Tosto Giuseppe, Monsell Sarah E, Hawes Stephen E, Mayeux Richard
The Taub Institute for Research on Alzheimer's Disease and the Aging Brain, Columbia University, New York, NY, USA.
Sergievsky Center, College of Physicians and Surgeons, Columbia University, New York, NY, USA.
J Neurol. 2015 Nov;262(11):2548-56. doi: 10.1007/s00415-015-7886-1. Epub 2015 Sep 4.
Patients with Alzheimer's disease (AD) often develop extrapyramidal signs (EPS), which increase in frequency as the disease progresses. We aimed to investigate the patterns of presentation of EPS in AD and their correlation with clinical and neuropathological features. 4284 subjects diagnosed with AD from the National Alzheimer's Coordinating Center (NACC) database with at least one abnormal Unified Parkinson's Disease Rating Scale (UPDRS) assessment were included. Individuals were assigned to a discovery sample and a sensitivity analysis sample (moderate and mild dementia, respectively) and a subset of subjects provided neuropathological data (n = 284). Individuals from the Washington Heights and Inwood Columbia Aging Project (WHICAP) served as validation sample. Patterns of presentation of EPS were identified employing categorical principal component analysis (CATPCA). Six principal components were identified in both mild and moderate AD samples: (I) hand movements, alternating movements, finger tapping, leg agility ("limbs bradykinesia"); (II) posture, postural instability, arising from chair, gait and body bradykinesia/hypokinesia ("axial"); (III) limb rigidity ("rigidity"); (IV) postural tremor; (V) resting tremor; (VI) speech and facial expression. Similar results were obtained in the WHICAP cohort. Individuals with hallucinations, apathy, aberrant night behaviors and more severe dementia showed higher axial and limb bradykinesia scores. "Limb bradykinesia" component was associated with a neuropathological diagnosis of Lewy body disease and "axial" component with reduced AD-type pathology. Patterns of EPS in AD show distinct clinical and neuropathological correlates; they share a pattern of presentation similar to that seen in Parkinson's disease, suggesting common pathogenic mechanisms across neurodegenerative diseases.
阿尔茨海默病(AD)患者常出现锥体外系症状(EPS),且随着疾病进展,其出现频率会增加。我们旨在研究AD中EPS的表现模式及其与临床和神经病理学特征的相关性。纳入了4284名来自国家阿尔茨海默病协调中心(NACC)数据库且被诊断为AD的受试者,这些受试者至少有一项异常的统一帕金森病评定量表(UPDRS)评估结果。个体被分为发现样本和敏感性分析样本(分别为中度和轻度痴呆),并且有一部分受试者提供了神经病理学数据(n = 284)。来自华盛顿高地和因伍德哥伦比亚衰老项目(WHICAP)的个体作为验证样本。采用分类主成分分析(CATPCA)确定EPS的表现模式。在轻度和中度AD样本中均确定了六个主成分:(I)手部动作、交替动作、手指轻敲、腿部敏捷性(“肢体运动迟缓”);(II)姿势、姿势不稳、从椅子上起身、步态以及身体运动迟缓/运动减少(“轴性”);(III)肢体僵硬(“僵硬”);(IV)姿势性震颤;(V)静止性震颤;(VI)言语和面部表情。在WHICAP队列中也获得了类似结果。有幻觉、冷漠、异常夜间行为以及更严重痴呆的个体表现出更高的轴性和肢体运动迟缓评分。“肢体运动迟缓”成分与路易体病的神经病理学诊断相关,而“轴性”成分与AD型病理学减少相关。AD中EPS的模式显示出明显的临床和神经病理学相关性;它们具有与帕金森病中所见相似的表现模式,提示跨神经退行性疾病存在共同的致病机制。