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Meta-analysis of genetic variants associated with human exceptional longevity

机译:与人类超常寿命相关的遗传变异的荟萃分析

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摘要

Despite evidence from family studies that there is a strong genetic influence upon exceptional longevity, relatively few genetic variants have been associated with this trait. One reason could be that many genes individually have such weak effects that they cannot meet standard thresholds of genome wide significance, but as a group in specific combinations of genetic variations, they can have a strong influence. Previously we reported that such genetic signatures of 281 genetic markers associated with about 130 genes can do a relatively good job of differentiating centenarians from non-centenarians particularly if the centenarians are 106 years and older. This would support our hypothesis that the genetic influence upon exceptional longevity increases with older and older (and rarer) ages. We investigated this list of markers using similar genetic data from 5 studies of centenarians from the USA, Europe and Japan. The results from the meta-analysis show that many of these variants are associated with survival to these extreme ages in other studies. Since many centenarians compress morbidity and disability towards the end of their lives, these results could point to biological pathways and therefore new therapeutics to increase years of healthy lives in the general population.
机译:尽管有家庭研究的证据表明,这种遗传对超长寿命有很强的影响力,但与这种性状相关的遗传变异相对较少。一个原因可能是许多基因单独具有如此弱的作用,以致于它们无法满足全基因组意义的标准阈值,但是作为一组特定的遗传变异组合,它们可能会产生强大的影响。以前我们报道过,与130个基因相关的281个遗传标记的遗传标记可以很好地区分百岁老人与非百岁老人,尤其是在百岁老人和106岁以上的情况下。这将支持我们的假设,即对超长寿命的遗传影响会随着年龄的增长而增加。我们使用了来自美国,欧洲和日本的5个百岁老人的相似遗传数据,调查了这一标记物清单。荟萃分析的结果表明,在其他研究中,许多这些变异与这些极端年龄的存活率有关。由于许多百岁老人在其生命的尽头都会压缩发病率和残疾,因此这些结果可能表明了生物学途径,因此提出了新的疗法来增加普通人群的健康寿命。

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