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Relationship between A1166C polymorphism of angiotensin II type 1 receptor gene and arteriosclerosis

机译:血管紧张素II型1受体基因和动脉硬化的1166C多态性的关系

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BACKGROUND:Arteriosclerosis has genetic correlation. Many studies have shown that angiotensin II type 1 receptor (AT1R) gene A1166C polymorphism is highly associated with arteriosclerosis, but there is no evidence-based basis. The purpose of this study is to systematically evaluate the relationship between AT1R gene A1166C polymorphism and arteriosclerosis.METHODS:The search time is set from the establishment of the database in December 2020 in this study. The search database include China National Knowledge Infrastructure (CNKI), Wanfang, VIP and China Biology Medicine disc (CBM), PubMed, EMBASE, Web of Science, and the Cochrane Library. The subjects are observational studies on the relationship between AGTR1 A1166C polymorphism and arteriosclerosis (including case-control study, cross-sectional study, and cohort study). 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 by Stata 16.0 software.RESULTS:This study will use pulse wave velocity as an index to evaluate arteriosclerosis to explore the relationship between AT1R gene A1166C polymorphism and arteriosclerosis.CONCLUSION:This study will provide evidence-based medicine for elucidating the genetic tendency of arteriosclerosis.ETHICS AND DISSEMINATION:Private information from individuals will not be published.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.OSF REGISTRATION NUMBER:DOI 10.17605/OSF.IO/V6E2Y.Copyright ? 2021 the Author(s). Published by Wolters Kluwer Health, Inc.
机译:背景:动脉硬化具有遗传相关性。许多研究表明,血管紧张素II型受体(AT1R)基因A1166C多态性与动脉硬化高,但没有基于循证的基础。本研究的目的是系统地评估AT1R基因A1166C多态性和动脉硬化之间的关系。方法:从该研究的2020年12月建立数据库的搜索时间。搜索数据库包括中国国家知识基础设施(CNKI),万方,VIP和中国生物学椎间盘(CBM),PubMed,EMBASE,科学网站和Cochrane图书馆。受试者是关于AGTR1 A1166C多态性和动脉硬化之间的关系的观察研究(包括案例对照研究,横截面研究和队列研究)。该语言仅限于英语和中文。提取包括的研究的数据,并通过2个研究人员独立评估文献质量。 STATA 16.0软件统计分析数据动脉硬化的遗传趋势。言语和传播:来自个人的私人信息不会出版。该系统审查也不涉及危及参与者权利。不需要道德批准。结果可以在同行评审的期刊中公布或在相关会议上传播.OSF注册号:DOI 10.17605 / OSF.IO / V6E2Y.COPYRIGHT? 2021提交人。由Wolters Kluwer Health,Inc。出版

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