|Title||Genome-wide Association Study of Parental Life Span.|
|Publication Type||Journal Article|
|Year of Publication||2017|
|Authors||Tanaka, T, Dutta, A, Pilling, LC, Xue, L, Lunetta, KL, Murabito, JM, Bandinelli, S, Wallace, RB, Melzer, D, Ferrucci, L|
|Journal||J Gerontol A Biol Sci Med Sci|
|Date Published||2017 Oct 01|
|Keywords||Aged, Aged, 80 and over, Chromosomes, Human, Pair 18, Female, Genome-Wide Association Study, Humans, Longevity, Male, Middle Aged, Parents, Phenotype, Polymorphism, Single Nucleotide, Trans-Activators|
Background: Having longer lived parents has been shown to be an important predictor of health trajectories and life span. As such, parental life span is an important phenotype that may uncover genes that affect longevity.
Methods: A genome-wide association study of parental life span in participants of European and African ancestry from the Health and Retirement Study was conducted.
Results: A genome-wide significant association was observed for rs35715456 (log10BF = 6.3) on chromosome 18 for the dichotomous trait of having at least one long-lived parent versus not having any long-lived parent. This association was not replicated in an independent sample from the InCHIANTI and Framingham Heart Study. The most significant association among single nucleotide polymorphisms in longevity candidate genes (APOE, MINIPP1, FOXO3, EBF1, CAMKIV, and OTOL1) was observed in the EBF1 gene region (rs17056207, p = .0002).
Conclusions: A promising genetic signal for parental life span was identified but was not replicated in independent samples.
|User Guide Notes|
|Alternate Journal||J. Gerontol. A Biol. Sci. Med. Sci.|
|PubMed Central ID||PMC5861941|
|Grant List||P30 CA086862 / CA / NCI NIH HHS / United States |
U01 AG009740 / AG / NIA NIH HHS / United States