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The Vicious Circle of Left Ventricular Dysfunction and Diabetes: From Pathophysiology to Emerging Treatments
Ilaria Cavallari1, Ernesto Maddaloni2, Silvia Pieralice3
1Department of Medicine, Unit of Cardiovascular Sciences, Campus Bio-Medico University of Rome, Italy.
Insights
Diabetes significantly increases heart failure (HF) risk and mortality. Sodium-glucose cotransporter 2 (SGLT2) inhibitors show promise in reducing HF outcomes for diabetic patients, representing a major therapeutic advance.
Area of Science:
- Cardiology
- Endocrinology
- Metabolic Diseases
Background:
- Diabetes mellitus and heart failure (HF) are prevalent, interconnected epidemic disorders.
- Diabetes is a frequent comorbidity in HF patients, increasing cardiovascular mortality.
- Complex molecular and cellular mechanisms link diabetes to cardiac dysfunction.
Purpose of the Study:
- To review the epidemiology, pathophysiology, clinical presentation, and treatment of HF in diabetic patients.
- To discuss the impact of diabetes on HF development and progression.
- To evaluate current and emerging therapeutic strategies for HF in the context of diabetes.
Main Methods:
- Literature search of relevant references up to February 2020 in PubMed.
- Quality assessment of observational studies using the Newcastle-Ottawa score.
- Quality assessment of randomized studies using the Cochrane Collaboration tool.
Main Results:
- Diabetes contributes to cardiac dysfunction through metabolic, neurohumoral, oxidative stress, and inflammatory pathways.
- Up to 42% of HF patients have diabetes, associated with a 34% increased risk of cardiovascular death.
- Sodium-glucose cotransporter 2 (SGLT2) inhibitors have demonstrated significant benefits in reducing HF outcomes in diabetic individuals.
Conclusions:
- The relationship between diabetes and HF is a detrimental, bidirectional cycle requiring preventive strategies and timely diagnosis.
- SGLT2 inhibitors represent a significant therapeutic advancement for HF in diabetes.
- Further research is needed to clarify the efficacy of SGLT2 inhibitors in HF with preserved ejection fraction, non-diabetic patients, and acute settings.
Context:
Diabetes and heart failure (HF) are 2 deadly and strictly related epidemic disorders. The aim of this review is to present an updated discussion of the epidemiology, pathophysiology, clinical presentation and treatment options for HF in diabetes.
Evidence Acquisition:
Relevant references published up to February 2020 were identified through searches in PubMed. Quality was graded using the Newcastle-Ottawa score in observational studies and the Cochrane Collaboration tool in randomized studies.
Evidence Synthesis:
Metabolic and neurohumoral derangements, oxidative stress, inflammation, micro- and macroangiopathy all contribute through complex molecular and cellular mechanisms to cardiac dysfunction in diabetes, which in turn, results as one the most frequent underlying conditions affecting up to 42% of patients with HF and causing a 34% increased risk of cardiovascular death. On top of traditional guideline-based HF medical and device therapies, equally effective in patients with and without diabetes, a new class of glucose-lowering agents acting through the sodium-glucose cotransporter 2 (SGLT2) inhibition showed impressive results in reducing HF outcomes in individuals with diabetes and represents an active area of investigation.
Conclusions:
Diabetes and HF are strictly linked in a bidirectional and deadly vicious circle difficult to break. Therefore, preventive strategies and a timely diagnosis are crucial to improve outcomes in such patients. SGLT2 inhibitors represent a major breakthrough with remarkably consistent findings. However, it is still not clear whether their benefits may be definitely extended to patients with HF with preserved ejection fraction, to those without diabetes and in the acute setting.
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