| Literature DB >> 29688278 |
Philip M C Davy1, D Craig Willcox2,3,4, Michio Shimabukuro5,6,7, Timothy A Donlon8, Trevor Torigoe1, Makoto Suzuki4, Moritake Higa7, Hiroaki Masuzaki9, Masataka Sata10, Randi Chen2, Rachel L Murkofsky11, Brian J Morris2,12, Eunjung Lim13, Richard C Allsopp1,14, Bradley J Willcox2,4,14.
Abstract
FOXO3 is one of the most prominent genes demonstrating a consistently reproducible genetic association with human longevity. The mechanisms by which these individual gene variants confer greater organismal lifespan are not well understood. We assessed the effect of longevity-associated FOXO3 alleles on age-related leukocyte telomere dynamics in a cross-sectional study comprised of samples from 121 healthy Okinawan-Japanese donors aged 21-95 years. We found that telomere length for carriers of the longevity associated allele of FOXO3 single nucleotide polymorphism rs2802292 displayed no significant correlation with age, an effect that was most pronounced in older (>50 years of age) participants. This is the first validated longevity gene variant identified to date showing an association with negligible loss of telomere length with age in humans in a cross-sectional study. Reduced telomere attrition may be a key mechanism for the longevity-promoting effect of the FOXO3 genotype studied.Entities:
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Year: 2018 PMID： 29688278 PMCID： PMC6175018 DOI： 10.1093/gerona/gly071
Source DB: PubMed Journal: J Gerontol A Biol Sci Med Sci ISSN： 1079-5006 Impact factor: 6.053