Li Ge, Larson Eric B, Shofer Jane B, Crane Paul K, Gibbons Laura E, McCormick Wayne, Bowen James D, Thompson Mary Lou
Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, Washington.
Geriatric Research, Education, and Clinical Center, VA Puget Sound Health Care System, Seattle, Washington.
J Am Geriatr Soc. 2017 Dec;65(12):2627-2633. doi: 10.1111/jgs.15077. Epub 2017 Sep 21.
BACKGROUND/OBJECTIVES: Longitudinal studies have shown an increase in cognitive decline many years before clinical diagnosis of dementia. We sought to estimate changes, relative to "normal" aging, in the trajectory of scores on a global cognitive function test-the Cognitive Abilities Screening Instrument (CASI).
A prospective cohort study.
Community-dwelling members of a U.S. health maintenance organization.
Individuals aged 65 and older who had no dementia diagnosis at baseline and had at least two visits with valid CASI test score (N = 4,315).
Average longitudinal trajectories, including changes in trajectory before clinical diagnosis in those who would be diagnosed with dementia, were estimated for CASI item response theory (IRT) scores. The impact of sex, education level, and APOE genotype on cognitive trajectories was assessed.
Increased cognitive decline relative to "normal" aging was evident in CASI IRT at least 10 years before clinical diagnosis. Male gender, lower education, and presence of ≥1 APOE ε4 alleles were associated with lower average IRT scores. In those who would be diagnosed with dementia, a trajectory change point was estimated at an average of 3.1 years (95% confidence interval 3.0-3.2) before clinical diagnosis, after which cognitive decline appeared to accelerate. The change point did not differ by sex, education level, or APOE ε4 genotype. There were subtle differences in trajectory slopes by sex and APOE ε4 genotype, but not by education.
Decline in average global cognitive function was evident at least 10 years before clinical diagnosis of dementia. The decline accelerated about 3 years before clinical diagnosis.
背景/目的:纵向研究表明,在痴呆临床诊断前许多年认知功能就已出现下降。我们试图评估在一项全球认知功能测试——认知能力筛查工具(CASI)上的得分轨迹相对于“正常”衰老的变化情况。
前瞻性队列研究。
美国一家健康维护组织的社区居民。
65岁及以上、基线时未被诊断为痴呆且至少有两次有效CASI测试得分的个体(N = 4315)。
对CASI项目反应理论(IRT)得分估计平均纵向轨迹,包括那些将被诊断为痴呆的个体在临床诊断前轨迹的变化。评估了性别、教育水平和APOE基因型对认知轨迹的影响。
相对于“正常”衰老,在临床诊断前至少10年,CASI的IRT得分就出现了认知功能下降加剧的情况。男性、低教育水平以及存在≥1个APOE ε4等位基因与较低的平均IRT得分相关。在那些将被诊断为痴呆的个体中,估计在临床诊断前平均3.1年(95%置信区间3.0 - 3.2)出现轨迹变化点,此后认知功能下降似乎加速。该变化点在性别、教育水平或APOE ε4基因型方面无差异。性别和APOE ε4基因型在轨迹斜率上存在细微差异,但教育水平无差异。
在痴呆临床诊断前至少10年,平均全球认知功能就已明显下降。在临床诊断前约3年下降加速。