[Diabetes and Heart Failure]

Walter Alarco1

  • 1Unidad de Insuficiencia Cardiaca, Trasplante Cardiaco e Hipertensión Pulmonar Instituto Nacional Cardiovascular INCOR. Lima, Perú.

Insights

Diabetes Mellitus (DM) significantly increases heart failure (HF) risk. Sodium-glucose cotransporter 2 inhibitors (SGLT2i) offer crucial benefits for diabetic patients with HF, improving outcomes beyond glycemic control.

Area of Science:

  • Cardiology and Endocrinology
  • Diabetic Cardiomyopathy
  • Cardio-metabolic disease research

Context:

  • Diabetes Mellitus (DM) is a chronic disease linked to severe cardiovascular complications, particularly heart failure (HF).
  • A complex bidirectional relationship exists between DM and HF, with HF often preceding other cardiovascular events in diabetic individuals.
  • DM contributes to HF through both atherosclerosis-mediated and non-atherosclerotic pathways, including direct myocardial effects (Diabetic Cardiomyopathy).

Purpose:

  • To review the mechanisms by which DM leads to HF.
  • To discuss current treatment strategies for HF in diabetic patients.
  • To highlight the role and benefits of SGLT2 inhibitors in managing HF within the diabetic population.

Summary:

  • HF treatment in diabetic patients with reduced ejection fraction mirrors non-diabetic guidelines, focusing on triple neurohumoral blockade.
  • For HF with preserved ejection fraction, specific therapies are still lacking.
  • Sodium-glucose cotransporter 2 inhibitors (SGLT2i) demonstrate significant advantages in diabetic HF patients, offering pleiotropic effects beyond glucose lowering.

Impact:

  • SGLT2 inhibitors provide metabolic, hemodynamic, and cellular viability benefits, preventing apoptosis and cell death in the myocardium.
  • Clinical trials like DAPA-HF show SGLT2 inhibitors' efficacy in HF with reduced ejection fraction, marking a therapeutic advancement.
  • These findings suggest SGLT2 inhibitors are pivotal in a new treatment paradigm for diabetic patients with heart failure.

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