Department of Biology, Mashhad Branch, Islamic Azad University, Mashhad, Iran.
Department of Nutrition and Integrative Physiology, Collogue of Health, University of Utah, Salt Lake City, UT, USA.
Eur J Clin Invest. 2021 Feb;51(2):e13448. doi: 10.1111/eci.13448. Epub 2020 Dec 5.
Several studies have been conducted on the diagnostic role of miR-223 in cancers related to the digestive system. However, the diagnostic role of this microRNA in gastrointestinal (GI) cancers has not been fully elucidated. This meta-analysis aimed to accurately assess the diagnostic role of circulating miR-223 in GI cancers.
A literature search was performed in PubMed/Medline, Science Direct, Web of Science, Google Scholar, Embase and Scopus, up to 1st May 2020 databases. Twelve studies were eligible and included in the analysis. Meta-Disc software was used to calculate the pooled sensitivity, specificity, positive likelihood ratio, negative likelihood ratio, diagnostic odds ratio, area under the curve (AUC) and the summary receiver operating characteristic (SROC) based on true positive, true negative, false negative and false positive for each gastrointestinal cancer separately and in total.
Twelve case-control studies were included with 1859 participants (1080 cases and 779 controls). Pooled sensitivity, specificity, positive likelihood ratio, negative likelihood ratio and diagnostic odds ratio were 0.77 (95% CI: 0.74-0.79), 0.75 (95% CI: 0.72-0.78), 3.04 (95% CI: 2.20-4.18), 0.31 (95% CI: 0.22-0.42) and 10.77 (95% CI: 5.96-19.47), respectively. AUC was 0.83, suggesting a high-grade diagnostic precision of miR-223 in gastrointestinal cancers. Besides, subgroup analyses were performed to assess the diagnostic power of miR-223 based on the type of gastrointestinal cancer, sample type and country via calculating pooled sensitivity, specificity, positive likelihood ratio, negative likelihood ratio and diagnostic odds ratio.
Our meta-analysis showed the value of circulating miR-223 levels in the early diagnosis of diverse digestive system carcinomas.
已有多项研究探讨了 miR-223 在消化系统相关癌症中的诊断作用。然而,这种 microRNA 在胃肠道(GI)癌症中的诊断作用尚未完全阐明。本荟萃分析旨在准确评估循环 miR-223 在 GI 癌症中的诊断作用。
检索 PubMed/Medline、Science Direct、Web of Science、Google Scholar、Embase 和 Scopus 数据库,时间截至 2020 年 5 月 1 日。共纳入 12 项符合条件的研究进行分析。采用 Meta-Disc 软件,分别和总体计算每种胃肠道癌症的真阳性、真阴性、假阴性和假阳性,以计算合并敏感度、特异度、阳性似然比、阴性似然比、诊断优势比、曲线下面积(AUC)和汇总受试者工作特征(SROC)。
共纳入 12 项病例对照研究,包含 1859 名参与者(1080 例病例和 779 例对照)。合并敏感度、特异度、阳性似然比、阴性似然比和诊断优势比分别为 0.77(95%CI:0.74-0.79)、0.75(95%CI:0.72-0.78)、3.04(95%CI:2.20-4.18)、0.31(95%CI:0.22-0.42)和 10.77(95%CI:5.96-19.47)。AUC 为 0.83,提示 miR-223 对胃肠道癌症具有较高的诊断精度。此外,还通过计算合并敏感度、特异度、阳性似然比、阴性似然比和诊断优势比,按胃肠道癌症类型、样本类型和国家进行亚组分析,以评估 miR-223 的诊断效能。
本荟萃分析表明,循环 miR-223 水平在多种消化系统癌的早期诊断中有一定价值。