Institute of Genetic Medicine, European Academy Bozen/Bolzano Research, Viale Druso/Drususallee, 1 39100 Bolzano/Bozen, Italy.
J Gerontol A Biol Sci Med Sci. 2011 Jan;66(1):26-37. doi: 10.1093/gerona/glq163. Epub 2010 Sep 24.
Although genetic factors are known to influence the human aging process, the proportion of life span and longevity variation explained by them is still controversial. We evaluated the genetic contribution to life span using historical data from three Alpine communities in South Tyrol, Italy. We estimated the heritability of life span and survival to old age (longevity), and we assessed the hypothesis of a common genetic background between life span and reproduction. The heritability of life span was 0.15 (SE = 0.02), whereas the heritability of longevity increased from 0.20 to 0.35 as the longevity threshold increased. Heritability estimates were little influenced by shared environment, most likely due to the homogeneity of lifestyle and environmental factors in our study population. Life span showed both positive association and genetic correlation with reproductive history factors. Our study demonstrates a general low inheritance of human life span, but which increases substantially when considering long-living individuals, and a common genetic background of life span and reproduction, in agreement with evolutionary theories of aging.
虽然遗传因素被认为会影响人类的衰老过程,但它们对寿命和长寿变异的解释比例仍存在争议。我们使用来自意大利南蒂罗尔的三个阿尔卑斯社区的历史数据评估了遗传因素对寿命的贡献。我们估计了寿命和老年生存(长寿)的遗传力,并评估了寿命和生殖之间存在共同遗传背景的假设。寿命的遗传力为 0.15(SE=0.02),而随着长寿阈值的增加,长寿的遗传力从 0.20 增加到 0.35。遗传力估计受共享环境的影响很小,这很可能是由于我们研究人群的生活方式和环境因素的同质性所致。寿命与生殖历史因素均呈正相关和遗传相关。我们的研究表明,人类寿命的遗传率普遍较低,但当考虑长寿个体时,遗传率会大幅增加,并且寿命和生殖之间存在共同的遗传背景,这与衰老的进化理论一致。