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| dc.contributor.author | Soler-Espejo, Eva | |
| dc.contributor.author | Marín, Francisco | |
| dc.contributor.author | López-Gálvez, Raquel | |
| dc.contributor.author | Ramos-Bratos, María-Pilar | |
| dc.contributor.author | Sánchez-Villalobos, María | |
| dc.contributor.author | Esteve-Pastor, María-Asunción | |
| dc.contributor.author | Lip, Gregory-Y-H | |
| dc.contributor.author | Rivera-Caravaca, José-Miguel | |
| dc.contributor.author | Roldán-Schilling, Vanessa | |
| dc.date.accessioned | 2026-03-06T14:04:36Z | |
| dc.date.available | 2026-03-06T14:04:36Z | |
| dc.date.issued | 2025-02 | |
| dc.identifier.citation | Soler-Espejo E, Marín F, López-Gálvez R, Ramos-Bratos MP, Sánchez-Villalobos M, Esteve-Pastor MA, et al. The Neutrophil-to-Lymphocyte Ratio Is an Independent Inflammatory Biomarker for Adverse Events in Patients With Atrial Fibrillation: Insights From the Murcia AF Project II (MAFP-II) Cohort Study. Clinical Cardiology. febrero de 2025;48(2):e70102. doi:10.1002/clc.70102 | |
| dc.identifier.issn | 0160-9289 | |
| dc.identifier.uri | https://sms.carm.es/ricsmur/handle/123456789/24589 | |
| dc.description.abstract | BACKGROUND: Systemic inflammation plays a central role in atrial fibrillation (AF). The neutrophil-to-lymphocyte ratio (NLR) is a simple hematological index that has been shown to be associated with prognosis in different pathologies. HYPOTHESIS: The NLR is associated with an increased risk of adverse events in patients with AF. METHODS: We included a prospective cohort of AF patients who started vitamin K antagonists (VKAs) therapy between July 2016 and June 2018. NLR was assessed at baseline and classified into three categories: low (< 3), moderate (3-5), and high (> 5). During a 2-year follow-up period, all cardiovascular deaths, all-cause deaths, and net clinical outcomes (NCO; either ischemic stroke/transient ischemic attack, major bleeding or all-cause death), were recorded. RESULTS: A total of 1050 patients were included (51.4% women; median age 77 years). NLR was available in 936 patients: 507 (54.2%) had low NLR (< 3), 239 (25.5%) had moderate NLR (3-5), and 190 (20.3%) had high NLR (> 5). The primary endpoint was significantly increased in the high NLR category (p = 0.002 for cardiovascular death; p < 0.001 for all-cause mortality, and p < 0.001 for NCO), with higher IRRs (all p < 0.001). Multivariate Cox regression analyses showed that high NLR was independently associated with an increased risk of cardiovascular death (aHR: 2.02; 95% CI: 1.04-3.92), all-cause mortality (aHR: 2.51; 95% CI: 1.58-3.97), and NCO (aHR: 1.99; 95% CI: 1.37-2.87), compared to low NLR. CONCLUSIONS: In this prospective AF cohort receiving VKAs, elevated NLR was significantly associated with an increased risk of adverse clinical outcomes. NLR has independent prognostic value beyond other classical risk factors. | |
| dc.language.iso | eng | |
| dc.publisher | WILEY | |
| dc.rights | Atribución/Reconocimiento 4.0 Internacional | * |
| dc.rights.uri | https://creativecommons.org/licenses/by/4.0/deed.es | * |
| dc.subject.mesh | Humans | |
| dc.subject.mesh | Atrial Fibrillation/blood/drug therapy/complications/mortality/diagnosis | |
| dc.subject.mesh | Female | |
| dc.subject.mesh | Neutrophils | |
| dc.subject.mesh | Male | |
| dc.subject.mesh | Aged | |
| dc.subject.mesh | Lymphocytes | |
| dc.subject.mesh | Prospective Studies | |
| dc.subject.mesh | Biomarkers/blood | |
| dc.subject.mesh | Prognosis | |
| dc.subject.mesh | Risk Factors | |
| dc.subject.mesh | Risk Assessment | |
| dc.subject.mesh | Inflammation/blood | |
| dc.subject.mesh | Follow-Up Studies | |
| dc.subject.mesh | Aged, 80 and over | |
| dc.subject.mesh | Middle Aged | |
| dc.subject.mesh | Cause of Death/trends | |
| dc.title | The Neutrophil-to-Lymphocyte Ratio Is an Independent Inflammatory Biomarker for Adverse Events in Patients With Atrial Fibrillation: Insights From the Murcia AF Project II (MAFP-II) Cohort Study | |
| dc.type | info:eu-repo/semantics/article | |
| dc.identifier.pmid | 39985306 | |
| dc.relation.publisherversion | https://onlinelibrary.wiley.com/doi/10.1002/clc.70102 | |
| dc.type.version | info:eu-repo/semantics/publishedVersion | |
| dc.identifier.doi | 10.1002/clc.70102 | |
| dc.journal.title | Clinical Cardiology | |
| dc.identifier.essn | 1932-8737 |