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Polymorphism of IFN-γ (+874 T/A) in Syrian patients with chronic hepatitis B

AIM: This study aimed to investigate the association of IFN- γ +874 (T/A) polymorphism with susceptibility to chronic HBV infection in the Syrian population. BACKGROUND: Accumulating evidence indicate that the inadequate immune responses are responsible for HBV persistency. Therefore, polymorphisms...

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Autores principales: Al Kadi, Mohamad, Monem, Fawza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shaheed Beheshti University of Medical Sciences 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346822/
https://www.ncbi.nlm.nih.gov/pubmed/28331562
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author Al Kadi, Mohamad
Monem, Fawza
author_facet Al Kadi, Mohamad
Monem, Fawza
author_sort Al Kadi, Mohamad
collection PubMed
description AIM: This study aimed to investigate the association of IFN- γ +874 (T/A) polymorphism with susceptibility to chronic HBV infection in the Syrian population. BACKGROUND: Accumulating evidence indicate that the inadequate immune responses are responsible for HBV persistency. Therefore, polymorphisms in genes encoding the cytokines, which are responsible for regulation of the immune response, can affect the course and outcome of the infection. The IFN-γ +874 T/A polymorphism affects the expression of IFN-γ, which has been shown to be crucial to HBV clearance. METHODS: In this case-control study, 140 samples were collected (70 healthy individuals, 70 chronic HBV patients), and genomic DNA was isolated. Sequencing and ARMS-PCR were performed to genotype the IFN-γ +874 T/A polymorphism. RESULTS: Results of this study showed an association between IFN- γ +874 T/A polymorphism and the susceptibility to chronic HBV infection (P < 0.05). In addition, results showed that the AA genotype increased the risk of chronicity (OR = 3.05, 95% CI = 1.35 – 6.89), whereas the AT and TT genotypes reduced the risk of chronicity (OR = 0.33, 95% CI = 0.150 – 0.753). CONCLUSION: Results of this study conclude that the IFN- γ +874 T/A polymorphism may be associated with the chronic HBV infection, according to the genetic model AA vs. AT&TT.
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spelling pubmed-53468222017-03-22 Polymorphism of IFN-γ (+874 T/A) in Syrian patients with chronic hepatitis B Al Kadi, Mohamad Monem, Fawza Gastroenterol Hepatol Bed Bench Original Article AIM: This study aimed to investigate the association of IFN- γ +874 (T/A) polymorphism with susceptibility to chronic HBV infection in the Syrian population. BACKGROUND: Accumulating evidence indicate that the inadequate immune responses are responsible for HBV persistency. Therefore, polymorphisms in genes encoding the cytokines, which are responsible for regulation of the immune response, can affect the course and outcome of the infection. The IFN-γ +874 T/A polymorphism affects the expression of IFN-γ, which has been shown to be crucial to HBV clearance. METHODS: In this case-control study, 140 samples were collected (70 healthy individuals, 70 chronic HBV patients), and genomic DNA was isolated. Sequencing and ARMS-PCR were performed to genotype the IFN-γ +874 T/A polymorphism. RESULTS: Results of this study showed an association between IFN- γ +874 T/A polymorphism and the susceptibility to chronic HBV infection (P < 0.05). In addition, results showed that the AA genotype increased the risk of chronicity (OR = 3.05, 95% CI = 1.35 – 6.89), whereas the AT and TT genotypes reduced the risk of chronicity (OR = 0.33, 95% CI = 0.150 – 0.753). CONCLUSION: Results of this study conclude that the IFN- γ +874 T/A polymorphism may be associated with the chronic HBV infection, according to the genetic model AA vs. AT&TT. Shaheed Beheshti University of Medical Sciences 2017 /pmc/articles/PMC5346822/ /pubmed/28331562 Text en ©2017 RIGLD, Research Institute for Gastroenterology and Liver Diseases This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Al Kadi, Mohamad
Monem, Fawza
Polymorphism of IFN-γ (+874 T/A) in Syrian patients with chronic hepatitis B
title Polymorphism of IFN-γ (+874 T/A) in Syrian patients with chronic hepatitis B
title_full Polymorphism of IFN-γ (+874 T/A) in Syrian patients with chronic hepatitis B
title_fullStr Polymorphism of IFN-γ (+874 T/A) in Syrian patients with chronic hepatitis B
title_full_unstemmed Polymorphism of IFN-γ (+874 T/A) in Syrian patients with chronic hepatitis B
title_short Polymorphism of IFN-γ (+874 T/A) in Syrian patients with chronic hepatitis B
title_sort polymorphism of ifn-γ (+874 t/a) in syrian patients with chronic hepatitis b
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346822/
https://www.ncbi.nlm.nih.gov/pubmed/28331562
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