Centre for Global Health Research, Usher Institute of Population Health Sciences and Informatics, University of Edinburgh, Edinburgh, United Kingdom.
Institute of Social and Preventive Medicine, University Hospital of Lausanne, Lausanne, Switzerland.
Elife. 2019 Jan 15;8:e39856. doi: 10.7554/eLife.39856.
We use a genome-wide association of 1 million parental lifespans of genotyped subjects and data on mortality risk factors to validate previously unreplicated findings near , , , , , and 13q21.31, and identify and replicate novel findings near , , and . We also validate previous findings near 5q33.3/ and , whilst finding contradictory evidence at other loci. Gene set and cell-specific analyses show that expression in foetal brain cells and adult dorsolateral prefrontal cortex is enriched for lifespan variation, as are gene pathways involving lipid proteins and homeostasis, vesicle-mediated transport, and synaptic function. Individual genetic variants that increase dementia, cardiovascular disease, and lung cancer - but not other cancers - explain the most variance. Resulting polygenic scores show a mean lifespan difference of around five years of life across the deciles.
This article has been through an editorial process in which the authors decide how to respond to the issues raised during peer review. The Reviewing Editor's assessment is that all the issues have been addressed (see decision letter).
我们使用了 100 万对经过基因分型的父母寿命的全基因组关联分析以及关于死亡率风险因素的数据,来验证先前在附近 、 、 、 、 和 13q21.31 处未被复制的发现,并鉴定和复制附近 、 和 处的新发现。我们还验证了先前在 5q33.3/ 和 处的发现,而在其他位置则发现了相互矛盾的证据。基因集和细胞特异性分析表明,在胎儿脑细胞和成人背外侧前额叶皮层中表达的寿命变异富集,涉及脂质蛋白和动态平衡、囊泡介导的运输和突触功能的基因途径也是如此。增加痴呆症、心血管疾病和肺癌(但不是其他癌症)风险的个体遗传变异解释了最大的变异。由此产生的多基因评分显示,在十分位数范围内,平均寿命差异约为五年。
本文经过编辑过程,作者决定如何处理同行评审中提出的问题。审稿人的评估是所有问题都已得到解决(见评审意见)。