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帕金森病生物标志物计划中RNA血液生物标志物的评估

Evaluation of RNA Blood Biomarkers in the Parkinson's Disease Biomarkers Program.

作者信息

Santiago Jose A, Bottero Virginie, Potashkin Judith A

机构信息

Department of Cellular and Molecular Pharmacology, The Chicago Medical School, Rosalind Franklin University of Medicine and Science, North Chicago, IL, United States.

出版信息

Front Aging Neurosci. 2018 May 29;10:157. doi: 10.3389/fnagi.2018.00157. eCollection 2018.

Abstract

There is a high misdiagnosis rate between Parkinson's disease (PD) and atypical parkinsonian disorders (APD), such as progressive supranuclear palsy (PSP), the second most common parkinsonian syndrome. In our earlier studies, we identified and replicated RNA blood biomarkers in several independent cohorts, however, replication in a cohort that includes PSP patients has not yet been performed. To this end, we evaluated the diagnostic potential of nine previously identified RNA biomarkers using quantitative PCR assays in 138 blood samples at baseline from PD, PSP and healthy controls (HCs) nested in the PD Biomarkers Program. Linear discriminant analysis showed that and distinguished PD from PSP patients with 62.5% accuracy. Five biomarkers, , , , and were useful for distinguishing PSP from controls with 69% accuracy. Several biomarkers correlated with clinical features in PD patients. correlated with Unified Parkinson's Disease Rating Scale total and part III scores. In addition, , and , correlated with Montreal Cognitive Assessment (MoCA). Interestingly, , and were downregulated in cognitively impaired (CI) compared to normal subjects. Linear discriminant analysis showed that age, , , , and distinguished CI from normal subjects with 65.9% accuracy. These results suggest that and are useful for distinguishing PD from PSP patients. In addition, the combination of , , , and is a useful signature for cognitive impairment. Evaluation of these biomarkers in a larger study will be a key to advancing these biomarkers into the clinic.

摘要

帕金森病(PD)与非典型帕金森综合征(APD),如进行性核上性麻痹(PSP,第二常见的帕金森综合征)之间的误诊率很高。在我们早期的研究中,我们在几个独立队列中识别并重复验证了血液RNA生物标志物,然而,尚未在包含PSP患者的队列中进行重复验证。为此,我们在帕金森病生物标志物项目中,对来自PD、PSP和健康对照(HC)的138份基线血液样本,使用定量PCR分析评估了9种先前识别的RNA生物标志物的诊断潜力。线性判别分析表明,[具体标志物1]和[具体标志物2]区分PD和PSP患者的准确率为62.5%。5种生物标志物,[具体标志物3]、[具体标志物4]、[具体标志物5]、[具体标志物6]和[具体标志物7]区分PSP和对照的准确率为69%。几种生物标志物与PD患者的临床特征相关。[具体标志物8]与统一帕金森病评定量表总分及第三部分得分相关。此外,[具体标志物9]、[具体标志物10]和[具体标志物11]与蒙特利尔认知评估(MoCA)相关。有趣的是,与正常受试者相比,[具体标志物12]、[具体标志物13]和[具体标志物14]在认知受损(CI)患者中表达下调。线性判别分析表明,年龄、[具体标志物15]、[具体标志物16]、[具体标志物17]、[具体标志物18]和[具体标志物19]区分CI和正常受试者的准确率为65.9%。这些结果表明,[具体标志物1]和[具体标志物2]有助于区分PD和PSP患者。此外,[具体标志物3]、[具体标志物4]、[具体标志物5]、[具体标志物6]和[具体标志物7]的组合是认知障碍的有用特征。在更大规模的研究中评估这些生物标志物将是将这些生物标志物推进临床应用的关键。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebb1/5986959/dc54b0f6d03d/fnagi-10-00157-g0001.jpg

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