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路易体痴呆的生物标志物和诊断,包括前驱期:实用方面。

Biomarkers and diagnosis of dementia with Lewy bodies including prodromal: Practical aspects.

机构信息

Hôpitaux Universitaire de Strasbourg, CM2R (Centre Mémoire de Ressource et de Recherche), Hôpital de jour, pôle de Gériatrie, Strasbourg, France; CNRS, laboratoire ICube UMR 7357 et FMTS (Fédération de Médecine Translationnelle de Strasbourg), équipe IMIS, Strasbourg, France.

CNRS, laboratoire ICube UMR 7357 et FMTS (Fédération de Médecine Translationnelle de Strasbourg), équipe IMIS, Strasbourg, France; Hôpitaux Universitaire de Strasbourg, Laboratoire de Biochimie et Biologie Moléculaire, Strasbourg, France.

出版信息

Rev Neurol (Paris). 2022 May;178(5):472-483. doi: 10.1016/j.neurol.2022.03.008. Epub 2022 Apr 28.

Abstract

Dementia with Lewy Bodies (DLB) is a common form of cognitive neurodegenerative disease. More than half of the patients affected are not or misdiagnosed because of the clinical similarity with Alzheimer's disease (AD), Parkinson's disease but also psychiatric diseases such as depression or psychosis. In this review, we evaluate the interest of different biomarkers in the diagnostic process: cerebrospinal fluid (CSF), brain MRI, FP-CIT SPECT, MIBG SPECT, perfusion SPECT, FDG-PET by focusing more specifically on differential diagnosis between DLB and AD. FP-CIT SPECT is of high interest to discriminate DLB and AD, but not at the prodromal stage. Brain MRI has shown differences in group study with lower grey matter concentration of the Insula in prodromal DLB, but its interest in clinical routine is not demonstrated. Among the AD biomarkers (t-Tau, phospho-Tau, Aβ42 and Aβ40) used routinely, t-Tau and phospho-Tau have shown excellent discrimination whatever the clinical stages severity. CSF Alpha-synuclein assay in the CSF has also an interest in the discrimination between DLB and AD but not in segregation between DLB and healthy elderly subjects. CSF synuclein RT-QuIC seems to be an excellent biomarker but its application in clinical routine remains to be demonstrated, given the non-automation of the process.

摘要

路易体痴呆(DLB)是一种常见的认知神经退行性疾病。由于与阿尔茨海默病(AD)、帕金森病相似,也与抑郁症或精神病等精神疾病相似,超过一半的受影响患者未被诊断或误诊。在这篇综述中,我们评估了不同生物标志物在诊断过程中的意义:脑脊液(CSF)、脑 MRI、FP-CIT SPECT、MIBG SPECT、灌注 SPECT、FDG-PET,并特别关注 DLB 和 AD 之间的鉴别诊断。FP-CIT SPECT 是区分 DLB 和 AD 的重要标志物,但在前驱期则不然。脑 MRI 在组研究中显示出差异,前驱期 DLB 的岛叶灰质浓度较低,但在临床常规中的意义尚未得到证明。在常规使用的 AD 生物标志物(总 Tau、磷酸化 Tau、Aβ42 和 Aβ40)中,无论疾病严重程度如何,t-Tau 和磷酸化 Tau 均具有出色的区分能力。CSF 中的α-突触核蛋白测定也有助于区分 DLB 和 AD,但不能区分 DLB 和健康老年人。CSF synuclein RT-QuIC 似乎是一种很好的生物标志物,但由于该过程尚未实现自动化,其在临床常规中的应用仍有待证明。

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