In chronic spontaneous urticaria, IgE and C-reactive protein are linked to distinct microRNAs and interleukin-31

dc.contributor.authorBakay, Ozge Sevil Karstarli
dc.contributor.authorDemir, Betul
dc.contributor.authorCicek, Demet
dc.contributor.authorErol, Deniz
dc.contributor.authorAsci Toraman, Zulal
dc.contributor.authorGural, Yunus
dc.contributor.authorMaurer, Marcus
dc.date.accessioned2026-08-12T17:38:18Z
dc.date.issued2023
dc.departmentFırat Üniversitesi
dc.description.abstractBackgroundChronic spontaneous urticaria (CSU) is a common and disabling disease. Assessments of IgE and C-reactive protein (CRP) are recommended in the diagnostic work-up, but the role and clinical relevance of these biomarkers are not well characterized. Moreover, it remains unknown if elevated levels of IgE or CRP are linked to CSU microRNA (miRNA) signatures or interleukin 31 (IL-31). MethodsWe measured IgE and CRP serum levels in 47 CSU patients (and 45 healthy controls) and determined CSU disease activity using the urticaria activity score (UAS7). Expression levels of miR-155 and miR-221 were assessed by RT-PCR, and IL-31 levels were determined by ELISA. ResultsTotal IgE and CRP levels were independently increased in CSU patients. IgE and CRP levels were highest and lowest in patients with high and mild disease activity. IgE levels correlated with miR-155 levels, whereas CRP levels correlated with miR-221 levels. miR-155 and miR-221 were significantly overexpressed in CSU patients. ROC analyses linked miRNA-155 and CSU with a sensitivity of 79% and specificity of 87%, and miRNA-221 and CSU with a sensitivity of 75% and specificity of 91%. High CRP and miR-221 expression levels were linked to elevated levels of IgG anti-TPO and IL-31. ConclusionIgE and CRP are useful biomarkers for disease activity in CSU, with distinct miRNA profiles. High CRP and miR-221 levels may point to autoimmune CSU and a role for IL-31.
dc.description.sponsorshipFirat University Coordinatorship of Scientific Research Projects [TF.16.36]
dc.description.sponsorshipACKNOWLEDGMENTS This work was supported by the Firat University Coordinatorship of Scientific Research Projects (No: TF.16.36). Open Access funding enabled and organized by Projekt DEAL.
dc.identifier.doi10.1002/clt2.12290
dc.identifier.issn2045-7022
dc.identifier.issue8
dc.identifier.orcid0000-0002-6190-5124
dc.identifier.orcid0000-0002-1523-3187
dc.identifier.orcid0000-0002-0572-453X
dc.identifier.orcid0000-0002-4121-481X
dc.identifier.orcid0000-0001-8405-7730
dc.identifier.orcid0000-0001-5202-8564
dc.identifier.pmid37632245
dc.identifier.scopus2-s2.0-85166758650
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.1002/clt2.12290
dc.identifier.urihttps://hdl.handle.net/11508/58399
dc.identifier.volume13
dc.identifier.wosWOS:001042060100001
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherWiley
dc.relation.ispartofClinical and Translational Allergy
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260511
dc.subjectCRP
dc.subjectIgE
dc.subjectinterleukin-31
dc.subjectmicro-RNA
dc.subjecturticaria
dc.titleIn chronic spontaneous urticaria, IgE and C-reactive protein are linked to distinct microRNAs and interleukin-31
dc.typeArticle

Dosyalar