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睡眠时间的多祖先遗传结构及其与其他睡眠和精神疾病表型的关系。

Multi-ancestry genetic architecture of sleep duration and its relationship to other sleep and psychiatric phenotypes.

作者信息

Austin-Zimmerman Isabelle, Levey Daniel F, Deak Joseph D, Galimberti Marco, Adhikari Keyrun, Coleman Jonathan R I, Buysse Daniel J, Wilson Peter W F, Sofer Tamar, Gaziano J Michael, Gottlieb Daniel J, Stein Murray B, Forti Marta Di, Gelernter Joel

机构信息

Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE5 8AF, UK.

Division of Human Genetics, Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.

出版信息

medRxiv. 2025 May 21:2025.05.19.25327902. doi: 10.1101/2025.05.19.25327902.

Abstract

Differences in sleep duration, quality, and timing are associated with variation in cognition, health outcomes, and quality of life. Genetic studies may help explain the underlying mechanisms of sleep and its relationships to other conditions. Our previous work highlighted risk loci associated with short (<6hrs) and long sleep (>9hrs), using data from the UK Biobank and the Million Veteran Program. We build on this work by conducting a genome wide association study (GWAS) and multi-ancestry meta-analysis of sleep duration as a quantitative trait. We used LD score regression (LDSC) to evaluate the correlation between sleep duration and other traits, and genomic structural equation modelling (genomicSEM) to consider the relationships between traits of interest. We identify 234 independent genome-wide significant loci for sleep duration, of which 143 are novel. The average impact of each risk variant amounts to approximately ±0.86minutes (sd=0.19), with a sum total of ± 220.5 minutes across all genome-wide significant loci. We support previous findings showing the most strongly associated gene is . Linkage disequilibrium score regression shows that the genetic architecture of sleep duration is largely distinct from other measures of sleep quality and sleep disorders. We see several examples of negative correlation between deleterious traits and the quantitative measure of sleep duration reported here, contrasting with positive associations with long and short sleep (e.g., depression, ADHD, cannabis use disorder, smoking). We derive genomic-SEM models that show short and long sleep load on separate factors, as does overall sleep duration loading alone. This is the largest available GWAS of sleep duration, and the first to extend analyses outside of European ancestry populations. We identify novel loci for sleep duration and provide insight to the shared and unique genetic architecture across multiple sleep and neuropsychiatric traits.

摘要

睡眠时间、质量和时间安排的差异与认知、健康结果及生活质量的变化相关。基因研究可能有助于解释睡眠的潜在机制及其与其他状况的关系。我们之前的研究利用英国生物银行和百万退伍军人计划的数据,突出了与短睡眠(<6小时)和长睡眠(>9小时)相关的风险位点。我们在此基础上开展了一项全基因组关联研究(GWAS)以及将睡眠时间作为定量性状的多祖先荟萃分析。我们使用连锁不平衡分数回归(LDSC)来评估睡眠时间与其他性状之间的相关性,并使用基因组结构方程模型(genomicSEM)来考量感兴趣的性状之间的关系。我们确定了234个全基因组显著的独立睡眠时间位点,其中143个是新发现的。每个风险变异的平均影响约为±0.86分钟(标准差=0.19),所有全基因组显著位点的总影响为±220.5分钟。我们支持之前的研究结果,即显示关联最强的基因是 。连锁不平衡分数回归表明,睡眠时间的遗传结构在很大程度上与睡眠质量和睡眠障碍的其他测量指标不同。我们看到了有害性状与本文报道的睡眠时间定量测量之间存在负相关的几个例子,这与长睡眠和短睡眠的正相关情况形成对比(例如,抑郁症、注意力缺陷多动障碍、大麻使用障碍、吸烟)。我们推导的基因组结构方程模型表明,短睡眠和长睡眠负荷于不同因素,整体睡眠时间单独负荷也是如此。这是目前关于睡眠时间最大规模的全基因组关联研究,也是首次将分析扩展到欧洲血统人群之外。我们确定了睡眠时间的新位点,并深入了解了多种睡眠和神经精神性状的共同和独特遗传结构。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0b2/12140527/4f22b9acda4a/nihpp-2025.05.19.25327902v1-f0001.jpg

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