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Clinical Characterization of Patients with Chronic Spontaneous Urticaria according to Anti-TPO IgE Levels

BACKGROUND: Chronic spontaneous urticaria (CSU) is a heterogeneous disease with some frequent comorbidities like autoimmune diseases, drug reactions, and inducible urticaria. IgE antibodies against thyroid peroxidase (anti-TPO IgE) could be associated with some of these clinical characteristics. OBJ...

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Autores principales: Sánchez, Jorge, Sánchez, Andres, Cardona, Ricardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6925798/
https://www.ncbi.nlm.nih.gov/pubmed/31886301
http://dx.doi.org/10.1155/2019/4202145
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author Sánchez, Jorge
Sánchez, Andres
Cardona, Ricardo
author_facet Sánchez, Jorge
Sánchez, Andres
Cardona, Ricardo
author_sort Sánchez, Jorge
collection PubMed
description BACKGROUND: Chronic spontaneous urticaria (CSU) is a heterogeneous disease with some frequent comorbidities like autoimmune diseases, drug reactions, and inducible urticaria. IgE antibodies against thyroid peroxidase (anti-TPO IgE) could be associated with some of these clinical characteristics. OBJECTIVE: To explore the clinical characteristics of CSU patients, according to the presence of anti-TPO IgE in serum. METHODS: Anti-TPO IgE levels were measured during the clinical control period (Urticaria Activity Score, 0 point) and exacerbation period (≥3 points) in 100 CSU patients. Patients with self-reported exacerbation of skin involvement by foods, nonsteroidal anti-inflammatory drugs (NSAIDs), and physical triggers underwent controlled challenge tests. RESULTS: We identified 2 groups of patients: (1) patients with anti-TPO IgE during the clinical control period or during an exacerbation, who had a higher frequency of atopy, asthma, and positive challenge test results with NSAIDs and (2) patients without anti-TPO IgE during any period, who had a higher frequency of positive challenge test results for inducible urticaria. Among the first group (anti-TPO IgE at any point), we identified 3 subgroups: patients with anti-TPO IgE during the clinical control period (n = 12); patients with anti-TPO IgE during the clinical control period and significantly increased levels during an urticaria exacerbation (n = 18); and patients with anti-TPO IgE only during an exacerbation (n = 13). None of the patients with self-reported food reactions had a positive challenge test result. CONCLUSION: Anti-TPO IgE is a useful biomarker for differentiating between clinical phenotypes of patients with CSU. Elevation of anti-TPO IgE during exacerbation periods supports an association between this autoantibody and the pathogenesis of urticaria.
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spelling pubmed-69257982019-12-29 Clinical Characterization of Patients with Chronic Spontaneous Urticaria according to Anti-TPO IgE Levels Sánchez, Jorge Sánchez, Andres Cardona, Ricardo J Immunol Res Research Article BACKGROUND: Chronic spontaneous urticaria (CSU) is a heterogeneous disease with some frequent comorbidities like autoimmune diseases, drug reactions, and inducible urticaria. IgE antibodies against thyroid peroxidase (anti-TPO IgE) could be associated with some of these clinical characteristics. OBJECTIVE: To explore the clinical characteristics of CSU patients, according to the presence of anti-TPO IgE in serum. METHODS: Anti-TPO IgE levels were measured during the clinical control period (Urticaria Activity Score, 0 point) and exacerbation period (≥3 points) in 100 CSU patients. Patients with self-reported exacerbation of skin involvement by foods, nonsteroidal anti-inflammatory drugs (NSAIDs), and physical triggers underwent controlled challenge tests. RESULTS: We identified 2 groups of patients: (1) patients with anti-TPO IgE during the clinical control period or during an exacerbation, who had a higher frequency of atopy, asthma, and positive challenge test results with NSAIDs and (2) patients without anti-TPO IgE during any period, who had a higher frequency of positive challenge test results for inducible urticaria. Among the first group (anti-TPO IgE at any point), we identified 3 subgroups: patients with anti-TPO IgE during the clinical control period (n = 12); patients with anti-TPO IgE during the clinical control period and significantly increased levels during an urticaria exacerbation (n = 18); and patients with anti-TPO IgE only during an exacerbation (n = 13). None of the patients with self-reported food reactions had a positive challenge test result. CONCLUSION: Anti-TPO IgE is a useful biomarker for differentiating between clinical phenotypes of patients with CSU. Elevation of anti-TPO IgE during exacerbation periods supports an association between this autoantibody and the pathogenesis of urticaria. Hindawi 2019-12-07 /pmc/articles/PMC6925798/ /pubmed/31886301 http://dx.doi.org/10.1155/2019/4202145 Text en Copyright © 2019 Jorge Sánchez et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Sánchez, Jorge
Sánchez, Andres
Cardona, Ricardo
Clinical Characterization of Patients with Chronic Spontaneous Urticaria according to Anti-TPO IgE Levels
title Clinical Characterization of Patients with Chronic Spontaneous Urticaria according to Anti-TPO IgE Levels
title_full Clinical Characterization of Patients with Chronic Spontaneous Urticaria according to Anti-TPO IgE Levels
title_fullStr Clinical Characterization of Patients with Chronic Spontaneous Urticaria according to Anti-TPO IgE Levels
title_full_unstemmed Clinical Characterization of Patients with Chronic Spontaneous Urticaria according to Anti-TPO IgE Levels
title_short Clinical Characterization of Patients with Chronic Spontaneous Urticaria according to Anti-TPO IgE Levels
title_sort clinical characterization of patients with chronic spontaneous urticaria according to anti-tpo ige levels
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6925798/
https://www.ncbi.nlm.nih.gov/pubmed/31886301
http://dx.doi.org/10.1155/2019/4202145
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