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dc.contributor.authorWechsler M.E
dc.contributor.authorScelo G
dc.contributor.authorLarenas-Linnemann D.E.S
dc.contributor.authorTorres-Duque C.A
dc.contributor.authorMaspero J
dc.contributor.authorTran T.N
dc.contributor.authorMurray R.B
dc.contributor.authorMartin N
dc.contributor.authorMenzies-Gow A.N
dc.date.accessioned2024-11-01T14:38:43Z
dc.date.available2024-11-01T14:38:43Z
dc.date.issued2024
dc.identifier.issn15354970
dc.identifier.otherhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85184138353&doi=10.1164%2frccm.202305-0808OC&partnerID=40&md5=9f4115af5a6656d2855e7084c0dd4c7c
dc.identifier.urihttp://hdl.handle.net/10818/62237
dc.description.abstractRationale: Previous studies investigating the impact of comorbidities on the effectiveness of biologic agents have been relatively small and of short duration and have not compared classes of biologic agents. Objectives: To determine the association between type 2-related comorbidities and biologic agent effectiveness in adults with severe asthma (SA). Methods: This cohort study used International Severe Asthma Registry data from 21 countries (2017-2022) to quantify changes in four outcomes before and after biologic therapy-annual asthma exacerbation rate, FEV1% predicted, asthma control, and long-term oral corticosteroid daily dose-in patients with or without allergic rhinitis, chronic rhinosinusitis (CRS) with or without nasal polyps (NPs), NPs, or eczema/atopic dermatitis. Measurements and Main Results: Of 1,765 patients, 1,257, 421, and 87 initiated anti-IL-5/5 receptor, anti-IgE, and anti-IL-4/13 therapies, respectively. In general, pre- versus post-biologic therapy improvements were noted in all four asthma outcomes assessed, irrespective of comorbidity status. However, patients with comorbid CRS with or without NPs experienced 23% fewer exacerbations per year (95% CI, 10-35%; P < 0.001) and had 59% higher odds of better post-biologic therapy asthma control (95% CI, 26-102%; P < 0.001) than those without CRS with or without NPs. Similar estimates were noted for those with comorbid NPs: 22% fewer exacerbations and 56% higher odds of better post-biologic therapy control. Patients with SA and CRS with or without NPs had an additional FEV1% predicted improvement of 3.2% (95% CI, 1.0-5.3; P = 0.004), a trend that was also noted in those with comorbid NPs. The presence of allergic rhinitis or atopic dermatitis was not associated with post-biologic therapy effect for any outcome assessed. Conclusions: These findings highlight the importance of systematic comorbidity evaluation. The presence of CRS with or without NPs or NPs alone may be considered a predictor of the effectiveness of biologic agents in patients with SA.en
dc.formatapplication/pdfes_CO
dc.language.isoenges_CO
dc.publisherAmerican journal of respiratory and critical care medicinees_CO
dc.relation.ispartofseriesAmerican journal of respiratory and critical care medicine Vol. 209 N° 3
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourceUniversidad de La Sabanaes_CO
dc.sourceIntellectum Repositorio Universidad de La Sabanaes_CO
dc.subject.otherBiological producten
dc.subject.otherAdulten
dc.subject.otherAllergic rhinitisen
dc.subject.otherAsthmaen
dc.subject.otherChronic diseaseen
dc.subject.otherCohort analysisen
dc.subject.otherComorbidityen
dc.titleAssociation between t2-related comorbidities and effectiveness of biologics in severe asthmaen
dc.typejournal articlees_CO
dc.type.hasVersionpublishedVersiones_CO
dc.rights.accessRightsopenAccesses_CO
dc.identifier.doi10.1164/rccm.202305-0808OC


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