An association study of FOXO3 variant and longevity

• Autor(a) principal: Silva-Sena,Geralda Gillian
• Data de Publicação: 2018
• Outros Autores: Camporez,Daniela, Santos,Lígia Ramos dos, Silva,Aline Sesana da, Sagrillo Pimassoni,Lúcia Helena, Tieppo,Alessandra, Pimentel Batitucci,Maria do Carmo, Morelato,Renato Lírio, Paula,Flavia de
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Genetics and Molecular Biology
• Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572018000300386
• topic: Lifespan; SNPs; environmental factors; oxidative stress; genomic damage

Abstract Human longevity is a polygenic and multifactorial trait. Pathways related to lifespan are complex and involve molecular, cellular, and environmental processes. In this analytical observational study, we evaluated the relationship between environment factors, oxidative stress status, DNA integrity level, and the association of FOXO3 (rs2802292), SOD2 (rs4880), APOE (rs429358 and rs7412), and SIRT1 (rs2273773) polymorphisms with longevity in oldest-old individuals from southeastern Brazil. We found an association between the FOXO3 GG genotype and gender. While lifestyle, anthropometric, and biochemical characteristics showed significant results, DNA damage and oxidative stress were not related to lifespan. We found that long-lived individuals with FOXO3 GT genotype had low levels of triglycerides. This study is the first to demonstrate that FOXO3 could be a candidate gene for longevity in the Brazilian population. These results are important in terms of provisions of health care for age-related diseases and lifespan, and provide insight for further research on epigenetic, gene regulation, and expression in oldest-old individuals.