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轻度认知障碍、阿尔茨海默病和路易体痴呆的精神运动迟缓:机制与诊断价值。

Psychomotor slowing in mild cognitive impairment, Alzheimer's disease and lewy body dementia: mechanisms and diagnostic value.

机构信息

Department of Neurology and the Laboratoire de Neurosciences Fonctionnelles et Pathologies (UMR CNRS 8160), University Hospital of Lille, Lille, and University Hospital of Amiens, Amiens, France.

出版信息

Dement Geriatr Cogn Disord. 2010;29(5):388-96. doi: 10.1159/000305095. Epub 2010 May 20.

DOI:10.1159/000305095
PMID:20484908
Abstract

BACKGROUND

Although psychomotor slowing is frequent in Alzheimer's disease (AD) and Lewy body dementia (LBD), its mechanism and diagnostic value have not been examined.

OBJECTIVE

To (i) assess psychomotor speed in patients with mild cognitive impairment (MCI), AD and LBD, (ii) determine the underlying mechanisms, and (iii) examine whether psychomotor slowing constitutes a useful diagnostic marker.

METHODS

Psychomotor speed was assessed in MCI (n = 11) and mild dementia due to AD (n = 23) or LBD (n = 18) and controls (n = 52) with visual inspection time (VIT), digital tapping, simple reaction time (SRT) and choice reaction time (CRT) tests.

RESULTS

MCI did not differ from controls. Both dementia groups showed different patterns. In AD, VIT (p = 0.0001), tapping (p = 0.021), SRT (p = 0.0001) and decision time (p = 0.0001) were impaired as compared to controls. In LBD, VIT (p = 0.0001) was very impaired and correlated with visual hallucinations (p = 0.001); SRT lengthening (p = 0.0001) was related to attentional disorders (p = 0.0001).

CONCLUSIONS

Psychomotor slowing of AD is due to slower perceptuomotor and decision processes. In LBD, psychomotor slowing is due to visual and attention disorders, and subtle visual disorders contribute to hallucinations. VIT and CRT are useful diagnostic markers.

摘要

背景

虽然运动迟缓在阿尔茨海默病(AD)和路易体痴呆(LBD)中很常见,但它的机制和诊断价值尚未得到检验。

目的

(i)评估轻度认知障碍(MCI)、AD 和 LBD 患者的运动速度,(ii)确定其潜在机制,以及(iii)检查运动迟缓是否构成有用的诊断标志物。

方法

使用视觉检查时间(VIT)、数字敲击、简单反应时间(SRT)和选择反应时间(CRT)测试,评估 MCI(n = 11)和轻度 AD 痴呆(n = 23)或 LBD 痴呆(n = 18)患者以及对照组(n = 52)的运动速度。

结果

MCI 与对照组无差异。两个痴呆组表现出不同的模式。在 AD 中,与对照组相比,VIT(p = 0.0001)、敲击(p = 0.021)、SRT(p = 0.0001)和决策时间(p = 0.0001)均受损。在 LBD 中,VIT(p = 0.0001)严重受损,与视觉幻觉相关(p = 0.001);SRT 延长(p = 0.0001)与注意力障碍有关(p = 0.0001)。

结论

AD 的运动迟缓是由于感知运动和决策过程较慢所致。在 LBD 中,运动迟缓是由于视觉和注意力障碍引起的,而微妙的视觉障碍导致幻觉。VIT 和 CRT 是有用的诊断标志物。

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