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路易体痴呆的神经生理学生物标志物

Neurophysiological biomarkers for Lewy body dementias.

作者信息

Cromarty Ruth A, Elder Greg J, Graziadio Sara, Baker Mark, Bonanni Laura, Onofrj Marco, O'Brien John T, Taylor John-Paul

机构信息

Institute of Neuroscience, Campus for Aging and Vitality, Newcastle University, Newcastle upon Tyne NE4 5PL, UK.

Institute of Neuroscience, Campus for Aging and Vitality, Newcastle University, Newcastle upon Tyne NE4 5PL, UK.

出版信息

Clin Neurophysiol. 2016 Jan;127(1):349-359. doi: 10.1016/j.clinph.2015.06.020. Epub 2015 Jun 27.

Abstract

OBJECTIVE

Lewy body dementias (LBD) include both dementia with Lewy bodies (DLB) and Parkinson's disease with dementia (PDD), and the differentiation of LBD from other neurodegenerative dementias can be difficult. Currently, there are few biomarkers which might assist early diagnosis, map onto LBD symptom severity, and provide metrics of treatment response. Traditionally, biomarkers in LBD have focussed on neuroimaging modalities; however, as biomarkers need to be simple, inexpensive and non-invasive, neurophysiological approaches might also be useful as LBD biomarkers.

METHODS

In this review, we searched PubMED and PsycINFO databases in a semi-systematic manner in order to identify potential neurophysiological biomarkers in the LBDs.

RESULTS

We identified 1491 studies; of these, 37 studies specifically examined neurophysiological biomarkers in LBD patients. We found that there was substantial heterogeneity with respect to methodologies and patient cohorts.

CONCLUSION

Generally, many of the findings have yet to be replicated, although preliminary findings reinforce the potential utility of approaches such as quantitative electroencephalography and motor cortical stimulation paradigms.

SIGNIFICANCE

Various neurophysiological techniques have the potential to be useful biomarkers in the LBDs. We recommend that future studies focus on maximising the diagnostic specificity and sensitivity of the most promising neurophysiological biomarkers.

摘要

目的

路易体痴呆(LBD)包括路易体痴呆(DLB)和帕金森病痴呆(PDD),将LBD与其他神经退行性痴呆区分开来可能具有挑战性。目前,几乎没有生物标志物可用于辅助早期诊断、反映LBD症状严重程度以及提供治疗反应指标。传统上,LBD中的生物标志物主要集中在神经影像学方法上;然而,由于生物标志物需要简单、廉价且无创,神经生理学方法也可能作为LBD生物标志物发挥作用。

方法

在本综述中,我们以半系统的方式检索了PubMED和PsycINFO数据库,以确定LBD中潜在的神经生理学生物标志物。

结果

我们共识别出1491项研究;其中,37项研究专门检查了LBD患者的神经生理学生物标志物。我们发现,在方法和患者队列方面存在很大的异质性。

结论

总体而言,尽管初步研究结果强化了定量脑电图和运动皮层刺激范式等方法的潜在效用,但许多研究结果尚未得到重复验证。

意义

各种神经生理学技术有可能成为LBD中有用的生物标志物。我们建议未来的研究专注于最大限度地提高最有前景的神经生理学生物标志物的诊断特异性和敏感性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aea2/4727506/31bb07266e62/gr1.jpg

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