Marquis Scott, Moore M Milar, Howieson Diane B, Sexton Gary, Payami Haydeh, Kaye Jeffrey A, Camicioli Richard
Department of Medicine (Neurology), University of Alberta, 2E3.08, 8440 112th St, Edmonton, Alberta, Canada T6G 2B7.
Arch Neurol. 2002 Apr;59(4):601-6. doi: 10.1001/archneur.59.4.601.
Several studies have shown that individually memory, hippocampal volume, and motor measures presage the onset of dementia. It is unclear if these independently contribute to the prediction of mild cognitive impairment.
To determine the ability of memory, hippocampal volume, and a gait speed to independently predict cognitive decline in healthy elderly persons.
A prospective, longitudinal, observational cohort study with a mean follow-up of 6 years.
One hundred eight optimally healthy elderly cognitively intact subjects.
Any cognitive impairment noted on the Clinical Dementia Rating Scale (score = 0.5) or persistent or progressive cognitive impairment. Cox modeling determined if time to onset of cognitive impairment was associated with baseline logical memory II test score (a measure of delayed recall), hippocampal volume (magnetic resonance imaging), or gait speed (time to walk 30 ft [9 m]) independent of age, sex, depression, or the allele producing the epsilon4 type of apolipoprotein E (APOE epsilon4).
Questionable dementia occurred in 48 participants in a mean (SD) of 3.7 (2.4) years. This progressed to persistent cognitive impairment in 38 of these participants in a mean (SD) of 4.4 (2.4) years. Logical memory II test performance and hippocampal volume each predicted onset of questionable dementia, independent of age and sex. Time to walk 30 ft additionally contributed independently to the prediction of time to onset of persistent cognitive impairment. Possessing the APOE epsilon4 allele and depression did not enter either model significantly.
Models combining multiple risk factors should refine the prediction of questionable dementia and persistent cognitive impairment, harbingers of dementia. Individuals at risk for cognitive impairment may represent a high-risk group for intervention.
多项研究表明,个体记忆、海马体积和运动指标可预示痴呆症的发病。目前尚不清楚这些因素是否独立有助于预测轻度认知障碍。
确定记忆、海马体积和步速对健康老年人认知功能下降的独立预测能力。
一项前瞻性、纵向观察队列研究,平均随访6年。
108名健康状况最佳、认知功能正常的老年人。
临床痴呆评定量表(得分=0.5)记录的任何认知障碍或持续性或进行性认知障碍。Cox模型确定认知障碍发病时间是否与基线逻辑记忆II测试得分(延迟回忆的指标)、海马体积(磁共振成像)或步速(行走30英尺[9米]的时间)相关,且独立于年龄、性别、抑郁或产生载脂蛋白E ε4型(APOE ε4)的等位基因。
48名参与者在平均(标准差)3.7(2.4)年时出现可疑痴呆。其中38名参与者在平均(标准差)4.4(2.4)年时病情进展为持续性认知障碍。逻辑记忆II测试表现和海马体积各自独立预测了可疑痴呆的发病,且独立于年龄和性别。行走30英尺的时间还独立地对持续性认知障碍发病时间的预测有贡献。携带APOE ε4等位基因和抑郁在两个模型中均未显著进入。
结合多种风险因素的模型应能优化对可疑痴呆和持续性认知障碍(痴呆的先兆)的预测。有认知障碍风险的个体可能是干预的高危人群。