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路易体痴呆的早期鉴别诊断。脑脊液和影像学生物标志物的新作用。

Early discriminatory diagnosis of dementia with Lewy bodies. The emerging role of CSF and imaging biomarkers.

作者信息

Aarsland Dag, Kurz Martin, Beyer Mona, Bronnick Kolbjørn, Piepenstock Nore Sabine, Ballard Clive

机构信息

Norwegian Centre for Movement Disorders, Stavanger University Hospital, Stavanger, Norway.

出版信息

Dement Geriatr Cogn Disord. 2008;25(3):195-205. doi: 10.1159/000113417. Epub 2008 Jan 17.

DOI:10.1159/000113417
PMID:18204253
Abstract

BACKGROUND

The clinical diagnostic criteria for dementia with Lewy bodies (DLB) have a low sensitivity, and there are no generally accepted biomarkers to distinguish DLB from other dementias. Our aim was to identify biomarkers that may differentiate DLB from Alzheimer's disease (AD).

METHOD

We performed a systematic literature search for studies of EEG, imaging techniques and genetic and CSF markers that provide sensitivity and specificity in the identification of DLB.

RESULTS

The best evidence was for scintigraphy of the striatal dopamine transporter system using FP-CIT SPECT. Several small scintigraphy studies of cardiovascular autonomic function using metaiodobenzylguanidine SPECT have reported promising results. Studies exploring innovative techniques based on CSF have reported interesting findings for the combination of amyloid beta (abeta) isoforms as well as alpha-synuclein, and there are interesting results emerging from preliminary studies applying proteomic techniques. Data from studies using structural MRI, perfusion SPECT, genetics and EEG studies show differences between DLB and AD but only at a group level.

CONCLUSION

Several potential biomarkers for the differential diagnosis of probable DLB and AD have shown good diagnostic accuracy in the research setting. Data from large multicentre studies and from studies with autopsy confirmation exist for scintigraphy of the dopamine transporter system. Future studies should explore its value in possible DLB and for clinical management and health economics.

摘要

背景

路易体痴呆(DLB)的临床诊断标准敏感性较低,且尚无普遍公认的生物标志物可用于区分DLB与其他痴呆症。我们的目的是识别可能区分DLB与阿尔茨海默病(AD)的生物标志物。

方法

我们对脑电图、成像技术以及基因和脑脊液标志物的研究进行了系统的文献检索,这些研究在DLB的识别中提供敏感性和特异性。

结果

最有力的证据是使用FP-CIT SPECT对纹状体多巴胺转运体系统进行闪烁扫描。几项使用间碘苄胍SPECT对心血管自主神经功能进行的小型闪烁扫描研究报告了有前景的结果。探索基于脑脊液的创新技术的研究报告了关于淀粉样β(Aβ)亚型以及α-突触核蛋白组合的有趣发现,并且应用蛋白质组学技术的初步研究也出现了有趣的结果。使用结构MRI、灌注SPECT、遗传学和脑电图研究的数据显示了DLB和AD之间的差异,但仅在组水平上。

结论

几种用于鉴别可能的DLB和AD的潜在生物标志物在研究环境中显示出良好的诊断准确性。多巴胺转运体系统闪烁扫描有来自大型多中心研究和尸检证实研究的数据。未来的研究应探索其在可能的DLB中的价值以及对临床管理和卫生经济学的价值。

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