| dc.contributor.author | Garate Viñas, Gabriel | |
| dc.contributor.author | Gangas, L. | |
| dc.contributor.author | De la Torre Hernández, José María | |
| dc.contributor.author | Muñoz San-Martín, M. | |
| dc.contributor.author | Pascual Gómez, Julio | |
| dc.contributor.author | González Quintanilla, Vicente | |
| dc.contributor.other | Universidad de Cantabria | es_ES |
| dc.date.accessioned | 2025-10-08T09:40:55Z | |
| dc.date.available | 2025-10-08T09:40:55Z | |
| dc.date.issued | 2025 | |
| dc.identifier.issn | 2297-055X | |
| dc.identifier.uri | https://hdl.handle.net/10902/37715 | |
| dc.description.abstract | Introduction: Calcitonin gene-related peptide (CGRP), particularly its alpha isoform, might play a role in restoring physiological cardiovascular functioning. While its involvement in acute myocardial infarction (AMI) pathophysiology has been suggested, human data remain scarce. This study analyzed circulating alpha-CGRP levels during AMI, comparing them to healthy controls (HC) and post-AMI resolution levels.
Methods: A total of 26 AMI patients and 26 age- and sex-matched HC were recruited. Blood samples were collected from patients within four hours of AMI onset and, when possible, six months post-event. Alpha-CGRP serum concentrations were measured using a validated ELISA assay.
Results: Alpha-CGRP levels were significantly higher in AMI patients at admission (mean±SD: 96.0±77.4 pg/ml) compared to HC (42.0±25.8 pg/ml, p<0.0001), with an average increase of 129%. Among nine patients available for follow-up, levels normalized to the HC range (45.1±26.7 pg/ml, p=0.011). Patients with poor outcomes had numerically lower alpha-CGRP levels (72.6±37.2 pg/ml) than those with a satisfactory resolution (100.3±82.5 70.6 pg/ml; p=0.241).
Discussion: Alpha-CGRP is acutely elevated during AMI, likely as a compensatory vasodilator response to ischemia. Its post-AMI normalization suggests a transient protective mechanism. Further research is needed to explore its role in AMI-related pathophysiology and usefulness as a therapeutic agent. | es_ES |
| dc.description.sponsorship | The author(s) declare that financial support was received for
the research and/or publication of this article. This study was
supported by grants PI20/01358, funded by the Instituto de
Salud Carlos III, and by grant JDC2022-048637-I, funded by
MCIN/AEI/10.13039/501100011033 and by the European Union
NextGenereationEU/PRTR. | es_ES |
| dc.format.extent | 6 p. | es_ES |
| dc.language.iso | eng | es_ES |
| dc.publisher | Frontiers Media S.A. | es_ES |
| dc.rights | © 2025 The author(s). This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). | es_ES |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
| dc.source | Frontiers in Cardiovascular Medicine, 2025, 12, 1581056 | es_ES |
| dc.subject.other | Alpha-CGRP | es_ES |
| dc.subject.other | Biomarker | es_ES |
| dc.subject.other | Myocardial infarction | es_ES |
| dc.subject.other | Cardiac cephalgia | es_ES |
| dc.subject.other | Response mediator | es_ES |
| dc.title | Alpha-CGRP as a specific response mediator during acute myocardial infarction in humans: findings from an observational longitudinal study | es_ES |
| dc.type | info:eu-repo/semantics/article | es_ES |
| dc.relation.publisherVersion | https://doi.org/10.3389/fcvm.2025.1581056 | es_ES |
| dc.rights.accessRights | openAccess | es_ES |
| dc.identifier.DOI | 10.3389/fcvm.2025.1581056 | |
| dc.type.version | publishedVersion | es_ES |