Hostname: page-component-5b777bbd6c-7sgmh Total loading time: 0 Render date: 2025-06-25T13:16:44.605Z Has data issue: false hasContentIssue false

Contemporary factors affecting serum 25-hydroxyvitamin D concentrations in Chinese children aged 2–6 years

Published online by Cambridge University Press:  04 June 2025

Qian Chen
Affiliation:
Department of Child Health Care, Children’s Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Health and Nutrition, Chongqing 400014, China
Ting Yang
Affiliation:
Department of Child Health Care, Children’s Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Health and Nutrition, Chongqing 400014, China
Yongfang Liu
Affiliation:
Department of Nutrition, Children’s Hospital of Chongqing Medical University, Chongqing, China
Jie Chen
Affiliation:
Department of Child Health Care, Children’s Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Health and Nutrition, Chongqing 400014, China
Qian Cheng*
Affiliation:
Department of Child Health Care, Children’s Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Health and Nutrition, Chongqing 400014, China
Tingyu Li*
Affiliation:
Department of Child Health Care, Children’s Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Health and Nutrition, Chongqing 400014, China
*
*Corresponding authors: Emails: tyli@vip.sina.com; chqq5@126.com
*Corresponding authors: Emails: tyli@vip.sina.com; chqq5@126.com
Rights & Permissions [Opens in a new window]

Abstract

Objective:

We investigated vitamin D (VitD) nutritional status in children aged 2–6 years to provide a basis for prevention and intervention strategies for VitD deficiency (VitDD) in Chinese children.

Design:

From November 2018 to September 2019, a total of 2192 healthy children aged 2–6 years were enrolled. The serum 25-hydroxyvitamin D (25(OH)D) concentrations were measured by liquid chromatography tandem MS.

Setting:

Twelve jurisdictions in eight provinces and cities across northern and southern China were selected through stratified cluster sampling.

Participants:

2192 children aged 2–6 years were enrolled.

Results:

(1) A serum 25(OH)D concentration of 23·87 (sd 8·24) ng/ml, a VitDS rate of 65·2 %, an insufficiency rate of 29·6 % and a deficiency rate of 5·2 % were noted. (2) Age (OR = 2·22, 95 % CI 1·86, 2·64) and spring (OR = 1·35, 95 % CI 0·91, 2·01) are risk factors for VitDD and VitDI. The male (OR = 0·68, 95 % CI 0·52, 0·90), the temperature (OR = 0·89, 95 % CI 0·86, 0·93), summer (OR = 0·25, 95 % CI 0·09, 0·68), autumn (OR = 0·26, 95 % CI 0·09, 0·74) the intake of VitD supplements (OR = 0·08, 95 % CI 0·03, 0·28), the intake frequency of dairy products (OR = 0·86, 95 % CI 0·78, 0·96) and egg products (OR = 0·83, 95 % CI 0·74, 0·93) are protective factors for VitDD and VitDI.

Conclusion:

VitDD in children aged 2–6 years is still prevalent in China, but the influencing factors of VitD nutrition have changed. Latitude is not the main factor in the 25(OH)D concentrations of children aged 2–6 years; temperature, intake of eggs and dairy products and sampling season have more obvious impacts.

Type
Research Paper
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
© The Author(s), 2025. Published by Cambridge University Press on behalf of The Nutrition Society

Vitamin D (VitD) is a class of lipid-soluble vitamins. VitD not only plays a role in regulating Ca and phosphorus metabolism and bone health but also has a wider range of extraosseous biological effects(Reference Marquina, Mousa and Scragg1). It is associated with obesity, muscle, CVD, endocrine and metabolism, infections, and immune diseases(Reference Marquina, Mousa and Scragg1,Reference Pramono, Jocken and Blaak2) . VitD deficiency (VitDD) in children may also be associated with many diseases in adulthood. Therefore, VitD status in childhood has received more attention(Reference Wang, Shen and Jiang3). With the intensification of air pollution and the corresponding reduction in outdoor activities, VitDD has become increasingly common in humans, especially children, and VitD insufficiency and deficiency have become a public health problem in developed and developing countries(Reference Zhang, Li and Wei4).

The metabolism and nutritional status of VitD in the human body are affected by various factors, such as race, region, sex and age(Reference Wang, Shen and Jiang3,Reference Cashman, Dowling and Škrabáková5Reference Fink, Peters and Koplin10) . China has a large inland area, a large span between north and south latitudes, and a large difference in altitude between east and west. There are significant differences in temperature between different regions. People in different regions receive different intensities of sunlight and have different dressing and outdoor activity habits, which directly affect the concentrations of 25-hydroxyvitamin D (25(OH)D) synthesis by the local residents. Even in the same province, the 25(OH)D concentration is still affected by different altitudes and light levels(Reference Fan, Wang and Li11). Therefore, it is very important to investigate the current nutritional status of VitD in China on a large scale, but the most recent national VitD survey in China was from 2010 to 2013(Reference Zhenyu12). It suggested that the VitDD rate of children aged 3–5 years in China was 8·9 %. In recent years, although there have been many studies on the nutritional status of VitD in China, they are all based on the physical examination data of children in local hospitals or healthcare centres(Reference Wang, Shen and Jiang3,Reference Zhang, Li and Wei4,Reference Yan, Thomson and Zhao13Reference Zhang, Chen and Jin16) , which have a significant bias. The most recent multicentre survey of VitD status in the general population was conducted in 2013–2015, and only people aged 6–18 years in six cities were surveyed(Reference Wang, Gao and Cheng17). Since 2013, there has been no multicentre survey based on VitD status in preschool children. Due to the lack of large-scale population data, the ‘Expert Consensus on the Clinical Application of Vitamin A and Vitamin D in Chinese Children’ published in China in 2021 still used the data from the 2010–2013 survey(18). A new population-based multicentre VitD nutrition survey in children is needed.

This study was a multicentre cross-sectional study. The VitD and dietary nutritional status of children aged 2–6 years in twelve regions of eight provinces and cities in China were sampled and analysed. The influencing factors of VitD nutritional status were analysed to understand the recent changes in VitD nutrition and its influencing factors in China and provide a basis for adjusting China’s VitD intervention policy.

Objectives and methods

Research subjects and sampling strategy

This study was a multicentre cross-sectional survey. The sampling period was November 2018 to September 2019. The methods were approved by the Ethics Committee.

The study sample size was calculated using the following formula based on relevant research reports on VitDD: $N = {{u_M^2\;p\left( {1 - p} \right)} \over {{\delta ^2}}}$ . The prevalence of VitDD (< 12 ng/ml) has been calculated at 8·9 %(Reference Zhenyu12). Given a probability of type I errors less than 0·05, the allowable errors between the sample prevalence and the overall prevalence were less than 5 %. This study needed a sample size of 125 based on the following calculation:

$${\rm{N}} = \left[ {1{\cdot}{{96}^2} \times 0{\cdot}089 \times 0{\cdot}911} \right]/0{\cdot}{05^2} \approx 125.$$

Assuming a loss-to-follow-up rate of 10 %, the minimum sample size was 138. Therefore, we selected 200 children from each sampling site.

Sampling sites were chosen from provinces/municipalities, and the sampled provinces ran from the north to the south of China. The northernmost region was the Altay Prefecture of Xinjiang, and the southernmost region was Yunnan. Cities with different geographical characteristics were selected near the same latitude: the coastal city of Fuzhou in Fujian Province and the inland cities of Guiyang and Kunming. From each area, twelve sampling points were randomly selected by computer-generated random numbers. The final selected regions were Chongqing (Bishan, Liangjiang New District, Changshou, Qianjiang and Wanzhou), Guizhou (Guiyang), Yunnan (Kunming), Sichuan (Mianyang), Qinghai (Xining), Shaanxi (Xianyang), Fujian (Fuzhou) and Xinjiang (Altay) (Fig. 1).

Fig. 1 Regions covered by this study

A cross-sectional study was conducted to enrol healthy children aged 2–6 years who lived in the zones mentioned above. Children of appropriate ages were randomly selected from randomly selected kindergartens. Hospitals in Wanzhou, Mianyang, Qianjiang and Kunming also enrolled eligible participants from their respective societies. The specific situation of this queue is described in detail in Chen Qian’s article published in 2021(Reference Chen, Liu and Chen19). The inclusion and exclusion criteria are also the same.

Four millilitres of postprandial venous blood were collected from the children in the morning, the serum was segregated by centrifugation and a third-party company quantified the 25(OH)D concentration. The 25(OH)D concentration, including 25(OH)D3 and 25(OH)D2, was determined with liquid-phase tandem MS (AB SCIEX Framingham). A triple-quad mass spectrometer equipped with an Agilent Zorbax Eclipse XDB C8 guard column was used in the testing. The standard reference material VitD in human serum are ‘740 217’ and ‘739 650’ from the company of Sigma. The limit of quantitation and limit of detection were 1·2 ng/ml and 0·4 ng/ml, respectively. The intraday and interday precision were 3·27 % and 5·97 %, respectively. The method is accredited by the Vitamin D External Quality Assessment Scheme. The sum of 25(OH)D3 and 25(OH)D2 equals the total plasma 25(OH)D concentrations among the participants.

Evaluation criteria

Due to the limited understanding of the physiological functions of VitD, the definition of VitD serum status has been controversial. Currently, the serum VitD concentration cut-off point published by the Institute of Medicine in 2011 is the most widely accepted. The ‘Expert Consensus on the Clinical Application of Vitamin A and Vitamin D in Chinese Children’ published in 2021 also recommends the use of this threshold(18).

  • VitD sufficiency (VitDS): serum 25-hydroxy-VitD (25(OH)D) ≥ 50 nmol/l (20 ng/ml),

  • VitD insufficiency (VitDI): serum 25(OH)D 30–50 nmol/l (12–20 ng/ml),

  • VitD insufficiency (VitDI): serum 25(OH)D 30–50 nmol/l (12–20 ng/ml),

  • VitD deficiency (VitDD): serum 25(OH)D < 30 nmol/l (12 ng/ml)(21)

  • VitD inadequate: VitDI + VitDD: serum 25(OH)D < 50 nmol/l (20 ng/ml)

    Units of measurement used internationally to quantify VitD include(Reference Fink, Peters and Koplin10):

  • Doses: 1 microgram (µg) = 2·5 nanomoles (nmol) = 40 international units (IU)

  • Concentrations: 1 ng/ml = 1 µg/l = 2·5 nmol/l

Natural environment data

Data on the children’s area of residence, including the elevation and latitude data of the various regions, came from the ‘Load Code for the Design of Building Structures (2006 Edition) (GB500092012) [S]’(22). The annual mean temperature data came from the National Earth System Science Data Sharing Service Platform.

Data processing and statistical methods

A predefined testing centre in each area carried out all the tests, and the data were double-entered into Excel 2007 software (Microsoft, Redmond, USA). Continuous data are expressed as the mean (sd), and Student’s t test was used to compare independent samples. To compare differences between three or more groups, we used one-way ANOVA. The χ 2 test was used to compare proportions between groups. In the logistic regression analysis, VitD nutritional status was the dependent variable (1 = VitD inadequate: VitDI + VitDD, 0 = VitDS). The final correction factors included in the logistic regression model were weight-for-age Z-score (WAZ), height-for-age Z-score (HAZ) and BMI Z-score (BMZ). The independent variables of each grade were assigned as follows: sex (1 = male, 0 = female), age, season (1 = spring, 2 = summer, 3 = autumn, 4 = winter), vitD intake (0 = without vitD supplementation, 1 = with vitD supplementation), and milk intake and egg intake (9 = eat every day, 8 = 3–5 times/week, 7 = 1–2 times/week, 6 = little, 5 = never).

The logistic regression model for evaluation was run after adjustment for the WAZ, HAZ and BMZ. A stepwise selection technique was applied to include variables with a significance level for entry > 0·10 and exclude those with a significance level to stay < 0·05. All statistical analyses were performed in SAS 9.4 software (SAS Institute). P < 0·05 was considered statistically significant.

Results

Overall demographic and vitamin D nutritional status of the sample

In this study, a total of 2192 subjects met the inclusion criteria. Their average age was 3·83 (sd 1·14) years. The boys numbered 1165, accounting for 53·1 %, and the sex composition ratio did not significantly differ from that expected. The average concentration of 25(OH)D in the total population was 23·87 (sd 8·24) ng/ml, 5·2 % of children had VitDD (25(OH)D < 12 ng/ml) and 29·6 % of children had VitD insufficiency (12 ng/ml ≤ 25(OH)D < 20 ng/ml). The 25(OH)D concentration in boys was higher than that in girls (24·3 (sd 8·33) ng/ml v. 22·66 (sd 7·98) ng/ml, P < 0·05), and the VitD sufficiency rate in boys was higher than that in girls (70·1 % v. 59·6 %, P < 0·05, Table 1). There were no significant differences in age, region of origin, blood collection season or dietary habits between males and females (Table 1).

Table 1 Basic demographic characteristics and dietary intake of participants (n 2192)

25(OH)D, 25-hydroxyvitamin D; HAZ, height-for-age Z-score; WAZ, weight-for-age Z-score.

Continuous variables are expressed as the mean (sd), and categorical variables are expressed as the number of samples (%).

VDS, vitamin D sufficiency: 25(OH)D > 20 ng/ml, VDI, vitamin D insufficient: 12–20 ng/ml, VDD, vitamin D deficiency < 12 ng/ml. #Significant difference in prevalence of VDD, VDI and VDS (P < 0·05).

Vitamin D nutritional status by age, season and region

When the children were grouped by age, the serum 25(OH)D concentration and VitD sufficiency rate of children aged 2–6 years gradually decreased with age (30·60 (sd 8·79) ng/ml, 91·4 %; 24·97 (sd 7·29) ng/ml, 72·7 %; 22·26 (sd 7·48) ng/ml, 58·0 %; and 21·22 (sd 7·24) ng/ml, 53·5 %). The 25(OH)D concentrations of the 2-year-old and 3-year-old groups were significantly different from those of the other groups (P < 0·05), and there was no significant difference between the 4-year-old and the 5–6-year-old groups (P > 0·05). With increasing age, the incidence of VitD deficiency and insufficiency gradually increased (P < 0·05) (Fig. 2(a)).

Fig. 2 (a) Vitamin D nutritional status by age, season and region. VDS, vitamin D sufficiency: 25(OH)D > 20 ng/ml; VDI, vitamin D insufficiency: 12–20 ng/ml; VDD, vitamin D deficiency: < 12 ng/ml. * Significant difference in prevalence of VitDD, VitDI, and VitDS (P < 0·05). †Significant difference in VitD concentrations between groups (P < 0·05). (b) The serum 25(OH)D concentration in different regions. VitD, vitamin D; VitDD, VitD deficiency; VitDI insufficiency; VitD sufficiency; 25(OH)D, 25-hydroxyvitamin D.

The serum 25(OH)D concentration varied with the season, and the prevalence of VitD deficiency and insufficiency showed the opposite trend (Fig. 2(a)). The 25(OH)D concentration was highest in summer (29·60 (sd 6·95) ng/ml, VitD sufficiency rate of 94·8 %), followed by 24·38 (sd 6·81) ng/ml in fall (VitD sufficiency rate of 71·9 %) and was lowest in winter (20·89 (sd 8·26) ng/ml, VitD sufficiency rate of 44·7 %) (P < 0·05).

Among the eight provinces studied, Fujian had the highest 25(OH)D concentration and VitD sufficiency rate (29·01 (sd 7·02) ng/ml, 93·4 %), followed by Xinjiang (26·89 (sd 6·50) ng/ml, 87·0 %). The lowest was found in Chongqing (22·19 (sd 8·70) ng/ml, 52·0 %) (Fig. 2(a)). There are significant differences in 25(OH)D concentration in some regions (Fig. 2(b)). The VitD nutritional statuses of children aged 2–6 years in various regions were significantly different (Table 5).

Vitamin D nutritional status in children with different dietary habits

The surveyed children ate relatively high amounts of milk, eggs and meat products. Different dietary habits had an impact on the serum 25(OH)D concentration and the VitDD rate (Table 2). The serum 25(OH)D concentration and VitD sufficiency rate of children with dairy intake ≥ 3 times/week, egg intake ≥ 3 times/week and aquatic product intake ≥ 3 times/week were all relatively high (24·22 (sd 8·42) ng/ml, 66·1 %; 23·98 (sd 8·48) ng/ml, 65·7 %; 25·80 (sd 8·54) ng/ml, 74·1 %) (P < 0·05).

Table 2 25(OH)D concentrations and VitD nutritional status of children with different dietary habits

25(OH)D, 25-hydroxyvitamin D; VitD, vitamin D.

Vitamin D supplementation and nutritional status

The overall VitD supplementation rate of the surveyed population was only 5·4 %. Before the age of 5 years, the VitD supplementation rate gradually decreased with age (Table 3). There was no significant difference in the VitD supplementation rate between the 4-year-old (3·3 %) and the 5–6-year-old groups (3·4 %). The serum 25(OH)D concentration in children with VitD supplementation was significantly higher than that in the non-supplemented population (29·37 (sd 6·80) ng/ml v. 23·15 (sd 8·16) ng/ml). Regardless of the dose, VitDD did not occur in the population receiving VitD supplementation (0·0 %, Table 3).

Table 3 VitD supplementation and nutritional status (n 1919)

VitD, vitamin D.

Geographical-environmental factors and vitamin D nutritional status at the sampling sites

Linear regression was used to analyse the effect of the latitude of the sampling sites and the monthly average temperature on VitD status in the population. There was a significant correlation between the monthly mean temperature and the serum 25(OH)D concentration in the population (25(OH)D = 16·779 + 0·3625 × temperature) (P < 0·05) (Fig. 3). The serum 25(OH)D concentration increased by 0·3625 ng/ml for every 1°C increase in temperature. From the broken-line graph of temperature and VitDS%, we can also see that at temperatures above 20°C, the proportion of VitD sufficiency gradually increased with increasing sampling temperature (Fig. 4); when the temperature was > 26°C, the proportion of VitD sufficiency often reached 100 %.

Fig. 3 Correlation analysis of monthly mean temperature and serum 25(OH)D concentration at the time of sampling. 25(OH)D, 25-hydroxyvitamin D.

Fig. 4 Monthly mean temperature at the time of sampling and the rate of VitD sufficiency. VitD, vitamin D.

There was no correlation between the latitude of the sampling site and the serum 25(OH)D concentration or the prevalence of VitDD (P > 0·05).

Risk factors for vitamin D deficiency and insufficient in preschool children

After adjusting for WAZ, HAZ and BMZ, we included sex, age, season, VitD intake, milk intake, egg intake, fish intake, latitude and temperature (monthly average temperature at the time of sampling) into the logistic regression analysis, and VitD status was the dependent variable (1 = VitD inadequacy: VitDI + VitDD; 0 = VitDS). The final correction factors included in the logistic regression model were WAZ, HAZ and BMZ. The results are shown in Tables 4a and 4b. Males have decreased odds of VitD inadequacy compared to females (OR, OR = 0·68, 95 % CI 0·52, 0·90). The odds of VitD inadequacy increase by 1·22 times for every year of age increase (OR = 2·22, 95 % CI 1·86, 2·64). Compared to winter, the odds of VitD inadequacy increase in spring (OR = 1·35, 95 % CI 0·91, 2·01) and decrease in summer (OR = 0·25, 95 % CI 0·09, 0·68) and autumn (OR = 0·26, 95 % CI 0·09, 0·74). Children who consume VitD supplements (OR = 0·08, 95 % CI 0·03, 0·28) and dairy (OR = 0·86, 95 % CI 0·78, 0·96) and egg products (OR = 0·83, 95 % CI 0·74, 0·93) more frequently have decreased odds of VitD inadequacy. When the monthly mean temperature at the sampling point varies between 11°C and 36°C, the odds of VitD inadequacy decrease by 11 % for every 1°C increase in temperature (OR = 0·89, 95 % CI 0·86, 0·93). All the above differences were statistically significant (P < 0·05) except for those associated with autumn. VitD status was not significantly correlated with household income or latitude (P > 0·05).

Table 4a The factors affecting VitDI and VitDD in children aged 2–6 (n 1447)

VitDI insufficiency; VitDD, VitD deficiency; VitD, vitamin D.

Variables entered into the m odel: sex, age, season, vitD intake, milk intake, egg intake, fish intake, latitude and temperaure (monthly average temperature at the time of sampling).

Covariate: weight-for-age Z-score (WAZ), height-for-age Z-score (HAZ), and BMI Z-score (BMZ). VitD status was the dependent variable (1 = Vitamin D inadequate: VitDI + VitDD; 0 = VitDS).

Independent variable: Sex (0 = female, 1 = male), Season (1 = spring, 2 = summer, 3 = autumn, 4 = winter), VitD intake (0 = without vitD supplementation, 1 = with vitD supplementation), Milk intake and egg intake (9 = eat every day, 8 = 3–5 times/week, 7 = 1–2 times/week, 6 = little, 5 = never), Temperature is a continuous variable from 11°C to 36°C.

Table 4b The factors affecting VitDI and VitDD in children aged 2–6 (n 1447)

VitDI insufficiency; VitDD, VitD deficiency; VitD, vitamin D.

Variables entered into the model: sex, age, season, VitD intake, milk intake, egg intake, fish intake, latitude and temperature (monthly average temperature at the time of sampling).

Covariates: weight-for-age Z-score (WAZ), height-for-age Z-score (HAZ), and BMI Z-score (BMZ). VitD status was the dependent variable (1 = Vitamin D inadequacy: VitDI + VitDD; 0 = VitDS).

Independent variable: Sex (0 = female, 1 = male), Season (1 = spring, 2 = summer, 3 = autumn, 4 = winter), VitD intake (0 = without VitD supplementation, 1 = with VitD supplementation), Milk intake and egg intake (9 = eat every day, 8 = 3–5 times/week, 7 = 1–2 times/week, 6 = little, 5 = never), Temperature is a continuous variable from 11°C to 36°C.

Table 5 VitD nutritional status of children in different regions

VitD, vitamin D.

Discussion

VitD includes VitD2 and VitD3(Reference Marino and Misra23). VitD2 is most common in plant food sources such as mushrooms and ergot and in fortified foods(Reference Jean, Souberbielle and Chazot24,Reference Gois, Ferreira and Olenski25) . During exposure to sunlight, 7-dehydrocholesterol in the skin is converted to VitD3(Reference Deluca26). In recent years, with the development of China’s economy, the proportion of urbanisation has further expanded, and people’s living habits have undergone major changes. Their diet is richer, and more attention is given to nutrient supplementation. At the same time, children enter kindergarten early, resulting in a significant reduction in outdoor activities. In recent years, there have been few large-scale population surveys of VitD status in China, especially of preschool children. Because of the difficulty of sampling, since the 2010–2013 national survey, there has been no multicentre VitD status survey of preschool children. The VitD nutritional status data of Chinese preschool children in the past 5 years were generated from outpatients(Reference Wang, Shen and Jiang3,Reference Zhang, Li and Wei4,Reference Yang, Mao and Ping14Reference Zhang, Chen and Jin16) .

This study used national large-scale multicentre data to analyse the epidemiological characteristics and influencing factors of the VitD nutritional status of children aged 2–6 years in China. The results showed that the rates of VitDD and insufficiency reached 5·2 % and 29·6 %, respectively, which were lower than the national multicentre data in 2013(Reference Zhenyu12), indicating that the overall VitD nutritional status has improved. Blood collection season, dietary habits, VitD supplementation and sampling temperature were correlated with VitD nutritional status.

Season is an important factor affecting 25(OH)D concentrations. Like previous studies, this study suggests that in almost all age groups, the 25(OH)D concentration is the lowest in winter and spring and highest in summer(Reference Wang, Shen and Jiang3,Reference Park, Hong and Chung7,Reference Hu, Chen and Wang8,Reference Herrick, Storandt and Afful27Reference Wang, Wang and Wen29) . The intrinsic reason for the difference in seasonal 25(OH)D concentration is the intensity of seasonal sunlight exposure, the outdoor activities of the population and the surface area of the skin exposed to sunlight. In summer, the UV intensity is relatively high, more of the skin is exposed to sun and so the skin makes relatively high amounts of VitD.

With increasing age, the serum 25(OH)D concentration gradually decreased, and the VitDD rate gradually increased, which is consistent with the data obtained by the healthcare departments of various hospitals in recent years(Reference Yang, Mao and Ping14Reference Zhang, Chen and Jin16). This may be related to the decrease in the VitD supplementation rate. The VitD supplementation rate of children after 2 years of age was generally low (5·4 %), and the supplementation rate further decreased with increasing age. With increasing age, children’s outdoor activities gradually decrease(Reference Wang, Gao and Cheng17). When VitD is gradually consumed by the body, the serum 25(OH)D concentration gradually decreases. This study also found that no VitDD occurred in the population who received VitD supplementation. We did not have any data on the amount of outdoor activities. More regional and population census data are needed, especially of preschool children.

The serum 25(OH)D concentrations and VitD sufficiency rates of boys were higher than those of girls, in line with previous studies(Reference Yang, Mao and Ping14,Reference Wang, Gao and Cheng17,Reference Yan, Zhang and Cheng30) . Previous studies have found a sex difference in VitD, which may be because boys have less body fat than girls(Reference Wang, Gao and Cheng17). However, in this study, there was no sex difference in the body fat distribution of preschool children, which may be because the amount of outdoor activities in boys is greater than that of girls, and girls pay more attention to sun protection when they go out. The relationship between sex and VitD is relatively complex, there are few studies on this aspect and further studies are needed.

Previous studies suggest that in high-latitude areas, especially north of 35°N, the UV intensity is relatively low in winter and spring, and the skin makes little VitD(Reference Cashman, Dowling and Škrabáková5Reference Park, Hong and Chung7,Reference Lane, Nisbet and Whiting9) . In this survey, after adjusting the sampling season, age, sex and other indicators, latitude did not have a significant effect on the VitD nutritional status, and there was no significant difference in the 25(OH)D concentration between the northern and southern regions. A cross-sectional survey conducted at a hospital in Taiyuan, China, also found that latitude had no significant effect on VitD nutritional status(Reference Yan, Thomson and Zhao13). China is a large country with relatively large differences in topography and culture. Even in the same latitude area, there was still a large difference in VitD status between cities, such as between Guizhou, Yunnan and Fujian, in this study. The sampling latitudes of Yunnan and Fujian were relatively close, and the annual average sunshine duration in Yunnan is longer than that in Fujian, but the serum 25(OH)D concentration in Fujian was significantly higher, which may be related to their higher consumption of fish. In this study, 21·55 % of children in Fujian (Fuzhou) ate fish daily, while only 4·48 % ate fish daily in Yunnan (Kunming). The annual average temperature in Fuzhou is higher than that in Kunming, and the skin exposure time is longer than that in Kunming, which may also be the reason for the difference. In the high-latitude regions of this survey, the VitDD rates in Qinghai (36·98°N) and Guizhou (26·58°N) were the same, and the serum 25(OH)D concentrations were similar. The 25(OH)D concentration in Chongqing was the lowest in the low-latitude regions, and the 25(OH)D concentration was the highest in Xinjiang (47·87°N), which completely contrasts with the previous results. With changes in human lifestyle, environmental pollution has been aggravated, and the amount of solar UVB that reaches the surface has decreased due to air pollution(Reference Chen, Chimeh and Lu31). Preschool children of all latitudes spend less time outdoors, so the influence of latitude is greatly reduced. Although Xinjiang is located in a high-latitude region, the sampled children were all Uyghurs, with lighter skin than Han Chinese. In addition, the annual average sunshine duration in Xinjiang is relatively long, the population eats large amount of dairy products and the sampling time was spring, so the 25(OH)D concentration was relatively high. Different studies have all found that the 25(OH)D concentration in Chongqing is relatively low(Reference Zhenyu12,Reference Wang, Gao and Cheng17) , which may be because the weather in Chongqing is humid and foggy, the surrounding mountains are relatively high and the sunshine duration at the sampling site is relatively short.

Previous studies have suggested that food sources of VitD are relatively small and have little effect on human VitD. Even so, this study found that the intake of dairy products and egg products had a significant impact on the VitD nutritional status. This may be because when there is less sunlight exposure and VitD supplementation, the relative influence of food on the nutritional status of human VitD increases. In this study, the proportion of aquatic product intake was relatively small, and only 15·6 % of the population ate aquatic products more than three times per week. Many inland areas were sampled, so freshwater fish and shrimp made up a greater proportion of the food intake. This may be one reason why aquatic products had no significant effect on VitD nutritional status in the logistic regression analysis.

Although latitude had little effect on 25(OH)D concentrations, the sampling area had a significant impact on the VitD nutritional status. Samples will be affected not only by the latitude and temperature of the sampling site but also by the economic and medical development status of the area and its health policy. The intake of VitD preparations had the greatest impact on VitD status (OR = 10·64). The monthly average temperature at the time of sampling showed a linear correlation with the serum 25(OH)D concentration. When the temperature was lower than 20°C, the relationship between air temperature and the percentage of VitD sufficiency (VitDS%) was not clear. This may be because the degree of skin exposure was lower when the temperature was too low, and the effect of sunlight on VitD nutrition was weaker. After the temperature reached higher than 25°C, only one person had VitDD. This study also investigated the effect of household income per capita on VitD nutritional status and found that after correction for many factors, household income per capita had no significant effect on the 25(OH)D concentrations of children aged 2–6 years.

With the development of Chinese society and changes in its environment and lifestyle, the factors affecting the VitD nutritional status have changed. Some primary care physicians still follow the guidelines of the Paediatrics Branch of the Chinese Medical Association and recommend that all children receive no less than 400 IU/d of VitD only from 2 weeks to 2 years after birth(32) and stop taking VitD supplements at the age of 2 years. At the same time, the Chinese public has doubts about long-term VitD supplementation(Reference Yan, Thomson and Zhao13) and believes that benefit of VitD is only to promote Ca absorption. Further strengthening the education of VitD supplementation, recommending regular monitoring of the 25(OH)D concentration in children and improving the awareness of the importance of VitD supplementation level among healthcare personnel and family members should all be addressed in our health efforts and in the development of health policies. The National Health Organization can tell doctors and parents which regions and populations are most likely to experience VitDD and need to strengthen supplementation. In China, many parents do not want to constantly provide their children with VitD supplementation. They are afraid of VitD overdose. In this study, VitDD rates were extremely low among preschool children in summer (0·4 %) and coastal cities (0·6 %). For these preschool children, VitD supplementation can be intermittent based on their level of exposure to sunlight during the summer in order to increase the long-term compliance with VitD supplementation.

Conclusion

VitDD in children aged 2–6 years is still prevalent in China. Although it is better than it was in 2010–2013, it is still an important public health problem. With changes in lifestyle, the influencing factors of VitD nutritional status have also changed. In China, latitude is not the main factor affecting the 25(OH)D concentration of preschool children; rather, the temperature at the time of sampling, the intake of eggs and dairy products, the sampling season, and the sampling area have more significant effects on the VitD nutritional status of children aged 2–6 years. It is necessary to further strengthen the education and policy development of VitD supplementation to improve the overall VitD nutritional status of Chinese children.

Acknowledgements

The authors thank all the staff of cooperative hospitals for helping in conducting interviews, carrying out measurements and sample collection: Qianjiang Central Hospital of Chongqing, Guizhou Provincial Maternal and Child Health Hospital, Three Gorges Central Hospital, Mianyang Central Hospital, Fuzhou Children’s Hospital of Fujian, Kunming Children’s Hospital, Xianyang Rainbow Hospital, Chongqing Changshou Maternal and Child Health Hospital, Urumqi Children’s Hospital of Xinjiang, Bishan Maternal and Child Health Hospital of Chongqing, Qinghai Provincial Women and Children’s Hospital, and the First People’s Hospital of Chongqing Liangjiang.

Financial support

Special fund for the development of science and technology guided by the central government: a multicentre cohort study of vitamin A-anemia intervention in children to the central and western regions

Conflicts of interest

There are no conflicts of interest.

Authorship

Qian Chen collected the data and validated the statistical results and wrote the initial draft of the manuscript. Tingyu Li and Qian Cheng conceived and designed the study and confirm the authenticity of all the raw data. Qian Cheng and Jie Chen and Ting Yang participated in the logistical planning of the study. Yongfang Liu provided statistical support for the sample size estimates and the design of the statistical analysis. All authors read and approved the final manuscript.

Ethics of human subject participation

This study was conducted according to the guidelines laid down in the Declaration of Helsinki, and all procedures involving research study participants were approved by the ethics committee of the Children’s Hospital of Chongqing Medical University. Written informed consent was obtained from all subjects.

References

Marquina, C, Mousa, A, Scragg, R et al. (2019) Vitamin D and cardiometabolic disorders: a review of current evidence, genetic determinants and pathomechanisms. Obes Rev 20, 262277.10.1111/obr.12793CrossRefGoogle ScholarPubMed
Pramono, A, Jocken, J & Blaak, EE (2019) Vitamin D deficiency in the aetiology of obesity-related insulin resistance. Diabetes Metab Res Rev 35, e3146.10.1002/dmrr.3146CrossRefGoogle ScholarPubMed
Wang, S, Shen, G, Jiang, S et al. (2017) Nutrient status of vitamin D among Chinese children. Nutrients 9, 319.10.3390/nu9040319CrossRefGoogle ScholarPubMed
Zhang, H, Li, Z, Wei, Y et al. (2020) Status and influential factors of vitamin D among children aged 0 to 6 years in a Chinese population. BMC Public Health 20, 429.10.1186/s12889-020-08557-0CrossRefGoogle Scholar
Cashman, KD, Dowling, KG, Škrabáková, Z et al. (2016) Vitamin D deficiency in Europe: pandemic. Am J Clin Nutr 103, 10331044.10.3945/ajcn.115.120873CrossRefGoogle ScholarPubMed
Vijayakumar, M, Bhatia, V & George, B (2020) Vitamin D status of children in Kerala, southern India. Public Health Nutr 23, 11791183.10.1017/S1368980018003622CrossRefGoogle ScholarPubMed
Park, JH, Hong, IY, Chung, JW et al. (2018) Vitamin D status in South Korean population: seven-year trend from the KNHANES. Medicine (Baltimore) 97, e11032.10.1097/MD.0000000000011032CrossRefGoogle ScholarPubMed
Hu, Y, Chen, J, Wang, R et al. (2017) Vitamin D nutritional status, its related factors for Chinese children, adolescents in 2010–2012. Nutrients 9, 1024.10.3390/nu9091024CrossRefGoogle ScholarPubMed
Lane, G, Nisbet, C, Whiting, SJ et al. (2019) Canadian newcomer children’s bone health and vitamin D status. Appl Physiol Nutr Metab 44, 796803.10.1139/apnm-2018-0705CrossRefGoogle ScholarPubMed
Fink, C, Peters, RL, Koplin, JJ et al. (2019) Factors affecting vitamin D status in infants. Children (Basel) 6, 7.Google ScholarPubMed
Fan, P, Wang, Q, Li, J et al. (2021) Poor status of vitamin D: a survey of area with lowest sunlight radiation in Sichuan, China. Front Endocrinol (Lausanne) 12, 626983.10.3389/fendo.2021.626983CrossRefGoogle ScholarPubMed
Zhenyu, Y. (2020) Report on Nutrition and Health Status of Chinese Residents (2010-2013) No.9- Nutrition and Health Status of Children Aged 0-5. Beijing: People’s Health Publishing House.Google Scholar
Yan, X, Thomson, JS, Zhao, R et al. (2017) Vitamin D status of residents in Taiyuan, China and influencing factors. Nutrients 9, 898.10.3390/nu9080898CrossRefGoogle ScholarPubMed
Yang, C, Mao, M, Ping, L et al. (2020) Prevalence of vitamin D deficiency and insufficiency among 460 537 children in 825 hospitals from 18 provinces in mainland China. Medicine (Baltimore) 99, e22463.Google Scholar
Guo, Y, Ke, HJ, Liu, Y et al. (2018) Prevalence of vitamin D insufficiency among children in southern China: a cross-sectional survey. Medicine (Baltimore) 97, e11030.10.1097/MD.0000000000011030CrossRefGoogle ScholarPubMed
Zhang, X, Chen, Y, Jin, S et al. (2020) Association of serum 25-Hydroxyvitamin D with Vitamin D intervention and outdoor activity among children in North China: an observational study. BMC Pediatr 20, 542.10.1186/s12887-020-02435-9CrossRefGoogle ScholarPubMed
Wang, HJ, Gao, AY, Cheng, H et al. (2021) [Association of vitamin D nutritional status with calcaneal bone mineral density in school-age children: a prospective cohort study]. Zhonghua Liu Xing Bing Xue Za Zhi 42, 462468. Chinese. doi: 10.3760/cma.j.cn112338-20200809-01048.Google Scholar
Children’s Health Branch of the Chinese Preventive Medicine Association (2021) Expert consensus on clinical application of vitamin A and vitamin D in Chinese children. Chinese. Journal of Children’s Health Care 29, 110116.Google Scholar
Chen, Q, Liu, Y, Chen, L et al. (2021) Vitamin A levels among pre-school children of central and Western China. Front Public Health 9, 694106.10.3389/fpubh.2021.694106CrossRefGoogle ScholarPubMed
World Health Organization (1982) Control of Vitamin A Deficiency and Xerophthalmia. World Health Organization Technical Report Series, No. 672. Geneva: WHO. pp. 170.Google Scholar
Institute of Medicine (2011) Dietary Reference Intakes for Calcium and Vitamin D. Washington, DC: National Academies Press (US).Google Scholar
GB500092012 (2012) Code for Load of Building Structures. [S] Ministry of Housing and Urban-Rural Development of the People’s Republic of China. https://www.mohurd.gov.cn/gongkai/zhengce/zhengcefilelib/201207/20120723_210754.html (accessed November 2024).Google Scholar
Marino, R & Misra, M (2019) Extra-skeletal effects of vitamin D. Nutrients 11, 1460.10.3390/nu11071460CrossRefGoogle ScholarPubMed
Jean, G, Souberbielle, JC & Chazot, C (2017) Vitamin D in chronic kidney disease and dialysis patients. Nutrients 9, 328.10.3390/nu9040328CrossRefGoogle ScholarPubMed
Gois, P, Ferreira, D, Olenski, S et al. (2017) Vitamin D and infectious diseases: simple bystander or contributing factor. Nutrients 9, 651.10.3390/nu9070651CrossRefGoogle ScholarPubMed
Deluca, HF (2014) History of the discovery of vitamin D and its active metabolites. Bonekey Rep 3, 479.10.1038/bonekey.2013.213CrossRefGoogle Scholar
Herrick, KA, Storandt, RJ, Afful, J et al. (2019) Vitamin D status in the United States, 2011–2014. Am J Clin Nutr 110, 150157.10.1093/ajcn/nqz037CrossRefGoogle ScholarPubMed
Alyahya, KO (2017) Vitamin D levels in schoolchildren: a cross-sectional study in Kuwait. BMC Pediatr 17, 213.10.1186/s12887-017-0963-0CrossRefGoogle ScholarPubMed
Wang, LL, Wang, HY, Wen, HK et al. (2016) Vitamin D status among infants, children, and adolescents in southeastern China. J Zhejiang Univ Sci B 17, 545552.10.1631/jzus.B1500285CrossRefGoogle ScholarPubMed
Yan, X, Zhang, N, Cheng, S et al. (2019) Gender differences in vitamin D status in China. Med Sci Monit 25, 70947099.10.12659/MSM.916326CrossRefGoogle ScholarPubMed
Chen, TC, Chimeh, F, Lu, Z et al. (2007) Factors that influence the cutaneous synthesis and dietary sources of vitamin D. Arch Biochem Biophys 460, 213217.10.1016/j.abb.2006.12.017CrossRefGoogle ScholarPubMed
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 (2008) Recommendation for prevention and treatment of rickets of vitamin D deficiency in childhood. Zhonghua Er Ke Za Zhi 46, 190191.Google Scholar
Figure 0

Fig. 1 Regions covered by this study

Figure 1

Table 1 Basic demographic characteristics and dietary intake of participants (n 2192)

Figure 2

Fig. 2 (a) Vitamin D nutritional status by age, season and region. VDS, vitamin D sufficiency: 25(OH)D > 20 ng/ml; VDI, vitamin D insufficiency: 12–20 ng/ml; VDD, vitamin D deficiency: < 12 ng/ml. * Significant difference in prevalence of VitDD, VitDI, and VitDS (P < 0·05). †Significant difference in VitD concentrations between groups (P < 0·05). (b) The serum 25(OH)D concentration in different regions. VitD, vitamin D; VitDD, VitD deficiency; VitDI insufficiency; VitD sufficiency; 25(OH)D, 25-hydroxyvitamin D.

Figure 3

Table 2 25(OH)D concentrations and VitD nutritional status of children with different dietary habits

Figure 4

Table 3 VitD supplementation and nutritional status (n 1919)

Figure 5

Fig. 3 Correlation analysis of monthly mean temperature and serum 25(OH)D concentration at the time of sampling. 25(OH)D, 25-hydroxyvitamin D.

Figure 6

Fig. 4 Monthly mean temperature at the time of sampling and the rate of VitD sufficiency. VitD, vitamin D.

Figure 7

Table 4a The factors affecting VitDI and VitDD in children aged 2–6 (n 1447)

Figure 8

Table 4b The factors affecting VitDI and VitDD in children aged 2–6 (n 1447)

Figure 9

Table 5 VitD nutritional status of children in different regions