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Relationship between Sleep Duration, Sun Exposure, and Serum 25-Hydroxyvitamin D Status: A Cross-sectional Study

Abstract

Normal-range sleep duration is an important factor for general health and metabolism, and insufficient or excessive sleep is associated with chronic metabolic disease. Among the many factors that affect sleep duration, sun exposure plays an important role in maintaining regular circadian rhythm and is also involved in the production and activation of 25-hydroxyvitamin D [25(OH)D], which regulates various functions in the body. However, 25(OH)D is available through food and various nutritional supplements without sun exposure, so it is important to find out the complex relationship among sun exposure, vitamin D status, and sleep duration. The relationship between sun exposure, vitamin D status, and sleep duration was analyzed in the nationwide survey and examination of 25,534 study populations, after adjusting for demographic characteristics, physical characteristics, lifestyle status, and socio-demographic variables. Vitamin D status alone did not show the relationship with sleep duration, although there were statistical relationships in the various factors including sun exposure with sleep duration. There was a statistical difference in 25(OH)D according to sleep duration, only in low sun exposure group. Subjects with low sun exposure and excessive sleep duration comparatively lower 25(OH)D than those with normal-range sleep, even after adjustment for potentially confounding factors. Individuals with limited exposure to sunlight should maintain adequate vitamin D status to have an appropriate sleep duration for health.

Introduction

Normal-range sleep duration is an important factor for general health and metabolism1. Insufficient or excessive sleep duration is associated with various chronic physical or mental illness, such as obesity, hypertension, diabetes, metabolic syndrome, depression, and other psychiatric disease2,3,4. Sleep insufficiency has been also associated with low thyroid hormone levels in rats and with high noradrenaline and cortisol levels in humans5. Sleep duration is mainly affected by circadian rhythm, and circadian rhythm is affected by the melatonin level controlled by the light exposure6,7,8. Therefore, sun exposure has an important role for determining sleep time9,10,11.

25-hydroxyvitamin D [25(OH)D], which is also greatly affected by sunlight exposure, regulates the metabolism of calcium and phosphorus, which contribute to the maintenance of a healthy musculoskeletal system. Recent studies have suggested that vitamin D status are associated with impaired glucose metabolism, cardiovascular disease, infectious/inflammatory disease, psychiatric disease, and cancer12,13,14,15,16. 25(OH)D is produced either through an endogenous pathway using UV light from sun exposure or an exogenous pathway through food intake. Vitamin D status are mainly regulated through serum phosphorus and parathyroid hormone, but are also affected by temperature, skin color, sunscreen use, clothing, obesity, and hepatic or renal function17. Serum vitamin D status, measured as 25(OH)D, are also implicated in an increasing number of physiological mechanisms, including sleep18. The 25(OH)D receptor is widely distributed among tissues, including the regions of the brain involved in sleep regulation and central nervous system inflammatory signaling19,20,21. The circadian phase of sleep can be delayed by vitamin D supplementation and by sun exposure22,23. Finally, serum vitamin D status have been related to daytime sleepiness24, and epidemiologic studies have indicated that vitamin D status are associated with the mid-point of sleep, sustained sleep, and sleep duration in the elderly25,26,27.

Modern human life often results in insufficient sun exposure, so it is important that 25(OH)D studies consider this factor. The complex metabolic process of production and activation of 25(OH)D by sun exposure, and the fact that 25(OH)D can be supplemented by exogenous methods, such as food or nutritional supplementation, without endogenous process of sun exposure implies that various related factors, including sun exposure, must be considered in analyzing the relationships between sleep duration and 25(OH)D. Therefore, we designed our study to analyze the relationship between vitamin D status, sleep duration, and sun exposure after controlling for a number of potentially confounding variables.

Methods

Study population

The Korean National Health and Nutrition Examination Survey (KNHANES) is a nationwide survey conducted by the Korea Centers for Disease Control and Prevention, in conjunction with the Korean Society of Otorhinolaryngology-Head and Neck Surgery (KORL-HNS) and other societies. KNHANES was initiated in 1998 to record the health and nutritional status of the Korean population and was designed as a multistage, cross-sectional, stratified sampling study without overlapping subjects. Teams of four medical experts, including an otolaryngologist, conducted the clinical examinations nationwide, using a specially equipped mobile examination vehicle. All questionnaires were completed, samples taken, and examinations performed for each subject in a single visit. KORL-HNS trained the survey teams to standardize the examinations. Our study was conducted on KNHANES data obtained between 2010 and 2012 (n = 25534). A total of 14490 participants were included in the final study population after the exclusion of participants aged less than 19 years (n = 5,935) and those with missing relevant data (n = 5,109). The mean age of study participants was 50.84 ± 16.26 years (range, 19–97 years) and the male to female ratio was 1:1.47. The survey protocol was approved by the institutional review board of the Korea Centers for Disease Control and Prevention (IRB Nos. 2010-02CON-21-C, 2011-02CON-06-C, and 201201EXP-01-2C). All study participants provided written informed consent as part of KNHANES.

Assessment of sleep duration and sun exposure

Self-reported sleep duration was assessed through a questionnaire. A KNHANES nurse asked survey participants “How many hours a day do you usually sleep?” and recorded their response28. From this response, sleep duration was divided into three groups: less than 6 hours, 6 to 9 hours, and more than 10 hours. To assess daily sun exposure, the participants were asked, “What is the average duration of your direct exposure to sun during the day?” for which participants were given the options: less than 2 hours, 2 to 5 hours, and 5 hours or more.

Measurement of serum 25-hydroxy vitamin D status

Blood samples were collected via the antecubital vein the morning after a minimum fast of 8 hours and refrigerated immediately. Samples were transported to the central testing facility in cold storage and analyzed within 24 h. Serum levels of 25(OH)D were measured by radioimmunoassay (25(OH)D 125I RIA Kit; DiaSorin, Still Water, MN) using a gamma-counter (1470 Wizard; PerkinElmer, Turku, Finland). The inter assay coefficients of variation were 11.7%, 10.5%, and 8.6% at 21.47, 56.66, and 82.37 nmol/L, respectively. KNHANES participates in the Vitamin D Standardization Program, so the measurement of 25(OH)D was standardized with the Belgian National Institute of Standards and Technology reference procedure recently developed by Ghent University29. Although there has been much debate over the definition of vitamin D deficiency, it is generally accepted that a 25(OH)D concentration of 20 ng/mL is an indication of deficiency30,31,32.

Statistical analysis

Statistical analyses were performed using the SAS survey procedure (ver. 9.4; SAS Institute, Cary, NC, USA) because of the complex sampling design and sampling weights from KNHANES. The procedure accommodated unequal probabilities of selection, oversampling, and non-response. Participants’ characteristics were analyzed using mean and standard error for continuous variables and value and percentage for categorical variables. To analyze differences in serum vitamin D status between sleep duration groups, the Rao-Scott chi-square test (using PROC SURVEYFREQ in SAS) was used. The exponentiated beta coefficients and 95% confidence intervals (CIs) for log-transformed vitamin D status were calculated.

Multiple logistic regression analysis (using PROC SURVEYLOGISTIC in SAS) was used to determine the association between 25(OH)D, sun exposure, and sleep duration. The crude dataset (model 1) was adjusted for age and sex (model 2). Model 2 was then adjusted for physical status (obesity, prevalent hypertension [HTN], prevalent diabetes [DM], and prevalent dyslipidemia) to generate model 3. Finally, model 3 was adjusted for lifestyle status (smoking status, drinking status, and regular exercise) and socio-demographic factors (family income, educational level, occupation, and region of residence), generating model 4. Two-tailed p values were generated, and a p < 0.05 was considered significant.

Ethical approval

All procedures performed in the studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

Informed consent

Informed consent was obtained from all individual participants included in the study.

Results

Baseline characteristics and associations with sleep duration

A total of 14490 enrolled participants were divided into three groups according to sleep duration: normal-range sleep group (‘6 to 9 hours’, 83.6%), sleep insufficient group (‘less than 6 hours’, 13%), and excessive sleep group (‘more than 10 hours’, 3.4%). Data were analyzed to identify statistical differences between groups in terms of age, sex, obesity, HTN, DM, dyslipidemia, smoking status, alcohol consumption, regular exercise, region of residence, family income, education level, occupation, exposure to sunlight, and vitamin D status (Table 1). All factors differed between groups apart from regular exercise and vitamin D status. In the excessive sleep group, participants were more likely to be younger, non-hypertensive, non-dyslipidemic, and menstruating women. In the sleep insufficient group, participants tended to be older, overweight, relatively hypotensive, DM, dyslipidemic, non-smokers, non-alcohol drinkers, and menopausal women. The percentage of residents living in urban areas was higher in the sleep insufficient group than in the excessive sleep group. Participants with low sun exposure were most likely to be in the normal-range sleep group than in the sleep insufficient or excessive sleep group. Vitamin D status were not significantly different between sleep duration groups prior to adjustment for potentially confounding factors.

Table 1 Baseline characteristics by sleep duration.

Association of vitamin D status with baseline characteristics and association of sleep duration with vitamin D sufficiency/deficiency

Vitamin D status in participants were analyzed with respect to age, sex, obesity, HTN, DM, dyslipidemia, smoking status, alcohol consumption, regular exercise, region of residence, family income, education level, occupation, and exposure to sunlight. Participants were also divided according to vitamin D status into a deficiency group (<20 ng/mL, 71.74%) and a sufficiency group (≥20 ng/mL, 28.26%), and groups were analyzed for an association with baseline characteristics (Table 2). Vitamin D status were higher in participants who were elderly, overweight, hypertensive, diabetic, and dyslipidemic and lower in menstruating women. Participants with appropriate vitamin D status were more likely to participate in regular exercise, live in a rural area, have a low familial income and educational level, be blue collar workers, and have adequate sun exposure. Vitamin D status were relatively high in the participants with sleep insufficiency.

Table 2 Vitamin D status by participant characteristics.

The vitamin D deficiency and sufficiency groups showed significant differences in terms of age, sex, obesity, HTN, DM, dyslipidemia, smoking status, alcohol consumption, regular exercise, region of residence, family income, education level, occupation, and exposure to sunlight. However, no significant difference was observed between 25(OH)D groups in terms of sleep duration.

Multiple logistic regression analyses of vitamin D status, sleep duration, and exposure to sunlight

Multiple logistic regression analyses were performed because of the conflicting evidence that there was no significant difference between the sleep duration groups and sun exposure, but there was a statistical difference in sleep duration within participants with low sun exposure (Table 3 and Fig. 1).

Table 3 Vitamin D status by sleep duration and sun exposure.
Figure 1
figure1

Distribution of Vit. D status.

To accurately assess the relationship between sleep duration, sun exposure, and vitamin D status, confounding factors of vitamin D status and sleep duration identified during this study were controlled through multiple logistic regression analysis. Differences in log-transformed vitamin D status between the sleep insufficient or excessive sleep groups and the normal-range sleep group were not significant. However, vitamin D status were significantly lower in the low exposure to sunlight group than in the adequate exposure to sunlight group, even after controlling for confounding variables (β = 0.91) (Table 4).

Table 4 Exponentiated beta coefficients and 95% confidence intervals of log-transformed vitamin D status.

Discussion

25(OH)D is known to be involved in the metabolism of calcium and phosphate for the maintenance of musculoskeletal health, but recent clinical studies have suggested it may also be involved in chronic metabolic disease. Research has shown that 25(OH)D receptors are present in most cells of the body and produce a variety of symptoms due to the hormone-like effects of 25(OH)D. Vitamin D deficiency is often overlooked because of the lack of outward symptoms. UV light exogenously triggers 25(OH)D production, and 25(OH)D can be supplemented through food intake. Differences in the bioavailability of 25(OH)D have been reported to depend on the form, route of administration, and activation pathway involved33. In modern society, it can be difficult to obtain adequate sun exposure because of an increase in indoor activities. Therefore, it is important to study the combined influence of low exposure to sunlight and other factors in vitamin D deficiency to indicate more achievable measures that can be taken against this condition. Our study investigated vitamin D deficiency from this angle, and in line with previous reports, we found that sun exposure and vitamin D status have a significant association. This is a natural consequence of the 25(OH)D activation pathway. However, unlike previous studies, we also analyzed the relationship between sleep duration and vitamin D status in detail. We found no significant difference between vitamin D status and sleep duration in individuals who were exposed to adequate sunlight. However, in participants with insufficient sun exposure, we found that individuals with excessive sleep duration had relatively low levels of 25(OH)D, even after controlling for potentially confounding variables.

A previous study reported that shorter sleep duration was associated with lower vitamin D status in the elderly34, though the data were limited by the age group of the study population and did not sufficiently control for sun exposure and other confounding factors. Another study found a relationship between sleep apnea and vitamin D status, but did not analyze other characteristics of sleep duration35. Although vitamin D supplements have been reported to improve sleep quality36, their effect on serum vitamin D status and sleep duration has not been assessed.

This study was based on a population-based epidemiologic dataset and controlled for the effect of sun exposure on vitamin D status to mimic life in a contemporary society. Results were statistically significant, even when potentially confounding variables were controlled. However, the factors such as adequate sleep duration and exposure to sunlight vary depending on the person and the given environment, so the lack of sufficient reflection of these factors may be a limitation of our research. In addition, because sleep duration and sun exposure were determined from participant responses to a questionnaire, the accuracy of these data may be limited by leading question bias or recall bias.

In this study, we found that low serum vitamin D status are associated with excessive sleep duration in individuals with low sun exposure. Therefore, in modern society where sun exposure is inevitably low, maintaining an adequate serum vitamin D status may be important for a healthy sleep duration.

Conclusion

Therefore, we analyzed the relationship between sleep duration and vitamin D status in the low exposure to sunlight group. There was no significant difference between vitamin D status in the sleep insufficiency and normal-range sleep groups. However, the excessive sleep group had significantly lower levels of 25(OH)D than the normal-range sleep group, even after controlling for confounding variables.

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Acknowledgements

This was not an industry-supported study. This work was supported by the National Research Foundation of Korea Grant funded by the Korean Government (NRF-2019R1A2C4002468). This study was also supported by the Soonchunhyang University Research Fund. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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Conceptualization: Do-Yang Park, Ji Ho Choi. Data curation: Dong Young Kim, Ji Ho Choi. Formal analysis: Bora Lee, Bumhee Park. Funding acquisition: Do-Yang Park, Ji Ho Choi. Methodology: Bora Lee, Bumhee Park. Supervision: Do-Yang Park. Validation: Jae Yong Lee, Hyun Jun Kim, Chang-Hoon Kim. Writing – original draft: Do-Yang Park, Ji Ho Choi. Writing – review & editing: Do-Yang Park, Ji Ho Choi.

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Correspondence to Do-Yang Park.

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Choi, J.H., Lee, B., Lee, J.Y. et al. Relationship between Sleep Duration, Sun Exposure, and Serum 25-Hydroxyvitamin D Status: A Cross-sectional Study. Sci Rep 10, 4168 (2020). https://doi.org/10.1038/s41598-020-61061-8

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