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Association of Paraoxonase 1 Gene Polymorphisms With the Risk of Hepatitis B Virus-related Liver Diseases in a Guangxi Population: A Case-control Study

Paraoxonase 1 (PON1), a liver-induced glycoprotein enzyme responsible for antioxidant defense against reactive oxygen species and anti-inflammatory, has been linked to various cancers. The objective of this study was to explore the association of PON1 rs662 and rs705382 with the risk of chronic hepa...

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Autores principales: Lao, Xianjun, Wang, Xiaogang, Liu, Yanqiong, Lu, Yu, Yang, Dongmei, Liu, Minyan, Zhang, Xiaolian, Rong, Chengzhi, Qin, Xue, Li, Shan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4674207/
https://www.ncbi.nlm.nih.gov/pubmed/26632904
http://dx.doi.org/10.1097/MD.0000000000002179
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author Lao, Xianjun
Wang, Xiaogang
Liu, Yanqiong
Lu, Yu
Yang, Dongmei
Liu, Minyan
Zhang, Xiaolian
Rong, Chengzhi
Qin, Xue
Li, Shan
author_facet Lao, Xianjun
Wang, Xiaogang
Liu, Yanqiong
Lu, Yu
Yang, Dongmei
Liu, Minyan
Zhang, Xiaolian
Rong, Chengzhi
Qin, Xue
Li, Shan
author_sort Lao, Xianjun
collection PubMed
description Paraoxonase 1 (PON1), a liver-induced glycoprotein enzyme responsible for antioxidant defense against reactive oxygen species and anti-inflammatory, has been linked to various cancers. The objective of this study was to explore the association of PON1 rs662 and rs705382 with the risk of chronic hepatitis B (CHB), hepatitis B virus-related liver cirrhosis (LC), and hepatocellular carcinoma (HCC) in patients living in the Guangxi region of southern China. The PON1 rs662 and rs705382 single-nucleotide polymorphisms (SNPs) were genotyped by polymerase chain reaction–restriction fragment length polymorphism (PCR-RFLP) in 99 CHB patients, 84 LC patients, 258 HCC patients, and 221 healthy controls. Significant associations with CHB risk were observed for the rs705382 SNP after adjusting for sex, age, ethnicity, smoking, alcohol consumption, and body mass index. When stratified by sex and age, this positive association was significantly strengthened among men and individuals over 40 years old. Moreover, a decreased risk of LC was associated with the rs705382 CG and the combined GG + CG genotypes among women, with borderline statistical significance. In haplotype analyses, the haplotype GA was associated with a 1.68-fold increase in the risk of HCC. Our results showed that the PON1 rs705382 SNP might be a risk factor for CHB in Guangxi populations.
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spelling pubmed-46742072015-12-14 Association of Paraoxonase 1 Gene Polymorphisms With the Risk of Hepatitis B Virus-related Liver Diseases in a Guangxi Population: A Case-control Study Lao, Xianjun Wang, Xiaogang Liu, Yanqiong Lu, Yu Yang, Dongmei Liu, Minyan Zhang, Xiaolian Rong, Chengzhi Qin, Xue Li, Shan Medicine (Baltimore) 5700 Paraoxonase 1 (PON1), a liver-induced glycoprotein enzyme responsible for antioxidant defense against reactive oxygen species and anti-inflammatory, has been linked to various cancers. The objective of this study was to explore the association of PON1 rs662 and rs705382 with the risk of chronic hepatitis B (CHB), hepatitis B virus-related liver cirrhosis (LC), and hepatocellular carcinoma (HCC) in patients living in the Guangxi region of southern China. The PON1 rs662 and rs705382 single-nucleotide polymorphisms (SNPs) were genotyped by polymerase chain reaction–restriction fragment length polymorphism (PCR-RFLP) in 99 CHB patients, 84 LC patients, 258 HCC patients, and 221 healthy controls. Significant associations with CHB risk were observed for the rs705382 SNP after adjusting for sex, age, ethnicity, smoking, alcohol consumption, and body mass index. When stratified by sex and age, this positive association was significantly strengthened among men and individuals over 40 years old. Moreover, a decreased risk of LC was associated with the rs705382 CG and the combined GG + CG genotypes among women, with borderline statistical significance. In haplotype analyses, the haplotype GA was associated with a 1.68-fold increase in the risk of HCC. Our results showed that the PON1 rs705382 SNP might be a risk factor for CHB in Guangxi populations. Wolters Kluwer Health 2015-12-07 /pmc/articles/PMC4674207/ /pubmed/26632904 http://dx.doi.org/10.1097/MD.0000000000002179 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle 5700
Lao, Xianjun
Wang, Xiaogang
Liu, Yanqiong
Lu, Yu
Yang, Dongmei
Liu, Minyan
Zhang, Xiaolian
Rong, Chengzhi
Qin, Xue
Li, Shan
Association of Paraoxonase 1 Gene Polymorphisms With the Risk of Hepatitis B Virus-related Liver Diseases in a Guangxi Population: A Case-control Study
title Association of Paraoxonase 1 Gene Polymorphisms With the Risk of Hepatitis B Virus-related Liver Diseases in a Guangxi Population: A Case-control Study
title_full Association of Paraoxonase 1 Gene Polymorphisms With the Risk of Hepatitis B Virus-related Liver Diseases in a Guangxi Population: A Case-control Study
title_fullStr Association of Paraoxonase 1 Gene Polymorphisms With the Risk of Hepatitis B Virus-related Liver Diseases in a Guangxi Population: A Case-control Study
title_full_unstemmed Association of Paraoxonase 1 Gene Polymorphisms With the Risk of Hepatitis B Virus-related Liver Diseases in a Guangxi Population: A Case-control Study
title_short Association of Paraoxonase 1 Gene Polymorphisms With the Risk of Hepatitis B Virus-related Liver Diseases in a Guangxi Population: A Case-control Study
title_sort association of paraoxonase 1 gene polymorphisms with the risk of hepatitis b virus-related liver diseases in a guangxi population: a case-control study
topic 5700
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4674207/
https://www.ncbi.nlm.nih.gov/pubmed/26632904
http://dx.doi.org/10.1097/MD.0000000000002179
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