sectional study, children with any illness that might affect hydroxylation of vitamin D, calcium, and phosphorus metabolism (rickets or hypocalcemia or abnormal liver or renal function) were excluded. Ethical approval (No. 20180413) was granted by Hangzhou Women’s Hospital Ethics Committee, and informed consent was obtained from the parents of all participants.

Serum 25(OH)D Level

Fasting blood samples were centrifuged at 1,000 revolutions/min for 10 min after collection, and then the serum was stored at −20°C until analysis. Before analysis, 100 μL of serum was mixed with 200 μL of methanol with internal standard and then vibrated for 5 min. The internal standards of vitamin D2 and D3 were 25-hydroxyvitamin D2–d3 and 25-hydroxyvitamin D3–d6, respectively. The supernatants were collected and extracted with 600 μL of n-hexane and then analyzed by liquid chromatography–mass spectrometry. The vitamin D level was the sum of serum 25(OH)D2 and serum 25(OH)D3.

Vitamin D status was determined based on the serum 25(OH)D level and categorized into three groups: vitamin D deficiency [serum 25(OH)D ≤ 20 ng/mL], vitamin D insufficiency (20–30 ng/mL), and vitamin D sufficiency ≥30 ng/mL).

Statistical Analyses

We used SPSS version 21.0 for all analyses. Categorical variables were summarized as the number and percentage, and continuous variables were summarized as the mean and standard deviation (SD). Independent-samples t-tests (gender, caries, and recurrent respiratory infection) and one-way analysis of variance (age, BMI) were used to compare the differences in vitamin D levels among groups. Pearson χ2 test was used to compare the differences in vitamin D status among groups. Spearman correlation analysis was used to examine the correlations between vitamin D level and child age and between vitamin D level and number of caries. Multiple linear regression was used to predict the effect of vitamin D level on caries, adjusted for gender, age, and BMI. Two-tailed p < 0.05 was considered statistically significant.

Results

Participant Characteristics

A total of 1,510 healthy children from 15 kindergartens in Hangzhou City participated in this cross-sectional study. A total of 54.2% of the children were boys, and the remaining children were girls. Their mean age was 44 ± 8.2 months (range = 24–72 months), and they were divided into four groups according to their ages: Group24−36M (24–36 months, n = 142), Group36−48M (36–48 months, n = 1,150), Group48−60M (48–60 months, n = 128), and Group60−72M (60–72 months, n = 90). Most of the children (87.2%) had a BMI within the normal range, but 1.4, 8.9, and 2.5% of them were underweight, overweight, and obese, respectively. In addition, 24.37% of the children (n = 368) had ECC. The characteristics of the participants are shown in Table 1.

TABLE 1
www.frontiersin.org

Table 1. The influence of host-related factors (gender, age, BMI) on serum 25(OH)D levels and vitamin D status in children.

Host-Related Factors Influencing Vitamin D Level/Status

The serum 25(OH)D concentrations of all 1,510 children were measured. The mean 25(OH)D levels of the children were 28.01 ± 7.29 ng/mL, and the levels ranged from 8.5 to 62.4 ng/mL. A total of 52.6% of children had vitamin D insufficiency, and another 11.4% had deficiency. Only 36.0% of them showed vitamin D sufficiency.

We found no significant difference in the mean vitamin D level or vitamin D status between boys and girls (p > 0.05). Similarly, there were also no significant differences among the different BMI groups (p > 0.05). However, it is worth noting that the 25(OH)D levels of children in the normal group were highest (28.16 ± 7.3 ng/mL), and those of the obese group were lowest (25.51 ± 7.4 ng/mL). The prevalence of vitamin D deficiency was also the highest in the obesity group (24.3%) and the lowest in the normal group (10.5%).

Significant differences in the 25(OH)D level and vitamin D status were found among different age groups (p < 0.05). Children aged 25–36 months had the highest 25(OH)D level (29.44 ± 7.3 ng/mL), and the mean level decreased with age. Similarly, the prevalence of vitamin D sufficiency decreased from 40.1 to 20.0% with age (Table 1). Spearman correlation analysis suggested a statistically significant negative correlation between 25(OH)D levels and children’s age (r = −0.144, p < 0.001) (Supplementary Table 1). Additionally, a simple linear regression was calculated to determine the effect of age on 25(OH)D levels in children (Figure 1). The coefficient of determination (R2) was 0.036, meaning that 3.6% of the variance in 25(OH)D levels was explained by children’s age. The regression equation showed that the 25(OH)D level was equal to −0.17 (age) + 35.45 (ng/mL) (p < 0.001; R2 = 0.036) and indicated that children’s 25(OH)D levels decreased by 0.17 ng/mL at every month of age.

FIGURE 1
www.frontiersin.org

Figure 1. The effect of age on 25(OH)D levels in children (n = 1,510).

Correlation of Vitamin D Level/Status and Related Health Outcomes

Obesity

Compared with those of non-obese children, the 25(OH)D levels of obese children were significantly lower (p = 0.035) at 28.07 ± 7.28 and 25.51 ± 7.34 ng/mL, respectively. Moreover, the prevalence of obesity in the group with vitamin D deficiency was significantly higher than that in the groups with vitamin D insufficiency and sufficiency (p = 0.043), at 5.23, 2.14, and 2.02%, respectively (Table 2).

TABLE 2
www.frontiersin.org

Table 2. Correlation of serum 25(OH)D level/vitamin D status and related health outcomes.

Early Childhood Caries

The prevalence of ECC among the 1,510 children was 24.4%, and the child with the most severe ECC had 14 decayed teeth. There were significant differences in the vitamin D levels and vitamin D statuses of children with and without ECC (p = 0.002). Compared with children who had vitamin D sufficiency (20.40%), children with vitamin D insufficiency and deficiency had a significantly higher prevalence of ECC (p = 0.016), at 25.95 and 29.65%, respectively (Table 2).

Figure 2 shows a negative correlation between 25(OH)D levels and the number of caries in children (r = −0.103, p < 0.001). After adjustment for gender, age and BMI, the results of multiple linear regression indicated that the number of caries in children increased by 0.08 per 1-ng/mL decrease in 25(OH)D (β = −0.08, p < 0.001) (Supplementary Table 2).

FIGURE 2
www.frontiersin.org

Figure 2. Correlation of serum 25(OH)D levels and the number of early childhood caries (n = 1,510). ECC, early childhood caries.

Respiratory Tract Infections

The results of the questionnaire survey show that among the 325 children surveyed, 316, 65, 25, and 39 children had URTI, trachea bronchitis, pneumonia, and recurrent respiratory infections in the last year, respectively.

For children who had URTI, trachea bronchitis, or pneumonia in the last year, their vitamin D levels were similar to those of healthy children. Interestingly, however, compared with healthy children, children who had recurrent respiratory infections in the last year had relatively higher vitamin D levels (p = 0.048), at 28.67 ± 7.41 vs. 31.65 ± 6.92 ng/mL, respectively. But after adjustment for gender, age, and BMI, the results of multiple linear regression indicated there were also no significant differences of vitamin D levels between children with recurrent respiratory infections and healthy children (p = 0.059) (Supplementary Table 3). In addition, no significant differences were found regarding the probability of children with different vitamin D statuses (sufficiency, insufficiency, and deficiency) suffering from respiratory tract infections (Table 2).

Discussion

Vitamin D deficiency and insufficiency are global public health problems. Although the importance of vitamin D to health has been a concern in recent years, there are few studies on vitamin D in preschool children. Table 3 summarizes the articles published in the last 5 years on vitamin D levels and risk factors for preschool children in PubMed, which indicate that vitamin D deficiency/insufficiency is a serious problem in preschool children in most parts of the world.

TABLE 3
www.frontiersin.org

Table 3. Prevalence and risk factors for low vitamin D (vitamin D deficiency and insufficiency) in preschool children worldwide.

In this study, we found that more than half of the preschool children (52.6%) in Hangzhou had vitamin D insufficiency. Compared with previous reports on preschool children in Asia, our study showed that preschoolers in Hangzhou had the lowest rate of vitamin D deficiency (11.4%), but the vitamin D sufficiency rate was lower than that in other cities in East China (Changsha and Wenzhou City) (11, 13). This difference may be related to the economy, latitude, and eating habits. Hangzhou is affluent, and the one-child policy in China makes parents eager to offer nutritious food to their babies, which may lead to a low rate of vitamin D deficiency among preschool children in Hangzhou. However, compared with the latitudes of Wenzhou and Changsha (27°03′ N and 27°51′ N, respectively), the latitude of Hangzhou is 2 degrees higher, at 30°33′ N. The higher latitude means more sun exposure and vitamin D synthesis. In addition, the diet of Wenzhou is dominated by ocean fish all year, which can provide children with sufficient vitamin D. It should be noted that our study may have overestimated the children’s overall vitamin D levels because it was conducted in the summer (1). Thus, more attention should be paid to the vitamin D statuses of preschool children, and supplementation with appropriate vitamin D is necessary in Hangzhou.

Consistent with many studies (1, 2), we found no significant difference in the vitamin D status between boys and girls. However, a study in Bahrain showed that the mean 25(OH)D levels of girls were significantly lower than those of boys and that girls had a higher prevalence of vitamin D deficiency (14). Similarly, a study in Saudi Arabia also reported that vitamin D deficiency was more serious among females than males (15). The difference might be due to different cultural factors and religious behaviors. Girls in Muslim countries with traditional dress have less sun exposure than boys, and boys tend to play outside and produce more vitamin D (14, 16).

Young age of children has often been found to be a potential risk factor for vitamin D deficiency and insufficiency. Most studies have shown significant differences in vitamin D levels among children of different ages, with the prevalence of vitamin D deficiency increasing with age (1, 11). These studies paid more attention to school-age children because of their less time spent outdoors (17) or because the age span of research participants was relatively large (e.g., 0 months to 16 years) (18). Considering that few studies have been conducted on preschoolers, in this study, our subjects were children aged 25–72 months who were divided into 12-month age groups. Previous research showed that there may be age-related functional alterations of gastrointestinal change based on the efficiency of vitamin D absorption (19), and we found the same results: the mean 25(OH)D levels and the prevalence of vitamin D sufficiency decreased with age. In addition, Spearman correlation analysis also suggested a significant inverse association between 25(OH)D levels and age. Even so, however, the association and mechanism between vitamin D and age are still unconfirmed (14). Further studies should be performed to determine how vitamin D status is affected by children’s age.

An inverse association between BMI and 25(OH)D levels among children has been widely reported (2, 20). A study conducted with preschoolers aged 2.5–6 years showed that after adjustment for gender, age, place of residence, season, and sun exposure, BMI continued to be associated with an increased odds ratio of vitamin D deficiency, and it was an independent predictor of vitamin D deficiency (20). Another study in Norway also indicated that preschoolers aged 4–6 years who were overweight had significantly lower 25(OH)D levels than non-overweight preschoolers, showing that overweight status increased the risk for vitamin D deficiency (2). In our study, however, no significant difference in the 25(OH)D level or vitamin D status was found among the four BMI groups. It is worth noting that the 25(OH)D levels of the children in the normal group were highest (28.16 ± 7.3 ng/mL), and those of the children in the obesity group were lowest (25.51 ± 7.4 ng/mL). Meanwhile, the prevalence of vitamin D deficiency was also highest in the obesity group (24.3%) and lowest in the normal group (10.5%). This finding may be due to the lack of power for this hypothesis (only 2.5% of the preschoolers in this study were obese) (2). Thus, we then divided the children into obesity group and non-obesity group, and the results showed that the mean 25(OH)D levels of the two groups were significantly different. Therefore, more attention should be paid to obese children for vitamin D supplementation.

Does obesity decrease vitamin D levels, does vitamin D deficiency promote obesity, or do they interact? On the one hand, researchers believe vitamin D bioavailability in obese individuals is decreased because of vitamin D deposition in body adipose tissue and altered expression levels of vitamin D–metabolizing enzymes (2, 7, 17). Moreover, obese children are less likely to engage in outdoor activities, which results in reduced vitamin D synthesis (21). On the other hand, studies found that vitamin D regulated multiple aspects of adipose biology, such as adipogenesis and metabolic and endocrine function of adipose tissues (7). This may be the reason for obesity and metabolic diseases caused by vitamin D deficiency. To date, however, the association between vitamin D deficiency and adiposity is still unclear (22). In our study, we analyzed the effect of vitamin D status on obesity. We found that compared with vitamin D sufficiency, vitamin D insufficiency had a slight effect on obesity in preschool children; only when vitamin D was <20 ng/mL did the prevalence of obesity increase significantly. Therefore, 20 ng/mL may be the vitamin D cutoff value for preventing obesity.

In addition to obesity, we also analyzed the possible association between vitamin D and ECC. We found a significant negative correlation between the 25(OH)D level and the number of caries. After adjustment for gender, age, and BMI, multiple linear regression indicated that the number of caries increased by 0.08 per 1-ng/mL decrease in 25(OH)D. Although few studies have focused on the relationship between vitamin D and ECC, especially in Asia (16), our results are still supported by some studies (23, 24). A cross-sectional study in the United States indicated a significant association between vitamin D and ECC in children aged 1–6 years and showed that children with suboptimal vitamin D (serum 25(OH)D level <75 nmol/L) were twice as likely to have ECC than children with optimal levels (23). Chhonkar et al. also showed that vitamin D deficiency was a risk factor both for the incidence and severity of ECC in children aged 3–6 years (24). This relationship between vitamin D and ECC may be explained by the mineralization and antibacterial function of vitamin D. On the one hand, vitamin D deficiency can induce defective tooth mineralization, resulting in dentin and enamel defects, which can increase the risk of dental caries (16). On the other hand, vitamin D can induce certain antimicrobial peptides that protect against oral pathogens, such as defensins and cathelicidins (25). Remarkably, recent studies have suggested that maternal 25(OH)D deficiency may increase the risk of enamel hypoplasia and the rates of ECC in infants (26). Although the mechanism of the effect of vitamin D on ECC is unclear, researchers tend to believe that sufficient vitamin D early in life (including pregnancy) is a promising preventive agent against ECC (27).

Considering the immunomodulatory properties of vitamin D, several studies have attempted to determine the association between vitamin D and infectious diseases of the respiratory system, such as acute otitis media, bronchiolitis, and pneumonia (28). A study from Maharashtra showed a significantly negative correlation between serum 25(OH)D concentrations and episodes of URTI in school-aged children and indicated that children with vitamin D sufficiency had fewer URTI episodes and shorter URTI durations than children with vitamin D insufficiency (29). Another study also indicated that low serum 25(OH)D levels could increase the risk of acute lower respiratory tract infections in newborn babies (6). In this study, we tried to understand the possible link between serum 25(OH)D levels and the occurrence of respiratory tract infection (URTI, trachea bronchitis, pneumonia, and recurrent respiratory infection) in preschoolers. However, our results did not suggest a significant association between lower 25(OH)D levels and the occurrence of all respiratory tract infections we investigated, which was in line with some studies (30). Sudfeld et al. reported no association between vitamin D status and the incidence of URTI and acute lower respiratory tract infection in children aged 6 months (31). A randomized, double-blind, placebo-controlled trial indicated that vitamin D–calcium supplementation exerted no effect on the occurrence of infections compared with the placebo (32). All of these conflicting results may have been induced by several confounding factors, such as seasonal and racial differences, populations of different ages, and different cutoffs of vitamin D (3). In this study, the number of respiratory infections in the last year was recalled by the children’s parents, and we cannot rule out the effect of recall bias on the results.

Conclusions

Our study suggested a high prevalence of low vitamin D levels (vitamin D insufficiency and deficiency) in preschool children in Hangzhou. The age and BMI of children possibly affected their vitamin D levels. More attention should be paid to older children and obesity children for vitamin D supplement. In addition, vitamin D deficiency increased the risk of obesity and ECC in preschool children, which means keeping sufficient vitamin D is essential for children’s health.

Data Availability Statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics Statement

The studies involving human participants were reviewed and approved by Hangzhou Women’s Hospital Ethics Committee. Written informed consent to participate in this study was provided by the participants’ legal guardian/next of kin.

Author Contributions

ZC, XQ, and TW were responsible for data collection. ZC was responsible for writing the first draft of the article and analyzing the data with XL. YZ and WH revised and finalized the article. All authors contributed to the article and approved the submitted version.

Funding

This work received financial support from the Basic Public Welfare Research Project Zhejiang Province (Grant Number: GD20H260003) and Social Development Scientific Research Projects of the Science and Technology Bureau of Hangzhou (20180417A02). The funding institution had no role in the design, data collection, analysis, interpretation and writing of the manuscript.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

The authors are grateful to all participants and the parents or guardians who took part in this project.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpubh.2021.675403/full#supplementary-material

References

1. Zhang H, Li Z, Wei Y, Fu J, Feng Y, 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. doi: 10.1186/s12889-020-08557-0

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Midtbo LK, Nygaard LB, Markhus MW, Kjellevold M, Lie O, Dahl L, et al. Vitamin D status in preschool children and its relations to vitamin D sources and body mass index-fish intervention studies-KIDS (FINS-KIDS). Nutrition. (2020) 70:110595. doi: 10.1016/j.nut.2019.110595

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Zisi D, Challa A, Makis A. The association between vitamin D status and infectious diseases of the respiratory system in infancy and childhood. Hormones. (2019) 18:353–63. doi: 10.1007/s42000-019-00155-z

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Luan Z, Ma Y, Xin Y, Qian J, Wang H. Possible molecular mechanisms by which vitamin D prevents inflammatory bowel disease and colitis-associated colorectal cancer. Curr Med Chem. (2017) 24:911–7. doi: 10.2174/0929867323666161202153028

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Dogan E, Sevinc E. The vitamin D status and serum eosinophilic cationic protein levels in infants with cow’s milk protein allergy. Am J Transl Res. (2020) 12:8208–15.

PubMed Abstract | Google Scholar

6. Dinlen N, Zenciroglu A, Beken S, Dursun A, Dilli D, Okumus N. Association of vitamin D deficiency with acute lower respiratory tract infections in newborns. J Matern Fetal Neonatal Med. (2016) 29:928–32. doi: 10.3109/14767058.2015.1023710

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Nimitphong H, Park E, Lee MJ. Vitamin D regulation of adipogenesis and adipose tissue functions. Nutr Res Pract. (2020) 14:553–67. doi: 10.4162/nrp.2020.14.6.553

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Roth DE, Abrams SA, Aloia J, Bergeron G, Bourassa MW, Brown KH, et al. Global prevalence and disease burden of vitamin D deficiency: a roadmap for action in low- and middle-income countries. Ann N Y Acad Sci. (2018) 1430:44–79. doi: 10.1111/nyas.13968

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Ni Chaoimh C, McCarthy EK, Hourihane JO, Kenny LC, Irvine AD, Murray DM, et al. Low vitamin D deficiency in Irish toddlers despite northerly latitude and a high prevalence of inadequate intakes. Eur J Nutr. (2018) 57:783–94. doi: 10.1007/s00394-016-1368-9

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Mutua AM, Nampijja M, Elliott AM, Pettifor JM, Williams TN, Abubakar A, et al. Vitamin D status is not associated with cognitive or motor function in pre-school Ugandan children. Nutrients. (2020) 12:1662. doi: 10.3390/nu12061662

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Wang LL, Wang HY, Wen HK, Tao HQ, Zhao XW. Vitamin D status among infants, children, and adolescents in southeastern China. J Zhejiang Univ Sci B. (2016) 17:545–52. doi: 10.1631/jzus.B1500285

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Sun T, Che H, Qi B, Wang Y, Dong Y, Xia X, et al. Characterization of vertical distribution and radiative forcing of ambient aerosol over the Yangtze River Delta during 2013-2015. Sci Total Environ. (2019) 650:1846–57. doi: 10.1016/j.scitotenv.2018.09.262

PubMed Abstract | CrossRef Full Text | Google Scholar

13. He Y, Cai M, Huang X. Prevalence of vitamin D insufficiency/deficiency among overweight and obese preschool children in Yuelu District of Changsha. Zhong Nan Da Xue Xue Bao Yi Xue Ban. (2017) 42:565–9. doi: 10.11817/j.issn.1672-7347.2017.05.014

PubMed Abstract | CrossRef Full Text | Google Scholar

14. 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. doi: 10.26719/emhj.19.084

PubMed Abstract | CrossRef Full Text | Google Scholar

15. 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. doi: 10.4274/jcrpe.3301

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Almoudi MM, Hussein AS, Abu Hassan MI, Schroth RJ. Dental caries and vitamin D status in children in Asia. Pediatr Int. (2019) 61:327–38. doi: 10.1111/ped.13801

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Roh YE, Kim BR, Choi WB, Kim YM, Cho MJ, Kim HY, et al. Vitamin D deficiency in children aged 6 to 12 years: single center’s experience in Busan. Ann Pediatr Endocrinol Metab. (2016) 21:149–54. doi: 10.6065/apem.2016.21.3.149

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Zhu Z, Zhan J, Shao J, Chen W, Chen L, Li W, et al. High prevalence of vitamin D deficiency among children aged 1 month to 16 years in Hangzhou, China. BMC Public Health. (2012) 12:126. doi: 10.1186/1471-2458-12-126

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Meza-Meza MR, Ruiz-Ballesteros AI, de la Cruz-Mosso U. Functional effects of vitamin D: from nutrient to immunomodulator. Crit Rev Food Sci Nutr. (2020) 23:1–21. doi: 10.1080/10408398.2020.1862753

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Esmaeili Dooki MR, Moslemi L, Moghadamnia AA, Alijanpour Aghamaleki M, Bijani A, Pornasrollah m, et al. Vitamin D status in preschool children: should vitamin D supplementation, preventing vitamin D deficiency be continued in children over 2 years? J Public Health. (2019) 41:575–82. doi: 10.1093/pubmed/fdy147

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Taylor SN. Vitamin D in toddlers, preschool children, and adolescents. Ann Nutr Metab. (2020) 76 (Suppl. 2):30–41. doi: 10.1159/000505635

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Bemanalizadeh M, Heidari-Beni M, Ejtahed HS, Heshmat R, Baygi F, Seif E, et al. Association of serum 25-hydroxyvitamin D concentration with anthropometric measures in children and adolescents: the CASPIAN-V study. Eat Weight Disord. (2020) 27. doi: 10.1007/s40519-020-01067-3

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Seminario AL, Jumani K, Velan E, Scott JM, Latimer J, Schroth RJ. Suboptimal serum vitamin D associated with early childhood caries in special health care needs children. J Dent Child. (2018) 85:93–101.

PubMed Abstract | Google Scholar

24. Chhonkar A, Gupta A, Arya V. Comparison of vitamin D level of children with severe early childhood caries and children with no caries. Int J Clin Pediatr Dent. (2018) 11:199–204. doi: 10.5005/jp-journals-10005-1511

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Botelho J, Machado V, Proenca L, Delgado AS, Mendes JJ. Vitamin D deficiency and oral health: a comprehensive review. Nutrients. (2020) 12:1471. doi: 10.3390/nu12051471

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Singleton R, Day G, Thomas T, Schroth R, Klejka J, Lenaker D, et al. Association of maternal vitamin D deficiency with early childhood caries. J Dent Res. (2019) 98:549–55. doi: 10.1177/0022034519834518

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Reed SG, Miller CS, Wagner CL, Hollis BW, Lawson AB. Toward preventing enamel hypoplasia: modeling maternal and neonatal biomarkers of human calcium homeostasis. Caries Res. (2020) 54:55–67. doi: 10.1159/000502793

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Zhang J, Sun RR, Yan ZX, Yi WX, Yue B. Correlation of serum vitamin A, D, and E with recurrent respiratory infection in children. Eur Rev Med Pharmacol Sci. (2019) 23:8133–8. doi: 10.26355/eurrev_201909_19033

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Mandlik R, Chiplonkar S, Kajale N, Khadilkar V, Khadilkar A. Infection status of rural schoolchildren and its relationship with vitamin D concentrations. Indian J Pediatr. (2019) 86:675–80. doi: 10.1007/s12098-019-02933-4

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Tse SM, Weiler H, Kovesi T. Food insecurity, vitamin D insufficiency and respiratory infections among Inuit children. Int J Circumpolar Health. (2016) 75:29954. doi: 10.3402/ijch.v75.29954

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Sudfeld CR, Manji KP, Smith ER, Aboud S, Kisenge R, Fawzi WW, et al. Vitamin D deficiency is not associated with growth or the incidence of common morbidities among Tanzanian infants. J Pediatr Gastroenterol Nutr. (2017) 65:467–74. doi: 10.1097/MPG.0000000000001658

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Mandlik R, Mughal Z, Khadilkar A, Chiplonkar S, Ekbote V, Kajale N, et al. Occurrence of infections in schoolchildren subsequent to supplementation with vitamin D-calcium or zinc: a randomized, double-blind, placebo-controlled trial. Nutr Res Pract. (2020) 14:117–26. doi: 10.4162/nrp.2020.14.2.117

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Petry N, Al-Maamary SA, Woodruff BA, Alghannami S, Al-Shammakhi SM, Al-Ghammari IK, et al. National prevalence of micronutrient deficiencies, anaemia, genetic blood disorders and over- and undernutrition in Omani women of reproductive age and preschool children. Sultan Qaboos Univ Med J. (2020) 20:e151–64. doi: 10.18295/squmj.2020.20.02.005

CrossRef Full Text | Google Scholar

34. Ando E, Morisaki N, Asakura K, Sasaki S, Fujiwara T, Horikawa R. Serum 25-hydroxyvitamin D levels showed strong seasonality but lacked association with vitamin D intake in 3-year-old Japanese children. Br J Nutr. (2018) 120:1034–44. doi: 10.1017/S0007114518002258

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Karin Z, Gilic B, Supe Domic D, Sarac Z, Ercegovic K, Zenic N, et al. Vitamin D status and analysis of specific correlates in preschool children: a cross-sectional study in Southern Croatia. Int J Environ Res Public Health. (2018) 15:2503. doi: 10.3390/ijerph15112503

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Houghton LA, Brown RC, Beaumont S, Jennings S, Bailey KB, Haszard JJ, et al. Micronutrient status differs among Maasai and Kamba preschoolers in a supplementary feeding programme in Kenya. Matern Child Nutr. (2019) 15:e12805. doi: 10.1111/mcn.12805

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Cairncross CT, Stonehouse W, Conlon CA, Grant CC, McDonald B, Houghton LA, et al. Predictors of vitamin D status in New Zealand preschool children. Matern Child Nutr. (2017) 13:e12340. doi: 10.1111/mcn.12340

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: vitamin D, preschool children, obesity, early children caries, respiratory tract infections

Citation: Chen Z, Lv X, Hu W, Qian X, Wu T and Zhu Y (2021) Vitamin D Status and Its Influence on the Health of Preschool Children in Hangzhou. Front. Public Health 9:675403. doi: 10.3389/fpubh.2021.675403

Received: 03 March 2021; Accepted: 30 March 2021;
Published: 17 May 2021.

Edited by:

Pietro Vajro, University of Salerno, Italy

Reviewed by:

Nasser M. Al-Daghri, King Saud University, Saudi Arabia
Khaled Saad, Assiut University Hospital, Egypt

Copyright © 2021 Chen, Lv, Hu, Qian, Wu and Zhu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Yunxia Zhu, 544039114@qq.com

These authors have contributed equally to this work

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.