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二甲双胍对冠心病患者全因和心血管死亡率的影响:系统评价和更新的荟萃分析。

Effect of metformin on all-cause and cardiovascular mortality in patients with coronary artery diseases: a systematic review and an updated meta-analysis.

机构信息

Department of Cardiology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China.

Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, 100005, China.

出版信息

Cardiovasc Diabetol. 2019 Jul 30;18(1):96. doi: 10.1186/s12933-019-0900-7.


DOI:10.1186/s12933-019-0900-7
PMID:31362743
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6668189/
Abstract

BACKGROUND: Metformin is the most widely prescribed drug to lower glucose and has a definitive effect on the cardiovascular system. The goal of this systematic review and meta-analysis is to assess the effects of metformin on mortality and cardiac function among patients with coronary artery disease (CAD). METHODS: Relevant studies reported before October 2018 was retrieved from databases including PubMed, EMBASE, Cochrane Library and Web of Science. Hazard ratio (HR) was calculated to evaluate the all-cause mortality, cardiovascular mortality and incidence of cardiovascular events (CV events), to figure out the level of left ventricular ejection fraction (LVEF), creatine kinase MB (CK-MB), type B natriuretic peptide (BNP) and to compare the average level of low density lipoprotein (LDL). RESULTS: In this meta-analysis were included 40 studies comprising 1,066,408 patients. The cardiovascular mortality, all-cause mortality and incidence of CV events were lowered to adjusted HR (aHR) = 0.81, aHR = 0.67 and aHR = 0. 83 respectively after the patients with CAD were given metformin. Subgroup analysis showed that metformin reduced all-cause mortality in myocardial infarction (MI) (aHR = 0.79) and heart failure (HF) patients (aHR = 0.84), the incidence of CV events in HF (aHR = 0.83) and type II diabetes mellitus (T2DM) patients (aHR = 0.83), but had no significant effect on MI (aHR = 0.87) and non-T2DM patients (aHR = 0.92). Metformin is superior to sulphonylurea (aHR = 0.81) in effects on lowering the incidence of CV events and in effects on patients who don't use medication. The CK-MB level in the metformin group was lower than that in the control group standard mean difference (SMD) = - 0.11). There was no significant evidence that metformin altered LVEF (MD = 2.91), BNP (MD = - 0.02) and LDL (MD = - 0.08). CONCLUSION: Metformin reduces cardiovascular mortality, all-cause mortality and CV events in CAD patients. For MI patients and CAD patients without T2DM, metformin has no significant effect of reducing the incidence of CV events. Metformin has a better effect of reducing the incidence of CV events than sulfonylureas.

摘要

背景:二甲双胍是降低血糖最广泛应用的药物,对心血管系统有明确的作用。本系统回顾和荟萃分析的目的是评估二甲双胍对冠心病(CAD)患者死亡率和心功能的影响。

方法:检索了包括 PubMed、EMBASE、Cochrane 图书馆和 Web of Science 在内的数据库中截至 2018 年 10 月之前发表的相关研究。计算风险比(HR)来评估全因死亡率、心血管死亡率和心血管事件(CV 事件)发生率,以确定左心室射血分数(LVEF)、肌酸激酶 MB(CK-MB)、B 型利钠肽(BNP)的水平,并比较低密度脂蛋白(LDL)的平均水平。

结果:本荟萃分析共纳入 40 项研究,包括 1066408 例患者。CAD 患者使用二甲双胍后,心血管死亡率、全因死亡率和 CV 事件发生率分别降低至调整后的 HR(aHR)=0.81、aHR=0.67 和 aHR=0.83。亚组分析显示,二甲双胍降低了心肌梗死(MI)(aHR=0.79)和心力衰竭(HF)(aHR=0.84)患者的全因死亡率,HF(aHR=0.83)和 2 型糖尿病(T2DM)(aHR=0.83)患者的 CV 事件发生率,但对 MI(aHR=0.87)和非 T2DM 患者(aHR=0.92)无显著影响。与磺脲类药物相比,二甲双胍在降低 CV 事件发生率和在未用药患者中的效果更优(aHR=0.81)。二甲双胍组 CK-MB 水平低于对照组的标准均数差(SMD)=-0.11。没有证据表明二甲双胍改变左心室射血分数(MD=2.91)、B 型利钠肽(MD=-0.02)和低密度脂蛋白(MD=-0.08)。

结论:二甲双胍降低 CAD 患者的心血管死亡率、全因死亡率和 CV 事件发生率。对于 MI 患者和无 T2DM 的 CAD 患者,二甲双胍降低 CV 事件发生率的效果不显著。与磺脲类药物相比,二甲双胍降低 CV 事件发生率的效果更好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3238/6668189/9ac823f6ddd9/12933_2019_900_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3238/6668189/57f72ca64477/12933_2019_900_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3238/6668189/459cfb9555ee/12933_2019_900_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3238/6668189/950d9548cd6d/12933_2019_900_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3238/6668189/9b87671e0b95/12933_2019_900_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3238/6668189/ce174908c5d7/12933_2019_900_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3238/6668189/9d088b6d6cfb/12933_2019_900_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3238/6668189/9ac823f6ddd9/12933_2019_900_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3238/6668189/57f72ca64477/12933_2019_900_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3238/6668189/459cfb9555ee/12933_2019_900_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3238/6668189/950d9548cd6d/12933_2019_900_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3238/6668189/9b87671e0b95/12933_2019_900_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3238/6668189/ce174908c5d7/12933_2019_900_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3238/6668189/9d088b6d6cfb/12933_2019_900_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3238/6668189/9ac823f6ddd9/12933_2019_900_Fig7_HTML.jpg

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