| Literature DB >> 17888441 |
Lucia A Hindorff1, Kenneth M Rice, Leslie A Lange, Paula Diehr, Indrani Halder, Jeremy Walston, Pui Kwok, Elad Ziv, Caroline Nievergelt, Steven R Cummings, Anne B Newman, Russell P Tracy, Bruce M Psaty, Alexander P Reiner.
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.Entities:
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Year: 2007 PMID: 17888441 PMCID: PMC2362133 DOI: 10.1016/j.atherosclerosis.2007.08.012
Source DB: PubMed Journal: Atherosclerosis ISSN: 0021-9150 Impact factor: 5.162