The impact of diabetes on heart failure development: The cardio-renal-metabolic connection
- PMID: 33895192
- DOI: 10.1016/j.diabres.2021.108831
The impact of diabetes on heart failure development: The cardio-renal-metabolic connection
Abstract
Heart failure (HF) and chronic kidney disease (CKD) are often associated in type 2 diabetes (T2D), aggravate each other and exert synergistic effects to increase the risk of cardiac and renal events. The risks of renal worsening in HF patients and HF in CKD patients need to be evaluated to tailor preventive therapy. The recent CV and renal trials enriched our knowledge about the natural history of HF and CKD in T2D and provided evidence for the benefit of sodium-glucose cotransporter 2 inhibitors (SGLT2is) in HF and renal decline prevention. SGLT-2is are the best choice in patients with HFrEF to improve CV prognosis and HF-related outcomes and also to prevent kidney-related outcomes, and in CKD patients to slow down renal failure and also reduce hospitalization for HF and CV death. In both situations the number of patients to treat in order to prevent such events in one patient is lower than in the general T2D population at high CV risk. GLP1-receptor agonists could be an alternative in a patient who is intolerant or has a contraindication to SGLT-2is. A tight collaboration between diabetologists, nephrologists and cardiologists should be encouraged for a holistic and effective strategy to reduce the burden of cardio-renal-metabolic interaction.
Keywords: Chronic kidney disease; Coronary artery disease; Diabetes; GLP1-receptor agonists; Heart failure; SGLT2 inhibitors.
Copyright © 2021. Published by Elsevier B.V.
Conflict of interest statement
Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: PV discloses the following potential conflicts of interest: lectures for Abbott, AstraZeneca, Bayer, Eli Lilly, Hikma Pharmaceuticals, Merck Sharp & Dohme, Novo Nordisk, Novartis, Pfizer, Sanofi; research grants from Abbott, Bristol-Myers-Squibb–AstraZeneca, Novo Nordisk; participation in expert committees for AstraZeneca, Boehringer Ingelheim, Novo Nordisk, Daiichi Sankyo, Sanofi, Servier, Stendo. GP discloses the potential following conflicts of interest: lectures for Abbott, AstraZeneca, Eli-Lilly, Merck-Sharp-Dohme, Novo Nordisk, Sanofi; participation to Expert Committees for Merck-Sharp-Dohme, Novo Nordisk, Sanofi. SP discloses no conflict of interest. JMH discloses the following potential conflicts of interest: consulting fees from Astra Zeneca, Alexion, Servier, Vifor Fresenius, Merck-Sharp-Dohme, Novo Nordisk, Boehringer Ingelheim France, Sanofi, Bayer. ED discloses the following potential conflicts of interest: consulting fees from AstraZeneca, General Electric Healthcare, Bristol-Myers-Squibb.
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