Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education.
Department of Obstetrics and Gynecology, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Medicine (Baltimore). 2021 Apr 9;100(14):e25477. doi: 10.1097/MD.0000000000025477.
Preeclampsia has genetic correlation. Many studies have shown that microRNA (miRNA) polymorphism is highly associated with preeclampsia, but the results are inconsistent. The purpose of this study is to systematically evaluate the relationship between miRNA polymorphism and preeclampsia.
In this study, the search time is set from the establishment of the database on January 2021. The search database include China National Knowledge Infrastructure (CNKI), Wanfang, VIP and China Biology Medicine disc (CBM), PubMed, EMBASE, and Web of Science, and the Cochrane Library. The subjects are case-control studies on the relationship between miRNA polymorphism and preeclampsia. The language is limited to English and Chinese. The data of the included study are extracted and the literature quality is evaluated by 2 researchers independently. The data are statistically analyzed through Stata 16.0 software. We also predicted the miRNA secondary structure and the binding sites of miRNA interaction with its target genes.
This review will be disseminated in print by peer-review.
This study will provide evidence-based medicine to elucidate the genetic tendency of preeclampsia.
Private information from individuals will not be published. This systematic review also does not involve endangering participant rights. Ethical approval will not be required. The results may be published in a peer-reviewed journal or disseminated at relevant conferences.
DOI 10.17605/OSF.IO/MJY2X.
子痫前期具有遗传相关性。许多研究表明 microRNA(miRNA)多态性与子痫前期高度相关,但结果不一致。本研究旨在系统评估 miRNA 多态性与子痫前期的关系。
本研究的检索时间设定为 2021 年 1 月数据库建立之时。检索数据库包括中国知网(CNKI)、万方、维普和中国生物医学文献数据库(CBM)、PubMed、EMBASE 和 Web of Science,以及 Cochrane 图书馆。研究对象为 miRNA 多态性与子痫前期关系的病例对照研究。语言限制为英语和中文。由 2 名研究者独立提取纳入研究的数据并评价文献质量。使用 Stata 16.0 软件对数据进行统计学分析。我们还预测了 miRNA 二级结构和 miRNA 与其靶基因相互作用的结合位点。
本综述将通过同行评议以印刷形式发表。
本研究将为阐明子痫前期的遗传倾向提供循证医学证据。
不会公布个人的隐私信息。本系统评价也不会危及参与者的权利。不需要伦理批准。研究结果可能发表在同行评议的期刊上,或在相关会议上传播。
OSF 注册号:DOI 10.17605/OSF.IO/MJY2X。