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与人类寿命相关的遗传变异的前瞻性分析。

A Prospective Analysis of Genetic Variants Associated with Human Lifespan.

机构信息

Calico Life Sciences LLC. 1170 Veterans Blvd, South San Francisco 94080.

Ancestry, San Francisco, California 94107, and.

出版信息

G3 (Bethesda). 2019 Sep 4;9(9):2863-2878. doi: 10.1534/g3.119.400448.

Abstract

We present a massive investigation into the genetic basis of human lifespan. Beginning with a genome-wide association (GWA) study using a de-identified snapshot of the unique database - more than 300,000 genotyped individuals linked to pedigrees of over 400,000,000 people - we mapped six genome-wide significant loci associated with parental lifespan. We compared these results to a GWA analysis of the traditional lifespan proxy trait, age, and found only one locus, , to be associated with both age and lifespan. By combining the results with those of an independent UK Biobank dataset, we conducted a meta-analysis of more than 650,000 individuals and identified fifteen parental lifespan-associated loci. Beyond just those significant loci, our genome-wide set of polymorphisms accounts for up to 8% of the variance in human lifespan; this value represents a large fraction of the heritability estimated from phenotypic correlations between relatives.

摘要

我们对人类寿命的遗传基础进行了大规模的研究。从使用独特的数据库的匿名快照进行全基因组关联(GWA)研究开始 - 超过 30 万名个体被基因分型,并与超过 4 亿人的家系相关联 - 我们绘制了与父母寿命相关的六个全基因组显著位点。我们将这些结果与传统寿命代理特征年龄的 GWA 分析进行了比较,发现只有一个位点,与年龄和寿命都相关。通过将这些结果与独立的英国生物银行数据集相结合,我们对超过 65 万名个体进行了荟萃分析,确定了 15 个与父母寿命相关的位点。除了这些显著的位点之外,我们全基因组范围内的多态性可以解释人类寿命变异的 8%;这个值代表了从亲属之间表型相关性估计的遗传力的很大一部分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9df0/6723124/9dadb9bc60b1/2863f1.jpg

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