Detailed Information

Cited 0 time in webofscience Cited 0 time in scopus
Metadata Downloads

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

Full metadata record
DC Field Value Language
dc.contributor.authorJones, Samuel E.-
dc.contributor.authorTyrrell, Jessica-
dc.contributor.authorWood, Andrew R.-
dc.contributor.authorBeaumont, Robin N.-
dc.contributor.authorRuth, Katherine S.-
dc.contributor.authorTuke, Marcus A.-
dc.contributor.authorYaghootkar, Hanieh-
dc.contributor.authorHu, Youna-
dc.contributor.authorTeder-Laving, Maris-
dc.contributor.authorHayward, Caroline-
dc.contributor.authorRoenneberg, Till-
dc.contributor.authorWilson, James F.-
dc.contributor.authorDel Greco, Fabiola-
dc.contributor.authorHicks, Andrew A.-
dc.contributor.authorShin, Chol-
dc.contributor.authorYun, Chang-Ho-
dc.contributor.authorLee, Seung Ku-
dc.contributor.authorMetspalu, Andres-
dc.contributor.authorByrne, Enda M.-
dc.contributor.authorGehrman, Philip R.-
dc.contributor.authorTiemeier, Henning-
dc.contributor.authorAllebrandt, Karla V.-
dc.contributor.authorFreathy, Rachel M.-
dc.contributor.authorMurray, Anna-
dc.contributor.authorHinds, David A.-
dc.contributor.authorFrayling, Timothy M.-
dc.contributor.authorWeedon, Michael N.-
dc.date.accessioned2021-09-03T21:44:41Z-
dc.date.available2021-09-03T21:44:41Z-
dc.date.created2021-06-18-
dc.date.issued2016-08-
dc.identifier.issn1553-7390-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/88019-
dc.description.abstractDisrupted 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.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherPUBLIC LIBRARY SCIENCE-
dc.subjectMENDELIAN RANDOMIZATION-
dc.subjectDIURNAL PREFERENCE-
dc.subjectCHRONOTYPE-
dc.subjectOBESITY-
dc.subjectGENES-
dc.subjectMETAANALYSIS-
dc.subjectCOMPONENT-
dc.subjectVARIANTS-
dc.subjectINSIGHTS-
dc.subjectGWAS-
dc.titleGenome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci-
dc.typeArticle-
dc.contributor.affiliatedAuthorShin, Chol-
dc.identifier.doi10.1371/journal.pgen.1006125-
dc.identifier.scopusid2-s2.0-84984916617-
dc.identifier.wosid000382394500004-
dc.identifier.bibliographicCitationPLOS GENETICS, v.12, no.8-
dc.relation.isPartOfPLOS GENETICS-
dc.citation.titlePLOS GENETICS-
dc.citation.volume12-
dc.citation.number8-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaGenetics & Heredity-
dc.relation.journalWebOfScienceCategoryGenetics & Heredity-
dc.subject.keywordPlusMENDELIAN RANDOMIZATION-
dc.subject.keywordPlusDIURNAL PREFERENCE-
dc.subject.keywordPlusCHRONOTYPE-
dc.subject.keywordPlusOBESITY-
dc.subject.keywordPlusGENES-
dc.subject.keywordPlusMETAANALYSIS-
dc.subject.keywordPlusCOMPONENT-
dc.subject.keywordPlusVARIANTS-
dc.subject.keywordPlusINSIGHTS-
dc.subject.keywordPlusGWAS-
Files in This Item
There are no files associated with this item.
Appears in
Collections
College of Medicine > Department of Medical Science > 1. Journal Articles

qrcode

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

Altmetrics

Total Views & Downloads

BROWSE