69.7 万人时间型的全基因组关联分析:揭示昼夜节律与疾病的联系
Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms, and links to disease
一句话摘要
对 697,828 人做时间型的全基因组关联分析,识别大量相关位点,并揭示时间型与精神及代谢疾病的遗传学关联。
为什么重要
把时间型从行为学量表提升为可做大规模遗传解析的数量性状,为「晨型—夜型有生物学基础而非习惯问题」提供了迄今最大样本的证据。
英文摘要原文
Being a morning person is a behavioural indicator of a person's underlying circadian rhythm. Using genome-wide data from 697,828 UK Biobank and 23andMe participants we increase the number of genetic loci associated with being a morning person from 24 to 351. Using data from 85,760 individuals with activity-monitor derived measures of sleep timing we find that the chronotype loci associate with sleep timing: the mean sleep timing of the 5% of individuals carrying the most morningness alleles is 25 min earlier than the 5% carrying the fewest. The loci are enriched for genes involved in circadian regulation, cAMP, glutamate and insulin signalling pathways, and those expressed in the retina, hindbrain, hypothalamus, and pituitary. Using Mendelian Randomisation, we show that being a morning person is causally associated with better mental health but does not affect BMI or risk of Type 2 diabetes. This study offers insights into circadian biology and its links to disease in humans.
所属章节
条目编号 P030 · 元数据经 Crossref / Europe PMC 回查