From sleep duration to childhood obesity—what are the pathways?

被引:0
作者
Claudia Börnhorst
Sabrina Hense
Wolfgang Ahrens
Antje Hebestreit
Lucia Reisch
Gianvincenzo Barba
Rüdiger von Kries
Otmar Bayer
机构
[1] University of Bremen,Department of Biometry and Data Management, BIPS
[2] University of Bremen, Institute for Epidemiology and Prevention Research
[3] Copenhagen Business School,Department of Epidemiological Methods and Etiologic Research, BIPS
[4] Institute for Intercultural Communication and Management, Institute for Epidemiology and Prevention Research
[5] Epidemiology and Population Genetics,National Research Council, Institute of Food Science
[6] Ludwig-Maximilians University of Munich,Institute for Social Paediatrics and Adolescent Medicine
[7] BIPS - Institute for Epidemiology and Prevention Research,undefined
来源
European Journal of Pediatrics | 2012年 / 171卷
关键词
Cross sectional study; BMI; Fat mass; Insulin; Children; Sleep duration;
D O I
暂无
中图分类号
学科分类号
摘要
Sleep duration has been identified as risk factor for obesity already in children. Besides investigating the role of fat mass (FM), this study addressed the question whether endocrine mechanisms act as intermediates in the association between sleep duration and overweight/obesity. Within the framework of the IDEFICS study, the present research was conducted in 609 German resident children aged 2–9 years with information on fasting insulin, C-reactive protein and cortisol levels next to anthropometric measurements and parental questionnaires. Emphasising methodological aspects, an age-specific measure of sleep duration was derived to account for alteration in sleep duration during childhood/period of growth. Multivariate linear regression and quantile regression models confirmed an inverse relationship between sleep duration and measures of overweight/obesity. The estimate for the association of sleep duration and body mass index (BMI) was approximately halved after adjustment for FM, but remained significant. The strength of this association was also markedly attenuated when adjusting for insulin mainly for the upper BMI quantiles (Q80, β = −0.36 vs. β = −0.26; Q95, β = −0.87 vs. β = −0.47). Adjustment for cortisol and CrP did not yield this attenuation. Conclusion: The inverse relationship between sleep duration and BMI is mainly explained by the association between sleep duration and FM. Insulin may explain part of this association, in particular at the upper tail of the BMI distribution.
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页码:1029 / 1038
页数:9
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