Multi-ancestry genome-wide analysis identifies shared genetic effects and common genetic variants for self-reported sleep duration.
Multi-ancestry genome-wide analysis identifies shared genetic effects and common genetic variants for self-reported sleep duration.
复制标题
多祖先全基因组分析确定了自我报告的睡眠持续时间的共同遗传效应和常见遗传变异。
DOI:
10.1093/hmg/ddad101
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发表时间:
2023
影响因子:
3.5
通讯作者:
Saxena,R
中科院分区:
文献类型:
--
作者:
Scammell,BH;Tchio,C;Song,Y;Nishiyama,T;Louie,TL;Dashti,HS;Nakatochi,M;Zee,PC;Daghlas,I;Momozawa,Y;Cai,J;Ollila,HM;Redline,S;Wakai,K;Sofer,T;Suzuki,S;Lane,JM;Saxena,R
Both short (≤6 h per night) and long sleep duration (≥9 h per night) are associated with increased risk of chronic diseases. Despite evidence linking habitual sleep duration and risk of disease, the genetic determinants of sleep duration in the general population are poorly understood, especially outside of European (EUR) populations. Here, we report that a polygenic score of 78 European ancestry sleep duration single-nucleotide polymorphisms (SNPs) is associated with sleep duration in an African (n= 7288;P =0.003), an East Asian (n =13 618;P =6 × 10−4) and a South Asian (n= 7485;P =0.025) genetic ancestry cohort, but not in a Hispanic/Latino cohort (n= 8726;P =0.71). Furthermore, in a pan-ancestry (N= 483 235) meta-analysis of genome-wide association studies (GWAS) for habitual sleep duration, 73 loci are associated with genome-wide statistical significance. Follow-up of five loci (nearHACD2,COG5,PRR12,SH3RF1andKCNQ5) identified expression-quantitative trait loci forPRR12andCOG5in brain tissues and pleiotropic associations with cardiovascular and neuropsychiatric traits. Overall, our results suggest that the genetic basis of sleep duration is at least partially shared across diverse ancestry groups.
影响因子:
1.6
作者:
C. G. Loosli
通讯作者:
C. G. Loosli
影响因子:
5.9
作者:
BAINE, WB;LUBY, JP;MARTIN, SM
通讯作者:
MARTIN, SM