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The Prevalence of Atopy in Biologically Treated Spondyloarthropathies: A Retrospective Study of 200 Patients

(1) Background: Recent data shed light on the association between atopic disorders (ADs) (atopic dermatitis, allergic asthma, allergic rhinitis) and spondyloarthropathies (SpAs), underpinning the critical role of T helper (Th)1-Th17/Th2-T regulatory cells disbalance. We evaluated the prevalence of A...

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Autores principales: Strugariu, Georgiana, Pomîrleanu, Cristina, Bran, Codruța, Costea, Andrei, Vicovan, Andrei, Tatarciuc, Diana, Eșanu, Irina, Ancuța, Eugen, Chirieac, Rodica, Ancuța, Codrina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745433/
https://www.ncbi.nlm.nih.gov/pubmed/35011793
http://dx.doi.org/10.3390/jcm11010055
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author Strugariu, Georgiana
Pomîrleanu, Cristina
Bran, Codruța
Costea, Andrei
Vicovan, Andrei
Tatarciuc, Diana
Eșanu, Irina
Ancuța, Eugen
Chirieac, Rodica
Ancuța, Codrina
author_facet Strugariu, Georgiana
Pomîrleanu, Cristina
Bran, Codruța
Costea, Andrei
Vicovan, Andrei
Tatarciuc, Diana
Eșanu, Irina
Ancuța, Eugen
Chirieac, Rodica
Ancuța, Codrina
author_sort Strugariu, Georgiana
collection PubMed
description (1) Background: Recent data shed light on the association between atopic disorders (ADs) (atopic dermatitis, allergic asthma, allergic rhinitis) and spondyloarthropathies (SpAs), underpinning the critical role of T helper (Th)1-Th17/Th2-T regulatory cells disbalance. We evaluated the prevalence of AD in axial SpAs (axSpAs) and psoriatic arthritis (PsA) and explored the potential association between atopic status, disease-related parameters, and biological therapy. (2) Methods: A monocentric, retrospective study was conducted that enrolled 200 patients taking biologics. Demographics, disease, and drug-related variables, along with a screening questionnaire focused on Ads, were systematically collected. (3) Results: Overall, 51 patients (25.5%) had atopy—namely, 24.4% of axSpA and 28% of PsA, with a higher frequency of rhinitis (43%) vs. atopic dermatitis (37.2%) or asthma (21.5%). We failed to demonstrate any statistically significant difference in demographics, SpA-related parameters excepting concomitant inflammatory bowel disease, and biologic drug exposure in patients with and without atopy (p > 0.05). However, significantly more non-atopic patients need only one TNF inhibitor (54%) vs. atopic patients (28%) (p < 0.05) to control active SpA. (4) Conclusions: We successfully demonstrated that AD is associated with one out of four SpA. Irrespective of the SpA subtype, atopic patients require more frequent switching among biologics, as significantly more non-atopic patients remain on their first anti-TNF.
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spelling pubmed-87454332022-01-11 The Prevalence of Atopy in Biologically Treated Spondyloarthropathies: A Retrospective Study of 200 Patients Strugariu, Georgiana Pomîrleanu, Cristina Bran, Codruța Costea, Andrei Vicovan, Andrei Tatarciuc, Diana Eșanu, Irina Ancuța, Eugen Chirieac, Rodica Ancuța, Codrina J Clin Med Article (1) Background: Recent data shed light on the association between atopic disorders (ADs) (atopic dermatitis, allergic asthma, allergic rhinitis) and spondyloarthropathies (SpAs), underpinning the critical role of T helper (Th)1-Th17/Th2-T regulatory cells disbalance. We evaluated the prevalence of AD in axial SpAs (axSpAs) and psoriatic arthritis (PsA) and explored the potential association between atopic status, disease-related parameters, and biological therapy. (2) Methods: A monocentric, retrospective study was conducted that enrolled 200 patients taking biologics. Demographics, disease, and drug-related variables, along with a screening questionnaire focused on Ads, were systematically collected. (3) Results: Overall, 51 patients (25.5%) had atopy—namely, 24.4% of axSpA and 28% of PsA, with a higher frequency of rhinitis (43%) vs. atopic dermatitis (37.2%) or asthma (21.5%). We failed to demonstrate any statistically significant difference in demographics, SpA-related parameters excepting concomitant inflammatory bowel disease, and biologic drug exposure in patients with and without atopy (p > 0.05). However, significantly more non-atopic patients need only one TNF inhibitor (54%) vs. atopic patients (28%) (p < 0.05) to control active SpA. (4) Conclusions: We successfully demonstrated that AD is associated with one out of four SpA. Irrespective of the SpA subtype, atopic patients require more frequent switching among biologics, as significantly more non-atopic patients remain on their first anti-TNF. MDPI 2021-12-23 /pmc/articles/PMC8745433/ /pubmed/35011793 http://dx.doi.org/10.3390/jcm11010055 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Strugariu, Georgiana
Pomîrleanu, Cristina
Bran, Codruța
Costea, Andrei
Vicovan, Andrei
Tatarciuc, Diana
Eșanu, Irina
Ancuța, Eugen
Chirieac, Rodica
Ancuța, Codrina
The Prevalence of Atopy in Biologically Treated Spondyloarthropathies: A Retrospective Study of 200 Patients
title The Prevalence of Atopy in Biologically Treated Spondyloarthropathies: A Retrospective Study of 200 Patients
title_full The Prevalence of Atopy in Biologically Treated Spondyloarthropathies: A Retrospective Study of 200 Patients
title_fullStr The Prevalence of Atopy in Biologically Treated Spondyloarthropathies: A Retrospective Study of 200 Patients
title_full_unstemmed The Prevalence of Atopy in Biologically Treated Spondyloarthropathies: A Retrospective Study of 200 Patients
title_short The Prevalence of Atopy in Biologically Treated Spondyloarthropathies: A Retrospective Study of 200 Patients
title_sort prevalence of atopy in biologically treated spondyloarthropathies: a retrospective study of 200 patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745433/
https://www.ncbi.nlm.nih.gov/pubmed/35011793
http://dx.doi.org/10.3390/jcm11010055
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