Memory Clinic, Department of Geriatrics, University Hospital, Basel, Switzerland.
J Alzheimers Dis. 2013;34(2):537-46. doi: 10.3233/JAD-121234.
We investigated the earliest neuropsychological changes in Alzheimer's disease (AD) by comparing the baseline performance of 29 individuals who subsequently developed AD within an average of 7.91 ± 2.70 years with 29 pairwise-matched individuals who remained cognitively healthy (NC). We hypothesized that subtle, qualitative changes in cognition precede clinical AD by several years, and therefore examined subjective as well as standard quantitative measures of cognition, in addition to subjective estimates of mood and medical status. Participants were selected from the 825 members of the longitudinal BASEL study (BAsel Study on the ELderly), all of whom had been ApoE-genotyped and received comprehensive bi-annual neuropsychological assessments. Within 13 years, 29 were diagnosed with probable AD. Each individual who progressed to AD (AD-P) was pairwise matched to a NC participant based on age, education, demographic status, observation period, and, importantly, ApoE genotype. A regression analysis using the lasso technique identified which of 115 neuropsychological variables best discriminated baseline NC from baseline AD-P performance. This analysis yielded eleven neuropsychological variables that optimally discriminated the two groups (correct classification rate: 60.4%): 1) Intrusions and 2) response bias in verbal learning and memory tasks; 3) delayed figure recall; 4-6) three Wechsler Adult Intelligence Scale (WAIS) Block Design subtest variables; 7-8) number of errors and repetitions on letter fluency; and 9-11) self-report of memory problems, a feeling of sadness, and cardiac problems. These results suggest that the preclinical neuropsychological cascade to AD includes subtle but identifiable qualitative impairments in verbal and visual memory, visuospatial processing, error control, and subjective neuropsychological complaints.
我们通过比较 29 名在平均 7.91±2.70 年内随后发展为 AD 的个体与 29 名配对的认知健康(NC)个体的基线表现,研究了阿尔茨海默病(AD)的最早神经心理学变化。我们假设,认知的细微、定性变化会在临床 AD 前几年出现,因此,除了主观的和标准的认知测量外,我们还检查了主观的情绪和医疗状况估计。参与者从纵向 BASEL 研究(巴塞尔老年人研究)的 825 名成员中选出,所有参与者均进行了 ApoE 基因分型,并接受了全面的两年一次的神经心理学评估。在 13 年内,29 人被诊断为可能的 AD。每个进展为 AD 的个体(AD-P)均与 NC 参与者进行配对,配对依据为年龄、教育程度、人口统计学状况、观察期,以及重要的是,ApoE 基因型。使用套索技术的回归分析确定了 115 个神经心理学变量中的哪一个最能区分基线 NC 与基线 AD-P 的表现。该分析产生了 11 个神经心理学变量,这些变量最佳区分了两组(正确分类率:60.4%):1)言语学习和记忆任务中的干扰和 2)反应偏差;3)延迟图形回忆;4-6)三个韦氏成人智力量表(WAIS)积木设计子测试变量;7-8)字母流畅性的错误和重复次数;以及 9-11)记忆问题、悲伤感和心脏问题的自我报告。这些结果表明,AD 的临床前神经心理学级联包括言语和视觉记忆、视空间处理、错误控制以及主观神经心理学投诉方面的微妙但可识别的定性损伤。