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SGLT2 inhibition and heart failure-current concepts
Joaquim Silva Custodio1,2, Andre Rodrigues Duraes3,4, Marconi Abreu5
1Department of Health Family, Medical School of Bahia, Federal University of Bahia, Praça XV de Novembro, s/n° - Largo do Terreiro de Jesus, Salvador, BA, 40026-010, Brazil. jocsjunior@uol.com.br.
Abstract:
Type 2 diabetes mellitus (T2DM) is a major risk factor for several cardiovascular (CV) conditions, including heart failure (HF). However, until recently, no therapy to treat patients with diabetes could also reduce CV risks related to HF. The EMPA-REG OUTCOME trial with empagliflozin was the first to demonstrate significant cardioprotective benefits in this population. Its impressive 35% reduction in hospitalizations for HF drew the attention of the scientific community to the possibility that pharmacologic sodium-glucose cotransporter 2 (SGLT2) inhibition could be part of the armamentarium for treating patients with HF, with and without diabetes. The recently published CANVAS Program (with canagliflozin) and real-life data from the CVD-Real Study (using dapagliflozin, empagliflozin, and canagliflozin) further strengthened this hypothesis, suggesting that the observed benefit is not restricted to a particular drug, but is rather a class effect. This review explores the effects of pharmacologic SGLT2 inhibitors' use in cardiac function and discusses the potential role of this class of medication as a treatment for HF.
Insights
Sodium-glucose cotransporter 2 (SGLT2) inhibitors, initially for type 2 diabetes, show significant heart failure (HF) benefits. This class of drugs may offer a new treatment strategy for heart failure in patients with and without diabetes.
Area of Science:
- Cardiology
- Endocrinology
- Pharmacology
Background:
- Type 2 diabetes mellitus (T2DM) significantly increases the risk of cardiovascular (CV) conditions, notably heart failure (HF).
- Historically, treatments for T2DM lacked dedicated cardioprotective benefits against HF.
- The EMPA-REG OUTCOME trial marked a turning point, revealing empagliflozin's cardioprotective effects in T2DM patients.
Purpose of the Study:
- To review the impact of pharmacologic sodium-glucose cotransporter 2 (SGLT2) inhibitors on cardiac function.
- To explore the potential of SGLT2 inhibitors as a therapeutic option for heart failure, irrespective of diabetic status.
Main Methods:
- Review of pivotal clinical trials, including EMPA-REG OUTCOME and the CANVAS Program.
- Analysis of real-world evidence from studies like CVD-Real, examining dapagliflozin, empagliflozin, and canagliflozin.
- Synthesis of findings to evaluate the class effect of SGLT2 inhibition on HF.
Main Results:
- Empagliflozin demonstrated a notable 35% reduction in HF hospitalizations.
- Subsequent studies (CANVAS, CVD-Real) corroborated these cardioprotective benefits.
- Evidence suggests the benefits of SGLT2 inhibition for HF are a class effect, not drug-specific.
Conclusions:
- Pharmacologic SGLT2 inhibition has emerged as a promising therapeutic strategy for managing heart failure.
- The cardioprotective effects observed extend beyond glycemic control, indicating a broader CV benefit.
- SGLT2 inhibitors represent a potential new class of medications for HF treatment in both diabetic and non-diabetic individuals.
Related Concept Videos
Heart Failure II: Pathophysiology
Pathophysiology of Heart Failure
Heart Failure I: Introduction
Heart Failure VI: Adjunct Therapies
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