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首页> 外文期刊>Reports of Biochemistry and Molecular Biology >Assessment of Correlation Between miR-210 Expression and Pre-Eclampsia Risk: A Meta-Analysis
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Assessment of Correlation Between miR-210 Expression and Pre-Eclampsia Risk: A Meta-Analysis

机译:miR-210表达与先兆子痫风险之间的相关性评估:一项荟萃分析

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Background: Pre-eclampsia (PE) is a pregnancy disorder characterized by hypertension and proteinuria. The evidence has suggested that microRNAs (miRs) are associated with pre-eclampsia pathogenesis; however, these results are inconsistent. The aim of this study was to assess the association between miR-210 expression and PE risk. Methods: Previous studies were selected using PubMed, Scopus, MEDLINE, EMBASE, Science Direct, Google Scholar, Directory of Open Access Journals (DOAJ), and Scientific Information Database (SID). This meta-analysis includes 12 studies associated with miR-210 and pre-eclampsia and necessary information was extracted. Results: The standardized mean differences [(SMD (0.32) 95% CI (014–0.49), p=0.97] and heterogeneity were determined with the chi-square test (Q=3.63 df =11 p= 0.97), which found no heterogeneity between these studies. Additionally, publication bias was evaluated by Egger’s and Begg′s tests. Visual inspection of the funnel plot graphically, and statistically with Egger’s weighted regression [(p= 0.35) (95% CI -0.90 – 2.29)] and Begg’s rank correlation (p= 0.21), found no important publication bias between studies within the meta-analysis. Conclusions: Our findings suggest that miR-210 contributes to the pathogenesis of PE; therefore, miR-210 could serve as a novel biomarker to predict PE pathophysiology. Further studies are required in this field to characterize the mechanism involved in this process.
机译:背景:先兆子痫(PE)是一种以高血压和蛋白尿为特征的妊娠疾病。有证据表明,microRNA(miRs)与子痫前期发病有关。但是,这些结果不一致。这项研究的目的是评估miR-210表达与PE风险之间的关联。方法:使用PubMed,Scopus,MEDLINE,EMBASE,Science Direct,Google Scholar,开放获取期刊目录(DOAJ)和科学信息数据库(SID)选择先前的研究。这项荟萃分析包括与miR-210和先兆子痫相关的12项研究,并提取了必要的信息。结果:采用卡方检验(Q = 3.63 df = 11 p = 0.97)确定了标准化的均数差[(SMD(0.32)95%CI(014-0.49),p = 0.97]和异质性),但未发现这些研究之间存在异质性,此外,通过Egger和Begg的检验评估了出版偏倚;以图形方式对漏斗图进行了目视检查,并通过Egger的加权回归进行了统计学检验[(p = 0.35)(95%CI -0.90 – 2.29)] Begg的秩相关性(p = 0.21),在荟萃分析中没有发现重要的出版偏倚结论:我们的发现表明miR-210可以促进PE的发病;因此,miR-210可以作为一种新的生物标志物预测PE的病理生理学,需要对该领域进行进一步的研究,以表征该过程涉及的机制。

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