From the Departments of Neurology (B.E.S., O.L.L., W.E.K.), Neurological Surgery (Y.C.), Medicine (D.L.T.), Radiology (B.J.L.), Psychiatry (A.D.C., H.J.A., W.E.K.), Human Genetics (M.I.K.), and Epidemiology (L.H.K.), University of Pittsburgh, PA; Department of Neurology (S.T.D.), University of Florida, Gainesville; and Department of Mental Health (M.C.C.), Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
Neurology. 2020 Aug 25;95(8):e984-e994. doi: 10.1212/WNL.0000000000010239. Epub 2020 Jul 22.
To explore long-term predictors of avoiding β-amyloid (Aβ) deposition and maintaining unimpaired cognition as outcomes in the oldest old.
In a longitudinal observational cohort study, 100 former participants of the Ginkgo Evaluation of Memory Study (GEMS; 2000-2008) completed biannual Pittsburgh compound B-PET imaging and annual clinical-cognitive evaluations beginning in 2010. Most recent Aβ status and cognitive status were selected for each participant. Longitudinal outcomes included change in serial Aβ and cognitive tests. Baseline predictors from GEMS included neuropsychological tests, daily functioning, genotype, lifestyle variables, occupational measures, health history, sleep, subjective memory, physical and cognitive activities, depressive symptoms, and physical performance and health indices, among others.
Mean age at the last cognitive evaluation was 92.0 (range 86-100) years. Mean follow-up time from baseline to last measured Aβ status was 12.3 (SD 1.9) years and to last cognitive evaluation was 14.1 (SD 1.9) years. The allele predicted last Aβ status (n = 34 Aβ negative vs n = 66 Aβ positive). Baseline cognition predicted cognitive status (n = 30 unimpaired vs n = 70 impaired). Predictors of cognitive status among Aβ-positive participants only (n = 14 normal cognition vs n = 52 impaired) were baseline cognitive test scores and smoking history. Baseline pulse pressure predicted longitudinal Aβ increase; paid work engagement and life satisfaction predicted less cognitive decline.
The allele and lower pulse pressure predict resistance to Aβ deposition in advanced aging. Cognitive test scores 14 years prior, likely reflecting premorbid abilities, predict cognitive status and maintenance of unimpaired cognition in the presence of Aβ. Several lifestyle factors appear protective.
探索作为结局的避免β-淀粉样蛋白(Aβ)沉积和保持认知不受损害的长期预测因素,这些结局在高龄人群中。
在一项纵向观察性队列研究中,2000-2008 年参加银杏评估记忆研究(GEMS)的 100 名前参与者从 2010 年开始每两年进行一次匹兹堡化合物 B-PET 成像,每年进行一次临床认知评估。为每位参与者选择了最近的 Aβ状态和认知状态。纵向结局包括连续 Aβ和认知测试的变化。GEMS 的基线预测因素包括神经心理学测试、日常功能、基因型、生活方式变量、职业措施、健康史、睡眠、主观记忆、身体和认知活动、抑郁症状以及身体表现和健康指数等。
最后一次认知评估时的平均年龄为 92.0 岁(范围 86-100 岁)。从基线到最后一次测量 Aβ状态的平均随访时间为 12.3 年(SD 1.9 年),从基线到最后一次认知评估的平均随访时间为 14.1 年(SD 1.9 年)。等位基因预测最后 Aβ状态(n=34 Aβ阴性与 n=66 Aβ阳性)。基线认知预测认知状态(n=30 认知正常与 n=70 认知受损)。仅在 Aβ阳性参与者中(n=14 认知正常与 n=52 认知受损),认知状态的预测因素是基线认知测试分数和吸烟史。基线脉搏压预测 Aβ的纵向增加;有薪工作参与度和生活满意度预测认知衰退较少。
等位基因和较低的脉搏压预测在高龄时对 Aβ沉积的抵抗。14 年前的认知测试分数,可能反映了发病前的能力,预测了 Aβ存在时的认知状态和认知不受损害的维持。几种生活方式因素似乎具有保护作用。