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Genetics of Human Longevity From Incomplete Data: New Findings From the Long Life Family Study

机译:来自不完整数据的人类寿命遗传学:长寿家族研究的新发现

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摘要

The special design of the Long Life Family Study provides a unique opportunity to investigate the genetics of human longevity by analyzing data on exceptional lifespans in families. In this article, we performed two series of genome wide association studies of human longevity which differed with respect to whether missing lifespan data were predicted or not predicted. We showed that the use of predicted lifespan is most beneficial when the follow-up period is relatively short. In addition to detection of strong associations of SNPs in APOE, TOMM40, NECTIN2, and APOC1 genes with longevity, we also detected a strong new association with longevity of rs1927465, located between the CYP26A1 and MYOF genes on chromosome 10. The association was confirmed using data from the Health and Retirement Study. We discuss the biological relevance of the detected SNPs to human longevity.
机译:长寿家庭研究的特殊设计通过分析家庭特殊寿命的数据,为研究人类长寿的遗传学提供了独特的机会。在本文中,我们对人类寿命进行了两个系列的全基因组关联研究,这些研究在是否预测缺少寿命数据方面有所不同。我们表明,在随访期相对较短时,使用预测寿命最为有益。除了检测具有长寿的APOE,TOMM40,NECTIN2和APOC1基因中SNP的强关联外,我们还检测到了与rs1927465的长寿强相关的新关联,该关联位于10号染色体上的CYP26A1和MYOF基因之间。来自健康与退休研究的数据。我们讨论检测到的SNPs与人类寿命的生物学相关性。

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