Early Treatment of Acute Myocardial Infarction with Melatonin: Effects on MMP-9 and Adverse Cardiac Events.

MMP-9 acute myocardial infarction major cardiovascular events melatonin primary percutaneous coronary intervention

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
30 Mar 2022
Historique:
received: 22 02 2022
revised: 23 03 2022
accepted: 27 03 2022
entrez: 12 4 2022
pubmed: 13 4 2022
medline: 13 4 2022
Statut: epublish

Résumé

Matrix metalloproteinase-9 (MMP-9) is crucial in tissue remodeling after an adverse cardiac event. In experimental studies, melatonin has been found to attenuate MMP-9 activation. The present study assessed the effects of systemic melatonin administration on the prognosis of patients with acute myocardial infarction (AMI) successfully treated with primary percutaneous coronary intervention, and to examine the effects on MMP-9 levels. We conducted a randomized controlled trial, enrolling patients who underwent primary percutaneous coronary intervention due to AMI. They were assigned to two groups for melatonin or placebo. The primary endpoint was a combined event of mortality and heart failure readmission at 2 years. The secondary endpoint was the levels of MMP-9 after the percutaneous coronary intervention. Ninety-four patients were enrolled, 45 in the melatonin group and 49 in the control group. At 2 years of follow-up, 13 (13.8%) patients suffered the primary endpoint (3 deaths and 10 readmissions due to heart failure), 3 patients in the melatonin group and 10 in the placebo group. The difference in the restricted mean survival time was 87.5 days ( This pilot study demonstrated that compared to placebo, melatonin administration was associated with better outcomes in AMI patients undergoing primary percutaneous coronary intervention.

Sections du résumé

BACKGROUND BACKGROUND
Matrix metalloproteinase-9 (MMP-9) is crucial in tissue remodeling after an adverse cardiac event. In experimental studies, melatonin has been found to attenuate MMP-9 activation. The present study assessed the effects of systemic melatonin administration on the prognosis of patients with acute myocardial infarction (AMI) successfully treated with primary percutaneous coronary intervention, and to examine the effects on MMP-9 levels.
METHODS METHODS
We conducted a randomized controlled trial, enrolling patients who underwent primary percutaneous coronary intervention due to AMI. They were assigned to two groups for melatonin or placebo. The primary endpoint was a combined event of mortality and heart failure readmission at 2 years. The secondary endpoint was the levels of MMP-9 after the percutaneous coronary intervention.
RESULTS RESULTS
Ninety-four patients were enrolled, 45 in the melatonin group and 49 in the control group. At 2 years of follow-up, 13 (13.8%) patients suffered the primary endpoint (3 deaths and 10 readmissions due to heart failure), 3 patients in the melatonin group and 10 in the placebo group. The difference in the restricted mean survival time was 87.5 days (
CONCLUSIONS CONCLUSIONS
This pilot study demonstrated that compared to placebo, melatonin administration was associated with better outcomes in AMI patients undergoing primary percutaneous coronary intervention.

Identifiants

pubmed: 35407517
pii: jcm11071909
doi: 10.3390/jcm11071909
pmc: PMC9000067
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Fundación Canaria de Investigación Sanitaria
ID : PIFUN11/18
Organisme : Sociedad Española de Cardiología
ID : SEC 2018 Grant

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Auteurs

Alberto Domínguez-Rodríguez (A)

Servicio de Cardiología, Hospital Universitario de Canarias, 38010 Santa Cruz de Tenerife, Spain.
Facultad de Ciencias de la Salud, Universidad Europea de Canarias, 38200 Santa Cruz de Tenerife, Spain.
CIBER de Enfermedades Cardiovasculares (CIBERCV), 28029 Madrid, Spain.

Daniel Hernández-Vaquero (D)

Área del Corazón, Hospital Universitario Central de Asturias, 33011 Oviedo, Spain.
Instituto de Investigación Sanitaria del Principado de Asturias, 33011 Oviedo, Spain.

Pedro Abreu-González (P)

Departamento de Fisiología, Facultad de Medicina, Universidad de La Laguna, 38200 Santa Cruz de Tenerife, Spain.

Néstor Báez-Ferrer (N)

Servicio de Cardiología, Hospital Universitario de Canarias, 38010 Santa Cruz de Tenerife, Spain.

Rocío Díaz (R)

Área del Corazón, Hospital Universitario Central de Asturias, 33011 Oviedo, Spain.
Instituto de Investigación Sanitaria del Principado de Asturias, 33011 Oviedo, Spain.

Pablo Avanzas (P)

Área del Corazón, Hospital Universitario Central de Asturias, 33011 Oviedo, Spain.
Instituto de Investigación Sanitaria del Principado de Asturias, 33011 Oviedo, Spain.
Departamento de Medicina, Universidad de Oviedo, 33003 Oviedo, Spain.

Fedor Simko (F)

Institute of Pathophysiology, Faculty of Medicine, Comenius University, 81108 Bratislava, Slovakia.

Virginia Domínguez-González (V)

School of Medicine, Facultad de Ciencias de la Salud, Universidad de La Laguna, 38200 Santa Cruz de Tenerife, Spain.

Ramaswamy Sharma (R)

Department of Cell Systems and Anatomy, Joe R. and Teresa Lozano Long School of Medicine, UT Health San Antonio, San Antonio, TX 78229, USA.

Russel J Reiter (RJ)

Department of Cell Systems and Anatomy, Joe R. and Teresa Lozano Long School of Medicine, UT Health San Antonio, San Antonio, TX 78229, USA.

Classifications MeSH