Comparing the efficacy of sodium-glucose co-transporter 2 inhibitors among non-older and older patients: A Systematic Review and Meta-Analysis.

IF 2.6 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Journal of Cardiovascular Pharmacology Pub Date : 2024-12-12 DOI:10.1097/FJC.0000000000001659
Izuki Yamashita, Tomohiro Fujisaki, Francisco J Romeo, Daisuke Sueta, Eiichiro Yamamoto, Kenichi Tsujita
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Abstract

Large scale randomized trials have shown that sodium-glucose co-transporter 2 (SGLT2) inhibitors can reduce cardiovascular events in patients with cardiovascular disease or with increased risks of cardiovascular disease. However, the evidence from older patients is limited. To compare the efficacy of SGLT2 inhibitors among non-older and older patients we have searched PubMed, Cochrane Central, and Embase until February 2023 for randomized controlled trials (RCTs) investigating SGLT2 inhibitors in older (age ≥ 65 years) patients with diabetes mellitus, chronic kidney disease, and chronic heart failure. The primary outcome was a composite outcome of cardiovascular death, acute myocardial infarction, and stroke. The secondary outcomes were exacerbation of heart failure, kidney disease progression, and a composite of cardiovascular death and heart failure. Our search identified 11 RCTs with a total of 79,370 patients. SGLT2 inhibitors were associated with a reduced risk of the primary outcome in the total cohort (HR: 0.91; CI [0.84-0.99]) with concordant results in both non-older and older populations (HR: 0.96; CI [0.88-1.05], HR: 0.87; CI [0.75-1.01], respectively) without subgroup differences (p=0.23), and a reduced risk of developing the composite of cardiovascular death and heart failure exacerbation in both non-older and older populations (HR: 0.77; CI [0.67-0.87], HR: 0.76; CI [0.71-0.82], respectively) without subgroup differences (p=0.96). A meta-analysis could not be performed for the other outcomes. These results suggested that SGLT2 inhibitors were similarly associated with a reduced risks of cardiovascular events across the spectrum of non-older and older patients with risk factors for developing cardiovascular disease.

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比较钠-葡萄糖共转运蛋白2抑制剂在非老年和老年患者中的疗效:一项系统回顾和荟萃分析
大规模随机试验表明,钠-葡萄糖共转运蛋白2 (SGLT2)抑制剂可以减少心血管疾病或心血管疾病风险增加的患者的心血管事件。然而,来自老年患者的证据有限。为了比较SGLT2抑制剂在非老年和老年患者中的疗效,我们检索了PubMed、Cochrane Central和Embase,直到2023年2月,研究SGLT2抑制剂在老年(年龄≥65岁)糖尿病、慢性肾脏疾病和慢性心力衰竭患者中的疗效的随机对照试验(RCTs)。主要结局是心血管死亡、急性心肌梗死和中风的复合结局。次要结局是心力衰竭加重、肾脏疾病进展、心血管死亡和心力衰竭的复合。我们的研究确定了11项随机对照试验,共计79,370例患者。在整个队列中,SGLT2抑制剂与主要结局风险降低相关(HR: 0.91;CI[0.84-0.99]),非老年人群和老年人群的结果一致(HR: 0.96;Ci [0.88-1.05], hr: 0.87;CI[0.75-1.01],无亚组差异(p=0.23),并且在非老年人群和老年人群中发生心血管死亡和心力衰竭加重复合的风险降低(HR: 0.77;Ci [0.67-0.87], hr: 0.76;CI[0.71-0.82]),无亚组差异(p=0.96)。其他结果无法进行荟萃分析。这些结果表明,SGLT2抑制剂与具有心血管疾病危险因素的非老年和老年患者的心血管事件风险降低相似。
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来源期刊
CiteScore
5.10
自引率
3.30%
发文量
367
审稿时长
1 months
期刊介绍: Journal of Cardiovascular Pharmacology is a peer reviewed, multidisciplinary journal that publishes original articles and pertinent review articles on basic and clinical aspects of cardiovascular pharmacology. The Journal encourages submission in all aspects of cardiovascular pharmacology/medicine including, but not limited to: stroke, kidney disease, lipid disorders, diabetes, systemic and pulmonary hypertension, cancer angiogenesis, neural and hormonal control of the circulation, sepsis, neurodegenerative diseases with a vascular component, cardiac and vascular remodeling, heart failure, angina, anticoagulants/antiplatelet agents, drugs/agents that affect vascular smooth muscle, and arrhythmias. Appropriate subjects include new drug development and evaluation, physiological and pharmacological bases of drug action, metabolism, drug interactions and side effects, application of drugs to gain novel insights into physiology or pathological conditions, clinical results with new and established agents, and novel methods. The focus is on pharmacology in its broadest applications, incorporating not only traditional approaches, but new approaches to the development of pharmacological agents and the prevention and treatment of cardiovascular diseases. Please note that JCVP does not publish work based on biological extracts of mixed and uncertain chemical composition or unknown concentration.
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