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MUC7 VNTR polymorphism and association with bronchial asthma in Egyptian children
Overproduction of mucins in the airways donates largely to airway blockage in asthma patients. Glycoprotein MUC7 plays a role in the clearance of bacteria and has anti-candidacidal criteria. Our goal was to investigate the association between the MUC7 variable number of tandem repeats (VNTR) polymor...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9640678/ https://www.ncbi.nlm.nih.gov/pubmed/36344553 http://dx.doi.org/10.1038/s41598-022-21631-4 |
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author | Saad, Entsar A. Elsaid, Afaf M. Shoaib, Rasha M. S. Megahed, Khaled F. Elsharawy, Amal N. |
author_facet | Saad, Entsar A. Elsaid, Afaf M. Shoaib, Rasha M. S. Megahed, Khaled F. Elsharawy, Amal N. |
author_sort | Saad, Entsar A. |
collection | PubMed |
description | Overproduction of mucins in the airways donates largely to airway blockage in asthma patients. Glycoprotein MUC7 plays a role in the clearance of bacteria and has anti-candidacidal criteria. Our goal was to investigate the association between the MUC7 variable number of tandem repeats (VNTR) polymorphism and bronchial asthma among Egyptian children. The MUC7 VNTR polymorphism was investigated among 100 children with bronchial asthma and 100 healthy controls using polymerase chain reaction (PCR) method. Serum levels of immunoglobulin E (IgE), tumor necrosis factor-alpha (TNF-α), and transforming growth factor-beta1 (TGF-β1) were assessed by enzyme-linked immunosorbent assay (ELISA) technique. The frequencies of 6*5 genotype, 5*5 genotype, (6*5 + 5*5) genotypes, and MUC7*5 allele of the MUC7 VNTR variant were significantly lower among asthmatic patients than controls (p < 0.015, OR = 0.39, 95% CI = 0.19–0.81; p = 0.03, OR = 0.18, 95% CI = 0.04–0.86; p < 0.001, OR = 0.29, 95% CI = 0.15–0.58; p < 0.001, OR = 0.3, 95% CI = 0.17–0.55, respectively). The (6*5 + 5*5) genotypes of the MUC7 VNTR variant were not associated with the clinical manifestations and serum levels of IgE, TNF-α, and TGF-β1 among asthmatic patients (p ˃ 0.05). In conclusion, the (6*5 + 5*5) genotypes of the MUC7 VNTR variant may have a protective role for bronchial asthma in Egyptian children. |
format | Online Article Text |
id | pubmed-9640678 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96406782022-11-15 MUC7 VNTR polymorphism and association with bronchial asthma in Egyptian children Saad, Entsar A. Elsaid, Afaf M. Shoaib, Rasha M. S. Megahed, Khaled F. Elsharawy, Amal N. Sci Rep Article Overproduction of mucins in the airways donates largely to airway blockage in asthma patients. Glycoprotein MUC7 plays a role in the clearance of bacteria and has anti-candidacidal criteria. Our goal was to investigate the association between the MUC7 variable number of tandem repeats (VNTR) polymorphism and bronchial asthma among Egyptian children. The MUC7 VNTR polymorphism was investigated among 100 children with bronchial asthma and 100 healthy controls using polymerase chain reaction (PCR) method. Serum levels of immunoglobulin E (IgE), tumor necrosis factor-alpha (TNF-α), and transforming growth factor-beta1 (TGF-β1) were assessed by enzyme-linked immunosorbent assay (ELISA) technique. The frequencies of 6*5 genotype, 5*5 genotype, (6*5 + 5*5) genotypes, and MUC7*5 allele of the MUC7 VNTR variant were significantly lower among asthmatic patients than controls (p < 0.015, OR = 0.39, 95% CI = 0.19–0.81; p = 0.03, OR = 0.18, 95% CI = 0.04–0.86; p < 0.001, OR = 0.29, 95% CI = 0.15–0.58; p < 0.001, OR = 0.3, 95% CI = 0.17–0.55, respectively). The (6*5 + 5*5) genotypes of the MUC7 VNTR variant were not associated with the clinical manifestations and serum levels of IgE, TNF-α, and TGF-β1 among asthmatic patients (p ˃ 0.05). In conclusion, the (6*5 + 5*5) genotypes of the MUC7 VNTR variant may have a protective role for bronchial asthma in Egyptian children. Nature Publishing Group UK 2022-11-07 /pmc/articles/PMC9640678/ /pubmed/36344553 http://dx.doi.org/10.1038/s41598-022-21631-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Saad, Entsar A. Elsaid, Afaf M. Shoaib, Rasha M. S. Megahed, Khaled F. Elsharawy, Amal N. MUC7 VNTR polymorphism and association with bronchial asthma in Egyptian children |
title | MUC7 VNTR polymorphism and association with bronchial asthma in Egyptian children |
title_full | MUC7 VNTR polymorphism and association with bronchial asthma in Egyptian children |
title_fullStr | MUC7 VNTR polymorphism and association with bronchial asthma in Egyptian children |
title_full_unstemmed | MUC7 VNTR polymorphism and association with bronchial asthma in Egyptian children |
title_short | MUC7 VNTR polymorphism and association with bronchial asthma in Egyptian children |
title_sort | muc7 vntr polymorphism and association with bronchial asthma in egyptian children |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9640678/ https://www.ncbi.nlm.nih.gov/pubmed/36344553 http://dx.doi.org/10.1038/s41598-022-21631-4 |
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