Detailed Information

Cited 231 time in webofscience Cited 242 time in scopus
Metadata Downloads

Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci

Authors
Jones, Samuel E.Tyrrell, JessicaWood, Andrew R.Beaumont, Robin N.Ruth, Katherine S.Tuke, Marcus A.Yaghootkar, HaniehHu, YounaTeder-Laving, MarisHayward, CarolineRoenneberg, TillWilson, James F.Del Greco, FabiolaHicks, Andrew A.Shin, CholYun, Chang-HoLee, Seung KuMetspalu, AndresByrne, Enda M.Gehrman, Philip R.Tiemeier, HenningAllebrandt, Karla V.Freathy, Rachel M.Murray, AnnaHinds, David A.Frayling, Timothy M.Weedon, Michael N.
Issue Date
Aug-2016
Publisher
PUBLIC LIBRARY SCIENCE
Citation
PLOS GENETICS, v.12, no.8
Indexed
SCI
SCIE
SCOPUS
Journal Title
PLOS GENETICS
Volume
12
Number
8
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/6194
DOI
10.1371/journal.pgen.1006125
ISSN
1553-7390
1553-7404
Abstract
Disrupted circadian rhythms and reduced sleep duration are associated with several human diseases, particularly obesity and type 2 diabetes, but until recently, little was known about the genetic factors influencing these heritable traits. We performed genome-wide association studies of self-reported chronotype (morning/evening person) and self-reported sleep duration in 128,266 white British individuals from the UK Biobank study. Sixteen variants were associated with chronotype (P<5x10(-8)), including variants near the known circadian rhythm genes RGS16 (1.21 odds of morningness, 95% CI [1.15, 1.27], P = 3x10(-12)) and PER2 (1.09 odds of morningness, 95% CI [1.06, 1.12], P = 4x10(-10)). The PER2 signal has previously been associated with iris function. We sought replication using self-reported data from 89,283 23andMe participants; thirteen of the chronotype signals remained associated at P<5x10(-8) on meta-analysis and eleven of these reached P< 0.05 in the same direction in the 23andMe study. We also replicated 9 additional variants identified when the 23andMe study was used as a discovery GWAS of chronotype (all P<0.05 and meta-analysis P<5x10(-8)). For sleep duration, we replicated one known signal in PAX8 (2.6 minutes per allele, 95% CI [1.9, 3.2], P = 5.7x10(-16)) and identified and replicated two novel associations at VRK2 (2.0 minutes per allele, 95% CI [1.3, 2.7], P = 1.2x10(-9); and 1.6 minutes per allele, 95% CI [1.1, 2.2], P = 7.6x10(-9)). Although we found genetic correlation between chronotype and BMI (rG = 0.056, P = 0.05); undersleeping and BMI (rG = 0.147, P = 1x10(-5)) and over-sleeping and BMI (rG = 0.097, P = 0.04), Mendelian Randomisation analyses, with limited power, provided no consistent evidence of causal associations between BMI or type 2 diabetes and chronotype or sleep duration. Our study brings the total number of loci associated with chronotype to 22 and with sleep duration to three, and provides new insights into the biology of sleep and circadian rhythms in humans.
Files in This Item
There are no files associated with this item.
Appears in
Collections
2. Clinical Science > Department of Pulmonary, Allergy, and Critical Care Medicine > 1. Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Related Researcher

Researcher Shin, Chol photo

Shin, Chol
Ansan Hospital (Department of Pulmonary, Allergy, and Critical Care Medicine, Ansan Hospital)
Read more

Altmetrics

Total Views & Downloads

BROWSE