Population-representative study reveals cardiovascular and metabolic disease biomarkers associated with misaligned sleep schedules
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F67985823%3A_____%2F23%3A00573072" target="_blank" >RIV/67985823:_____/23:00573072 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/68378025:_____/23:00573072
Výsledek na webu
<a href="https://doi.org/10.1093/sleep/zsad037" target="_blank" >https://doi.org/10.1093/sleep/zsad037</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1093/sleep/zsad037" target="_blank" >10.1093/sleep/zsad037</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Population-representative study reveals cardiovascular and metabolic disease biomarkers associated with misaligned sleep schedules
Popis výsledku v původním jazyce
Study ObjectivesSocial 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.MethodsAdult respondents participated in a nationally representative longitudinal survey of Czech households (individuals in each wave: n(2018/19/20) = 5132/1957/1533), which included Munich ChronoType Questionnaire to evaluate chronotype and social jetlag. A subset provided blood samples (n(2019) = 1957) for detection of nine biomarkers and was surveyed in three successive years (social jetlag calculated for n(2018/19/20) = 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.ResultsHigher 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: p(CHL) = 0.0005, p(LDL) = 0.0009, women: p(CHL) = 0.0079, p(LDL) = 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.ConclusionsWe report significant associations between sleep phase preference, social jetlag, and cardio-metabolic biomarkers.
Název v anglickém jazyce
Population-representative study reveals cardiovascular and metabolic disease biomarkers associated with misaligned sleep schedules
Popis výsledku anglicky
Study ObjectivesSocial 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.MethodsAdult respondents participated in a nationally representative longitudinal survey of Czech households (individuals in each wave: n(2018/19/20) = 5132/1957/1533), which included Munich ChronoType Questionnaire to evaluate chronotype and social jetlag. A subset provided blood samples (n(2019) = 1957) for detection of nine biomarkers and was surveyed in three successive years (social jetlag calculated for n(2018/19/20) = 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.ResultsHigher 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: p(CHL) = 0.0005, p(LDL) = 0.0009, women: p(CHL) = 0.0079, p(LDL) = 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.ConclusionsWe report significant associations between sleep phase preference, social jetlag, and cardio-metabolic biomarkers.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
30105 - Physiology (including cytology)
Návaznosti výsledku
Projekt
Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2023
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Sleep
ISSN
0161-8105
e-ISSN
1550-9109
Svazek periodika
46
Číslo periodika v rámci svazku
6
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
14
Strana od-do
zsad037
Kód UT WoS článku
000973377000001
EID výsledku v databázi Scopus
2-s2.0-85162244955