Sebastiani Paola, Gurinovich Anastasia, Bae Harold, Andersen Stacy, Malovini Alberto, Atzmon Gil, Villa Francesco, Kraja Aldi T, Ben-Avraham Danny, Barzilai Nir, Puca Annibale, Perls Thomas T
Department of Biostatistics, Boston University School of Public Health, Massachusetts.
Bioinformatics Program, Boston University, Massachusetts.
J Gerontol A Biol Sci Med Sci. 2017 Oct 12;72(11):1453-1464. doi: 10.1093/gerona/glx027.
The search for the genetic determinants of extreme human longevity has been challenged by the phenotype's rarity and its nonspecific definition by investigators. To address these issues, we established a consortium of four studies of extreme longevity that contributed 2,070 individuals who survived to the oldest one percentile of survival for the 1900 U.S. birth year cohort. We conducted various analyses to discover longevity-associated variants (LAV) and characterized those LAVs that differentiate survival to extreme age at death (eSAVs) from those LAVs that become more frequent in centenarians because of mortality selection (eg, survival to younger years). The analyses identified new rare variants in chromosomes 4 and 7 associated with extreme survival and with reduced risk for cardiovascular disease and Alzheimer's disease. The results confirm the importance of studying truly rare survival to discover those combinations of common and rare variants associated with extreme longevity and longer health span.
对人类极端长寿的基因决定因素的探索,因该表型的罕见性以及研究者对其非特异性定义而受到挑战。为解决这些问题,我们建立了一个由四项极端长寿研究组成的联盟,该联盟贡献了2070名个体,他们在1900年美国出生队列中存活至生存的最老百分之一。我们进行了各种分析,以发现与长寿相关的变异(LAV),并对那些将死亡时极端年龄生存(eSAV)与因死亡率选择(例如,存活至较年轻年龄)而在百岁老人中变得更常见的LAV区分开来的LAV进行了特征描述。这些分析在4号和7号染色体上鉴定出与极端生存以及心血管疾病和阿尔茨海默病风险降低相关的新的罕见变异。结果证实了研究真正罕见的生存情况以发现与极端长寿和更长健康寿命相关的常见和罕见变异组合的重要性。