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前驱帕金森病 MDS 研究标准的更新。

Update of the MDS research criteria for prodromal Parkinson's disease.

机构信息

Department of Neurology, Christian-Albrechts-University, Kiel, Germany.

Department of Neurodegeneration, Hertie Institute for Clinical Brain Research, University of Tuebingen, Tuebingen, Germany.

出版信息

Mov Disord. 2019 Oct;34(10):1464-1470. doi: 10.1002/mds.27802. Epub 2019 Aug 14.

Abstract

The MDS Research Criteria for Prodromal PD allow the diagnosis of prodromal Parkinson's disease using an evidence-based conceptual framework, which was designed to be updated as new evidence becomes available. New prospective evidence of predictive values of risk and prodromal markers published since 2015 was reviewed and integrated into the criteria. Many of the predictive values (likelihood ratios, LR) remain unchanged. The positive likelihood ratio notably increase for olfactory loss and decreased for substantia nigra hyperechogenicity. Negative likelihood ratio remained largely unchanged for all markers. New levels of diagnostic certainty for neurogenic and symptomatic orthostatic hypotension have been added, which substantially differ in positive likelihood ratio from the original publication. For intermediate strength genetic variants, their age-related penetrance is now incorporated in the calculation of the positive likelihood ratio. Moreover, apart from prospective studies, evidence from cross-sectional case-control genome-wide association studies is also considered (given their likely lack of confounding and reverse causation), and to account for the effect of multiple low-penetrance genetic variants polygenic risk scores are added to the model. Diabetes, global cognitive deficit, physical inactivity, and low plasma urate levels in men enter the criteria as new markers. A web-based prodromal PD risk calculator allows the calculation of probabilities of prodromal PD for individuals. Several promising candidate markers may improve the diagnostic accuracy of prodromal PD in the future. © 2019 International Parkinson and Movement Disorder Society.

摘要

MDS 前驱期帕金森病研究标准采用基于证据的概念框架,允许使用前驱期帕金森病的诊断,该框架旨在随着新证据的出现而更新。审查并整合了自 2015 年以来发表的关于风险和前驱期标志物预测值的新前瞻性证据,这些证据纳入了标准。许多预测值(似然比,LR)保持不变。嗅觉丧失的阳性似然比显著增加,而黑质超声回声过高的阳性似然比降低。所有标志物的阴性似然比基本保持不变。增加了神经源性和症状性直立性低血压的新诊断确定性水平,其阳性似然比与原始出版物有很大不同。对于中等强度的遗传变异,现在将其与年龄相关的外显率纳入阳性似然比的计算中。此外,除了前瞻性研究外,还考虑了横断面病例对照全基因组关联研究的证据(考虑到它们可能缺乏混杂和反向因果关系),并为了考虑多个低外显率遗传变异多基因风险评分对模型进行了补充。糖尿病、总体认知缺陷、身体活动不足和男性血浆尿酸水平低作为新标志物纳入标准。一个基于网络的前驱期帕金森病风险计算器可计算个体前驱期帕金森病的概率。一些有前途的候选标志物可能会提高前驱期帕金森病的诊断准确性。

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