Author/Authors :
Lucia A. Hindorff، نويسنده , , Kenneth M. Rice، نويسنده , , Leslie A. Lange، نويسنده , , Paula Diehr، نويسنده , , Indrani Halder، نويسنده , , Jeremy Walston، نويسنده , , Pui Kwok، نويسنده , , Elad Ziv، نويسنده , , Caroline Nievergelt، نويسنده , , Steven R. Cummings، نويسنده , , Anne B. Newman، نويسنده , , Russell P. Tracy، نويسنده , , Bruce M. Psaty، نويسنده , , Alexander P. Reiner، نويسنده ,
Abstract :
Common polymorphisms in the CRP gene are associated with plasma CRP levels in population-based studies, but associations with age-related events are uncertain. A previous study of CRP haplotypes in older adults was broadened to include longevity and cause-specific mortality (all-cause, noncardiovascular (non-CV), and cardiovascular (CV)). Common haplotypes were inferred from four tagSNPs in 4512 whites and five tagSNPs in 812 blacks from the Cardiovascular Health Study, a longitudinal cohort of adults over age 65. Exploratory analyses addressed early versus late mortality. CRP haplotypes were not associated with all-cause mortality or longevity overall in either population, but associations with all-cause mortality differed during early and late periods. In blacks, the haplotype tagged by 3872A (rs1205) was associated with increased risk of non-CV mortality, relative to other haplotypes (adjusted hazard ratio for each additional copy: 1.42, 95% CI: 1.07, 1.87). Relative to other haplotypes, this haplotype was associated with decreased risk of early but not decreased risk of late CV mortality in blacks; among whites, a haplotype tagged by 2667C (rs1800947) gave similar but nonsignificant findings. If confirmed, CRP genetic variants may be weakly associated with CV and non-CV mortality in older adults, particularly in self-identified blacks.
Keywords :
aging , C-reactive protein , polymorphism , Genetic , susceptibility , Aged , mortality , longevity