Efficacy of Sodium-Glucose Cotransporter-2 Inhibitors in Patients With Acute Myocardial Infarction: A Meta-Analysis of Randomised Controlled Trials

IF 2.7 Q3 ENDOCRINOLOGY & METABOLISM
Mushood Ahmed, Hritvik Jain, Hira Javaid, Areeba Ahsan, Szabolcs Szilagyi, Adeel Ahmad, Raheel Ahmed
{"title":"Efficacy of Sodium-Glucose Cotransporter-2 Inhibitors in Patients With Acute Myocardial Infarction: A Meta-Analysis of Randomised Controlled Trials","authors":"Mushood Ahmed,&nbsp;Hritvik Jain,&nbsp;Hira Javaid,&nbsp;Areeba Ahsan,&nbsp;Szabolcs Szilagyi,&nbsp;Adeel Ahmad,&nbsp;Raheel Ahmed","doi":"10.1002/edm2.514","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background</h3>\n \n <p>Sodium-glucose cotransporter 2 (SGLT2) inhibitors improve cardiovascular (CV) outcomes in patients with or without Type 2 diabetes and heart failure (HF). However, studies have shown conflicting evidence regarding their efficacy in patients following acute myocardial infarction (MI). We conducted a pilot systematic review and meta-analysis to synthesise the available evidence regarding the effectiveness of SGLT2 inhibitors in MI.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>A systematic literature search was conducted using PubMed/MEDLINE, the Cochrane Library and Embase databases to identify randomised controlled trials (RCTs) that compared clinical outcomes of SGLT2 inhibitors with placebo following MI. We conducted the statistical analysis using RevMan, version 5.4 and pooled risk ratios (RRs) along the corresponding 95% confidence interval (CI) for all outcomes.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Five RCTs reporting data for 11,211 patients were included in our study. The mean follow-up duration was 43.8 weeks. Our pooled analysis showed that SGLT2 inhibitors significantly reduced the risk of hospitalisations for heart failure (HHF) (RR = 0.76, 95% CI: 0.61–0.88, <i>p</i> = 0.001) in patients with MI. However, the risk of all-cause mortality (RR = 1.05, 95% CI: 0.78–1.41, <i>p</i> = 0.76), CV mortality (RR = 1.04, 95% CI = 0.84–1.29, <i>p</i> = 0.73) and all-cause hospitalisations (RR = 1.06, 95% CI: 0.96–1.17, <i>p</i> = 0.25) remained comparable across the two groups.</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>SGLT2 inhibitors reduce HHF without affecting all-cause mortality, CV mortality and all-cause hospitalisations. However, further evidence is required to reach a definitive conclusion.</p>\n </section>\n </div>","PeriodicalId":36522,"journal":{"name":"Endocrinology, Diabetes and Metabolism","volume":null,"pages":null},"PeriodicalIF":2.7000,"publicationDate":"2024-08-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/edm2.514","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Endocrinology, Diabetes and Metabolism","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/edm2.514","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0

Abstract

Background

Sodium-glucose cotransporter 2 (SGLT2) inhibitors improve cardiovascular (CV) outcomes in patients with or without Type 2 diabetes and heart failure (HF). However, studies have shown conflicting evidence regarding their efficacy in patients following acute myocardial infarction (MI). We conducted a pilot systematic review and meta-analysis to synthesise the available evidence regarding the effectiveness of SGLT2 inhibitors in MI.

Methods

A systematic literature search was conducted using PubMed/MEDLINE, the Cochrane Library and Embase databases to identify randomised controlled trials (RCTs) that compared clinical outcomes of SGLT2 inhibitors with placebo following MI. We conducted the statistical analysis using RevMan, version 5.4 and pooled risk ratios (RRs) along the corresponding 95% confidence interval (CI) for all outcomes.

Results

Five RCTs reporting data for 11,211 patients were included in our study. The mean follow-up duration was 43.8 weeks. Our pooled analysis showed that SGLT2 inhibitors significantly reduced the risk of hospitalisations for heart failure (HHF) (RR = 0.76, 95% CI: 0.61–0.88, p = 0.001) in patients with MI. However, the risk of all-cause mortality (RR = 1.05, 95% CI: 0.78–1.41, p = 0.76), CV mortality (RR = 1.04, 95% CI = 0.84–1.29, p = 0.73) and all-cause hospitalisations (RR = 1.06, 95% CI: 0.96–1.17, p = 0.25) remained comparable across the two groups.

Conclusion

SGLT2 inhibitors reduce HHF without affecting all-cause mortality, CV mortality and all-cause hospitalisations. However, further evidence is required to reach a definitive conclusion.

Abstract Image

钠-葡萄糖共转运体-2 抑制剂对急性心肌梗死患者的疗效:随机对照试验的 Meta 分析。
背景:钠-葡萄糖共转运体 2(SGLT2)抑制剂可改善患有或不患有 2 型糖尿病和心力衰竭(HF)患者的心血管(CV)预后。然而,有关其对急性心肌梗死(MI)患者疗效的研究证据却相互矛盾。我们进行了一项试验性系统综述和荟萃分析,以综合有关 SGLT2 抑制剂对心肌梗死疗效的现有证据:我们使用 PubMed/MEDLINE、Cochrane Library 和 Embase 数据库进行了系统性文献检索,以确定在心肌梗死后比较 SGLT2 抑制剂和安慰剂临床疗效的随机对照试验 (RCT)。我们使用 RevMan 5.4 版进行了统计分析,并对所有结果的风险比 (RR) 以及相应的 95% 置信区间 (CI) 进行了汇总:我们的研究共纳入了五项研究,报告了 11,211 名患者的数据。平均随访时间为 43.8 周。我们的汇总分析显示,SGLT2 抑制剂可显著降低心肌梗死患者因心力衰竭(HHF)住院的风险(RR = 0.76,95% CI:0.61-0.88,p = 0.001)。然而,两组患者的全因死亡风险(RR = 1.05,95% CI:0.78-1.41,p = 0.76)、CV 死亡率(RR = 1.04,95% CI = 0.84-1.29,p = 0.73)和全因住院风险(RR = 1.06,95% CI:0.96-1.17,p = 0.25)仍然相当:结论:SGLT2 抑制剂可降低 HHF,但不会影响全因死亡率、CV 死亡率和全因住院率。结论:SGLT2 抑制剂可降低 HHF,但不会影响全因死亡率、冠心病死亡率和全因住院率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Endocrinology, Diabetes and Metabolism
Endocrinology, Diabetes and Metabolism Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
5.00
自引率
0.00%
发文量
66
审稿时长
6 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信