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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

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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


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