Treatment of heart failure in patients with diabetes mellitus
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Updated: Oct 2, 2026

Modeling and Evaluation of Murine Diabetic Cardiomyopathy Model
Published on: November 29, 2024
Steven J Lavine1, Steven D Gellman
1Harper Hospital, Wayne State University, Detroit, Michigan, USA. Steven.Lvine@jax.ufl.edu
Insights
Diabetic patients face higher risks of cardiovascular disease, particularly congestive heart failure (CHF). Early intervention with beta-blockers and ACE inhibitors can significantly reduce morbidity and mortality in this high-risk group.
Area of Science:
- Cardiology
- Endocrinology
- Pharmacology
Background:
- Diabetes mellitus significantly increases cardiovascular disease morbidity and mortality.
- Congestive heart failure (CHF) and coronary artery disease are primary contributors to adverse cardiovascular events in diabetic patients.
- Diabetes and hypertension are key causes of left ventricular (LV) dysfunction and CHF, with diabetes causing metabolic/ultrastructural changes and hypertension causing fibrosis.
Purpose of the Study:
- To review the pathophysiology of CHF in diabetic patients.
- To examine the neurohormonal mechanisms underlying LV dysfunction and CHF in diabetes.
- To discuss the role of insulin and current therapeutic strategies, highlighting the need for further research.
Main Methods:
- Review of existing literature on CHF pathophysiology in diabetes.
- Analysis of experimental animal data on diabetes-induced biochemical and ultrastructural changes.
- Evaluation of available clinical data on insulin's role and therapeutic interventions.
Main Results:
- Diabetes contributes to metabolic and ultrastructural LV dysfunction, while hypertension leads to fibrosis.
- Insulin shows potential in reversing metabolic and structural changes, supported by experimental and limited clinical data.
- Current CHF therapy in diabetics mirrors non-diabetic treatment, focusing on beta-blockers and ACE inhibitors.
Conclusions:
- Diabetic patients with CHF have higher mortality rates, presenting a critical subgroup for clinical impact.
- Beta-blockers and ACE inhibitors offer significant benefits for diabetic patients with ischemia and CHF.
- Further clinical trials specifically designed for diabetic subgroups with hypertension and LV dysfunction are essential.
Abstract:
Patients with diabetes mellitus have an increased morbidity and mortality from cardiovascular disease. Both coronary artery disease and congestive heart failure (CHF) are largely responsible for the increased cardiovascular adverse events in patients with diabetes. This review discusses the pathophysiology of CHF, the mechanisms of left ventricular (LV) dysfunction and the neurohormonal mechanisms involved in both LV dysfunction and CHF. Diabetes with and without hypertension is an important cause of LV dysfunction and CHF. Diabetes may be responsible for the metabolic and ultrastructural causes of LV dysfunction, while hypertension may be responsible for the marked fibrotic changes that are found. Experimental induction of diabetes in animals has shed light on the biochemical and ultrastructural changes seen. The role of insulin to reverse both metabolic and structural changes is reviewed both from experimental data and with the limited amount of clinical data available. The therapy of CHF in patients with diabetes is similar to that of patients without diabetes, with therapy directed toward the use of beta-blockers and angiotensin converting enzyme (ACE) inhibitors. As the morbidity and mortality are higher in patients with diabetes, several studies have pointed out the importance of this subgroup where the opportunity to make a significant clinical impact exists. A significant opportunity exists to reduce morbidity and mortality with beta-blockers and ACE inhibitors when ischaemia and CHF are both present. However, studies in patients diabetes have been limited to post hoc subgroup analyses and rarely as predefined subgroups. Clinical trials involving patients with diabetes with and without hypertension and LV dysfunction are clearly needed in the future to adequately address the needs of this high risk subgroup.
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