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Efficacy of Pidotimod use in treating allergic rhinitis in a pediatric population

BACKGROUND: Allergic rhinitis (AR) and adenoidal hypertrophy (AH) are the most frequent causative disorders of nasal obstruction in children, leading to recurrent respiratory infections. Both nasal cavities are colonized by a stable microbial community susceptible to environmental changes and Staphy...

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Autores principales: Brindisi, Giulia, Zicari, Anna Maria, Schiavi, Laura, Gori, Alessandra, Conte, Maria Pia, Marazzato, Massimiliano, De Castro, Giovanna, Leonardi, Lucia, Duse, Marzia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7341603/
https://www.ncbi.nlm.nih.gov/pubmed/32635938
http://dx.doi.org/10.1186/s13052-020-00859-8
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author Brindisi, Giulia
Zicari, Anna Maria
Schiavi, Laura
Gori, Alessandra
Conte, Maria Pia
Marazzato, Massimiliano
De Castro, Giovanna
Leonardi, Lucia
Duse, Marzia
author_facet Brindisi, Giulia
Zicari, Anna Maria
Schiavi, Laura
Gori, Alessandra
Conte, Maria Pia
Marazzato, Massimiliano
De Castro, Giovanna
Leonardi, Lucia
Duse, Marzia
author_sort Brindisi, Giulia
collection PubMed
description BACKGROUND: Allergic rhinitis (AR) and adenoidal hypertrophy (AH) are the most frequent causative disorders of nasal obstruction in children, leading to recurrent respiratory infections. Both nasal cavities are colonized by a stable microbial community susceptible to environmental changes and Staphylococcus aureus seems to play the major role. Furthermore, nasal microbiota holds a large number and variety of viruses with upper respiratory tract infections. This local microbiota deserves attention because its modification could induce a virtuous cross-talking with the immune system, with a better clearance of pathogens. Although AR and AH present a different etiopathogenesis, they have in common a minimal chronic inflammation surrounding nasal obstruction; hence it would be challenging to evaluate the effect of an immunomodulator on this minimal chronic inflammation with possible clinical and microbiological effects. The aim of this study is therefore to evaluate the efficacy of an immunomoldulator (Pidotimod) on nasal obstruction in children with AR and/or AH and whether its action involves a variation of nasal microbiota. METHODS: We enrolled 76 children: those with allergic rhinitis (AR) sensitized to dust mites entered the AR group, those with adenoidal hypertrophy (AH) the AH group, those with both conditions the AR/AH group and those without AR ± AH as controls (CTRL). At the first visit they performed: skin prick tests, nasal fiberoptic endoscopy, anterior rhinomanometry, nasal swabs. Children with. AR ± AH started treatment with Pidotimod. After 1 month they were re-evaluated performing the same procedures. The primary outcome was the evaluation of nasal obstruction after treatment and the secondary outcome was the improvement of symptoms and the changes in nasal microflora. RESULTS: All patients improved their mean nasal flow (mNF) in respect to the baseline. In AR children mNF reached that one of CTRL. In AH children±AR the mNF was lower in respect to CTRL and AR group. We did not find any differences among all the groups at the two different time points in nasal microflora. CONCLUSIONS: Pidotimod is able to give an improvement in nasal obstruction, especially in AR children but this effect seems to be not mediated by changes in nasal microbiota.
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spelling pubmed-73416032020-07-14 Efficacy of Pidotimod use in treating allergic rhinitis in a pediatric population Brindisi, Giulia Zicari, Anna Maria Schiavi, Laura Gori, Alessandra Conte, Maria Pia Marazzato, Massimiliano De Castro, Giovanna Leonardi, Lucia Duse, Marzia Ital J Pediatr Research BACKGROUND: Allergic rhinitis (AR) and adenoidal hypertrophy (AH) are the most frequent causative disorders of nasal obstruction in children, leading to recurrent respiratory infections. Both nasal cavities are colonized by a stable microbial community susceptible to environmental changes and Staphylococcus aureus seems to play the major role. Furthermore, nasal microbiota holds a large number and variety of viruses with upper respiratory tract infections. This local microbiota deserves attention because its modification could induce a virtuous cross-talking with the immune system, with a better clearance of pathogens. Although AR and AH present a different etiopathogenesis, they have in common a minimal chronic inflammation surrounding nasal obstruction; hence it would be challenging to evaluate the effect of an immunomodulator on this minimal chronic inflammation with possible clinical and microbiological effects. The aim of this study is therefore to evaluate the efficacy of an immunomoldulator (Pidotimod) on nasal obstruction in children with AR and/or AH and whether its action involves a variation of nasal microbiota. METHODS: We enrolled 76 children: those with allergic rhinitis (AR) sensitized to dust mites entered the AR group, those with adenoidal hypertrophy (AH) the AH group, those with both conditions the AR/AH group and those without AR ± AH as controls (CTRL). At the first visit they performed: skin prick tests, nasal fiberoptic endoscopy, anterior rhinomanometry, nasal swabs. Children with. AR ± AH started treatment with Pidotimod. After 1 month they were re-evaluated performing the same procedures. The primary outcome was the evaluation of nasal obstruction after treatment and the secondary outcome was the improvement of symptoms and the changes in nasal microflora. RESULTS: All patients improved their mean nasal flow (mNF) in respect to the baseline. In AR children mNF reached that one of CTRL. In AH children±AR the mNF was lower in respect to CTRL and AR group. We did not find any differences among all the groups at the two different time points in nasal microflora. CONCLUSIONS: Pidotimod is able to give an improvement in nasal obstruction, especially in AR children but this effect seems to be not mediated by changes in nasal microbiota. BioMed Central 2020-07-07 /pmc/articles/PMC7341603/ /pubmed/32635938 http://dx.doi.org/10.1186/s13052-020-00859-8 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Brindisi, Giulia
Zicari, Anna Maria
Schiavi, Laura
Gori, Alessandra
Conte, Maria Pia
Marazzato, Massimiliano
De Castro, Giovanna
Leonardi, Lucia
Duse, Marzia
Efficacy of Pidotimod use in treating allergic rhinitis in a pediatric population
title Efficacy of Pidotimod use in treating allergic rhinitis in a pediatric population
title_full Efficacy of Pidotimod use in treating allergic rhinitis in a pediatric population
title_fullStr Efficacy of Pidotimod use in treating allergic rhinitis in a pediatric population
title_full_unstemmed Efficacy of Pidotimod use in treating allergic rhinitis in a pediatric population
title_short Efficacy of Pidotimod use in treating allergic rhinitis in a pediatric population
title_sort efficacy of pidotimod use in treating allergic rhinitis in a pediatric population
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7341603/
https://www.ncbi.nlm.nih.gov/pubmed/32635938
http://dx.doi.org/10.1186/s13052-020-00859-8
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