Evaluation of the Effects of the Sodium–Glucose Cotransporter 2 Inhibitors and Sacubitril/Valsartan Combined Therapy in Patients with HFrEF: An Echocardiographic Study
Sodium–glucose cotransporter 2 inhibitors (iSGLT2) have become the fourth pillar of the medical treatment for heart failure with reduced ejection fraction (HFrEF). However, the mechanisms of action of iSGLT2 remain poorly understood. The effectiveness of combined ARNI and iSGLT2 therapy in left vent...
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Published in | International journal of molecular sciences Vol. 26; no. 12; p. 5651 |
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Abstract | Sodium–glucose cotransporter 2 inhibitors (iSGLT2) have become the fourth pillar of the medical treatment for heart failure with reduced ejection fraction (HFrEF). However, the mechanisms of action of iSGLT2 remain poorly understood. The effectiveness of combined ARNI and iSGLT2 therapy in left ventricular (LV) remodeling is still under study. We aim to investigate the effects of ARNI + iSGLT2 combination therapy in patients affected by HFrEF in terms of ventricular remodeling using speckle tracking echocardiography (STE). In this observational study, 136 patients with HFrEF taking ARNI were enrolled. All patients were evaluated at baseline (before iSGLT2), at 3 months and at 12 months from the beginning of iSGLT2 therapy. Echocardiographic parameters, including STE analysis and volumetric and LV contractile function indices, were collected at the three timepoints. The objectives were (1) to evaluate the effects of ARNI + iSGLT2 combination therapy on ultrasound (US) measurements; (2) to evaluate the effects on the variation of laboratory data indicative of HF (NT-pro-BNP); and (3) to evaluate the medium-long term impact of the ARNI + iSGLT2 combination therapy in terms of major cardiovascular events (MACVE). After only three months of combined ARNI + iSGLT2 therapy, we reported a significant improvement in ventricular and atrial volumetric indices, systolic function indices and myocardial deformation parameters assessed by STE. We also reported a significant decrease in NTproBNP levels. This trend was confirmed at 12 months follow-up. Furthermore, narrowing down the analysis to patients who were already treated with ARNI when they started taking iSGLT2, we reported similar results in the improvement of US parameters and NTproBNP levels. Our study has shown that the ARNI + iSGLT2 combination therapy leads to a clinical improvement and positive ventricular remodeling. Even the single introduction of additional iSGLT-2 in HFrEF patients on an otherwise optimized therapy resulted in a significant improvement in US and laboratory variables. The results of our study suggest implementing iSGLT-2 therapy as soon as possible, as the structural and functional cardiac improvements achieved by these drugs are achieved in the short term and maintained in the long term. |
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AbstractList | Sodium–glucose cotransporter 2 inhibitors (iSGLT2) have become the fourth pillar of the medical treatment for heart failure with reduced ejection fraction (HFrEF). However, the mechanisms of action of iSGLT2 remain poorly understood. The effectiveness of combined ARNI and iSGLT2 therapy in left ventricular (LV) remodeling is still under study. We aim to investigate the effects of ARNI + iSGLT2 combination therapy in patients affected by HFrEF in terms of ventricular remodeling using speckle tracking echocardiography (STE). In this observational study, 136 patients with HFrEF taking ARNI were enrolled. All patients were evaluated at baseline (before iSGLT2), at 3 months and at 12 months from the beginning of iSGLT2 therapy. Echocardiographic parameters, including STE analysis and volumetric and LV contractile function indices, were collected at the three timepoints. The objectives were (1) to evaluate the effects of ARNI + iSGLT2 combination therapy on ultrasound (US) measurements; (2) to evaluate the effects on the variation of laboratory data indicative of HF (NT-pro-BNP); and (3) to evaluate the medium-long term impact of the ARNI + iSGLT2 combination therapy in terms of major cardiovascular events (MACVE). After only three months of combined ARNI + iSGLT2 therapy, we reported a significant improvement in ventricular and atrial volumetric indices, systolic function indices and myocardial deformation parameters assessed by STE. We also reported a significant decrease in NTproBNP levels. This trend was confirmed at 12 months follow-up. Furthermore, narrowing down the analysis to patients who were already treated with ARNI when they started taking iSGLT2, we reported similar results in the improvement of US parameters and NTproBNP levels. Our study has shown that the ARNI + iSGLT2 combination therapy leads to a clinical improvement and positive ventricular remodeling. Even the single introduction of additional iSGLT-2 in HFrEF patients on an otherwise optimized therapy resulted in a significant improvement in US and laboratory variables. The results of our study suggest implementing iSGLT-2 therapy as soon as possible, as the structural and functional cardiac improvements achieved by these drugs are achieved in the short term and maintained in the long term. Sodium-glucose cotransporter 2 inhibitors (iSGLT2) have become the fourth pillar of the medical treatment for heart failure with reduced ejection fraction (HFrEF). However, the mechanisms of action of iSGLT2 remain poorly understood. The effectiveness of combined ARNI and iSGLT2 therapy in left ventricular (LV) remodeling is still under study. We aim to investigate the effects of ARNI + iSGLT2 combination therapy in patients affected by HFrEF in terms of ventricular remodeling using speckle tracking echocardiography (STE). In this observational study, 136 patients with HFrEF taking ARNI were enrolled. All patients were evaluated at baseline (before iSGLT2), at 3 months and at 12 months from the beginning of iSGLT2 therapy. Echocardiographic parameters, including STE analysis and volumetric and LV contractile function indices, were collected at the three timepoints. The objectives were (1) to evaluate the effects of ARNI + iSGLT2 combination therapy on ultrasound (US) measurements; (2) to evaluate the effects on the variation of laboratory data indicative of HF (NT-pro-BNP); and (3) to evaluate the medium-long term impact of the ARNI + iSGLT2 combination therapy in terms of major cardiovascular events (MACVE). After only three months of combined ARNI + iSGLT2 therapy, we reported a significant improvement in ventricular and atrial volumetric indices, systolic function indices and myocardial deformation parameters assessed by STE. We also reported a significant decrease in NTproBNP levels. This trend was confirmed at 12 months follow-up. Furthermore, narrowing down the analysis to patients who were already treated with ARNI when they started taking iSGLT2, we reported similar results in the improvement of US parameters and NTproBNP levels. Our study has shown that the ARNI + iSGLT2 combination therapy leads to a clinical improvement and positive ventricular remodeling. Even the single introduction of additional iSGLT-2 in HFrEF patients on an otherwise optimized therapy resulted in a significant improvement in US and laboratory variables. The results of our study suggest implementing iSGLT-2 therapy as soon as possible, as the structural and functional cardiac improvements achieved by these drugs are achieved in the short term and maintained in the long term.Sodium-glucose cotransporter 2 inhibitors (iSGLT2) have become the fourth pillar of the medical treatment for heart failure with reduced ejection fraction (HFrEF). However, the mechanisms of action of iSGLT2 remain poorly understood. The effectiveness of combined ARNI and iSGLT2 therapy in left ventricular (LV) remodeling is still under study. We aim to investigate the effects of ARNI + iSGLT2 combination therapy in patients affected by HFrEF in terms of ventricular remodeling using speckle tracking echocardiography (STE). In this observational study, 136 patients with HFrEF taking ARNI were enrolled. All patients were evaluated at baseline (before iSGLT2), at 3 months and at 12 months from the beginning of iSGLT2 therapy. Echocardiographic parameters, including STE analysis and volumetric and LV contractile function indices, were collected at the three timepoints. The objectives were (1) to evaluate the effects of ARNI + iSGLT2 combination therapy on ultrasound (US) measurements; (2) to evaluate the effects on the variation of laboratory data indicative of HF (NT-pro-BNP); and (3) to evaluate the medium-long term impact of the ARNI + iSGLT2 combination therapy in terms of major cardiovascular events (MACVE). After only three months of combined ARNI + iSGLT2 therapy, we reported a significant improvement in ventricular and atrial volumetric indices, systolic function indices and myocardial deformation parameters assessed by STE. We also reported a significant decrease in NTproBNP levels. This trend was confirmed at 12 months follow-up. Furthermore, narrowing down the analysis to patients who were already treated with ARNI when they started taking iSGLT2, we reported similar results in the improvement of US parameters and NTproBNP levels. Our study has shown that the ARNI + iSGLT2 combination therapy leads to a clinical improvement and positive ventricular remodeling. Even the single introduction of additional iSGLT-2 in HFrEF patients on an otherwise optimized therapy resulted in a significant improvement in US and laboratory variables. The results of our study suggest implementing iSGLT-2 therapy as soon as possible, as the structural and functional cardiac improvements achieved by these drugs are achieved in the short term and maintained in the long term. |
Audience | Academic |
Author | Pitocco, Dario Burzotta, Francesco Fumarulo, Isabella Pellizzeri, Bianca Sten, Andriy Aspromonte, Nadia Vaccarella, Marcello Pasquini, Annalisa Garramone, Barbara Ravenna, Salvatore Emanuele La Vecchia, Giulia Lombardo, Antonella |
AuthorAffiliation | 2 Department of Cardiovascular Sciences, Catholic University of the Sacred Heart, 00168 Rome, Italy 6 Diabetes Care Unit, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Rome, Italy 5 Department of Life Science, Health and Health Professions, Università degli Studi Link, 00165 Rome, Italy 1 Department of Cardiovascular Sciences, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Rome, Italy; isabella.fumarulo@guest.policlinicogemelli.it (I.F.) 3 Operative Unit of Diagnostic Interventional Cardiology, Isola Tiberina-Gemelli Isola, 00186 Rome, Italy 4 Division of Cardiology, Azienda Ospedaliero Universitaria Policlinico “G. Rodolico-San Marco”, University of Catania, 95100 Catania, Italy |
AuthorAffiliation_xml | – name: 3 Operative Unit of Diagnostic Interventional Cardiology, Isola Tiberina-Gemelli Isola, 00186 Rome, Italy – name: 4 Division of Cardiology, Azienda Ospedaliero Universitaria Policlinico “G. Rodolico-San Marco”, University of Catania, 95100 Catania, Italy – name: 1 Department of Cardiovascular Sciences, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Rome, Italy; isabella.fumarulo@guest.policlinicogemelli.it (I.F.) – name: 2 Department of Cardiovascular Sciences, Catholic University of the Sacred Heart, 00168 Rome, Italy – name: 6 Diabetes Care Unit, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Rome, Italy – name: 5 Department of Life Science, Health and Health Professions, Università degli Studi Link, 00165 Rome, Italy |
Author_xml | – sequence: 1 givenname: Isabella orcidid: 0009-0006-9800-0480 surname: Fumarulo fullname: Fumarulo, Isabella – sequence: 2 givenname: Annalisa orcidid: 0000-0002-8015-6923 surname: Pasquini fullname: Pasquini, Annalisa – sequence: 3 givenname: Giulia orcidid: 0000-0002-4324-6348 surname: La Vecchia fullname: La Vecchia, Giulia – sequence: 4 givenname: Bianca surname: Pellizzeri fullname: Pellizzeri, Bianca – sequence: 5 givenname: Andriy surname: Sten fullname: Sten, Andriy – sequence: 6 givenname: Barbara surname: Garramone fullname: Garramone, Barbara – sequence: 7 givenname: Marcello orcidid: 0000-0003-1287-3952 surname: Vaccarella fullname: Vaccarella, Marcello – sequence: 8 givenname: Salvatore Emanuele surname: Ravenna fullname: Ravenna, Salvatore Emanuele – sequence: 9 givenname: Antonella orcidid: 0000-0003-3162-1830 surname: Lombardo fullname: Lombardo, Antonella – sequence: 10 givenname: Francesco surname: Burzotta fullname: Burzotta, Francesco – sequence: 11 givenname: Dario surname: Pitocco fullname: Pitocco, Dario – sequence: 12 givenname: Nadia surname: Aspromonte fullname: Aspromonte, Nadia |
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Snippet | Sodium–glucose cotransporter 2 inhibitors (iSGLT2) have become the fourth pillar of the medical treatment for heart failure with reduced ejection fraction... Sodium-glucose cotransporter 2 inhibitors (iSGLT2) have become the fourth pillar of the medical treatment for heart failure with reduced ejection fraction... |
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SubjectTerms | Aged Aminobutyrates - administration & dosage Aminobutyrates - pharmacology Aminobutyrates - therapeutic use Biphenyl Compounds - therapeutic use Cardiomyopathy Cardiovascular disease Dapagliflozin Development and progression Dextrose Diabetes Diuretics Drug Combinations Drug therapy Drug Therapy, Combination Drugs Echocardiography Ejection fraction Female Glucose Heart failure Heart Failure - diagnostic imaging Heart Failure - drug therapy Heart Failure - physiopathology Humans Ischemia Male Medical research Medicine, Experimental Middle Aged Mortality Natriuretic Peptide, Brain - blood Patients Peptide Fragments Pulmonary arteries Sodium-Glucose Transporter 2 Inhibitors - pharmacology Sodium-Glucose Transporter 2 Inhibitors - therapeutic use Stroke Volume - drug effects Treatment Outcome Valsartan - administration & dosage Valsartan - pharmacology Valsartan - therapeutic use Ventricular Remodeling - drug effects |
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Title | Evaluation of the Effects of the Sodium–Glucose Cotransporter 2 Inhibitors and Sacubitril/Valsartan Combined Therapy in Patients with HFrEF: An Echocardiographic Study |
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