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氧化应激基因对心血管事件的总影响:一项 7 年随访研究。

Total impact of oxidative stress genes on cardiovascular events-a 7-year follow-up study.

机构信息

First Department of Cardiology, Medical University of Gdansk, Ul. Smoluchowskiego 17, 80-214, Gdańsk, Poland.

Department of Molecular Biotechnology and Microbiology, Gdansk University of Technology, Ul. Narutowicza 11/12, 80-233, Gdańsk, Poland.

出版信息

J Appl Genet. 2023 May;64(2):319-327. doi: 10.1007/s13353-022-00741-9. Epub 2023 Jan 23.

DOI:10.1007/s13353-022-00741-9
PMID:36683124
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10076362/
Abstract

Cardiovascular (CV) events are the number one cause of lifetime disability and deaths worldwide. It is well known that traditional risk factors do not fully correlate with clinical outcomes; therefore, searching for other markers that would explain CV events' occurrence seems essential. Of importance, one of the main factors at the origin of CV events is oxidative stress, causing inflammation and atherosclerotic plaque instability. Therefore, the present study was conducted to evaluate eight carefully selected genetic polymorphisms related to oxidative stress as risk modifiers for CV events. A cohort of 1020 patients with coronary atherosclerosis was analysed in a 7-year follow-up observational study. The following end points were assessed: CV death, myocardial infarction (MI) and a combined end point of CV death/MI/stroke. Our results show that single polymorphisms are not significant cardiovascular disease risk factors, but genetic risk score (GRS), defined as the accumulation of our eight studied polymorphisms, was significantly associated with the three. Specifically, low GRS was associated with a higher risk of CV death, MI and CV death/MI/stroke. In conclusion, when regarding CV events, GRS investigated here can become clinically meaningful and undoubtedly adds to the knowledge in stratifying the risk of CV events.

摘要

心血管(CV)事件是全球导致终身残疾和死亡的首要原因。众所周知,传统的风险因素并不能完全与临床结果相关;因此,寻找其他可以解释 CV 事件发生的标志物似乎至关重要。重要的是,CV 事件的主要原因之一是氧化应激,导致炎症和动脉粥样硬化斑块不稳定。因此,本研究旨在评估与氧化应激相关的八个精心挑选的遗传多态性,以评估其作为 CV 事件的风险修饰因子。对 1020 名冠状动脉粥样硬化患者进行了为期 7 年的随访观察研究。评估了以下终点:CV 死亡、心肌梗死(MI)和 CV 死亡/MI/中风的联合终点。我们的结果表明,单一多态性不是心血管疾病的显著危险因素,但遗传风险评分(GRS),定义为我们研究的八个多态性的累积,与这三个终点显著相关。具体来说,低 GRS 与 CV 死亡、MI 和 CV 死亡/MI/中风的风险增加相关。总之,在考虑 CV 事件时,这里研究的 GRS 可以具有临床意义,无疑增加了 CV 事件风险分层的知识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2b9/10076362/30679ca69f22/13353_2022_741_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2b9/10076362/e4327378ff47/13353_2022_741_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2b9/10076362/b45f07b03c62/13353_2022_741_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2b9/10076362/94f7630a3f6e/13353_2022_741_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2b9/10076362/68df7435df4f/13353_2022_741_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2b9/10076362/30679ca69f22/13353_2022_741_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2b9/10076362/e4327378ff47/13353_2022_741_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2b9/10076362/b45f07b03c62/13353_2022_741_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2b9/10076362/94f7630a3f6e/13353_2022_741_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2b9/10076362/68df7435df4f/13353_2022_741_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2b9/10076362/30679ca69f22/13353_2022_741_Fig5_HTML.jpg

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