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失用症缺陷可预测生物标志物验证的阿尔茨海默病病理患者的一般认知障碍。

Apraxic deficits predict general cognitive impairment in patients with biomarker-verified Alzheimer's pathology.

作者信息

Schmidt Claudia C, Bardakan Michella M, Jaeger Elena, Richter Nils, Bischof Gérard N, Giehl Kathrin, Onur Oezguer A, Jessen Frank, Fink Gereon R, Drzezga Alexander, Weiss Peter H

机构信息

Cognitive Neuroscience, Institute of Neurosciences and Medicine (INM-3), Forschungszentrum Jülich, Jülich, Germany.

Department of Nuclear Medicine, Faculty of Medicine, University Hospital Cologne, University of Cologne, Cologne, Germany.

出版信息

J Neurol. 2025 Sep 25;272(10):654. doi: 10.1007/s00415-025-13401-9.

Abstract

Apraxia represents a core feature of Alzheimer's disease (AD), a neurodegenerative disorder characterised by the accumulation of β-amyloid plaques and tau deposition. However, systematic descriptions of apraxic deficits in AD patients remain scarce. Here, we comprehensively investigate apraxia profiles and their link with cognitive impairment in patients with biomarker-verified Alzheimer's pathology. We characterised the frequency and patterns of apraxic deficits in patients with biomarker-verified Alzheimer's pathology using a battery of standardised apraxia tests. Demographic variables and apraxia scores were related to patients' general cognitive impairment using hierarchical regression analysis. Apraxic deficits were found in 67% of patients with biomarker-verified Alzheimer's pathology (n = 63). Patients with Alzheimer's pathology were more impaired in imitating finger gestures (than hand gestures: 89.2% vs. 80.0%, p < 0.001) and imitating complex hand movements (than single hand movements: 97.4% vs. 78.5%, p < 0.001), even when controlling for general cognitive impairment. Apraxia assessments explained about 60% of the variance in dementia severity, with performance in the KAS subtest of pantomiming object use (beta coefficient: 0.47, p = 0.001) and the DATE subtest for limb apraxia (beta coefficient: 0.37, p = 0.005) constituting significant predictors of general cognitive impairment. These findings emphasise the relevance of apraxia in patients with biomarker-verified Alzheimer's pathology, revealing that praxis deficits predict general cognitive impairment in AD. Further research is warranted into the role of apraxia as a potential early diagnostic criterion in AD.

摘要

失用症是阿尔茨海默病(AD)的核心特征之一,AD是一种神经退行性疾病,其特征是β-淀粉样蛋白斑块的积累和tau蛋白沉积。然而,对AD患者失用症缺陷的系统描述仍然很少。在这里,我们全面研究了生物标志物验证的阿尔茨海默病病理患者的失用症特征及其与认知障碍的联系。我们使用一系列标准化失用症测试来表征生物标志物验证的阿尔茨海默病病理患者失用症缺陷的频率和模式。使用层次回归分析,将人口统计学变量和失用症得分与患者的一般认知障碍相关联。在67%的生物标志物验证的阿尔茨海默病病理患者(n = 63)中发现了失用症缺陷。即使在控制了一般认知障碍的情况下,患有阿尔茨海默病病理的患者在模仿手指手势(比模仿手部动作:89.2%对80.0%,p < 0.001)和模仿复杂手部动作(比单手动作:97.4%对78.5%,p < 0.001)方面受损更严重。失用症评估解释了痴呆严重程度约60%的方差,使用物体模仿的KAS子测试(β系数:0.47,p = 0.001)和肢体失用症的DATE子测试(β系数:0.37,p = 0.005)的表现构成了一般认知障碍的重要预测因素。这些发现强调了失用症在生物标志物验证的阿尔茨海默病病理患者中的相关性,揭示了实践缺陷可预测AD中的一般认知障碍。有必要进一步研究失用症作为AD潜在早期诊断标准的作用。

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