The tumor necrosis factor α (-308 A/G) polymorphism is associated with cystic fibrosis in Mexican patients.

<h4>Unlabelled</h4>Environmental and genetic factors may modify or contribute to the phenotypic differences observed in multigenic and monogenic diseases, such as cystic fibrosis (CF). An analysis of modifier genes can be helpful for estimating patient prognosis and directing preventive...

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Autores principales: Celia N Sanchez-Dominguez, Miguel A Reyes-Lopez, Adriana Bustamante, Ricardo M Cerda-Flores, Maria Del C Villalobos-Torres, Hugo L Gallardo-Blanco, Augusto Rojas-Martinez, Herminia G Martinez-Rodriguez, Hugo A Barrera-Saldaña, Rocio Ortiz-Lopez
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Publicado: Public Library of Science (PLoS) 2014
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spelling oai:doaj.org-article:b271aec9d93a4daca8f8f59b74fbe4722021-11-18T08:29:19ZThe tumor necrosis factor α (-308 A/G) polymorphism is associated with cystic fibrosis in Mexican patients.1932-620310.1371/journal.pone.0090945https://doaj.org/article/b271aec9d93a4daca8f8f59b74fbe4722014-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24603877/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Unlabelled</h4>Environmental and genetic factors may modify or contribute to the phenotypic differences observed in multigenic and monogenic diseases, such as cystic fibrosis (CF). An analysis of modifier genes can be helpful for estimating patient prognosis and directing preventive care. The aim of this study is to determine the association between seven genetic variants of four modifier genes and CF by comparing their corresponding allelic and genotypic frequencies in CF patients (n = 81) and control subjects (n = 104). Genetic variants of MBL2 exon 1 (A, B, C and D), the IL-8 promoter (-251 A/T), the TNFα promoter (TNF1/TNF2), and SERPINA1 (PI*Z and PI*S) were tested in CF patients and control subjects from northeastern Mexico by PCR-RFLP.<h4>Results</h4>The TNF2 allele (P = 0.012, OR 3.43, 95% CI 1.25-9.38) was significantly associated with CF under the dominant and additive models but was not associated with CF under the recessive model. This association remained statistically significant after adjusting for multiple tests using the Bonferroni correction (P = 0.0482). The other tested variants and genotypes did not show any association with the disease.<h4>Conclusion</h4>An analysis of seven genetic variants of four modifier genes showed that one variant, the TNF2 allele, appears to be significantly associated with CF in Mexican patients.Celia N Sanchez-DominguezMiguel A Reyes-LopezAdriana BustamanteRicardo M Cerda-FloresMaria Del C Villalobos-TorresHugo L Gallardo-BlancoAugusto Rojas-MartinezHerminia G Martinez-RodriguezHugo A Barrera-SaldañaRocio Ortiz-LopezPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 9, Iss 3, p e90945 (2014)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Celia N Sanchez-Dominguez
Miguel A Reyes-Lopez
Adriana Bustamante
Ricardo M Cerda-Flores
Maria Del C Villalobos-Torres
Hugo L Gallardo-Blanco
Augusto Rojas-Martinez
Herminia G Martinez-Rodriguez
Hugo A Barrera-Saldaña
Rocio Ortiz-Lopez
The tumor necrosis factor α (-308 A/G) polymorphism is associated with cystic fibrosis in Mexican patients.
description <h4>Unlabelled</h4>Environmental and genetic factors may modify or contribute to the phenotypic differences observed in multigenic and monogenic diseases, such as cystic fibrosis (CF). An analysis of modifier genes can be helpful for estimating patient prognosis and directing preventive care. The aim of this study is to determine the association between seven genetic variants of four modifier genes and CF by comparing their corresponding allelic and genotypic frequencies in CF patients (n = 81) and control subjects (n = 104). Genetic variants of MBL2 exon 1 (A, B, C and D), the IL-8 promoter (-251 A/T), the TNFα promoter (TNF1/TNF2), and SERPINA1 (PI*Z and PI*S) were tested in CF patients and control subjects from northeastern Mexico by PCR-RFLP.<h4>Results</h4>The TNF2 allele (P = 0.012, OR 3.43, 95% CI 1.25-9.38) was significantly associated with CF under the dominant and additive models but was not associated with CF under the recessive model. This association remained statistically significant after adjusting for multiple tests using the Bonferroni correction (P = 0.0482). The other tested variants and genotypes did not show any association with the disease.<h4>Conclusion</h4>An analysis of seven genetic variants of four modifier genes showed that one variant, the TNF2 allele, appears to be significantly associated with CF in Mexican patients.
format article
author Celia N Sanchez-Dominguez
Miguel A Reyes-Lopez
Adriana Bustamante
Ricardo M Cerda-Flores
Maria Del C Villalobos-Torres
Hugo L Gallardo-Blanco
Augusto Rojas-Martinez
Herminia G Martinez-Rodriguez
Hugo A Barrera-Saldaña
Rocio Ortiz-Lopez
author_facet Celia N Sanchez-Dominguez
Miguel A Reyes-Lopez
Adriana Bustamante
Ricardo M Cerda-Flores
Maria Del C Villalobos-Torres
Hugo L Gallardo-Blanco
Augusto Rojas-Martinez
Herminia G Martinez-Rodriguez
Hugo A Barrera-Saldaña
Rocio Ortiz-Lopez
author_sort Celia N Sanchez-Dominguez
title The tumor necrosis factor α (-308 A/G) polymorphism is associated with cystic fibrosis in Mexican patients.
title_short The tumor necrosis factor α (-308 A/G) polymorphism is associated with cystic fibrosis in Mexican patients.
title_full The tumor necrosis factor α (-308 A/G) polymorphism is associated with cystic fibrosis in Mexican patients.
title_fullStr The tumor necrosis factor α (-308 A/G) polymorphism is associated with cystic fibrosis in Mexican patients.
title_full_unstemmed The tumor necrosis factor α (-308 A/G) polymorphism is associated with cystic fibrosis in Mexican patients.
title_sort tumor necrosis factor α (-308 a/g) polymorphism is associated with cystic fibrosis in mexican patients.
publisher Public Library of Science (PLoS)
publishDate 2014
url https://doaj.org/article/b271aec9d93a4daca8f8f59b74fbe472
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