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Polymorphism in the EREG gene confers susceptibility to tuberculosis

BACKGROUND: Host genetic factors affect the immune response to Mycobacterium tuberculosis (Mtb) infection as well as the progression of the disease. Epiregulin (EREG) belongs to the epidermal growth factor (EGF) family, which binds to the epidermal growth factor receptor (EGFR) to regulate the immun...

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Autores principales: Cao, Wen, Luo, Liu-lin, Chen, Wei-wei, Liang, Li, Zhang, Ran-ran, Zhao, Yan-lin, Chen, Jin, Yue, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329172/
https://www.ncbi.nlm.nih.gov/pubmed/30634928
http://dx.doi.org/10.1186/s12881-018-0729-z
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author Cao, Wen
Luo, Liu-lin
Chen, Wei-wei
Liang, Li
Zhang, Ran-ran
Zhao, Yan-lin
Chen, Jin
Yue, Jun
author_facet Cao, Wen
Luo, Liu-lin
Chen, Wei-wei
Liang, Li
Zhang, Ran-ran
Zhao, Yan-lin
Chen, Jin
Yue, Jun
author_sort Cao, Wen
collection PubMed
description BACKGROUND: Host genetic factors affect the immune response to Mycobacterium tuberculosis (Mtb) infection as well as the progression of the disease. Epiregulin (EREG) belongs to the epidermal growth factor (EGF) family, which binds to the epidermal growth factor receptor (EGFR) to regulate the immune response of the host during infections. Our study aimed to compare EREG levels in tuberculosis (TB) patients and healthy controls and assess whether polymorphisms in EREG increase the risk of TB. METHODS: We used ELISA to determine the plasma EREG level from 30 healthy controls and 50 tuberculosis patients. By evaluating the EREG gene from 624 TB patients and 600 healthy controls, we determined the allelic and genotypic frequencies for association with susceptibility to TB infections in this group. RESULTS: This paper shows that the pulmonary tuberculosis (PTB) and extrapulmonary tuberculosis (EPTB) groups showed a significantly higher plasma EREG level (1014 ± 733.9 pg/ml, 700.2 ± 676.6 pg/ml, respectively) than the healthy controls (277 ± 105.4 pg/ml). The rs2367707 polymorphism was associated with a higher risk of PTB and EPTB (P = 0.00051, P = 0.0012). Analyses of haplotype frequencies found that people with the haplotype CACAT had a higher risk of PTB and EPTB (P = 0.00031, OR = 1.43; P = 0.000053, OR = 1.65). Moreover, the rs6446993 polymorphism of the EREG gene was found to be associated with EPTB (P = 0.00087, OR = 1.54; 95% CI = 1.23–1.94). CONCLUSIONS: Compared to that of healthy controls, the level of EREG in the plasma of TB patients increased significantly. Based on these data, we demonstrated that EREG polymorphisms are genetic factors for susceptibility to TB and various forms of TB.
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spelling pubmed-63291722019-01-16 Polymorphism in the EREG gene confers susceptibility to tuberculosis Cao, Wen Luo, Liu-lin Chen, Wei-wei Liang, Li Zhang, Ran-ran Zhao, Yan-lin Chen, Jin Yue, Jun BMC Med Genet Research Article BACKGROUND: Host genetic factors affect the immune response to Mycobacterium tuberculosis (Mtb) infection as well as the progression of the disease. Epiregulin (EREG) belongs to the epidermal growth factor (EGF) family, which binds to the epidermal growth factor receptor (EGFR) to regulate the immune response of the host during infections. Our study aimed to compare EREG levels in tuberculosis (TB) patients and healthy controls and assess whether polymorphisms in EREG increase the risk of TB. METHODS: We used ELISA to determine the plasma EREG level from 30 healthy controls and 50 tuberculosis patients. By evaluating the EREG gene from 624 TB patients and 600 healthy controls, we determined the allelic and genotypic frequencies for association with susceptibility to TB infections in this group. RESULTS: This paper shows that the pulmonary tuberculosis (PTB) and extrapulmonary tuberculosis (EPTB) groups showed a significantly higher plasma EREG level (1014 ± 733.9 pg/ml, 700.2 ± 676.6 pg/ml, respectively) than the healthy controls (277 ± 105.4 pg/ml). The rs2367707 polymorphism was associated with a higher risk of PTB and EPTB (P = 0.00051, P = 0.0012). Analyses of haplotype frequencies found that people with the haplotype CACAT had a higher risk of PTB and EPTB (P = 0.00031, OR = 1.43; P = 0.000053, OR = 1.65). Moreover, the rs6446993 polymorphism of the EREG gene was found to be associated with EPTB (P = 0.00087, OR = 1.54; 95% CI = 1.23–1.94). CONCLUSIONS: Compared to that of healthy controls, the level of EREG in the plasma of TB patients increased significantly. Based on these data, we demonstrated that EREG polymorphisms are genetic factors for susceptibility to TB and various forms of TB. BioMed Central 2019-01-11 /pmc/articles/PMC6329172/ /pubmed/30634928 http://dx.doi.org/10.1186/s12881-018-0729-z Text en © The Author(s). 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Research Article
Cao, Wen
Luo, Liu-lin
Chen, Wei-wei
Liang, Li
Zhang, Ran-ran
Zhao, Yan-lin
Chen, Jin
Yue, Jun
Polymorphism in the EREG gene confers susceptibility to tuberculosis
title Polymorphism in the EREG gene confers susceptibility to tuberculosis
title_full Polymorphism in the EREG gene confers susceptibility to tuberculosis
title_fullStr Polymorphism in the EREG gene confers susceptibility to tuberculosis
title_full_unstemmed Polymorphism in the EREG gene confers susceptibility to tuberculosis
title_short Polymorphism in the EREG gene confers susceptibility to tuberculosis
title_sort polymorphism in the ereg gene confers susceptibility to tuberculosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329172/
https://www.ncbi.nlm.nih.gov/pubmed/30634928
http://dx.doi.org/10.1186/s12881-018-0729-z
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