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Interaction Between the FOXO1A-209 Genotype and Tea Drinking Is Significantly Associated with Reduced Mortality at Advanced Ages

机译:FOXO1A-209基因型与饮茶之间的相互作用与高龄时死亡率降低显着相关

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摘要

On the basis of the genotypic/phenotypic data from Chinese Longitudinal Healthy Longevity Survey (CLHLS) and Cox proportional hazard model, the present study demonstrates that interactions between carrying FOXO1A-209 genotypes and tea drinking are significantly associated with lower risk of mortality at advanced ages. Such a significant association is replicated in two independent Han Chinese CLHLS cohorts (p = 0.028–0.048 in the discovery and replication cohorts, and p = 0.003–0.016 in the combined dataset). We found the associations between tea drinking and reduced mortality are much stronger among carriers of the FOXO1A-209 genotype compared to non-carriers, and drinking tea is associated with a reversal of the negative effects of carrying FOXO1A-209 minor alleles, that is, from a substantially increased mortality risk to substantially reduced mortality risk at advanced ages. The impacts are considerably stronger among those who carry two copies of the FOXO1A minor allele than those who carry one copy. On the basis of previously reported experiments on human cell models concerning FOXO1A-by-tea-compounds interactions, we speculate that results in the present study indicate that tea drinking may inhibit FOXO1A-209 gene expression and its biological functions, which reduces the negative impacts of FOXO1A-209 gene on longevity (as reported in the literature) and offers protection against mortality risk at oldest-old ages. Our empirical findings imply that the health outcomes of particular nutritional interventions, including tea drinking, may, in part, depend upon individual genetic profiles, and the research on the effects of nutrigenomics interactions could potentially be useful for rejuvenation therapies in the clinic or associated healthy aging intervention programs.
机译:根据中国纵向健康长寿调查(CLHLS)和Cox比例风险模型的基因型/表型数据,本研究表明,携带FOXO1A-209基因型与饮茶之间的相互作用与高龄死亡风险显着相关。在两个独立的汉族CLHLS队列中复制了这种显着关联(发现和复制队列中p = 0.028-0.048,组合数据集中p = 0.003-0.016)。我们发现,与非携带者相比,FOXO1A-209基因型携带者中饮茶与死亡率降低之间的关联要强得多,并且饮茶与携带FOXO1A-209次要等位基因的负面影响逆转有关,也就是说,从大幅增加的死亡率风险到大幅降低的老年死亡率风险。携带两个FOXO1A次要等位基因的人比携带一个拷贝的人的影响要大得多。根据先前报道的有关人细胞模型中FOXO1A-by-tea-compounds相互作用的实验,我们推测本研究结果表明饮茶可能抑制FOXO1A-209基因表达及其生物学功能,从而减少负面影响FOXO1A-209基因对寿命的影响(如文献报道),并提供了针对最大年龄的死亡风险的保护。我们的经验发现表明,特定的营养干预措施(包括喝茶)的健康结果可能部分取决于个体的遗传特征,并且有关营养素相互作用的影响的研究可能对诊所或相关健康人群的复兴疗法有用。老化干预计划。

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