人口队列遗传结构随年龄增长而变化:人类衰老和寿命遗传分析的意义。

Anatoliy I Yashin, Deqing Wu, Konstantin G Arbeev, Liubov S Arbeeva, Igor Akushevich, Alexander Kulminski, Irina Culminskaya, Eric Stallard, Svetlana V Ukraintseva
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引用次数: 0

摘要

背景:校正群体分层的潜在影响是复杂性状全基因组关联研究(GWAS)中的一个重要问题。研究群体遗传结构的主成分分析(PCA),随后在GWAS回归模型中加入前几个主成分(PCs),通常用于此目的。问题:对于长寿相关的性状,这样的修正可能会对基因分析的准确性产生负面影响。这是因为在遗传异质性群体中,pc可能捕获由死亡率选择过程引起的遗传结构。数据和方法:我们使用弗雷明汉心脏研究的寿命和个体遗传背景数据来构建两套pc。一个是为了将由于祖先差异造成的群体分层与由死亡率选择引起的群体分层区分开来。另一个是利用不同年龄个体的遗传数据构建的,没有试图将祖先效应与死亡率选择效应分开。使用每个选择集的前20个pc进行人类寿命的GWASs,以控制可能的群体分层。结果:结果表明,使用PC集分离由祖先差异引起的死亡率选择引起的群体分层的GWAS比不使用PC集分离的GWAS产生更强的遗传信号。结论:在控制群体分层可能产生的影响时,考虑死亡率选择引起的遗传结构变化,可以提高GWAS遗传估计的质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Genetic Structures of Population Cohorts Change with Increasing Age: Implications for Genetic Analyses of Human aging and Life Span.

Background: Correcting for the potential effects of population stratification is an important issue in genome wide association studies (GWAS) of complex traits. Principal component analysis (PCA) of the genetic structure of the population under study with subsequent incorporation of the first several principal components (PCs) in the GWAS regression model is often used for this purpose.

Problem: For longevity related traits such a correction may negatively affect the accuracy of genetic analyses. This is because PCs may capture genetic structure induced by mortality selection processes in genetically heterogeneous populations.

Data and methods: We used the Framingham Heart Study data on life span and on individual genetic background to construct two sets of PCs. One was constructed to separate population stratification due to differences in ancestry from that induced by mortality selection. The other was constructed using genetic data on individuals of different ages without attempting to separate the ancestry effects from the mortality selection effects. The GWASs of human life span were performed using the first 20 PCs from each of the selected sets to control for possible population stratification.

Results: The results indicated that the GWAS that used the PC set separating population stratification induced by mortality selection from differences in ancestry produced stronger genetic signals than the GWAS that used PCs without such separation.

Conclusion: The quality of genetic estimates in GWAS can be improved when changes in genetic structure caused by mortality selection are taken into account in controlling for possible effects of population stratification.

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