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    MACE or death risk in obstructive sleep apnoea and the effect of positive airway pressure

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    Identificadores
    URI: https://hdl.handle.net/10902/37384
    DOI: 10.1183/13993003.00519-2025
    ISSN: 0903-1936
    ISSN: 1399-3003
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    Autoría
    Divo, Miguel J.; Martínez-García, Miguel A.; González Martínez, MónicaAutoridad Unican; Campos-Rodríguez, Francisco; Lloberes, Patricia; Marín-Oto, Marta; Forner, Marta; Sanz-Rubio, David; Nieto, David; Celli, Bartolomé R.; Marín, José M.
    Fecha
    2025-08-21
    Derechos
    © European Respiratory Society. This is an author-submitted, peer-reviewed version of a manuscript that has been accepted for publication in the European Respiratory Journal, prior to copy-editing, formatting and typesetting. This version of the manuscript may not be duplicated or reproduced without prior permission from the copyright owner, the European Respiratory Society. The publisher is not responsible or liable for any errors or omissions in this version of the manuscript or in any version derived from it by any other parties. The final, copy-edited, published article, which is the version of record, is available without a subscription 18 months after the date of issue publication.
    Publicado en
    European Respiratory Journal, 2025, 2500519, 1-115
    Editorial
    European Respiratory Society
    Disponible después de
    2027-02-01
    Enlace a la publicación
    https://doi.org/10.1183/13993003.00519-2025
    Resumen/Abstract
    Rationale: Evidence regarding the efficacy of positive airway pressure (PAP) therapy in reducing the risks of non-fatal major cardiovascular events (NF-MACE) and mortality in patients with obstructive sleep apnoea (OSA) remains controversial. Objectives: This study aims to quantify the impact of PAP therapy on these risks and develop a predictive risk estimator. Methods: We conducted a multicentre, observational, prospective study involving 5358 individuals diagnosed with OSA, with a median follow-up of 14 years (IQR 10-15 years). We derived and validated a risk estimator of NF-MACE (including myocardial infarction, stroke, revascularisation procedures, and congestive heart failure) and all-cause mortality, incorporating PAP adherence alongside clinical and sleep-related data. Results: The cohort's mean (sd) for age was 55±11 years, the Body Mass Index 32.0±5.4 Kg·m-2, and an apnoea-hypopnea index (AHI) of 35 (±22) events/hour; 26% were females, and 1467 (37%) were PAP adherent. Over the follow-up period, 754 participants experienced NF-MACE, while 858 deaths were recorded. Significant predictors included prior cardiovascular events, non-HDL cholesterol 200 mg·dL-1, COPD diagnosis, AHI >30 events/hr, and age >60 years. PAP adherence was protective (OR 0.46; 95% CI: 0.38 to 0.56), and the absolute risk reduction varied depending on the baseline risk (median of 16%, IQR 12-18). The risk estimator yielded an AUROC of 0.75 and a Brier score of 0.17, with 64% sensitivity and 75% specificity. Conclusions: PAP therapy is associated with long-term risk reduction of NF-MACE and mortality in OSA patients, while the developed risk estimator enhances clinical decision-making regarding therapy initiation.
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    UNIVERSIDAD DE CANTABRIA

    Repositorio realizado por la Biblioteca Universitaria utilizando DSpace software
    Contacto | Sugerencias
    Metadatos sujetos a:licencia de Creative Commons Reconocimiento 4.0 España