| Literature DB >> 24997674 |
Andrea L Metti1, Kristine Yaffe2, Robert M Boudreau3, Eleanor M Simonsick4, Ryan M Carnahan5, Suzanne Satterfield6, Tamara B Harris7, Hilsa N Ayonayon8, Caterina Rosano3, Jane A Cauley3.
Abstract
We aimed to examine trajectories of inflammatory markers and cognitive decline over 10 years. Cox proportional hazards models were used to examine the association between interleukin-6 and C-reactive protein (CRP) trajectory components (slope, variability, and baseline level) and cognitive decline among 1323 adults, aged 70-79 years in the Health, Aging, and Body Composition Study. We tested for interactions by sex and apolipoprotein E (APOE) genotype. In models adjusted for multiple covariates and comorbidities, extreme CRP variability was significantly associated with cognitive decline (hazard ratio [HR] 1.6, 95% confidence interval [CI]: 1.1-2.3). This association was modified by sex and APOE e4 (p < 0.001 for both), such that the association remained among women (HR = 1.8; 95% CI: 1.1, 3.0) and among those with no APOE e4 allele (HR = 1.6; 95% CI: 1.1, 2.5). There were no significant associations between slope or baseline level of CRP and cognitive decline nor between interleukin-6 and cognitive decline. We believe CRP variability likely reflects poor control of or greater changes in vascular or metabolic disease over time, which in turn is associated with cognitive decline.Entities:
Keywords: C-reactive protein; Cognitive decline; Inflammatory markers; Interleukin-6
Mesh:
Substances:
Year: 2014 PMID: 24997674 PMCID: PMC4252870 DOI: 10.1016/j.neurobiolaging.2014.05.030
Source DB: PubMed Journal: Neurobiol Aging ISSN: 0197-4580 Impact factor: 4.673