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Absence of Oral Opportunistic Infections in Patients with Inflammatory Bowel Disease Receiving Anti-TNF-α and Anti-Integrin-α(4)β(7) Therapy

Biological therapy of inflammatory bowel disease (IBD) carries an increased risk for the development of opportunistic infections due to immunomodulation. The aim of this study was to determine the prevalence and types of oral infections in IBD patients treated with biological (anti-TNF-α and anti-in...

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Autores principales: Saltović, Ema, Mijandrušić-Sinčić, Brankica, Braut, Alen, Škrobonja, Ivana, Sever, Ella, Glažar, Irena, Pezelj-Ribarić, Sonja, Muhvić-Urek, Miranda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8947472/
https://www.ncbi.nlm.nih.gov/pubmed/35323234
http://dx.doi.org/10.3390/dj10030032
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author Saltović, Ema
Mijandrušić-Sinčić, Brankica
Braut, Alen
Škrobonja, Ivana
Sever, Ella
Glažar, Irena
Pezelj-Ribarić, Sonja
Muhvić-Urek, Miranda
author_facet Saltović, Ema
Mijandrušić-Sinčić, Brankica
Braut, Alen
Škrobonja, Ivana
Sever, Ella
Glažar, Irena
Pezelj-Ribarić, Sonja
Muhvić-Urek, Miranda
author_sort Saltović, Ema
collection PubMed
description Biological therapy of inflammatory bowel disease (IBD) carries an increased risk for the development of opportunistic infections due to immunomodulation. The aim of this study was to determine the prevalence and types of oral infections in IBD patients treated with biological (anti-TNF-α and anti-integrin-α(4)β(7)) and conventional medication protocols. The study included 20 IBD patients receiving anti-TNF-α therapy, 20 IBD patients receiving anti-integrin-α(4)β(7) therapy and 20 IBD patients without immunomodulatory therapy. Participants completed questionnaires on medical information, oral lesions and symptoms. For each patient, clinical examination and a salivary flow rate test were performed, followed by a swab of the oral mucosa. The swab samples were cultured to identify Candida spp. and oral bacteria. No bacterial opportunistic infections were detected. Candidiasis was detected in four participants, with no significant difference between groups (p = 0.765). Hyposalivation was most common in the anti-TNF-α group, with a significant difference between groups (p = 0.036). There were no significant differences between groups in self-reported oral mucosal lesions and symptoms (p > 0.05), or in the distribution of oral mucosal lesions (p > 0.05). This study suggests that IBD patients receiving biological therapy are at no greater risk of developing oral opportunistic infections than IBD patients not receiving immunomodulatory therapy.
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spelling pubmed-89474722022-03-25 Absence of Oral Opportunistic Infections in Patients with Inflammatory Bowel Disease Receiving Anti-TNF-α and Anti-Integrin-α(4)β(7) Therapy Saltović, Ema Mijandrušić-Sinčić, Brankica Braut, Alen Škrobonja, Ivana Sever, Ella Glažar, Irena Pezelj-Ribarić, Sonja Muhvić-Urek, Miranda Dent J (Basel) Article Biological therapy of inflammatory bowel disease (IBD) carries an increased risk for the development of opportunistic infections due to immunomodulation. The aim of this study was to determine the prevalence and types of oral infections in IBD patients treated with biological (anti-TNF-α and anti-integrin-α(4)β(7)) and conventional medication protocols. The study included 20 IBD patients receiving anti-TNF-α therapy, 20 IBD patients receiving anti-integrin-α(4)β(7) therapy and 20 IBD patients without immunomodulatory therapy. Participants completed questionnaires on medical information, oral lesions and symptoms. For each patient, clinical examination and a salivary flow rate test were performed, followed by a swab of the oral mucosa. The swab samples were cultured to identify Candida spp. and oral bacteria. No bacterial opportunistic infections were detected. Candidiasis was detected in four participants, with no significant difference between groups (p = 0.765). Hyposalivation was most common in the anti-TNF-α group, with a significant difference between groups (p = 0.036). There were no significant differences between groups in self-reported oral mucosal lesions and symptoms (p > 0.05), or in the distribution of oral mucosal lesions (p > 0.05). This study suggests that IBD patients receiving biological therapy are at no greater risk of developing oral opportunistic infections than IBD patients not receiving immunomodulatory therapy. MDPI 2022-02-23 /pmc/articles/PMC8947472/ /pubmed/35323234 http://dx.doi.org/10.3390/dj10030032 Text en © 2022 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
Saltović, Ema
Mijandrušić-Sinčić, Brankica
Braut, Alen
Škrobonja, Ivana
Sever, Ella
Glažar, Irena
Pezelj-Ribarić, Sonja
Muhvić-Urek, Miranda
Absence of Oral Opportunistic Infections in Patients with Inflammatory Bowel Disease Receiving Anti-TNF-α and Anti-Integrin-α(4)β(7) Therapy
title Absence of Oral Opportunistic Infections in Patients with Inflammatory Bowel Disease Receiving Anti-TNF-α and Anti-Integrin-α(4)β(7) Therapy
title_full Absence of Oral Opportunistic Infections in Patients with Inflammatory Bowel Disease Receiving Anti-TNF-α and Anti-Integrin-α(4)β(7) Therapy
title_fullStr Absence of Oral Opportunistic Infections in Patients with Inflammatory Bowel Disease Receiving Anti-TNF-α and Anti-Integrin-α(4)β(7) Therapy
title_full_unstemmed Absence of Oral Opportunistic Infections in Patients with Inflammatory Bowel Disease Receiving Anti-TNF-α and Anti-Integrin-α(4)β(7) Therapy
title_short Absence of Oral Opportunistic Infections in Patients with Inflammatory Bowel Disease Receiving Anti-TNF-α and Anti-Integrin-α(4)β(7) Therapy
title_sort absence of oral opportunistic infections in patients with inflammatory bowel disease receiving anti-tnf-α and anti-integrin-α(4)β(7) therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8947472/
https://www.ncbi.nlm.nih.gov/pubmed/35323234
http://dx.doi.org/10.3390/dj10030032
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