Lin Feng, Lo Raymond Y, Cole Daniel, Ducharme Simon, Chen Ding-Geng, Mapstone Mark, Porsteinsson Anton
Department of Psychiatry, University of Rochester, Rochester, N.Y., USA ; Department of School of Nursing, University of Rochester, Rochester, N.Y., USA.
Department of Neurology, Buddhist Tzu Chi General Hospital, Tzu Chi University, Hualien, Taiwan, ROC.
Dement Geriatr Cogn Dis Extra. 2014 Jun 28;4(2):184-94. doi: 10.1159/000363285. eCollection 2014 May.
BACKGROUND/AIMS: This study examines the longitudinal effect of metabolic syndrome (MetS) on brain-aging indices among cognitively normal (CN) and amnestic mild cognitive impairment (aMCI) groups [single-domain aMCI (saMCI) and multiple-domain aMCI (maMCI)].
The study population included 739 participants (CN = 226, saMCI = 275, and maMCI = 238) from the Alzheimer's Disease Neuroimaging Initiative, a clinic-based, multi-center prospective cohort. Confirmatory factor analysis was employed to determine a MetS latent composite score using baseline data of vascular risk factors. We examined the changes of two Alzheimer's disease (AD) biomarkers, namely [(18)F]fluorodeoxyglucose (FDG)-positron emission tomography (PET) regions of interest and medial temporal lobe volume over 5 years. A cerebrovascular aging index, cerebral white matter (cWM) volume, was examined as a comparison.
The vascular risk was similar in all groups. Applying generalized estimating equation modeling, all brain-aging indices declined significantly over time. Higher MetS scores were associated with a faster decline of cWM in the CN and maMCI groups but with a slower decrement of regional glucose metabolism in FDG-PET in the saMCI and maMCI groups.
At the very early stage of cognitive decline, the vascular burden such as MetS may be in parallel with or independent of AD pathology in contributing to cognitive impairment in terms of accelerating the disclosure of AD pathology.
背景/目的:本研究探讨代谢综合征(MetS)对认知正常(CN)组和遗忘型轻度认知障碍(aMCI)组[单领域aMCI(saMCI)和多领域aMCI(maMCI)]脑老化指标的纵向影响。
研究人群包括来自阿尔茨海默病神经影像倡议的739名参与者(CN = 226,saMCI = 275,maMCI = 238),这是一个基于诊所的多中心前瞻性队列。采用验证性因子分析,利用血管危险因素的基线数据确定MetS潜在综合评分。我们研究了两种阿尔茨海默病(AD)生物标志物在5年中的变化,即[(18)F]氟脱氧葡萄糖(FDG)-正电子发射断层扫描(PET)感兴趣区域和内侧颞叶体积。作为对照,研究了脑血管老化指数,即脑白质(cWM)体积。
所有组的血管风险相似。应用广义估计方程模型,所有脑老化指标均随时间显著下降。较高的MetS评分与CN组和maMCI组中cWM的更快下降相关,但与saMCI组和maMCI组中FDG-PET区域葡萄糖代谢的较慢下降相关。
在认知衰退的早期阶段,诸如MetS之类的血管负担在加速AD病理表现方面,可能与AD病理并行或独立地导致认知障碍。