Therapies for patients with coexisting heart failure with reduced ejection fraction and non-alcoholic fatty liver disease

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Heart failure with reduced ejection fraction (HFrEF) and nonalcoholic fatty liver disease (NAFLD) are two common comorbidities that share similar pathophysiological mechanisms. There is a growing interest in the potential of targeted therapies to improve outcomes in patients with coexisting HFrEF an...

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Detalles Bibliográficos
Autores: Arriola-Montenegro, Jose, Beas, Renato, Cerna-Viacava, Renato, Chaponan-Lavalle, Andres, Hernandez Randich, Karla, Chambergo-Michilot, Diego, Flores Sanga, Herson, Mutirangura, Pornthira
Formato: artículo
Fecha de Publicación:2023
Institución:Universidad Peruana de Ciencias Aplicadas
Repositorio:UPC-Institucional
Lenguaje:inglés
OAI Identifier:oai:repositorioacademico.upc.edu.pe:10757/669048
Enlace del recurso:http://hdl.handle.net/10757/669048
Nivel de acceso:acceso abierto
Materia:Cardiovascular disease
Heart Failure
Heart failure reduced ejection fraction
Non-alcoholic fatty liver disease
Novel therapies
HFrEF (Heart Failure with Reduced Ejection Fraction)
NAFLD (Nonalcoholic Fatty Liver Disease)
Comorbidities
Targeted Therapies
Angiotensin-Converting Enzyme Inhibitors (ACEi)
Angiotensin Receptor Blockers (ARBs)
Mineralocorticoid Receptor Antagonist
Sodium-Glucose Cotransporter-2 Inhibitors (SGLT2i)
Multidisciplinary Approach
Novel Therapies
Descripción
Sumario:Heart failure with reduced ejection fraction (HFrEF) and nonalcoholic fatty liver disease (NAFLD) are two common comorbidities that share similar pathophysiological mechanisms. There is a growing interest in the potential of targeted therapies to improve outcomes in patients with coexisting HFrEF and NAFLD. This manuscript reviews current and potential therapies for patients with coexisting HFrEF and NAFLD. Pharmacological therapies, including angiotensin-converting enzyme inhibitors/angiotensin receptor blockers, mineralocorticoids receptor antagonist, and sodium-glucose cotransporter-2 inhibitors, have been shown to reduce fibrosis and fat deposits in the liver. However, there are currently no data showing the beneficial effects of sacubitril/valsartan, ivabradine, hydralazine, isosorbide nitrates, digoxin, or beta blockers on NAFLD in patients with HFrEF. This study highlights the importance of considering HFrEF and NAFLD when developing treatment plans for patients with these comorbidities. Further research is needed in patients with coexisting HFrEF and NAFLD, with an emphasis on novel therapies and the importance of a multidisciplinary approach for managing these complex comorbidities.
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