Cargando…

Interferon gamma polymorphisms and hepatitis B virus-related liver cirrhosis risk in a Chinese population

BACKGROUND: Previous studies proved that interferon gamma (IFN-γ) gene polymorphisms were associated with the risk of hepatitis B virus (HBV) infection. However, the association between IFN-γ polymorphisms and HBV-related liver cirrhosis (HBV-LC) risk is still unclear. METHODS: IFN-γ +874 T/A and +2...

Descripción completa

Detalles Bibliográficos
Autores principales: Sun, Yifan, Lu, Yu, Xie, Li, Deng, Yan, Li, Shan, Qin, Xue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4389711/
https://www.ncbi.nlm.nih.gov/pubmed/25861244
http://dx.doi.org/10.1186/s12935-015-0184-2
_version_ 1782365605235523584
author Sun, Yifan
Lu, Yu
Xie, Li
Deng, Yan
Li, Shan
Qin, Xue
author_facet Sun, Yifan
Lu, Yu
Xie, Li
Deng, Yan
Li, Shan
Qin, Xue
author_sort Sun, Yifan
collection PubMed
description BACKGROUND: Previous studies proved that interferon gamma (IFN-γ) gene polymorphisms were associated with the risk of hepatitis B virus (HBV) infection. However, the association between IFN-γ polymorphisms and HBV-related liver cirrhosis (HBV-LC) risk is still unclear. METHODS: IFN-γ +874 T/A and +2109G/A genotypes were determined in 126 HBV-LC patients, 129 chronic hepatitis B(CHB) patients, and 173 early HBV infection controls using a sequence-specific primer-polymerase chain reaction and a polymerase chain reaction-restriction fragment length polymorphism, respectively. RESULTS: Significant associations were observed between +2109A/G polymorphisms and HBV-LC risk in the co-dominant model (GG vs. AA: OR = 0.321, 95% CI = 0.130-0.793, P = 0.014), the allelic model (OR = 0.565, 95% CI = 0.388-0.825, P = 0.003), the dominant model (OR = 0.551, 95% CI = 0.344-0.883, P = 0.013), and the recessive model (OR = 0.385, 95% CI = 0.159-0.930, P = 0.034). In addition, haplotype analysis indicated that the T(+874)G(+2109) haplotype significantly decreased the HBV-LC risk (OR = 0.106, 95% CI = 0.022-0.502, P = 0.000), and A(+874)A(+2109) haplotype significantly increased the LC risk (OR = 1.485, 95% CI = 1.065-2.070, P = 0.019). No significant associations were observed between IFN-γ +874 T/A polymorphisms and HBV-LC risk, as well as the two single-nucleotide polymorphisms (SNPs) and CHB risk (P > 0.05). CONCLUSIONS: Our observations suggested a significant association of IFN-γ polymorphisms with HBV-LC risk in the Chinese population.
format Online
Article
Text
id pubmed-4389711
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-43897112015-04-09 Interferon gamma polymorphisms and hepatitis B virus-related liver cirrhosis risk in a Chinese population Sun, Yifan Lu, Yu Xie, Li Deng, Yan Li, Shan Qin, Xue Cancer Cell Int Primary Research BACKGROUND: Previous studies proved that interferon gamma (IFN-γ) gene polymorphisms were associated with the risk of hepatitis B virus (HBV) infection. However, the association between IFN-γ polymorphisms and HBV-related liver cirrhosis (HBV-LC) risk is still unclear. METHODS: IFN-γ +874 T/A and +2109G/A genotypes were determined in 126 HBV-LC patients, 129 chronic hepatitis B(CHB) patients, and 173 early HBV infection controls using a sequence-specific primer-polymerase chain reaction and a polymerase chain reaction-restriction fragment length polymorphism, respectively. RESULTS: Significant associations were observed between +2109A/G polymorphisms and HBV-LC risk in the co-dominant model (GG vs. AA: OR = 0.321, 95% CI = 0.130-0.793, P = 0.014), the allelic model (OR = 0.565, 95% CI = 0.388-0.825, P = 0.003), the dominant model (OR = 0.551, 95% CI = 0.344-0.883, P = 0.013), and the recessive model (OR = 0.385, 95% CI = 0.159-0.930, P = 0.034). In addition, haplotype analysis indicated that the T(+874)G(+2109) haplotype significantly decreased the HBV-LC risk (OR = 0.106, 95% CI = 0.022-0.502, P = 0.000), and A(+874)A(+2109) haplotype significantly increased the LC risk (OR = 1.485, 95% CI = 1.065-2.070, P = 0.019). No significant associations were observed between IFN-γ +874 T/A polymorphisms and HBV-LC risk, as well as the two single-nucleotide polymorphisms (SNPs) and CHB risk (P > 0.05). CONCLUSIONS: Our observations suggested a significant association of IFN-γ polymorphisms with HBV-LC risk in the Chinese population. BioMed Central 2015-03-31 /pmc/articles/PMC4389711/ /pubmed/25861244 http://dx.doi.org/10.1186/s12935-015-0184-2 Text en © Sun et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Primary Research
Sun, Yifan
Lu, Yu
Xie, Li
Deng, Yan
Li, Shan
Qin, Xue
Interferon gamma polymorphisms and hepatitis B virus-related liver cirrhosis risk in a Chinese population
title Interferon gamma polymorphisms and hepatitis B virus-related liver cirrhosis risk in a Chinese population
title_full Interferon gamma polymorphisms and hepatitis B virus-related liver cirrhosis risk in a Chinese population
title_fullStr Interferon gamma polymorphisms and hepatitis B virus-related liver cirrhosis risk in a Chinese population
title_full_unstemmed Interferon gamma polymorphisms and hepatitis B virus-related liver cirrhosis risk in a Chinese population
title_short Interferon gamma polymorphisms and hepatitis B virus-related liver cirrhosis risk in a Chinese population
title_sort interferon gamma polymorphisms and hepatitis b virus-related liver cirrhosis risk in a chinese population
topic Primary Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4389711/
https://www.ncbi.nlm.nih.gov/pubmed/25861244
http://dx.doi.org/10.1186/s12935-015-0184-2
work_keys_str_mv AT sunyifan interferongammapolymorphismsandhepatitisbvirusrelatedlivercirrhosisriskinachinesepopulation
AT luyu interferongammapolymorphismsandhepatitisbvirusrelatedlivercirrhosisriskinachinesepopulation
AT xieli interferongammapolymorphismsandhepatitisbvirusrelatedlivercirrhosisriskinachinesepopulation
AT dengyan interferongammapolymorphismsandhepatitisbvirusrelatedlivercirrhosisriskinachinesepopulation
AT lishan interferongammapolymorphismsandhepatitisbvirusrelatedlivercirrhosisriskinachinesepopulation
AT qinxue interferongammapolymorphismsandhepatitisbvirusrelatedlivercirrhosisriskinachinesepopulation