循环微RNA是诊断帕金森病的潜在生物标记物:荟萃分析

W.T. Zhang , Y.J. Wang , Y.F. Yao , G.X. Zhang , Y.N. Zhang , S.S. Gao
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引用次数: 0

摘要

背景和目的帕金森病(PD)是最常见的神经退行性疾病之一。许多研究者证实了利用循环 miRNAs 诊断帕金森病的可能性。然而,结果并不一致。方法我们根据PRISMA声明仔细检索了PubMed、Embase、Web of Science、Cochrane图书馆、万方数据库和中国国家知识基础设施的相关研究(截至2022年1月1日)。通过计算汇总的敏感性、特异性、阳性似然比(PLR)、阴性似然比(NLR)、诊断几率比(DOR)和曲线下面积(AUC)来检验诊断准确性。此外,还进行了亚组分析以确定潜在的异质性来源,并使用 Deeks' 漏斗图不对称检验来评估潜在的发表偏倚。结果本次荟萃分析共纳入了 16 篇文章中符合条件的 44 项研究(3298 例帕金森病患者和 2529 例健康对照)。汇总灵敏度为0.79(95% CI:0.76-0.81),特异性为0.82(95% CI:0.78-0.84),PLR为4.3(95% CI:3.6-5.0),NLR为0.26(95% CI:0.23-0.30),DOR为16(95% CI:13-21),AUC为0.87(95% CI:0.84-0.90)。亚组分析表明,miRNA 聚类比 miRNA 单一显示出更好的诊断准确性。结论循环 miRNAs 作为诊断 PD 的新型非侵入性生物标记物具有巨大潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Circulating microRNAs as potential biomarkers for the diagnosis of Parkinson's disease: A meta-analysis

Background and objective

Parkinson's disease (PD) is the one of the most common neurodegenerative diseases. Many investigators have confirmed the possibility of using circulating miRNAs to diagnose PD. However, the results were inconsistent. Therefore, the aim of this meta-analysis was to systematically evaluate the diagnostic accuracy of circulating miRNAs in the diagnosis of PD.

Methods

We carefully searched PubMed, Embase, Web of Science, Cochrane Library, Wanfang database and China National Knowledge Infrastructure for relevant studies (up to January 1, 2022) based on PRISMA statement. The pooled sensitivity, specificity, positive likelihood ratio (PLR), negative likelihood ratio (NLR), the diagnostic odds ratio (DOR), and area under the curve (AUC) were calculated to test the diagnostic accuracy. Furthermore, subgroup analyses were performed to identify the potential sources of heterogeneity, and the Deeks’ funnel plot asymmetry test was used to evaluate the potential publication bias.

Results

Forty-four eligible studies from 16 articles (3298 PD patients and 2529 healthy controls) were included in the current meta-analysis. The pooled sensitivity was 0.79 (95% CI: 0.76–0.81), specificity was 0.82 (95% CI: 0.78–0.84), PLR was 4.3 (95% CI: 3.6–5.0), NLR was 0.26 (95% CI: 0.23–0.30), DOR was 16 (95% CI: 13–21), and AUC was 0.87 (95% CI: 0.84–0.90). Subgroup analysis suggested that miRNA cluster showed a better diagnostic accuracy than miRNA simple. Moreover, there was no significant publication bias.

Conclusions

Circulating miRNAs have great potential as novel non-invasive biomarkers for PD diagnosis.

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