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Association of tumor necrosis factor-α and -β gene polymorphisms in inflammatory bowel disease
Inflammatory bowel disease (IBD) is a complex, multifactorial, chronic inflammatory disorder of the gastrointestinal tract in which immune dysregulation caused by genetic and/or environmental factors plays an important role. The aim of this case–control study was to evaluate the association of tumor...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918894/ https://www.ncbi.nlm.nih.gov/pubmed/27382325 http://dx.doi.org/10.2147/JIR.S101225 |
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author | Al-Meghaiseeb, Ebtissam Saleh Al-Robayan, Abdulrahman A Al-Otaibi, Mulfi Mubarak Arfin, Misbahul Al-Asmari, Abdulrahman K |
author_facet | Al-Meghaiseeb, Ebtissam Saleh Al-Robayan, Abdulrahman A Al-Otaibi, Mulfi Mubarak Arfin, Misbahul Al-Asmari, Abdulrahman K |
author_sort | Al-Meghaiseeb, Ebtissam Saleh |
collection | PubMed |
description | Inflammatory bowel disease (IBD) is a complex, multifactorial, chronic inflammatory disorder of the gastrointestinal tract in which immune dysregulation caused by genetic and/or environmental factors plays an important role. The aim of this case–control study was to evaluate the association of tumor necrosis factor-alpha (TNF-α) (308) and -β (+252) polymorphisms with susceptibility of IBD. A total of 379 Saudi subjects including 179 IBD patients (ulcerative colitis (UC) =84 and Crohn’s disease (CD) =95) and 200 age- and sex-matched healthy controls were recruited. TNF-α and TNF-β genes were amplified using an amplification refractory mutation systems polymerase chain reaction methodology to detect TNF-α (−308) and -β (+252) polymorphisms. The frequency of the GA genotype of TNF-α (−308G/A) was higher, and the frequencies of the GG and AA genotypes were significantly lower in IBD patients compared with those in controls, indicating that genotype GA-positive individuals are susceptible to IBD and that the GG and AA genotypes exert a protective effect. The frequency of allele A of TNF-α (−308G/A) was significantly higher and that of allele G was lower in IBD patients compared with those in controls, indicating an association of allele A with IBD risk in Saudi patients. On stratification of IBD patients into UC and CD, an almost similar pattern was noticed in both the groups. The results of TNF-β (+252A/G) polymorphisms showed a significant increase in the frequency of the GG genotype in IBD patients, suggesting a positive association of GG genotype with IBD risk. On stratification of IBD patients into UC and CD, the genotype GG of TNF-β was associated with susceptibility risk to UC but not CD. The frequencies of alleles and genotypes of both TNF-α and-β polymorphisms are not affected by sex or type of IBD (familial or sporadic). TNF-α (−308G/A) and TNF-β (+252A/G) polymorphisms are associated with risk of developing IBD in Saudi population. |
format | Online Article Text |
id | pubmed-4918894 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-49188942016-07-05 Association of tumor necrosis factor-α and -β gene polymorphisms in inflammatory bowel disease Al-Meghaiseeb, Ebtissam Saleh Al-Robayan, Abdulrahman A Al-Otaibi, Mulfi Mubarak Arfin, Misbahul Al-Asmari, Abdulrahman K J Inflamm Res Original Research Inflammatory bowel disease (IBD) is a complex, multifactorial, chronic inflammatory disorder of the gastrointestinal tract in which immune dysregulation caused by genetic and/or environmental factors plays an important role. The aim of this case–control study was to evaluate the association of tumor necrosis factor-alpha (TNF-α) (308) and -β (+252) polymorphisms with susceptibility of IBD. A total of 379 Saudi subjects including 179 IBD patients (ulcerative colitis (UC) =84 and Crohn’s disease (CD) =95) and 200 age- and sex-matched healthy controls were recruited. TNF-α and TNF-β genes were amplified using an amplification refractory mutation systems polymerase chain reaction methodology to detect TNF-α (−308) and -β (+252) polymorphisms. The frequency of the GA genotype of TNF-α (−308G/A) was higher, and the frequencies of the GG and AA genotypes were significantly lower in IBD patients compared with those in controls, indicating that genotype GA-positive individuals are susceptible to IBD and that the GG and AA genotypes exert a protective effect. The frequency of allele A of TNF-α (−308G/A) was significantly higher and that of allele G was lower in IBD patients compared with those in controls, indicating an association of allele A with IBD risk in Saudi patients. On stratification of IBD patients into UC and CD, an almost similar pattern was noticed in both the groups. The results of TNF-β (+252A/G) polymorphisms showed a significant increase in the frequency of the GG genotype in IBD patients, suggesting a positive association of GG genotype with IBD risk. On stratification of IBD patients into UC and CD, the genotype GG of TNF-β was associated with susceptibility risk to UC but not CD. The frequencies of alleles and genotypes of both TNF-α and-β polymorphisms are not affected by sex or type of IBD (familial or sporadic). TNF-α (−308G/A) and TNF-β (+252A/G) polymorphisms are associated with risk of developing IBD in Saudi population. Dove Medical Press 2016-06-17 /pmc/articles/PMC4918894/ /pubmed/27382325 http://dx.doi.org/10.2147/JIR.S101225 Text en © 2016 Al-Meghaiseeb et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Al-Meghaiseeb, Ebtissam Saleh Al-Robayan, Abdulrahman A Al-Otaibi, Mulfi Mubarak Arfin, Misbahul Al-Asmari, Abdulrahman K Association of tumor necrosis factor-α and -β gene polymorphisms in inflammatory bowel disease |
title | Association of tumor necrosis factor-α and -β gene polymorphisms in inflammatory bowel disease |
title_full | Association of tumor necrosis factor-α and -β gene polymorphisms in inflammatory bowel disease |
title_fullStr | Association of tumor necrosis factor-α and -β gene polymorphisms in inflammatory bowel disease |
title_full_unstemmed | Association of tumor necrosis factor-α and -β gene polymorphisms in inflammatory bowel disease |
title_short | Association of tumor necrosis factor-α and -β gene polymorphisms in inflammatory bowel disease |
title_sort | association of tumor necrosis factor-α and -β gene polymorphisms in inflammatory bowel disease |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918894/ https://www.ncbi.nlm.nih.gov/pubmed/27382325 http://dx.doi.org/10.2147/JIR.S101225 |
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