Publication:
T2 Biomarkers as Predictors of Exacerbations of Chronic Obstructive Pulmonary Disease.

dc.contributor.authorAlcázar-Navarrete, Bernardino
dc.contributor.authorDíaz-Lopez, Jose Manuel
dc.contributor.authorGarcía-Flores, Paula
dc.contributor.authorOrtega-Antelo, Marina
dc.contributor.authorAguilar-Cruz, Ivan
dc.contributor.authorRuiz-Rodríguez, Oliverio
dc.contributor.authorSantiago-Diaz, Pablo
dc.contributor.authorRomero Palacios, Pedro José
dc.date.accessioned2023-05-03T14:45:23Z
dc.date.available2023-05-03T14:45:23Z
dc.date.issued2021-11-27
dc.description.abstractType 2 (T2) biomarkers such as blood eosinophil count (BEC) and FeNO have been related to a higher risk of exacerbations in COPD. It is unknown whether combining these biomarkers could be useful in forecasting COPD exacerbations. COPD patients were enrolled in this prospective, multicenter, observational study and followed up for 1 year, during which BEC were analysed at baseline (V0) while FeNO analyses were performed at baseline (V0), 6 months (V1) and 12 months (V2). The risk of moderate or severe exacerbation during follow up was assessed by Cox regression analysis, and the predictive capacity of both measurements was assessed by ROC curves and the DeLong test. Statistical significance was assumed at P Of the 322 COPD patients initially recruited, 287 were followed up. At baseline, 28.0% were active smokers, and experienced moderate airflow limitation (mean FEV1 56.4%±17.0% predicted). Patients with at least one elevated T2 biomarker (n=125, 42.5%) were at increased risk of COPD exacerbation (HR 1.75, 95% CI 1.25-2.45, P=.001) and of shorter time to first COPD exacerbation. There was no difference between BEC and FeNO regarding the predictive capacity for moderate to severe exacerbation (AUC 0.584 vs 0.576, P=.183) but FeNO predicted severe episodes more accurately than BEC (AUC 0.607 vs 0.539, P Both eosinophil count and FeNO have limited utility for predicting COPD exacerbations. Combining these T2 biomarkers could enhance the detection of future COPD exacerbations.
dc.identifier.doi10.1016/j.arbres.2021.11.006
dc.identifier.essn1579-2129
dc.identifier.pmid35312535
dc.identifier.urihttp://hdl.handle.net/10668/22003
dc.issue.number8
dc.journal.titleArchivos de bronconeumologia
dc.journal.titleabbreviationArch Bronconeumol
dc.language.isoen
dc.language.isoes
dc.organizationAPES Hospital de Poniente de Almería
dc.organizationHospital Universitario San Cecilio
dc.organizationHospital Universitario Virgen de las Nieves
dc.page.number595-600
dc.pubmedtypeJournal Article
dc.pubmedtypeMulticenter Study
dc.pubmedtypeObservational Study
dc.subjectBiomarkers
dc.subjectCOPD
dc.subjectEosinophil
dc.subjectFeNO
dc.subjectType 2 inflammation
dc.subject.meshBiomarkers
dc.subject.meshDisease Progression
dc.subject.meshEosinophils
dc.subject.meshHumans
dc.subject.meshProspective Studies
dc.subject.meshPulmonary Disease, Chronic Obstructive
dc.titleT2 Biomarkers as Predictors of Exacerbations of Chronic Obstructive Pulmonary Disease.
dc.typeresearch article
dc.volume.number58
dspace.entity.typePublication

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