Population-representative study reveals cardiovascular and metabolic disease biomarkers associated with misaligned sleep schedules
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
36827078
PubMed Central
PMC10262187
DOI
10.1093/sleep/zsad037
PII: 7056767
Knihovny.cz E-resources
- Keywords
- Biomarkers, Cholesterol, Chronotype, Circadian Rhythm, Humans, Lipoproteins, HDL, Lipoproteins, LDL, Models, Statistical, Social jetlag,
- MeSH
- Biomarkers MeSH
- Cholesterol MeSH
- Circadian Rhythm * MeSH
- Adult MeSH
- Jet Lag Syndrome MeSH
- Humans MeSH
- Metabolic Diseases * complications MeSH
- Surveys and Questionnaires MeSH
- Sleep MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Biomarkers MeSH
- Cholesterol MeSH
STUDY OBJECTIVES: Social jetlag manifests as a difference in sleep timing on workdays and free days. Social jetlag is often associated with shorter, lower-quality sleep, so it is unclear how much the chronic circadian misalignment contributes to observed negative health outcomes. We aimed to (1) investigate associations between social jetlag, chronotype (one of its determinants), and the levels of health markers, (2) describe factors associated with social jetlag, and (3) examine whether working from home can reduce social jetlag. METHODS: Adult respondents participated in a nationally representative longitudinal survey of Czech households (individuals in each wave: n2018/19/20 = 5132/1957/1533), which included Munich ChronoType Questionnaire to evaluate chronotype and social jetlag. A subset provided blood samples (n2019 = 1957) for detection of nine biomarkers and was surveyed in three successive years (social jetlag calculated for n2018/19/20 = 3930/1601/1237). Data were analyzed by nonparametric univariate tests and mixed effects multivariate regression with social jetlag, chronotype, sex, age, body-mass index, and reported diseases as predictors and biomarker levels as outcomes. RESULTS: Higher social jetlag (≥0.65 h) was significantly associated with increased levels of total cholesterol and low-density lipoprotein cholesterol, particularly in participants older than 50 years (Mann-Whitney, men: pCHL = 0.0005, pLDL = 0.0009; women: pCHL = 0.0079, pLDL = 0.0068). Extreme chronotypes were associated with cardiovascular disease risk markers regardless of social jetlag (Kruskal-Wallis, p < 0.0001). Commuting to work and time stress were identified as important contributors to social jetlag. Individual longitudinal data showed that working from home decreased social jetlag and prolonged sleep. CONCLUSIONS: We report significant associations between sleep phase preference, social jetlag, and cardio-metabolic biomarkers.
Institute of Physiology The Czech Academy of Sciences Prague Czech Republic
Institute of Sociology The Czech Academy of Sciences Prague Czech Republic
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Circadian dysfunction and cardio-metabolic disorders in humans