He Yong-Han, Lu Xiang, Yang Li-Qin, Xu Liang-You, Kong Qing-Peng
State Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, the Chinese Academy of Sciences, Kunming 650223, China. KIZ/CUHK Joint Laboratory of Bioresources and Molecular Research in Common Diseases, Kunming 650223, China.
Dujiangyan Longevity Research Centre, Dujiangyan 611830, China.
Aging (Albany NY). 2014 Nov;6(11):944-56. doi: 10.18632/aging.100703.
Human lifespan is determined greatly by genetic factors and some investigations have identified putative genes implicated in human longevity. Although some genetic loci have been associated with longevity, most of them are difficult to replicate due to ethnic differences. In this study, we analyzed the association of 18 reported gene single nucleotide polymorphisms (SNPs) with longevity in 1075 samples consisting of 567 nonagenarians/centenarians and 508 younger controls using the GenomeLab SNPstream Genotyping System. Our results confirm the association of the forkhead box O3 (FOXO3) variant (rs13217795) and the ATM serine/threonine kinase (ATM) variant (rs189037) genotypes with longevity (p=0.0075 and p=0.026, using the codominant model and recessive model, respectively). Of note is that we first revealed the association of insulin-like growth factor binding protein 3 (IGFBP-3) gene polymorphism rs11977526 with longevity in Chinese nonagenarians/centenarians (p=0.033 using the dominant model and p=0.035 using the overdominant model). The FOXO3 and IGFBP-3 form important parts of the insulin/insulin-like growth factor-1 signaling pathway (IGF-1) implicated in human longevity, and the ATM gene is involved in sensing DNA damage and reducing oxidative stress, therefore our results highlight the important roles of insulin pathway and oxidative stress in the longevity in the Chinese population.
人类寿命很大程度上由遗传因素决定,一些研究已经确定了与人类长寿相关的假定基因。尽管一些基因位点与长寿有关,但由于种族差异,其中大多数难以复制。在本研究中,我们使用GenomeLab SNPstream基因分型系统,分析了18个已报道的基因单核苷酸多态性(SNP)与1075个样本中长寿的关联,这些样本包括567名九旬老人/百岁老人和508名年轻对照。我们的结果证实了叉头框O3(FOXO3)变体(rs13217795)和ATM丝氨酸/苏氨酸激酶(ATM)变体(rs189037)基因型与长寿的关联(分别使用共显性模型和隐性模型时,p = 0.0075和p = 0.026)。值得注意的是,我们首次揭示了胰岛素样生长因子结合蛋白3(IGFBP - 3)基因多态性rs11977526与中国九旬老人/百岁老人长寿的关联(使用显性模型时p = 0.033,使用超显性模型时p = 0.035)。FOXO3和IGFBP - 3构成了与人类长寿相关的胰岛素/胰岛素样生长因子 - 1信号通路(IGF - 1)的重要部分,而ATM基因参与感知DNA损伤并减少氧化应激,因此我们的结果突出了胰岛素通路和氧化应激在中国人群长寿中的重要作用。