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The Presence of T Allele (rs35705950) of the MUC5B Gene Predicts Lower Baseline Forced Vital Capacity and Its Subsequent Decline in Patients with Hypersensitivity Pneumonitis

Hypersensitivity pneumonitis (HP) is an exposure-related interstitial lung disease with two phenotypes—fibrotic and non-fibrotic. Genetic predisposition is an important factor in the disease pathogenesis and fibrosis development. Several genes are supposed to be associated with the fibrosing cascade...

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Autores principales: Lewandowska, Katarzyna B., Szturmowicz, Monika, Lechowicz, Urszula, Franczuk, Monika, Błasińska, Katarzyna, Falis, Maria, Błaszczyk, Kamila, Sobiecka, Małgorzata, Wyrostkiewicz, Dorota, Siemion-Szcześniak, Izabela, Bartosiewicz, Małgorzata, Radwan-Röhrenschef, Piotr, Roży, Adriana, Chorostowska-Wynimko, Joanna, Tomkowski, Witold Z.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10341926/
https://www.ncbi.nlm.nih.gov/pubmed/37445925
http://dx.doi.org/10.3390/ijms241310748
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author Lewandowska, Katarzyna B.
Szturmowicz, Monika
Lechowicz, Urszula
Franczuk, Monika
Błasińska, Katarzyna
Falis, Maria
Błaszczyk, Kamila
Sobiecka, Małgorzata
Wyrostkiewicz, Dorota
Siemion-Szcześniak, Izabela
Bartosiewicz, Małgorzata
Radwan-Röhrenschef, Piotr
Roży, Adriana
Chorostowska-Wynimko, Joanna
Tomkowski, Witold Z.
author_facet Lewandowska, Katarzyna B.
Szturmowicz, Monika
Lechowicz, Urszula
Franczuk, Monika
Błasińska, Katarzyna
Falis, Maria
Błaszczyk, Kamila
Sobiecka, Małgorzata
Wyrostkiewicz, Dorota
Siemion-Szcześniak, Izabela
Bartosiewicz, Małgorzata
Radwan-Röhrenschef, Piotr
Roży, Adriana
Chorostowska-Wynimko, Joanna
Tomkowski, Witold Z.
author_sort Lewandowska, Katarzyna B.
collection PubMed
description Hypersensitivity pneumonitis (HP) is an exposure-related interstitial lung disease with two phenotypes—fibrotic and non-fibrotic. Genetic predisposition is an important factor in the disease pathogenesis and fibrosis development. Several genes are supposed to be associated with the fibrosing cascade in the lungs. One of the best-recognized and most prevalent is the common MUC5B gene promoter region polymorphism variant rs35705950. The aim of our study was to establish the frequency of the minor allele of the MUC5B gene in the population of patients with HP and to find the relationship between the MUC5B promoter region polymorphism and the development of lung fibrosis, the severity of the disease course, and the response to the treatment in patients with HP. Eighty-six consecutive patients with HP were tested for the genetic variant rs35705950 of the MUC-5B gene. Demographic, radiological, and functional parameters were collected. The relationship between the presence of the T allele and lung fibrosis, pulmonary function test parameters, and the treatment response were analyzed. The minor allele frequency in the study group was 17%, with the distribution of the genotypes GG in 69.8% of subjects and GT/TT in 30.2%. Patients with the GT/TT phenotype had significantly lower baseline forced vital capacity (FVC) and significantly more frequently had a decline in FVC with time. The prevalence of lung fibrosis in high-resolution computed tomography (HRCT) was not significantly increased in GT/TT variant carriers compared to GG ones. The patients with the T allele tended to respond worse to immunomodulatory treatment and more frequently received antifibrotic drugs. In conclusions: The frequency of MUC5B polymorphism in HP patients is high. The T allele may indicate a worse disease course, worse immunomodulatory treatment response, and earlier need for antifibrotic treatment.
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spelling pubmed-103419262023-07-14 The Presence of T Allele (rs35705950) of the MUC5B Gene Predicts Lower Baseline Forced Vital Capacity and Its Subsequent Decline in Patients with Hypersensitivity Pneumonitis Lewandowska, Katarzyna B. Szturmowicz, Monika Lechowicz, Urszula Franczuk, Monika Błasińska, Katarzyna Falis, Maria Błaszczyk, Kamila Sobiecka, Małgorzata Wyrostkiewicz, Dorota Siemion-Szcześniak, Izabela Bartosiewicz, Małgorzata Radwan-Röhrenschef, Piotr Roży, Adriana Chorostowska-Wynimko, Joanna Tomkowski, Witold Z. Int J Mol Sci Article Hypersensitivity pneumonitis (HP) is an exposure-related interstitial lung disease with two phenotypes—fibrotic and non-fibrotic. Genetic predisposition is an important factor in the disease pathogenesis and fibrosis development. Several genes are supposed to be associated with the fibrosing cascade in the lungs. One of the best-recognized and most prevalent is the common MUC5B gene promoter region polymorphism variant rs35705950. The aim of our study was to establish the frequency of the minor allele of the MUC5B gene in the population of patients with HP and to find the relationship between the MUC5B promoter region polymorphism and the development of lung fibrosis, the severity of the disease course, and the response to the treatment in patients with HP. Eighty-six consecutive patients with HP were tested for the genetic variant rs35705950 of the MUC-5B gene. Demographic, radiological, and functional parameters were collected. The relationship between the presence of the T allele and lung fibrosis, pulmonary function test parameters, and the treatment response were analyzed. The minor allele frequency in the study group was 17%, with the distribution of the genotypes GG in 69.8% of subjects and GT/TT in 30.2%. Patients with the GT/TT phenotype had significantly lower baseline forced vital capacity (FVC) and significantly more frequently had a decline in FVC with time. The prevalence of lung fibrosis in high-resolution computed tomography (HRCT) was not significantly increased in GT/TT variant carriers compared to GG ones. The patients with the T allele tended to respond worse to immunomodulatory treatment and more frequently received antifibrotic drugs. In conclusions: The frequency of MUC5B polymorphism in HP patients is high. The T allele may indicate a worse disease course, worse immunomodulatory treatment response, and earlier need for antifibrotic treatment. MDPI 2023-06-28 /pmc/articles/PMC10341926/ /pubmed/37445925 http://dx.doi.org/10.3390/ijms241310748 Text en © 2023 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
Lewandowska, Katarzyna B.
Szturmowicz, Monika
Lechowicz, Urszula
Franczuk, Monika
Błasińska, Katarzyna
Falis, Maria
Błaszczyk, Kamila
Sobiecka, Małgorzata
Wyrostkiewicz, Dorota
Siemion-Szcześniak, Izabela
Bartosiewicz, Małgorzata
Radwan-Röhrenschef, Piotr
Roży, Adriana
Chorostowska-Wynimko, Joanna
Tomkowski, Witold Z.
The Presence of T Allele (rs35705950) of the MUC5B Gene Predicts Lower Baseline Forced Vital Capacity and Its Subsequent Decline in Patients with Hypersensitivity Pneumonitis
title The Presence of T Allele (rs35705950) of the MUC5B Gene Predicts Lower Baseline Forced Vital Capacity and Its Subsequent Decline in Patients with Hypersensitivity Pneumonitis
title_full The Presence of T Allele (rs35705950) of the MUC5B Gene Predicts Lower Baseline Forced Vital Capacity and Its Subsequent Decline in Patients with Hypersensitivity Pneumonitis
title_fullStr The Presence of T Allele (rs35705950) of the MUC5B Gene Predicts Lower Baseline Forced Vital Capacity and Its Subsequent Decline in Patients with Hypersensitivity Pneumonitis
title_full_unstemmed The Presence of T Allele (rs35705950) of the MUC5B Gene Predicts Lower Baseline Forced Vital Capacity and Its Subsequent Decline in Patients with Hypersensitivity Pneumonitis
title_short The Presence of T Allele (rs35705950) of the MUC5B Gene Predicts Lower Baseline Forced Vital Capacity and Its Subsequent Decline in Patients with Hypersensitivity Pneumonitis
title_sort presence of t allele (rs35705950) of the muc5b gene predicts lower baseline forced vital capacity and its subsequent decline in patients with hypersensitivity pneumonitis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10341926/
https://www.ncbi.nlm.nih.gov/pubmed/37445925
http://dx.doi.org/10.3390/ijms241310748
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