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胶质瘤中循环微小RNA作为潜在诊断生物标志物的综合荟萃分析。

A comprehensive meta-analysis of circulation miRNAs in glioma as potential diagnostic biomarker.

作者信息

Ma Chenkai, Nguyen Hong P T, Luwor Rodney B, Stylli Stanley S, Gogos Andrew, Paradiso Lucia, Kaye Andrew H, Morokoff Andrew P

机构信息

Department of Surgery, The University of Melbourne, The Royal Melbourne Hospital, Parkville, Victoria, Australia.

Department of Neurosurgery, The Royal Melbourne Hospital, Parkville, Victoria, Australia.

出版信息

PLoS One. 2018 Feb 14;13(2):e0189452. doi: 10.1371/journal.pone.0189452. eCollection 2018.

Abstract

Glioma is the most common malignant intracranial tumour. Recently, several publications have suggested that miRNAs can be used as potential diagnostic biomarkers of glioma. Here we performed a meta-analysis to identify the diagnostic accuracy of differentially expressed circulating miRNAs in gliomas. Using PubMed, Medline and Cochrane databases, we searched for studies which evaluated a single or panel of miRNAs from circulating blood as potential biomarkers of glioma. Sixteen publications involving 23 studies of miRNAs from serum or plasma met our criteria and were included in this meta-analysis. The pooled diagnostic parameters were calculated by random effect models and overall diagnostic performance of altered miRNAs was illustrated by the summary receiver operator characteristic (SROC) curves. The pooled sensitivity, specificity, positive likelihood ratio (PLR) and negative likelihood ratio (NLR) from each study were calculated. The pooled PLR, NLR and Diagnostic Odds Ratio were 6.39 (95% CI, 4.61-8.87), 0.15 (95% CI, 0.11-0.21) and 41.91 (95% CI, 23.15-75.88), respectively. The pooled sensitivity, specificity and area under the curve (AUC) were 0.87 (95% CI, 0.82-0.91), 0.86 (95% CI, 0.82-0.90) and 0.93 (95% CI, 0.91-0.95), respectively. This meta-analysis demonstrated that circulating miRNAs are capable of distinguishing glioma from healthy controls. Circulating miRNAs are promising diagnostic biomarkers for glioma and can potentially be used as a non-invasive early detection.

摘要

胶质瘤是最常见的颅内恶性肿瘤。最近,有几篇出版物表明,微小RNA(miRNAs)可作为胶质瘤潜在的诊断生物标志物。在此,我们进行了一项荟萃分析,以确定胶质瘤中差异表达的循环miRNAs的诊断准确性。通过PubMed、Medline和Cochrane数据库,我们搜索了评估来自循环血液中的单个或一组miRNAs作为胶质瘤潜在生物标志物的研究。16篇涉及23项关于血清或血浆中miRNAs研究的出版物符合我们的标准,并被纳入本荟萃分析。通过随机效应模型计算合并诊断参数,并通过汇总接受者操作特征(SROC)曲线说明改变的miRNAs的总体诊断性能。计算每项研究的合并敏感性、特异性、阳性似然比(PLR)和阴性似然比(NLR)。合并的PLR、NLR和诊断比值比分别为6.39(95%CI,4.61 - 8.87)、0.15(95%CI,0.11 - 0.21)和41.91(95%CI,23.15 - 75.88)。合并的敏感性、特异性和曲线下面积(AUC)分别为0.87(95%CI,0.82 - 0.91)、0.86(95%CI,0.82 - 0.90)和0.93(95%CI,0.91 - 0.95)。这项荟萃分析表明,循环miRNAs能够区分胶质瘤与健康对照。循环miRNAs是有前景的胶质瘤诊断生物标志物,有可能用作非侵入性早期检测手段。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f4f/5812551/26b0d9971050/pone.0189452.g001.jpg

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