Grober E, Lipton R B, Hall C, Crystal H
Department of Neurology, Albert Einstein College of Medicine and Montefiore Medical Center, Bronx, NY 10461, USA.
Neurology. 2000 Feb 22;54(4):827-32. doi: 10.1212/wnl.54.4.827.
To estimate the relative rates of dementia in initially nondemented subjects with and without memory impairment defined by baseline free recall from the Free and Cued Selective Reminding (FCSR) test.
Our approach to identifying persons at high risk for future dementia is to show the presence of memory impairment not caused by other cognitive deficits by using a memory test that controls attention and cognitive processing. When the conditions of testing are not adequately controlled, prediction is reduced because age-associated memory deficits due to other cognitive deficits are confused with dementia-associated memory deficits.
Longitudinal evaluation of 264 initially nondemented, elderly community volunteers from the Einstein Aging Study with clinical and psychometric examinations every 12 to 18 months for up to 10 years.
Dementia was defined by an algorithmic definition that required a Blessed Information Memory and Concentration score >8 and clinical evidence of functional decline.
Thirty-two incident cases of dementia developed during follow-up. Survival analyses indicated that subjects with impaired free recall at baseline had dementia develop (relative risk = 75.2, 95% CI = 9.9 to 567) over 5 years of follow-up at dramatically higher rates than subjects with intact free recall after adjusting for age, gender, and education.
Poor performance on free recall from FCSR predicts future dementia. These findings support the existence of a preclinical phase of dementia characterized by memory impairment, which is present for at least 5 years before diagnosis.
通过自由和线索选择回忆(FCSR)测试中基线自由回忆所定义的有无记忆障碍,来估计初始无痴呆受试者中痴呆的相对发生率。
我们识别未来痴呆高危人群的方法是,通过使用一种能控制注意力和认知加工的记忆测试,来显示存在并非由其他认知缺陷引起的记忆障碍。当测试条件控制不充分时,预测能力会降低,因为由其他认知缺陷导致的与年龄相关的记忆缺陷会与痴呆相关的记忆缺陷相混淆。
对来自爱因斯坦衰老研究的264名初始无痴呆的老年社区志愿者进行纵向评估,每12至18个月进行临床和心理测量检查,为期长达10年。
痴呆由一种算法定义,该定义要求Blessed信息记忆与注意力得分>8以及功能衰退的临床证据。
随访期间出现了32例痴呆新发病例。生存分析表明,在调整年龄、性别和教育程度后,基线自由回忆受损的受试者在5年随访期间患痴呆的发生率(相对风险=75.2,95%可信区间=9.9至567)显著高于自由回忆正常的受试者。
FCSR测试中自由回忆表现不佳可预测未来痴呆。这些发现支持了痴呆临床前期的存在,其特征为记忆障碍,在诊断前至少存在5年。