Genetic associations with longevity in a Calabrian cohort: an exploratory genome-wide study.

Abstract

Human longevity is a complex trait shaped by genetic background and population-specific factors. Calabria, a region in Southern Italy with a high prevalence of centenarians and relative genetic isolation, is a valuable model for investigating the genetic architecture of extreme survival. Here, we performed a genome-wide association study of longevity in 705 Calabrian individuals, comparing long-lived subjects to younger controls using a mixed-model approach that accounts for relatedness and population structure. We identified 22 suggestive risk loci, among which one reached genome-wide significance. Although most loci did not replicate in external datasets, an intronic variant regulating proteasome-related gene expression was confirmed by meta-analysis. Based on the nominal significance of gene- and pathway-based analyses, it is possible to hypothesize that the biological processes potentially affecting longevity in this cohort might include proteostasis, maintenance of genome integrity, apoptosis, and insulin- and inflammation-related pathways. Notably, established longevity loci such as APOE and FOXO3 were not associated, underscoring population-specific genetic effects. Overall, our preliminary findings suggest that longevity in the Calabrian population arises from a combination of unique genetic influences and conserved aging-related mechanisms, providing new insights into the molecular basis of human lifespan extension.