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CATT polymorphism in MIF gene promoter is closely related to human pulmonary tuberculosis in a southwestern China population
Macrophage migration inhibitory factor (MIF) is deemed as an immunoregulatory and proinflammatory cytokine related to the progression of tuberculosis. A CATT short tandem repeat (STR) polymorphism at position −794 in the MIF gene promoter region is associated with the susceptibility to tuberculosis...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5977431/ https://www.ncbi.nlm.nih.gov/pubmed/29809055 http://dx.doi.org/10.1177/2058738418777108 |
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author | Liu, Aihua Bao, Fukai Voravuthikunchai, Supayang P |
author_facet | Liu, Aihua Bao, Fukai Voravuthikunchai, Supayang P |
author_sort | Liu, Aihua |
collection | PubMed |
description | Macrophage migration inhibitory factor (MIF) is deemed as an immunoregulatory and proinflammatory cytokine related to the progression of tuberculosis. A CATT short tandem repeat (STR) polymorphism at position −794 in the MIF gene promoter region is associated with the susceptibility to tuberculosis (TB). To investigate whether macrophage MIF gene mif CATT variants are associated with susceptibility to retreatment cases of TB and drug-resistant TB prevalence, genotyping of MIF −794 CATT polymorphism and quantifying of serum MIF were performed to associate MIF−794 CATT polymorphism with new patients and retreatment cases. Significant increases in MIF −794 CATT genotypes 7/8 and allele CATT 8 were observed in TB patients. Significant differences in the genotypic frequencies of MIF −794 CATT (5/X + 6/X vs 7/7 + 7/8) were demonstrated upon comparing the total cases and the new cases of TB with the controls. Significant differences in the allelic frequencies of MIF −794 CATT (5 + 6 vs 7 + 8) were observed in the total cases and new cases of TB. No differences in the genotypic frequencies of the MIF −794 CATT (5/X + 6/X vs 7/7 + 7/8) were observed between the retreatment cases and the controls or between the new cases and retreatment cases. In conclusion, the MIF −794 CATT genotypes 7/8 and allele CATT 8 were highly associated with TB; no differences in the genotypic frequencies of the MIF −794 CATT (5/X + 6/X vs 7/7 + 7/8) were observed between the new cases and retreatment cases. |
format | Online Article Text |
id | pubmed-5977431 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-59774312019-03-14 CATT polymorphism in MIF gene promoter is closely related to human pulmonary tuberculosis in a southwestern China population Liu, Aihua Bao, Fukai Voravuthikunchai, Supayang P Int J Immunopathol Pharmacol Letter to the Editor Macrophage migration inhibitory factor (MIF) is deemed as an immunoregulatory and proinflammatory cytokine related to the progression of tuberculosis. A CATT short tandem repeat (STR) polymorphism at position −794 in the MIF gene promoter region is associated with the susceptibility to tuberculosis (TB). To investigate whether macrophage MIF gene mif CATT variants are associated with susceptibility to retreatment cases of TB and drug-resistant TB prevalence, genotyping of MIF −794 CATT polymorphism and quantifying of serum MIF were performed to associate MIF−794 CATT polymorphism with new patients and retreatment cases. Significant increases in MIF −794 CATT genotypes 7/8 and allele CATT 8 were observed in TB patients. Significant differences in the genotypic frequencies of MIF −794 CATT (5/X + 6/X vs 7/7 + 7/8) were demonstrated upon comparing the total cases and the new cases of TB with the controls. Significant differences in the allelic frequencies of MIF −794 CATT (5 + 6 vs 7 + 8) were observed in the total cases and new cases of TB. No differences in the genotypic frequencies of the MIF −794 CATT (5/X + 6/X vs 7/7 + 7/8) were observed between the retreatment cases and the controls or between the new cases and retreatment cases. In conclusion, the MIF −794 CATT genotypes 7/8 and allele CATT 8 were highly associated with TB; no differences in the genotypic frequencies of the MIF −794 CATT (5/X + 6/X vs 7/7 + 7/8) were observed between the new cases and retreatment cases. SAGE Publications 2018-05-29 /pmc/articles/PMC5977431/ /pubmed/29809055 http://dx.doi.org/10.1177/2058738418777108 Text en © The Author(s) 2018 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Letter to the Editor Liu, Aihua Bao, Fukai Voravuthikunchai, Supayang P CATT polymorphism in MIF gene promoter is closely related to human pulmonary tuberculosis in a southwestern China population |
title | CATT polymorphism in MIF gene promoter
is closely related to human pulmonary tuberculosis in a southwestern China
population |
title_full | CATT polymorphism in MIF gene promoter
is closely related to human pulmonary tuberculosis in a southwestern China
population |
title_fullStr | CATT polymorphism in MIF gene promoter
is closely related to human pulmonary tuberculosis in a southwestern China
population |
title_full_unstemmed | CATT polymorphism in MIF gene promoter
is closely related to human pulmonary tuberculosis in a southwestern China
population |
title_short | CATT polymorphism in MIF gene promoter
is closely related to human pulmonary tuberculosis in a southwestern China
population |
title_sort | catt polymorphism in mif gene promoter
is closely related to human pulmonary tuberculosis in a southwestern china
population |
topic | Letter to the Editor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5977431/ https://www.ncbi.nlm.nih.gov/pubmed/29809055 http://dx.doi.org/10.1177/2058738418777108 |
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