The X-ray repair cross complementing protein 1 (XRCC1) rs25487 polymorphism and susceptibility to cirrhosis in Brazilian patients with chronic viral hepatitis

Introduction. The progression of hepatic disease in chronic viral hepatitis is accompanied by an increased production of reactive oxygen species (ROS), as well as an accumulation of oxidative DNA damage, which is primarily repaired through base excision repair. XRCC1 (X-ray repair cross complementin...

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Main Authors: Samantha Therezinha Almeida Pereira Leite, Nathália Marques-Guimarães, Júlio César Silva-Oliveira, Francisco José Dutra-Souto, Raquel Alves-dos-Santos, Carmen Lucia Bassi-Branco
Format: Article
Language:English
Published: Elsevier 2013-09-01
Series:Annals of Hepatology
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1665268119313146
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spelling doaj-bcc250321cba45998f82676a6d76daaf2021-06-09T05:54:06ZengElsevierAnnals of Hepatology1665-26812013-09-01125733739The X-ray repair cross complementing protein 1 (XRCC1) rs25487 polymorphism and susceptibility to cirrhosis in Brazilian patients with chronic viral hepatitisSamantha Therezinha Almeida Pereira Leite0Nathália Marques-Guimarães1Júlio César Silva-Oliveira2Francisco José Dutra-Souto3Raquel Alves-dos-Santos4Carmen Lucia Bassi-Branco5Pós-graduação em Ciencias da Saúde, Faculdade de Medicina (FM/UFMT), Cuiabá, BrazilFM/UFMT, Cuiabá, BrazilFM/UFMT, Cuiabá, BrazilDepartamento de Clínica Médica, FM/UFMT, Cuiabá, BrazilPós-graduação em Ciencias, Universidade de Franca (UNIFRAN), Franca, BrazilDepartamento de Ciências Básicas em Saúde, FM/UFMT, Cuiabá, Brazil; Correspondence and reprint request:Introduction. The progression of hepatic disease in chronic viral hepatitis is accompanied by an increased production of reactive oxygen species (ROS), as well as an accumulation of oxidative DNA damage, which is primarily repaired through base excision repair. XRCC1 (X-ray repair cross complementing protein 1) is one of the most important proteins involved in this repair pathway. The present study was carried out to verify the possible association of the XRCC1 rs25487 polymorphism with cirrhosis in patients from Central-West Brazil.Material and methods. A total of 227 individuals with viral hepatitis, 53 cirrhotic and 174 non-cirrhotic, were genotyped for the XRCC1 rs25487 polymorphism using PCR-RFLP. Results: There were significantly higher frequencies of both the Arg/Gln genotype and of individuals with at least one Gln allele (Arg/ Gln+Gln/Gln) among cirrhotic patients (56.6% and 69.8%) compared with non-cirrhotic patients (25.8% and 37.9%). Both conditions were significantly associated with cirrhosis, independent of age, sex, alcohol intake or tobacco use (adjusted OR = 3.5, CI = 1.7–7.4, p = 0.001 and adjusted OR = 3.1, CI = 1.5–6.3, p = 0.002, respectively). Similar results were obtained for a group of HCV-infected patients but not for HBV-in-fected patients. Conclusions. The XRCC1 rs25487 polymorphism may influence the development of cirrhosis in viral hepatitis patients, and additional investigation will be necessary.http://www.sciencedirect.com/science/article/pii/S1665268119313146DNA repairChronic hepatitis BChronic hepatitis CLiver cirrhosisSingle nucleotide polymorphism
collection DOAJ
language English
format Article
sources DOAJ
author Samantha Therezinha Almeida Pereira Leite
Nathália Marques-Guimarães
Júlio César Silva-Oliveira
Francisco José Dutra-Souto
Raquel Alves-dos-Santos
Carmen Lucia Bassi-Branco
spellingShingle Samantha Therezinha Almeida Pereira Leite
Nathália Marques-Guimarães
Júlio César Silva-Oliveira
Francisco José Dutra-Souto
Raquel Alves-dos-Santos
Carmen Lucia Bassi-Branco
The X-ray repair cross complementing protein 1 (XRCC1) rs25487 polymorphism and susceptibility to cirrhosis in Brazilian patients with chronic viral hepatitis
Annals of Hepatology
DNA repair
Chronic hepatitis B
Chronic hepatitis C
Liver cirrhosis
Single nucleotide polymorphism
author_facet Samantha Therezinha Almeida Pereira Leite
Nathália Marques-Guimarães
Júlio César Silva-Oliveira
Francisco José Dutra-Souto
Raquel Alves-dos-Santos
Carmen Lucia Bassi-Branco
author_sort Samantha Therezinha Almeida Pereira Leite
title The X-ray repair cross complementing protein 1 (XRCC1) rs25487 polymorphism and susceptibility to cirrhosis in Brazilian patients with chronic viral hepatitis
title_short The X-ray repair cross complementing protein 1 (XRCC1) rs25487 polymorphism and susceptibility to cirrhosis in Brazilian patients with chronic viral hepatitis
title_full The X-ray repair cross complementing protein 1 (XRCC1) rs25487 polymorphism and susceptibility to cirrhosis in Brazilian patients with chronic viral hepatitis
title_fullStr The X-ray repair cross complementing protein 1 (XRCC1) rs25487 polymorphism and susceptibility to cirrhosis in Brazilian patients with chronic viral hepatitis
title_full_unstemmed The X-ray repair cross complementing protein 1 (XRCC1) rs25487 polymorphism and susceptibility to cirrhosis in Brazilian patients with chronic viral hepatitis
title_sort x-ray repair cross complementing protein 1 (xrcc1) rs25487 polymorphism and susceptibility to cirrhosis in brazilian patients with chronic viral hepatitis
publisher Elsevier
series Annals of Hepatology
issn 1665-2681
publishDate 2013-09-01
description Introduction. The progression of hepatic disease in chronic viral hepatitis is accompanied by an increased production of reactive oxygen species (ROS), as well as an accumulation of oxidative DNA damage, which is primarily repaired through base excision repair. XRCC1 (X-ray repair cross complementing protein 1) is one of the most important proteins involved in this repair pathway. The present study was carried out to verify the possible association of the XRCC1 rs25487 polymorphism with cirrhosis in patients from Central-West Brazil.Material and methods. A total of 227 individuals with viral hepatitis, 53 cirrhotic and 174 non-cirrhotic, were genotyped for the XRCC1 rs25487 polymorphism using PCR-RFLP. Results: There were significantly higher frequencies of both the Arg/Gln genotype and of individuals with at least one Gln allele (Arg/ Gln+Gln/Gln) among cirrhotic patients (56.6% and 69.8%) compared with non-cirrhotic patients (25.8% and 37.9%). Both conditions were significantly associated with cirrhosis, independent of age, sex, alcohol intake or tobacco use (adjusted OR = 3.5, CI = 1.7–7.4, p = 0.001 and adjusted OR = 3.1, CI = 1.5–6.3, p = 0.002, respectively). Similar results were obtained for a group of HCV-infected patients but not for HBV-in-fected patients. Conclusions. The XRCC1 rs25487 polymorphism may influence the development of cirrhosis in viral hepatitis patients, and additional investigation will be necessary.
topic DNA repair
Chronic hepatitis B
Chronic hepatitis C
Liver cirrhosis
Single nucleotide polymorphism
url http://www.sciencedirect.com/science/article/pii/S1665268119313146
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