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Association analyses of insulin signaling pathway gene polymorphisms with healthy aging and longevity in Americans of Japanese ancestry

机译:日裔美国人胰岛素信号通路基因多态性与健康衰老和长寿的关联分析

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摘要

Evidence from model organisms suggests that the insulin/IGF-1 signaling pathway has an important, evolutionarily conserved influence over rate of aging and thus longevity. In humans, the FOXO3 gene is the only widely replicated insulin/IGF-1 signaling pathway gene associated with longevity across multiple populations. Therefore, we conducted a nested case-control study of other insulin/IGF-1 signaling genes and longevity, utilizing a large, homogeneous, long-lived population of American men of Japanese ancestry, well characterized for aging phenotypes. Genotyping was performed of single nucleotide polymorphisms, tagging most of the genetic variation across several genes in the insulin/IGF-1 signaling pathway or related gene networks that may be influenced by FOXO3, namely, ATF4, CBL, CDKN2, EXO1, and JUN. Two initial, marginal associations with longevity did not remain significant after correction for multiple comparisons, nor were they correlated with aging-related phenotypes.
机译:来自模型生物的证据表明,胰岛素/ IGF-1信号通路对衰老率和寿命具有重要的,进化上保守的影响。在人类中,FOXO3基因是唯一被广泛复制的胰岛素/ IGF-1信号通路基因,与多个人群的寿命有关。因此,我们利用大量的,均质的,长寿的日本血统美国男性,对其他胰岛素/ IGF-1信号基因和寿命进行了嵌套的病例对照研究,其特征是衰老的表型。对单核苷酸多态性进行基因分型,在胰岛素/ IGF-1信号传导途径或可能受FOXO3影响的相关基因网络(即ATF4,CBL,CDKN2,EXO1和JUN)的几个相关基因网络中标记大部分遗传变异。经过多次比较校正后,两个具有长寿的初始边缘关联并不显着,也不与衰老相关的表型相关。

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