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微小RNA作为重症肌无力的诊断生物标志物:系统评价与荟萃分析

MicroRNAs as Diagnostic Biomarkers of Myasthenia Gravis: A Systematic Review and Meta-Analysis.

作者信息

Paudel Prayash, Sah Asutosh, Paudel Poonam

机构信息

Bachelor of Medicine and Bachelor of Surgery, Maharajgunj Medical Campus, Institute of Medicine, Tribhuvan University Teaching Hospital, Maharajgunj Rd, Kathmandu, 44600, Bagmati, Nepal.

Department of Biochemistry, Pokhara University School of Health and Allied Sciences, Pokhara, 33700, Gandaki, Nepal.

出版信息

Cell Mol Neurobiol. 2025 Jul 18;45(1):71. doi: 10.1007/s10571-025-01585-7.

Abstract

Myasthenia gravis (MG) is an autoimmune neuromuscular disorder characterized by fluctuating muscle weakness. MicroRNAs (miRNAs) have emerged as potential biomarkers for MG diagnosis, offering noninvasive and reliable detection. This systematic review and meta-analysis evaluated the diagnostic accuracy of miRNAs in MG. A comprehensive search of PubMed, Embase, and Google Scholar was conducted up to March 9, 2025. Eligible studies assessing miRNAs as MG biomarkers were selected on the basis of predefined criteria. Pooled sensitivity, specificity, and diagnostic odds ratios (DORs) were calculated via random effects model. Heterogeneity was assessed via I, and publication bias was evaluated via Deeks' funnel plot. Nine studies including 1,797 participants were analysed. The pooled sensitivity and specificity were 0.80 (95% CI: 0.75-0.84) and 0.71 (95% CI: 0.65-0.77), respectively, with an area under the curve (AUC) of 0.83. Bivariate heterogeneity analysis indicated moderate variability, the cause of which were identified using subgroup analysis with region, clinical subtypes and seropositivity as subgroups. miRNAs demonstrate strong diagnostic potential for MG, with good sensitivity and specificity. However, standardized methodologies and further validation in large, multicentre studies is warranted.

摘要

重症肌无力(MG)是一种自身免疫性神经肌肉疾病,其特征为肌肉无力波动。微小RNA(miRNA)已成为重症肌无力诊断的潜在生物标志物,可提供无创且可靠的检测。本系统评价和荟萃分析评估了miRNA在重症肌无力中的诊断准确性。截至2025年3月9日,对PubMed、Embase和谷歌学术进行了全面检索。根据预定义标准选择评估miRNA作为重症肌无力生物标志物的合格研究。通过随机效应模型计算合并敏感性、特异性和诊断比值比(DOR)。通过I²评估异质性,并通过Deeks漏斗图评估发表偏倚。分析了包括1797名参与者的9项研究。合并敏感性和特异性分别为0.80(95%CI:0.75 - 0.84)和0.71(95%CI:0.65 - 0.77),曲线下面积(AUC)为0.83。双变量异质性分析表明存在中度变异性,使用以地区、临床亚型和血清学阳性为亚组的亚组分析确定其原因。miRNA对重症肌无力显示出强大的诊断潜力,具有良好的敏感性和特异性。然而,需要标准化方法并在大型多中心研究中进一步验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a769/12274162/c0891b8d31a9/10571_2025_1585_Fig1_HTML.jpg

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