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dc.contributor.authorKocatürk, Emek
dc.contributor.authorBülbül Başkan, Emel
dc.contributor.authorKüçük, Özlem Su
dc.contributor.authorÖzdemir, Mustafa
dc.contributor.authorÖrnek, Sinem
dc.contributor.authorCan, Pelin Kuteyla
dc.contributor.authorHaşal, Eda
dc.contributor.authorEngin, Burhan
dc.contributor.authorAtakan, Nilgün
dc.contributor.authorAlpsoy, Erkan
dc.date.accessioned2022-11-24T13:02:07Z
dc.date.available2022-11-24T13:02:07Z
dc.date.issued2022en_US
dc.identifier.citationKocatürk, E., Bülbül Başkan, E., Küçük, Ö. S., Özdemir, M., Örnek, S., Can, P. K. ... Alpsoy, E. (2022). Omalizumab versus cyclosporin-A for the treatment of chronic spontaneous urticaria: Can we define better-responding endotypes? Anais Brasileiros de Dermatologia, 97(5), 592-600. https://doi.org/10.1016/j.abd.2022.03.003en_US
dc.identifier.issn0365-0596
dc.identifier.issn1806-4841
dc.identifier.urihttps://doi.org/10.1016/j.abd.2022.03.003
dc.identifier.urihttps://hdl.handle.net/20.500.12511/10026
dc.description.abstractBackground: Chronic Spontaneous Urticaria (CSU) is characterized by recurrent wheals and/or angioedema for longer than 6-weeks. Guidelines recommend Omalizumab (Oma) as first-line and Cyclosporine-A (Cs-A) as second-line treatment in antihistamine resistant CSU. This step-wise algorithm might be time-consuming and costly. Objective: To determine indicators of response to Oma or Cs-A in CSU patients. Methods: We retrospectively analyzed data from seven centers in Turkey; the inclusion criteria for patients were to receive both Oma and Cs-A treatment (not concurrently) at some point in time during their follow-up. Clinical and laboratory features were compared between groups. Results: Among 110 CSU patients; 47 (42.7%) were Oma-responders, 15 (13.6%) were Cs-A-responders, and 24 (21.8%) were both Oma and Cs-A responders and 24 (21.8%) were non-responders to either drug. High CRP levels were more frequent in Cs-A-responders (72.7% vs. 40.3%; p = 0.055). Oma-responders had higher baseline UCT (Urticaria Control Test) scores (6 vs. 4.5; p = 0.045). Responders to both drugs had less angioedema and higher baseline UCT scores compared to other groups (33.3% vs. 62.8%; p = 0.01 and 8 vs. 5; p = 0.017). Non-responders to both drugs had an increased frequency in the female gender and lower baseline UCT scores compared to other groups (87.5% vs. 61.6%; p = 0.017 and 5 vs. 7; p = 0.06). Study Limitations: Retrospective nature, limited number of patients, no control group, the lack of the basophil activation (BAT) or BHRA (basophil histamine release assay) tests. Conclusions: Baseline disease activity assessment, which considers the presence of angioedema and disease activity scores, gender, and CRP levels might be helpful to predict treatment outcomes in CSU patients and to choose the right treatment for each patient. Categorizing patients into particular endotypes could provide treatment optimization and increase treatment success.en_US
dc.language.isoengen_US
dc.publisherElsevier Science Incen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAttribution 4.0 International*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subjectBiomarkeren_US
dc.subjectChronic Urticariaen_US
dc.subjectCyclosporineen_US
dc.subjectOmalizumaben_US
dc.titleOmalizumab versus cyclosporin-A for the treatment of chronic spontaneous urticaria: Can we define better-responding endotypes?en_US
dc.typearticleen_US
dc.relation.ispartofAnais Brasileiros de Dermatologiaen_US
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Deri ve Zührevi Hastalıklar Ana Bilim Dalıen_US
dc.authorid0000-0002-7022-913Xen_US
dc.identifier.volume97en_US
dc.identifier.issue5en_US
dc.identifier.startpage592en_US
dc.identifier.endpage600en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1016/j.abd.2022.03.003en_US
dc.institutionauthorÖzdemir, Mustafa
dc.identifier.wosqualityQ3en_US
dc.identifier.wos000882887400005en_US
dc.identifier.scopus2-s2.0-85134262805en_US
dc.identifier.pmid35853771en_US
dc.identifier.scopusqualityQ3en_US


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