Association of autoantibodies targeting endothelin type-A receptors with no-reflow in ST-elevation myocardial infarction.


Journal

Atherosclerosis
ISSN: 1879-1484
Titre abrégé: Atherosclerosis
Pays: Ireland
ID NLM: 0242543

Informations de publication

Date de publication:
08 2023
Historique:
received: 05 05 2023
revised: 23 06 2023
accepted: 27 06 2023
medline: 14 8 2023
pubmed: 9 7 2023
entrez: 8 7 2023
Statut: ppublish

Résumé

No-reflow (NR), where the coronary artery is patent after treatment of ST-elevation myocardial infarction (STEMI) but tissue perfusion is not restored, is associated with worse outcomes. We aimed to investigate the relationship between autoantibodies activating endothelin-1 receptor type A (ETAR-AAs) and NR after primary percutaneous coronary intervention (PPCI) in STEMI. We studied 50 patients (age 59 ± 11 years, 40 males) with STEMI who underwent PPCI within 6 h after the onset of symptoms. Blood samples were obtained from all patients within 12 h following PPCI for ETAR-AA level measurement. The seropositive threshold was provided by the manufacturer (>10 U/ml). NR was assessed by cardiac magnetic resonance imaging (MVO, microvascular obstruction). As a control group, 40 healthy subjects matched for age and sex were recruited from the general population. MVO was observed in 24 patients (48%). The prevalence of MVO was higher in patients with ETAR-AAs seropositivity (72% vs. 38%, p = 0.03). ETAR-AAs were higher in patients with MVO (8.9 U/mL (interquartile range [IQR] 6.8-16.2 U/mL) vs. 5.7 U/mL [IQR 4.3-7.7 U/mL], p = 0.003). ETAR-AAs seropositivity was independently associated with MVO (OR 3.2, 95% CI 1.3-7.1; p = 0.03). We identified ≥6.74 U/mL as the best cut-off for prediction of MVO (sensitivity 79%; specificity 65%; NPV 71%; PPV 74%; accuracy 72%). The ETAR-AAs seropositivity is associated with NR in STEMI patients. These findings may open up new options in the management of myocardial infarction even if confirmation in a larger trial is needed.

Sections du résumé

BACKGROUND AND AIMS
No-reflow (NR), where the coronary artery is patent after treatment of ST-elevation myocardial infarction (STEMI) but tissue perfusion is not restored, is associated with worse outcomes. We aimed to investigate the relationship between autoantibodies activating endothelin-1 receptor type A (ETAR-AAs) and NR after primary percutaneous coronary intervention (PPCI) in STEMI.
METHODS
We studied 50 patients (age 59 ± 11 years, 40 males) with STEMI who underwent PPCI within 6 h after the onset of symptoms. Blood samples were obtained from all patients within 12 h following PPCI for ETAR-AA level measurement. The seropositive threshold was provided by the manufacturer (>10 U/ml). NR was assessed by cardiac magnetic resonance imaging (MVO, microvascular obstruction). As a control group, 40 healthy subjects matched for age and sex were recruited from the general population.
RESULTS
MVO was observed in 24 patients (48%). The prevalence of MVO was higher in patients with ETAR-AAs seropositivity (72% vs. 38%, p = 0.03). ETAR-AAs were higher in patients with MVO (8.9 U/mL (interquartile range [IQR] 6.8-16.2 U/mL) vs. 5.7 U/mL [IQR 4.3-7.7 U/mL], p = 0.003). ETAR-AAs seropositivity was independently associated with MVO (OR 3.2, 95% CI 1.3-7.1; p = 0.03). We identified ≥6.74 U/mL as the best cut-off for prediction of MVO (sensitivity 79%; specificity 65%; NPV 71%; PPV 74%; accuracy 72%).
CONCLUSIONS
The ETAR-AAs seropositivity is associated with NR in STEMI patients. These findings may open up new options in the management of myocardial infarction even if confirmation in a larger trial is needed.

Identifiants

pubmed: 37422357
pii: S0021-9150(23)05073-6
doi: 10.1016/j.atherosclerosis.2023.06.970
pii:
doi:

Substances chimiques

Receptor, Endothelin A 0
Autoantibodies 0
Endothelins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

117179

Informations de copyright

Copyright © 2023 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Francesco Tona (F)

Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padua, Italy. Electronic address: francesco.tona@unipd.it.

Marta Vadori (M)

Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padua, Italy.

Giovanni Civieri (G)

Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padua, Italy.

Giulia Masiero (G)

Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padua, Italy.

Laura Iop (L)

Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padua, Italy.

Giorgia Antonelli (G)

Department of Medicine-DIMED, University of Padua, Padua, Italy.

Martina Perazzolo Marra (M)

Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padua, Italy.

Federica Bianco (F)

Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padua, Italy.

Annagrazia Cecere (A)

Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padua, Italy.

Giulia Lorenzoni (G)

Unit of Biostatistics, Epidemiology and Public Health, Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padua, Padua, Italy.

Natalia Naumova (N)

Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padua, Italy.

Giacomo Bernava (G)

Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padua, Italy.

Daniela Basso (D)

Department of Medicine-DIMED, University of Padua, Padua, Italy.

Mario Plebani (M)

Department of Medicine-DIMED, University of Padua, Padua, Italy.

Emanuele Cozzi (E)

Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padua, Italy.

Sabino Iliceto (S)

Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padua, Italy.

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