Association of Angiotensin II Receptor Type 1 and Endothelin‐1 Receptor Type A Agonistic Autoantibodies With Adverse Remodeling and Cardiovascular Events After Acute Myocardial Infarction

Background The left ventricular remodeling (LVR) process has limited the effectiveness of therapies after myocardial infarction. The relationship between autoantibodies activating AT1R‐AAs (angiotensin II receptor type 1‐AAs) and ETAR‐AAs (autoantibodies activating endothelin‐1 receptor type A) with...

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Main Authors: Francesco Tona, Giovanni Civieri, Marta Vadori, Giulia Masiero, Laura Iop, Martina Perazzolo Marra, Valentina Perin, Elisa Cuciz, Annagrazia Cecere, Giacomo Bernava, Donatella Tansella, Nataliia Naumova, Simran Grewal, Emanuele Cozzi, Sabino Iliceto
Format: Article
Language:English
Published: Wiley 2024-02-01
Series:Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
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Online Access:https://www.ahajournals.org/doi/10.1161/JAHA.123.032672
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author Francesco Tona
Giovanni Civieri
Marta Vadori
Giulia Masiero
Laura Iop
Martina Perazzolo Marra
Valentina Perin
Elisa Cuciz
Annagrazia Cecere
Giacomo Bernava
Donatella Tansella
Nataliia Naumova
Simran Grewal
Emanuele Cozzi
Sabino Iliceto
author_facet Francesco Tona
Giovanni Civieri
Marta Vadori
Giulia Masiero
Laura Iop
Martina Perazzolo Marra
Valentina Perin
Elisa Cuciz
Annagrazia Cecere
Giacomo Bernava
Donatella Tansella
Nataliia Naumova
Simran Grewal
Emanuele Cozzi
Sabino Iliceto
author_sort Francesco Tona
collection DOAJ
description Background The left ventricular remodeling (LVR) process has limited the effectiveness of therapies after myocardial infarction. The relationship between autoantibodies activating AT1R‐AAs (angiotensin II receptor type 1‐AAs) and ETAR‐AAs (autoantibodies activating endothelin‐1 receptor type A) with myocardial infarction has been described. Among patients with ST‐segment–elevation myocardial infarction, we investigated the relationship between these autoantibodies with LVR and subsequent major adverse cardiac events. Methods and Results In this prospective observational study, we included 131 patients with ST‐segment–elevation myocardial infarction (61±11 years of age, 112 men) treated with primary percutaneous coronary intervention. Within 48 hours of admission, 2‐dimensional transthoracic echocardiography was performed, and blood samples were obtained. The seropositive threshold for AT1R‐AAs and ETAR‐AAs was >10 U/mL. Patients were followed up at 6 months, when repeat transthoracic echocardiography was performed. The primary end points were LVR, defined as a 20% increase in left ventricular end‐diastolic volume index, and major adverse cardiac event occurrence at follow‐up, defined as cardiac death, nonfatal re‐myocardial infarction, and hospitalization for heart failure. Forty‐one (31%) patients experienced LVR. The prevalence of AT1R‐AAs and ETAR‐AAs seropositivity was higher in patients with versus without LVR (39% versus 11%, P<0.001 and 37% versus 12%, P=0.001, respectively). In multivariable analysis, AT1R‐AAs seropositivity was significantly associated with LVR (odds ratio [OR], 4.66; P=0.002) and represented a risk factor for subsequent major adverse cardiac events (OR, 19.6; P=0.002). Conclusions AT1R‐AAs and ETAR‐AAs are associated with LVR in patients with ST‐segment–elevation myocardial infarction. AT1R‐AAs are also significantly associated with recurrent major adverse cardiac events. These initial observations may set the stage for a better pathophysiological understanding of the mechanisms contributing to LVR and ST‐segment–elevation myocardial infarction prognosis.
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spelling doaj.art-4fa0c8351ee04bb5934875925d9a95062024-11-05T14:15:40ZengWileyJournal of the American Heart Association: Cardiovascular and Cerebrovascular Disease2047-99802024-02-0113410.1161/JAHA.123.032672Association of Angiotensin II Receptor Type 1 and Endothelin‐1 Receptor Type A Agonistic Autoantibodies With Adverse Remodeling and Cardiovascular Events After Acute Myocardial InfarctionFrancesco Tona0Giovanni Civieri1Marta Vadori2Giulia Masiero3Laura Iop4Martina Perazzolo Marra5Valentina Perin6Elisa Cuciz7Annagrazia Cecere8Giacomo Bernava9Donatella Tansella10Nataliia Naumova11Simran Grewal12Emanuele Cozzi13Sabino Iliceto14Department of Cardiac, Thoracic, Vascular Sciences, and Public Health University of Padua Padua ItalyDepartment of Cardiac, Thoracic, Vascular Sciences, and Public Health University of Padua Padua ItalyDepartment of Cardiac, Thoracic, Vascular Sciences, and Public Health University of Padua Padua ItalyDepartment of Cardiac, Thoracic, Vascular Sciences, and Public Health University of Padua Padua ItalyDepartment of Cardiac, Thoracic, Vascular Sciences, and Public Health University of Padua Padua ItalyDepartment of Cardiac, Thoracic, Vascular Sciences, and Public Health University of Padua Padua ItalyDepartment of Cardiac, Thoracic, Vascular Sciences, and Public Health University of Padua Padua ItalyDepartment of Cardiac, Thoracic, Vascular Sciences, and Public Health University of Padua Padua ItalyDepartment of Cardiac, Thoracic, Vascular Sciences, and Public Health University of Padua Padua ItalyDepartment of Cardiac, Thoracic, Vascular Sciences, and Public Health University of Padua Padua ItalyDepartment of Cardiac, Thoracic, Vascular Sciences, and Public Health University of Padua Padua ItalyDepartment of Cardiac, Thoracic, Vascular Sciences, and Public Health University of Padua Padua ItalyPenn State Hershey Medical Center Hershey PA USADepartment of Cardiac, Thoracic, Vascular Sciences, and Public Health University of Padua Padua ItalyDepartment of Cardiac, Thoracic, Vascular Sciences, and Public Health University of Padua Padua ItalyBackground The left ventricular remodeling (LVR) process has limited the effectiveness of therapies after myocardial infarction. The relationship between autoantibodies activating AT1R‐AAs (angiotensin II receptor type 1‐AAs) and ETAR‐AAs (autoantibodies activating endothelin‐1 receptor type A) with myocardial infarction has been described. Among patients with ST‐segment–elevation myocardial infarction, we investigated the relationship between these autoantibodies with LVR and subsequent major adverse cardiac events. Methods and Results In this prospective observational study, we included 131 patients with ST‐segment–elevation myocardial infarction (61±11 years of age, 112 men) treated with primary percutaneous coronary intervention. Within 48 hours of admission, 2‐dimensional transthoracic echocardiography was performed, and blood samples were obtained. The seropositive threshold for AT1R‐AAs and ETAR‐AAs was >10 U/mL. Patients were followed up at 6 months, when repeat transthoracic echocardiography was performed. The primary end points were LVR, defined as a 20% increase in left ventricular end‐diastolic volume index, and major adverse cardiac event occurrence at follow‐up, defined as cardiac death, nonfatal re‐myocardial infarction, and hospitalization for heart failure. Forty‐one (31%) patients experienced LVR. The prevalence of AT1R‐AAs and ETAR‐AAs seropositivity was higher in patients with versus without LVR (39% versus 11%, P<0.001 and 37% versus 12%, P=0.001, respectively). In multivariable analysis, AT1R‐AAs seropositivity was significantly associated with LVR (odds ratio [OR], 4.66; P=0.002) and represented a risk factor for subsequent major adverse cardiac events (OR, 19.6; P=0.002). Conclusions AT1R‐AAs and ETAR‐AAs are associated with LVR in patients with ST‐segment–elevation myocardial infarction. AT1R‐AAs are also significantly associated with recurrent major adverse cardiac events. These initial observations may set the stage for a better pathophysiological understanding of the mechanisms contributing to LVR and ST‐segment–elevation myocardial infarction prognosis.https://www.ahajournals.org/doi/10.1161/JAHA.123.032672antibodiesimmunologyprognosisremodelingSTEMI
spellingShingle Francesco Tona
Giovanni Civieri
Marta Vadori
Giulia Masiero
Laura Iop
Martina Perazzolo Marra
Valentina Perin
Elisa Cuciz
Annagrazia Cecere
Giacomo Bernava
Donatella Tansella
Nataliia Naumova
Simran Grewal
Emanuele Cozzi
Sabino Iliceto
Association of Angiotensin II Receptor Type 1 and Endothelin‐1 Receptor Type A Agonistic Autoantibodies With Adverse Remodeling and Cardiovascular Events After Acute Myocardial Infarction
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
antibodies
immunology
prognosis
remodeling
STEMI
title Association of Angiotensin II Receptor Type 1 and Endothelin‐1 Receptor Type A Agonistic Autoantibodies With Adverse Remodeling and Cardiovascular Events After Acute Myocardial Infarction
title_full Association of Angiotensin II Receptor Type 1 and Endothelin‐1 Receptor Type A Agonistic Autoantibodies With Adverse Remodeling and Cardiovascular Events After Acute Myocardial Infarction
title_fullStr Association of Angiotensin II Receptor Type 1 and Endothelin‐1 Receptor Type A Agonistic Autoantibodies With Adverse Remodeling and Cardiovascular Events After Acute Myocardial Infarction
title_full_unstemmed Association of Angiotensin II Receptor Type 1 and Endothelin‐1 Receptor Type A Agonistic Autoantibodies With Adverse Remodeling and Cardiovascular Events After Acute Myocardial Infarction
title_short Association of Angiotensin II Receptor Type 1 and Endothelin‐1 Receptor Type A Agonistic Autoantibodies With Adverse Remodeling and Cardiovascular Events After Acute Myocardial Infarction
title_sort association of angiotensin ii receptor type 1 and endothelin 1 receptor type a agonistic autoantibodies with adverse remodeling and cardiovascular events after acute myocardial infarction
topic antibodies
immunology
prognosis
remodeling
STEMI
url https://www.ahajournals.org/doi/10.1161/JAHA.123.032672
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