Metti Andrea L, Yaffe Kristine, Boudreau Robert M, Simonsick Eleanor M, Carnahan Ryan M, Satterfield Suzanne, Harris Tamara B, Ayonayon Hilsa N, Rosano Caterina, Cauley Jane A
Department of Epidemiology, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
Department of Psychiatry, University of California San Francisco, San Francisco, CA, USA; Department of Neurology, University of California San Francisco, San Francisco, CA, USA; Department of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, CA, USA.
Neurobiol Aging. 2014 Dec;35(12):2785-2790. doi: 10.1016/j.neurobiolaging.2014.05.030. Epub 2014 Jun 6.
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.
我们旨在研究10年间炎症标志物和认知衰退的轨迹。在健康、衰老和身体成分研究中,我们使用Cox比例风险模型来检验白细胞介素-6和C反应蛋白(CRP)轨迹成分(斜率、变异性和基线水平)与1323名70至79岁成年人认知衰退之间的关联。我们按性别和载脂蛋白E(APOE)基因型检验了交互作用。在针对多种协变量和合并症进行调整的模型中,极端的CRP变异性与认知衰退显著相关(风险比[HR]为1.6,95%置信区间[CI]:1.1至2.3)。这种关联在性别和APOE e4基因(两者p均<0.001)的影响下有所改变,即这种关联在女性中仍然存在(HR = 1.8;95% CI:1.1,3.0),在没有APOE e4等位基因的人群中也存在(HR = 1.6;95% CI:1.1,2.5)。CRP的斜率或基线水平与认知衰退之间以及白细胞介素-6与认知衰退之间均无显著关联。我们认为CRP变异性可能反映了随着时间推移血管或代谢疾病控制不佳或变化更大,而这反过来又与认知衰退相关。