| Literature DB >> 30060062 |
Paola Sebastiani1, Anastasia Gurinovich1,2, Marianne Nygaard3, Takashi Sasaki4, Benjamin Sweigart1, Harold Bae5, Stacy L Andersen6, Francesco Villa7, Gil Atzmon8,9, Kaare Christensen3, Yasumichi Arai4, Nir Barzilai9, Annibale Puca7,10, Lene Christiansen3, Nobuyoshi Hirose4, Thomas T Perls6.
Abstract
We assembled a collection of 28,297 participants from seven studies of longevity and healthy aging comprising New England Centenarian, Long Life Family, Longevity Gene Population, Southern Italian Centenarian, Japanese Centenarian, the Danish Longevity, and the Health and Retirement Studies to investigate the association between the APOE alleles ε2ε3 and ε4 and extreme human longevity and age at death. By using three different genetic models and two definitions of extreme longevity based on either a threshold model or age at death, we show that ε4 is associated with a substantially decreased odds for extreme longevity, and increased risk for death that persists even beyond ages reached by less than 1% of the population. We also show that carrying the ε2ε2 or ε2ε3 genotype is associated with significantly increased odds to reach extreme longevity, with decreased risk for death compared with carrying the genotype ε3ε3 but with only a modest reduction in risk for death beyond an age reached by less than 1% of the population.Entities:
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Year: 2019 PMID: 30060062 PMCID: PMC6298189 DOI: 10.1093/gerona/gly174
Source DB: PubMed Journal: J Gerontol A Biol Sci Med Sci ISSN: 1079-5006 Impact factor: 6.053