Poor sleep associated with 2X increase risk of Metabolic problems (both low Vitamin D)

Cross-sectional and Prospective Associations of Actigraphy-Assessed Sleep Regularity With Metabolic Abnormalities: The Multi-Ethnic Study of Atherosclerosis

Diabetes Care 2019 May; https://doi.org/10.2337/dc19-0596

Tianyi Huang, Susan Redline

This study found associations Possible relationships include * Low Vitamin D ==> Poor Sleep ==> Metabolic problems * Poor Sleep ==> Low Vitamin D ==> Metabolic Problems But, more important, Add Vitamin D ==> improves sleep AND Add Vitamin D ==> Reduces Metabolic problems Items in both categories Metabolic Syndrome and Intervention: {category} Items in both categories Sleep and Intervention: {category} See other studies in VitaminDWiki * Vitamin D deficiency increases risk of Metabolic Syndrome – 1998 * Metabolic Syndrome risk increases about 70 percent if poor Vitamin D Receptor * Poor sleep 1.5 X more likely if less than 20 ng of Vitamin D – meta-analysis Oct 2018 * Shift workers have low vitamin D, poorer sleep, and are more depressed – March 2019 * Sleep may be regulated by Vitamin D via two pathways – Nov 2018

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OBJECTIVE To cross-sectionally and prospectively investigate the association between irregular sleep patterns, a potential marker for circadian disruption, and metabolic abnormalities.

RESEARCH DESIGN AND METHODS In the Multi-Ethnic Study of Atherosclerosis, participants completed 7-day actigraphy at exam 5 (2010–2013) and were prospectively followed throughout exam 6 (2016 to 2017). Sleep regularity was quantified by the 7-day SD of actigraphy-assessed sleep duration and sleep onset timing. Metabolic abnormalities were defined by 1) the National Cholesterol Education Program Adult Treatment Panel III criteria and 2) a data-driven clustering of metabolic factors.

RESULTS In the exam 5 cross-sectional analysis adjusted for sociodemographic and lifestyle factors (n = 2,003), every 1-h increase in the sleep duration SD was associated with 27% (95% CI 1.10, 1.47) higher odds of metabolic syndrome, and every 1-h increase in the sleep timing SD was associated with 23% (95% CI 1.06, 1.42) higher odds. The associations remained significant, with additional adjustment for sleep-related factors including sleep duration. In the prospective analysis (n = 970), the corresponding fully adjusted odds ratio (OR) (95% CI) was 1.27 (0.97, 1.65) for sleep duration and 1.36 (1.03, 1.80) for sleep timing. Compared with the cluster of few metabolic changes, every 1-h increase in sleep variability was associated with almost doubled odds for the cluster characterized by incidence of

  • multiple metabolic abnormalities (OR 1.97 [95% CI 1.18, 3.30] for sleep duration and

  • OR 2.10 [95% CI 1.25, 3.53] for sleep timing).

CONCLUSIONS Increased variability in sleep duration and timing was associated with higher prevalence and incidence of metabolic abnormalities even after considering sleep duration and other lifestyle factors.