Cardiovascular outcomes of SGLT-2 Inhibitors Across BMI Spectrum in Heart Failure Patients: An Updated Systematic Review and Meta-Analysis

IF 2.6 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Lingyan Zhou, Huang Zijia, Zeng Ya, Zhang Ying
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Abstract

Sodium-glucose cotransporter 2 (SGLT-2) inhibitors have shown efficacy in improving cardiovascular outcomes in patients with chronic heart failure (HF). However, their impact on HF patients with varying BMI levels remains uncertain. To explore potential interactions between baseline BMI and the cardiovascular benefits of SGLT-2 inhibitors, we conducted a systematic review of studies from PubMed, Scopus, and the Cochrane Library database spanning from inception to March 2024. Eligible studies reported cardiovascular outcomes according to baseline BMI in HF patients treated with SGLT-2 inhibitors. Ultimately, our analysis included four studies encompassing 20,723 patients. We conducted separate random-effects meta-analyses for the composite outcome of first hospitalization for heart failure (HHF) or cardiovascular death (CVD), total HHF, CVD, and all-cause mortality. Compared with placebo, SGLT-2 inhibitors significantly reduced the risk of the composite outcome of first HHF or CVD (HR = 0.78, 95% CI: 0.72-0.83) and total HHF (HR = 0.73, 95% CI: 0.61-0.83), with consistent effects observed across different BMI categories (test for subgroup differences: P = 0.63 and P = 0.56, respectively). Furthermore, no statistical heterogeneity was found in the effects of SGLT-2 inhibitors on CVD (P = 0.84, I 2 = 0%) as well as all-cause mortality (P = 0.52, I 2 = 0%) across each baseline BMI subgroup in HF patients. No significant difference in safety was found between the placebo and SGLT-2 inhibitor arms. In conclusion, our findings suggest that the cardiovascular benefits of SGLT-2 inhibitors appear to be independent of baseline BMI in HF patients.
SGLT-2抑制剂对不同BMI指数的心衰患者的心血管疗效:最新系统综述和元分析
钠-葡萄糖共转运体 2(SGLT-2)抑制剂在改善慢性心力衰竭(HF)患者的心血管预后方面已显示出疗效。然而,它们对不同体重指数水平的心力衰竭患者的影响仍不确定。为了探索基线体重指数与 SGLT-2 抑制剂对心血管的益处之间的潜在相互作用,我们对 PubMed、Scopus 和 Cochrane Library 数据库中从开始到 2024 年 3 月的研究进行了系统性回顾。符合条件的研究报告了接受 SGLT-2 抑制剂治疗的高血压患者根据基线体重指数得出的心血管结果。最终,我们的分析包括了四项研究,涉及 20,723 名患者。我们对首次心衰(HHF)住院或心血管死亡(CVD)、总HHF、CVD和全因死亡率的复合结果分别进行了随机效应荟萃分析。与安慰剂相比,SGLT-2 抑制剂可显著降低首次 HHF 或 CVD(HR = 0.78,95% CI:0.72-0.83)和总 HHF(HR = 0.73,95% CI:0.61-0.83)综合结果的风险,在不同 BMI 类别中观察到一致的效果(亚组差异检验:分别为 P = 0.63 和 P = 0.56)。此外,SGLT-2抑制剂对心血管疾病(P = 0.84,I 2 = 0%)和全因死亡率(P = 0.52,I 2 = 0%)的影响在高血压患者的每个基线BMI亚组中均未发现统计学异质性。安慰剂组和 SGLT-2 抑制剂组在安全性方面无明显差异。总之,我们的研究结果表明,SGLT-2 抑制剂对心血管的益处似乎与心房颤动患者的基线体重指数无关。
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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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