Rajan Kumar B, Wilson Robert S, Weuve Jennifer, Barnes Lisa L, Evans Denis A
From the Department of Internal Medicine, Rush Institute for Healthy Aging (K.B.R., J.W., D.A.E.), Rush Alzheimer Disease Center (R.S.W., L.L.B.), and Departments of Neurological Sciences (R.S.W., L.L.B.) and Behavioral Sciences (R.S.W., L.L.B.), Rush University Medical Center, Chicago, IL.
Neurology. 2015 Sep 8;85(10):898-904. doi: 10.1212/WNL.0000000000001774. Epub 2015 Jun 24.
To examine the relation of performance on brief cognitive tests to development of clinically diagnosed Alzheimer disease (AD) dementia over the following 18 years in a sample of African Americans and European Americans.
A composite cognitive test score based on tests of episodic memory, executive function, and global cognition was constructed in a prospective population-based sample of 2,125 participants (55% African American and 61% female) aged 65 years and older residing in 4 Chicago neighborhoods. Time before AD dementia diagnosis was categorized into 6 groups corresponding to data collection periods: 0.1-0.9, 1.0-3.9, 4.0-6.9, 7.0-9.9, 10.0-12.9, and 13.0-17.9 years.
Of 2,125 participants without clinical AD dementia, 442 (21%) developed clinical AD dementia over 18 years of follow-up. Lower composite cognitive test scores were associated with the development of AD dementia over the duration of the study. The magnitude of association between composite cognitive test score and development of AD dementia increased from an odds ratio of 3.39 (95% confidence interval 1.72, 6.67; p < 0.001) at 13.0-17.9 years to 9.84 (95% confidence interval 7.41, 13.06; p < 0.001) at 0.1-0.9 years, per SD increment. These associations were consistently larger among European Americans than among African Americans. Performance on individual cognitive tests of episodic memory, executive function, and global cognition also significantly predicted the development of AD dementia, with associations exhibiting a similar trend over 18 years.
Our findings suggest that cognitive impairment may manifest in the preclinical phase of AD dementia substantially earlier than previously established.
在非裔美国人和欧裔美国人样本中,研究简短认知测试表现与接下来18年临床诊断的阿尔茨海默病(AD)痴呆症发展之间的关系。
在一个基于人群的前瞻性样本中,对居住在芝加哥4个社区的2125名65岁及以上参与者(55%为非裔美国人,61%为女性)进行了基于情景记忆、执行功能和整体认知测试的综合认知测试评分。AD痴呆症诊断前的时间被分为6组,对应数据收集期:0.1 - 0.9年、1.0 - 3.9年、4.0 - 6.9年、7.0 - 9.9年、10.0 - 12.9年和13.0 - 17.9年。
在2125名无临床AD痴呆症的参与者中,442名(21%)在18年随访期间发展为临床AD痴呆症。在研究期间,较低的综合认知测试分数与AD痴呆症的发展相关。综合认知测试分数与AD痴呆症发展之间的关联强度从13.0 - 17.9年时的优势比3.39(95%置信区间1.72, 6.67;p < 0.001)增加到0.1 - 0.9年时的9.84(95%置信区间7.41, 13.06;p < 0.001),每标准差增加。这些关联在欧裔美国人中始终比在非裔美国人中更大。情景记忆、执行功能和整体认知的个体认知测试表现也显著预测了AD痴呆症的发展,在18年中关联呈现相似趋势。
我们的研究结果表明,认知障碍可能在AD痴呆症临床前期比先前确定的时间更早出现。