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Gene-by-environment interactions of the CLOCK, PEMT, and GHRELIN loci with average sleep duration in relation to obesity traits using a cohort of 643 New Zealand European children.
- Source :
-
Sleep medicine [Sleep Med] 2017 Sep; Vol. 37, pp. 19-26. Date of Electronic Publication: 2017 Jun 24. - Publication Year :
- 2017
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Abstract
- Objectives: Modern technology may have desensitised the 'biological clock' to environmental cues, disrupting the appropriate co-ordination of metabolic processes. Susceptibility to misalignment of circadian rhythms may be partly genetically influenced and effects on sleep quality and duration could predispose to poorer health outcomes. Shorter sleep duration is associated with obesity traits, which are brought on by an increased opportunity to eat and/or a shift of hormonal profile promoting hunger. We hypothesised that increased sleep duration will offset susceptible genetic effects, resulting in reduced obesity risk.<br />Methods: We recruited 643 (male: 338; female: 305) European children born to participants in the New Zealand centre of the International Screening for Pregnancy Endpoints sleep study. Ten genes directly involved in the circadian rhythm machinery and a further 20 genes hypothesised to be driven by cyclic oscillations were evaluated by Sequenom assay. Multivariable regression was performed to test the interaction between gene variants and average sleep length (derived from actigraphy), in relation to obesity traits (body mass index (BMI) z-scores and percentage body fat (PBF)).<br />Results: No association was found between average sleep length and BMI z-scores (p = 0.056) or PBF (p = 0.609). Uncorrected genotype associations were detected between STAT-rs8069645 (p = 0.0052) and ADIPOQ-rs266729 (p = 0.019) with differences in average sleep duration. Evidence for uncorrected gene-by-sleep interactions of the CLOCK-rs4864548 (p = 0.0039), PEMT-936108 (p = 0.016) and GHRELIN-rs696217 (p = 0.046) were found in relation to BMI z-scores but not for PBF.<br />Conclusion: Our results indicate that children may have different genetic susceptibility to the effects of sleep duration on obesity. Further confirmatory studies are required in other population cohorts of different age groups.<br /> (Copyright © 2017 Elsevier B.V. All rights reserved.)
- Subjects :
- Actigraphy
Adiposity genetics
Body Mass Index
Child
Child, Preschool
Female
Genetic Association Studies
Genetic Loci
Genetic Predisposition to Disease
Humans
Male
Multivariate Analysis
New Zealand
Obesity epidemiology
Obesity physiopathology
Prospective Studies
Sleep physiology
Time Factors
White People genetics
CLOCK Proteins genetics
Gene-Environment Interaction
Ghrelin genetics
Obesity genetics
Phosphatidylethanolamine N-Methyltransferase genetics
Sleep genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1878-5506
- Volume :
- 37
- Database :
- MEDLINE
- Journal :
- Sleep medicine
- Publication Type :
- Academic Journal
- Accession number :
- 28899534
- Full Text :
- https://doi.org/10.1016/j.sleep.2017.05.017