Use of disease-modifying drugs in diabetic patients with heart failure with reduced ejection fraction

Heart Fail Rev. 2023 May;28(3):657-665. doi: 10.1007/s10741-021-10189-4. Epub 2021 Nov 3.

Abstract

Type 2 diabetes mellitus and heart failure are closely related, patients with type 2 diabetes mellitus have a higher risk of developing heart failure, and those with heart failure are at increased risk of developing type 2 diabetes. Although no specific randomized clinical trials have been conducted to test the effect of cardiovascular therapies (drugs and/or devices) in diabetic patients with heart failure, a lot of evidence shows that all interventions effective in improving prognosis in patients with heart failure reduced ejection fraction are equally beneficial in patients with and without diabetes. However, the use of disease-modifying drugs in patients with diabetes and heart failure reduced ejection fraction is a clinical challenge due to the increased risk of adverse effects. For example, β-blockers are underutilized in diabetic patients due to the theoretical unfavorable effects on glucose metabolism as well as the use of drugs that interact with the renin-angiotensin system can be challenged in patients with diabetic nephropathy because of the risk of hyperkalemia. This review outlines the current use of disease-modifying drugs in diabetic patients with heart failure reduced ejection fraction. In addition, the role of novel pharmacologic agents as type 2 sodium-glucose co-transporter inhibitors (SGLT2ii) is discussed.

Keywords: Heart failure reduced ejection fraction; Sacubitril/valsartan; Sodium-glucose co-transporter inhibitors; Type II diabetes mellitus; β-blockers.

Publication types

  • Review

MeSH terms

  • Angiotensin Receptor Antagonists / adverse effects
  • Diabetes Mellitus, Type 2* / complications
  • Diabetes Mellitus, Type 2* / drug therapy
  • Heart Failure* / chemically induced
  • Heart Failure* / complications
  • Heart Failure* / drug therapy
  • Humans
  • Renin-Angiotensin System
  • Stroke Volume

Substances

  • Angiotensin Receptor Antagonists