SGLT-2 Inhibitors in Heart Failure and Type-2 Diabetes: Hitting Two Birds with One Stone?

Diogo Santos-Ferreira1,2, Pedro Gonçalves-Teixeira1,2, Ricardo Fontes-Carvalho3,4

  • 1Serviço de Cardiologia, Centro Hospitalar Vila Nova de Gaia/Espinho, Porto, Portugal.

Cardiology
|December 23, 2019
PubMed

Insights

Sodium-glucose cotransporter-2 inhibitors (SGLT-2i) effectively manage type 2 diabetes mellitus (T2DM) and heart failure (HF). These drugs show promise in reducing heart failure hospitalizations for patients with T2DM.

Area of Science:

  • Cardiology
  • Endocrinology
  • Pharmacology

Background:

  • Type 2 diabetes mellitus (T2DM) and heart failure (HF) are significant global health issues.
  • T2DM and HF are mutually exacerbating conditions, leading to poorer prognoses when co-occurring.
  • Historically, T2DM and HF have been treated as independent pathologies.

Purpose of the Study:

  • To explore the intricate relationship between T2DM and HF.
  • To discuss the concept of diabetic cardiomyopathy.
  • To summarize the impact of sodium-glucose cotransporter-2 inhibitors (SGLT-2i) on HF hospitalizations and their mechanisms.

Main Methods:

  • Review of recent cardiovascular outcome trials.
  • Analysis of pathophysiological mechanisms linking T2DM and HF.
  • Synthesis of data on SGLT-2i efficacy in managing co-morbid T2DM and HF.

Main Results:

  • SGLT-2 inhibitors demonstrate efficacy in managing both T2DM and HF.
  • Evidence suggests SGLT-2i reduce HF hospitalizations in patients with T2DM.
  • Proposed pathophysiological mechanisms underlying these effects are explored.

Conclusions:

  • The treatment paradigm for T2DM and HF is evolving with the advent of SGLT-2i.
  • SGLT-2i represent a significant therapeutic advancement for patients with both conditions.
  • Further research into the mechanisms of SGLT-2i in diabetic cardiomyopathy is warranted.

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