<?xml version="1.0" encoding="UTF-8"?>
<collection>
<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1016/j.arbres.2024.12.005</dc:identifier><dc:language>eng</dc:language><dc:creator>Sanz-Rubio, David</dc:creator><dc:creator>Martín-Burriel, Inmaculada</dc:creator><dc:creator>Rodríguez, Jorge</dc:creator><dc:creator>Marín-Oto, Marta</dc:creator><dc:creator>Khalyfa, Abdelnaby</dc:creator><dc:creator>Sánchez-de-la-Torre, Manuel</dc:creator><dc:creator>Gozal, David</dc:creator><dc:creator>Marin, Jose M.</dc:creator><dc:title>Circulating Exosomal MicroRNAs and Subclinical Atherosclerosis in Obstructive Sleep Apnea</dc:title><dc:identifier>ART-2024-141351</dc:identifier><dc:description>Background. Obstructive sleep apnea (OSA) has been associated with thepathogenesis of atherogenesis. Exosomes and their microRNA (miRNA) cargocould play a major role in this process.Objectives. To determine plasma exosomal miRNA and their relationship withatherosclerosis in patients with OSA.Methods. From the EPIOSA cohort, we selected 50 OSA patients (apnea-hypopnea index–AHI ≥ 10) and 16 age- and sex-matched healthy subjects (AHI≤ 10) for the derivation analysis. The validation assay was composed by 88 OSApatients and 24 matched controls. OSA patients were categorized according toprevalent subclinical atherosclerosis (SA) as defined by ≥ 1 plaque in carotidultrasound. All participants were free of prevalent chronic comorbid conditions.Plasma-derived exosomes were isolated by precipitation, and miRNAs wereevaluated by real-time quantitative PCR.Results. SA was present in 34% of OSA patients. Three exosomal miRNAs wereoverexpressed in patients with OSA and SA at the derivation study: miR-21(relative expression, RE = 2.91), miR-145 (RE = 2.12) and miR-320a (RE =4.06). ROC curve analysis showed a high predictive value for SA of miR-320a(area under curve AUC = 0.813). In the validation cohort, miR-320a alsoexhibited an overexpression of RE = 2.66 among patients with OSA and SA, withan AUC of 0.798. Together with AHI and APO B, miR-320a, was independentlyassociated with SA. In addition, miR-320a correlate with the progression of intimamedia thickness from baseline to after 1 year of follow-up. Finally, miR-320a wasnot reduced after 1 year of follow-up independiently of the treatment with CPAP.3Conclusions. In patients with OSA, exosomal miR-320a is associated to thepresence of subclinical atherosclerosis and could be a useful marker ofcardiovascular risk in these patients</dc:description><dc:date>2024</dc:date><dc:source>http://zaguan.unizar.es/record/148617</dc:source><dc:doi>10.1016/j.arbres.2024.12.005</dc:doi><dc:identifier>http://zaguan.unizar.es/record/148617</dc:identifier><dc:identifier>oai:zaguan.unizar.es:148617</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA/B22-20R</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/DGA-CUS/1466-2020</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/ISCIII CD22-00033</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/ISCIII/PI15-01441</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/ISCIII/PI18-01524</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/ISCIII/PI21-01954</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MICINN/RYC2019--027831-I</dc:relation><dc:identifier.citation>Archivos de Bronconeumologia 61, 4 (2024), 235-238</dc:identifier.citation><dc:rights>by-nc-nd</dc:rights><dc:rights>https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

</collection>