Shift of conventional paradigm of heart failure treatment: from angiotensin receptor neprilysin inhibitor to sodium-glucose co-transporter 2 inhibitors?
- 30 November 2020
- journal article
- review article
- Published by Taylor & Francis Ltd in Future Cardiology
- Vol. 17 (3), 497-506
- https://doi.org/10.2217/fca-2020-0178
Abstract
Current clinical guidelines for heart failure (HF) contain a brand new therapeutic strategy for HF with reduced ejection fraction (HFrEF), which is based on neurohumoral modulation through the use of angiotensin receptor neprilysin inhibitors. There is a large body of evidence for the fact that sodium-glucose co-transporter 2 inhibitors may significantly improve all-cause mortality, cardiovascular mortality and hospitalization for HF in patients with HFrEF who received renin-angiotensin system blockers including angiotensin receptor neprilysin inhibitors, beta-blockers and mineralocorticoid receptor antagonists. The review discusses that sodium-glucose co-transporter 2 inhibitors have a wide spectrum of favorable molecular effects and contribute to tissue protection, improving survival in HFrEF patients. Lay Current clinical guidelines for heart failure (HF) contain a new therapeutic strategy for a certain type of HF. There is a large body of evidence for the fact that certain types of drugs called sodium-glucose co-transporter 2 inhibitors may significantly improve outcomes in patients with this type of HF who received a different group of drugs. The review discusses the features of sodium-glucose co-transporter 2 inhibitors that make them successful in improving the outcomes in patients with HF.Keywords
This publication has 74 references indexed in Scilit:
- The Emerging Epidemic of Heart Failure with Preserved Ejection FractionCurrent Heart Failure Reports, 2013
- Forecasting the Impact of Heart Failure in the United StatesCirculation: Heart Failure, 2013
- Loss of ACE2 Exaggerates High-Calorie Diet–Induced Insulin Resistance by Reduction of GLUT4 in MiceDiabetes, 2012
- B-Raf Associates with and Activates the NHE1 Isoform of the Na+/H+ ExchangerOnline Journal of Public Health Informatics, 2011
- Molecular determinants of renal glucose reabsorption. Focus on “Glucose transport by human renal Na+/d-glucose cotransporters SGLT1 and SGLT2”American Journal of Physiology-Cell Physiology, 2011
- Epidemiology and risk profile of heart failureNature Reviews Cardiology, 2010
- Angiotensin I–Converting Enzyme Type 2 (ACE2) Gene Therapy Improves Glycemic Control in Diabetic MiceDiabetes, 2010
- Activation of Na + /H + Exchanger 1 Is Sufficient to Generate Ca 2+ Signals That Induce Cardiac Hypertrophy and Heart FailureCirculation Research, 2008
- High-glucose-induced regulation of intracellular ANG II synthesis and nuclear redistribution in cardiac myocytesAmerican Journal of Physiology-Heart and Circulatory Physiology, 2007
- Parathyroid Hormone and Parathyroid Hormone-related Peptide Inhibit the Apical Na+/H+ Exchanger NHE-3 Isoform in Renal Cells (OK) via a Dual Signaling Cascade Involving Protein Kinase A and COnline Journal of Public Health Informatics, 1995