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间歇性记忆衰退可预测社区居住的老年人群的皮质淀粉样蛋白状态。

Episodic memory decline predicts cortical amyloid status in community-dwelling older adults.

机构信息

CogState Ltd, Melbourne, Australia.

出版信息

J Alzheimers Dis. 2011;27(3):627-37. doi: 10.3233/JAD-2011-110818.

DOI:10.3233/JAD-2011-110818
PMID:21876253
Abstract

Intra-individual decline in memory and cognition is characteristic of prodromal Alzheimer's disease (AD) and may allow detection of very early AD pathology. Episodic memory task scores on a brief computerized cognitive battery (CogState) were prospectively evaluated at baseline, and 3-, 6-, 9-, 12-, and 24-months post-baseline. Linear mixed models were conducted to compute age-adjusted slopes. Subjects with slopes declining ≥90th percentile ("memory decliners") and age- and gender-matched subjects without such decline ("non-decliners") were studied with clinical, neuropsychological, and neuroimaging evaluations. Of 195 who completed 24-month evaluation (age 51 to 80 years), 15 memory decliners (mean age 62.7 years, SD 7.6) were identified, and matched with 33 non-decliners (mean age 63.3 years, SD 8.2). Amyloid-PET imaging was qualitatively abnormal with excess cortical amyloid accumulation in 7 memory decliners (46.7%) and 4 (12.1%) non-decliners (odds ratio 6.34), and quantitatively abnormal with standardized uptake value ratios >1.4 in 5 memory decliners (33.3%) and 2 (6.1%) non-decliners (odds ratio 8.3). One of the memory decliners and none of the non-decliners fulfilled criteria for mild cognitive impairment, but the groups did not differ with respect to subjective memory impairment, neuropsychological evidence of episodic memory impairment, or MRI imaging abnormalities. Intra-individual decline in episodic memory can be detected using a brief computerized cognitive performance test optimized to detect change in community-dwelling non-demented older persons and appears predictive of the presence of cerebral amyloid in about half of these persons. This approach may help detect early prodromal AD pathology in wider-scale community screening programs.

摘要

个体内记忆和认知能力的下降是前驱期阿尔茨海默病(AD)的特征,并且可能允许检测到非常早期的 AD 病理学。在基线、3 个月、6 个月、9 个月、12 个月和 24 个月时,使用简短的计算机化认知电池(CogState)对情景记忆任务评分进行前瞻性评估。使用线性混合模型计算年龄调整斜率。对斜率下降≥第 90 个百分位数的受试者(“记忆下降者”)和没有这种下降的年龄和性别匹配的受试者(“非下降者”)进行临床、神经心理学和神经影像学评估。在完成 24 个月评估的 195 名受试者中(年龄 51 至 80 岁),确定了 15 名记忆下降者(平均年龄 62.7 岁,SD 7.6),并与 33 名非下降者(平均年龄 63.3 岁,SD 8.2)相匹配。15 名记忆下降者中有 7 名(46.7%)和 4 名(12.1%)非下降者(比值比 6.34)的淀粉样蛋白-PET 成像呈定性异常,皮质淀粉样蛋白堆积过多,5 名记忆下降者中有 5 名(33.3%)和 2 名(6.1%)非下降者(比值比 8.3)的标准化摄取值比>1.4 定量异常。1 名记忆下降者符合轻度认知障碍标准,而无一名非下降者符合标准,但两组在主观记忆障碍、情景记忆损害的神经心理学证据或 MRI 成像异常方面无差异。使用专门优化用于检测社区居住的非痴呆老年人认知变化的简短计算机化认知测试,可以检测到个体内情景记忆的下降,并且似乎可以预测其中约一半人的大脑淀粉样蛋白的存在。这种方法可能有助于在更广泛的社区筛查计划中检测早期前驱期 AD 病理学。

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