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微小 RNA 作为非典型帕金森综合征的候选生物标志物:系统文献综述。

MicroRNA as Candidate Biomarkers in Atypical Parkinsonian Syndromes: Systematic Literature Review.

机构信息

1st Department of Neurology, Eginition Hospital, Medical School, National and Kapodistrian University of Athens, 72-74 Vassilisis Sofia's Avenue, 11528 Athens, Greece.

出版信息

Medicina (Kaunas). 2022 Mar 26;58(4):483. doi: 10.3390/medicina58040483.

Abstract

Multiple system atrophy (MSA) and progressive supranuclear palsy (PSP) are rare atypical parkinsonian syndromes, characterized by motor and cognitive symptoms. Their clinical diagnosis is challenging because there are no established biomarkers. Dysregulation of microRNAs (miRNAs/miRs) has been reported to serve an important role in neurodegenerative diseases. However, the miRNA profiles of MSA and PSP patients are rarely reported. The aim of this study was to critically review the role of miRNAs as diagnostic biomarkers to differentiate these atypical parkinsonian disorders and their role in disease pathogenesis. A systematic literature search of PubMed was conducted up to February 2022 according the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. A total of 15 studies were analyzed. Three studies have shown that miR-9-3p, miR-19a, miR-19b, and miR-24 are potential biomarkers for MSA. In two studies, miR-132 was downregulated, whereas miR-147a and miR-518e were upregulated in the brain tissue of PSP patients. The potential of miRNA is still uncertain as a potential differential diagnostic marker to identify these disorders. Pre-analytical and analytical factors of included studies were important limitations to justify the introduction of miRNAs into clinical practice.

摘要

多系统萎缩(MSA)和进行性核上性麻痹(PSP)是罕见的非典型帕金森综合征,其特征为运动和认知症状。由于没有既定的生物标志物,因此其临床诊断具有挑战性。据报道,微小 RNA(miRNAs/miRs)的失调在神经退行性疾病中发挥着重要作用。然而,MSA 和 PSP 患者的 miRNA 图谱很少有报道。本研究旨在批判性地回顾 miRNA 作为区分这些非典型帕金森病的诊断生物标志物的作用及其在疾病发病机制中的作用。根据系统评价和荟萃分析的首选报告项目(PRISMA)指南,对 PubMed 进行了系统的文献检索,检索截至 2022 年 2 月。共分析了 15 项研究。三项研究表明,miR-9-3p、miR-19a、miR-19b 和 miR-24 是 MSA 的潜在生物标志物。在两项研究中,PSP 患者脑组织中 miR-132 下调,而 miR-147a 和 miR-518e 上调。miRNA 作为潜在的鉴别诊断标志物来识别这些疾病的潜力仍然不确定。纳入研究的分析前和分析因素是将 miRNA 引入临床实践的重要限制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1668/9025474/edf1a9bf8be4/medicina-58-00483-g001.jpg

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