Kim Ji Suk, Pak Kyoungjune, Goh Tae Sik, Jeong Dae Cheon, Han Myoung Eun, Kim Jihyun, Oh Sae Ock, Kim Chi Dae, Kim Yun Hak
BEER, Busan Society of Evidence-based Mdicine and Research, Busan, Korea.
Department of Family Medicine, BHS Han Seo Hospital, Busan, Korea.
Yonsei Med J. 2018 Jun;59(4):495-500. doi: 10.3349/ymj.2018.59.4.495.
Coronary artery diseases (CADs) are the leading causes of death in the world. Recent studies have reported that differentially expressed microRNAs (miRNAs) are associated with prognosis or major adverse cardiac events (MACEs) in CAD patients. In a previous meta-analysis, the authors made serious mistakes that we aimed to correct through an updated systematic review and meta-analysis of the prognostic value of altered miRNAs in patients with CADs.
We performed a systematic search of MEDLINE (from inception to May 2017) and EMBASE (from inception to May 2017) for English-language publications. Studies of CADs with results on miRNAs that reported survival data or MACEs were included. Data were extracted from each publication independently by two reviewers.
After reviewing 515 articles, a total eight studies were included in this study. We measured pooled hazard ratios (HRs) and 95% confidence intervals (CIs) of miRNA 133a with a fixed-effect model (pooled HR, 2.35; 95% CI, 1.56-3.55). High expression of miRNA 133a, 208b, 126, 197, 223, and 122-5p were associated with high mortality. Additionally, high levels of miRNA 208b, 499-5p, 134, 328, and 34a were related with MACEs.
The present study confirmed that miRNA 133a, which was associated with high mortality in CAD patients, holds prognostic value in CAD. More importantly, this study corrected issues raised against a prior meta-analysis and provides accurate information.
冠状动脉疾病(CAD)是全球主要的死亡原因。最近的研究报告称,差异表达的微小RNA(miRNA)与CAD患者的预后或主要不良心脏事件(MACE)相关。在之前的一项荟萃分析中,作者犯了严重错误,我们旨在通过对CAD患者中miRNA改变的预后价值进行更新的系统评价和荟萃分析来纠正这些错误。
我们对MEDLINE(从创刊到2017年5月)和EMBASE(从创刊到2017年5月)进行了系统检索,以查找英文出版物。纳入了关于CAD且有miRNA结果并报告生存数据或MACE的研究。由两名审阅者独立从每篇出版物中提取数据。
在审阅了515篇文章后,本研究共纳入了八项研究。我们使用固定效应模型测量了miRNA 133a的合并风险比(HR)和95%置信区间(CI)(合并HR,2.35;95%CI,1.56 - 3.55)。miRNA 133a、208b、126、'197、223和122 - 5p的高表达与高死亡率相关。此外,miRNA
208b、499 - 5p、134、328和34a的高水平与MACE相关。
本研究证实,与CAD患者高死亡率相关的miRNA 133a在CAD中具有预后价值。更重要的是,本研究纠正了先前荟萃分析中提出的问题并提供了准确信息。