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Variations in DEPDC5 gene and its association with chronic hepatitis C virus infection in Saudi Arabia
BACKGROUND: Variations at DEPDC5 gene have been recently reported as genetic markers associated with hepatocellular carcinoma (HCC) progression in chronic HCV-infected patients. This study was conducted to assess the association of DEPDC5 variants with advanced liver cirrhosis and HCC development am...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4311515/ https://www.ncbi.nlm.nih.gov/pubmed/25551790 http://dx.doi.org/10.1186/s12879-014-0632-y |
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author | Al-Anazi, Mashael R Matou-Nasri, Sabine Abdo, Ayman A Sanai, Faisal M Khan, Mohammed Q Albenmousa, Ali Al-Ashgar, Hamad I Khalaf, Nisreen Z Al-Ahdal, Mohammed N Al-Qahtani, Ahmed A |
author_facet | Al-Anazi, Mashael R Matou-Nasri, Sabine Abdo, Ayman A Sanai, Faisal M Khan, Mohammed Q Albenmousa, Ali Al-Ashgar, Hamad I Khalaf, Nisreen Z Al-Ahdal, Mohammed N Al-Qahtani, Ahmed A |
author_sort | Al-Anazi, Mashael R |
collection | PubMed |
description | BACKGROUND: Variations at DEPDC5 gene have been recently reported as genetic markers associated with hepatocellular carcinoma (HCC) progression in chronic HCV-infected patients. This study was conducted to assess the association of DEPDC5 variants with advanced liver cirrhosis and HCC development among chronic HCV-infected patients in Saudi Arabian population. METHODS: Six-hundred and one HCV-infected patients were genotyped for DEPDC5 polymorphisms (rs1012068 and rs5998152), in comparison with 592 non-infected healthy control subjects. The allelic frequency and genotype distribution of both DEPDC5 polymorphisms were determined followed by haplotype frequency estimation and multiple logistic regression analysis. RESULTS: The frequency of the risk alleles of both rs1012068 and rs5998152 was shown to be more in healthy control subjects than in patients (p = 0.0001, OR = 0.704, CI = 0.591-0.839; p = 0.002, OR = 0.761, CI = 0. 0.639-0.907, respectively). Also, our results revealed that GT for SNP rs1012068 (OR =1.715; 95% CI 1.132-2.597; p = 0.0104) and CT for SNP rs5998152 (OR = 1.932; 95% CI 1.276-2.925; p = 0.0017) showed significant association with development of cirrhosis compared with the GG and CC genotypes, respectively. The data also revealed that subjects with the T allele of both SNPs appeared to have a lower susceptibility to HCV-related cirrhosis/HCC than those with the G allele of rs1012068 (p = 0.038, OR = 1.353, 95 % CI 1.017-1.800) and C allele of rs5998152 (p = 0.043, OR = 1.342, 95 % CI 1.010-1.784). Haplotype analysis showed that a combination of T-T alleles of rs1012068 and rs5998152 was significantly associated with liver cirrhosis (frequency = 71.3% and p = 0.027) and with cirrhosis/HCC (frequency = 71.4% and P = 0.045). Also, multiple logistic regression analysis showed that rs5998152 (OR = 2.844, 95% CI 1.333-6.069 and p = 0.007), rs1012068 (OR = 2.793, 95% CI 1.316-5.928 and p = 0.010), age (OR = 1.029, 95% CI 1.001-1.057 and p = 0.041) and HCV genotypes (OR = 0.247, 95% CI 0.097-0.630 and p = 0.003) were independently associated with chronicity of HCV infection. CONCLUSION: Genetic variations in DEPDC5 gene region may influence HCV-associated liver cirrhosis and/or HCC development. |
format | Online Article Text |
id | pubmed-4311515 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43115152015-01-31 Variations in DEPDC5 gene and its association with chronic hepatitis C virus infection in Saudi Arabia Al-Anazi, Mashael R Matou-Nasri, Sabine Abdo, Ayman A Sanai, Faisal M Khan, Mohammed Q Albenmousa, Ali Al-Ashgar, Hamad I Khalaf, Nisreen Z Al-Ahdal, Mohammed N Al-Qahtani, Ahmed A BMC Infect Dis Research Article BACKGROUND: Variations at DEPDC5 gene have been recently reported as genetic markers associated with hepatocellular carcinoma (HCC) progression in chronic HCV-infected patients. This study was conducted to assess the association of DEPDC5 variants with advanced liver cirrhosis and HCC development among chronic HCV-infected patients in Saudi Arabian population. METHODS: Six-hundred and one HCV-infected patients were genotyped for DEPDC5 polymorphisms (rs1012068 and rs5998152), in comparison with 592 non-infected healthy control subjects. The allelic frequency and genotype distribution of both DEPDC5 polymorphisms were determined followed by haplotype frequency estimation and multiple logistic regression analysis. RESULTS: The frequency of the risk alleles of both rs1012068 and rs5998152 was shown to be more in healthy control subjects than in patients (p = 0.0001, OR = 0.704, CI = 0.591-0.839; p = 0.002, OR = 0.761, CI = 0. 0.639-0.907, respectively). Also, our results revealed that GT for SNP rs1012068 (OR =1.715; 95% CI 1.132-2.597; p = 0.0104) and CT for SNP rs5998152 (OR = 1.932; 95% CI 1.276-2.925; p = 0.0017) showed significant association with development of cirrhosis compared with the GG and CC genotypes, respectively. The data also revealed that subjects with the T allele of both SNPs appeared to have a lower susceptibility to HCV-related cirrhosis/HCC than those with the G allele of rs1012068 (p = 0.038, OR = 1.353, 95 % CI 1.017-1.800) and C allele of rs5998152 (p = 0.043, OR = 1.342, 95 % CI 1.010-1.784). Haplotype analysis showed that a combination of T-T alleles of rs1012068 and rs5998152 was significantly associated with liver cirrhosis (frequency = 71.3% and p = 0.027) and with cirrhosis/HCC (frequency = 71.4% and P = 0.045). Also, multiple logistic regression analysis showed that rs5998152 (OR = 2.844, 95% CI 1.333-6.069 and p = 0.007), rs1012068 (OR = 2.793, 95% CI 1.316-5.928 and p = 0.010), age (OR = 1.029, 95% CI 1.001-1.057 and p = 0.041) and HCV genotypes (OR = 0.247, 95% CI 0.097-0.630 and p = 0.003) were independently associated with chronicity of HCV infection. CONCLUSION: Genetic variations in DEPDC5 gene region may influence HCV-associated liver cirrhosis and/or HCC development. BioMed Central 2014-12-31 /pmc/articles/PMC4311515/ /pubmed/25551790 http://dx.doi.org/10.1186/s12879-014-0632-y Text en © Al-Anazi et al.; licensee Biomed Central. 2014 This article is published under license to BioMed Central Ltd. 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 | Research Article Al-Anazi, Mashael R Matou-Nasri, Sabine Abdo, Ayman A Sanai, Faisal M Khan, Mohammed Q Albenmousa, Ali Al-Ashgar, Hamad I Khalaf, Nisreen Z Al-Ahdal, Mohammed N Al-Qahtani, Ahmed A Variations in DEPDC5 gene and its association with chronic hepatitis C virus infection in Saudi Arabia |
title | Variations in DEPDC5 gene and its association with chronic hepatitis C virus infection in Saudi Arabia |
title_full | Variations in DEPDC5 gene and its association with chronic hepatitis C virus infection in Saudi Arabia |
title_fullStr | Variations in DEPDC5 gene and its association with chronic hepatitis C virus infection in Saudi Arabia |
title_full_unstemmed | Variations in DEPDC5 gene and its association with chronic hepatitis C virus infection in Saudi Arabia |
title_short | Variations in DEPDC5 gene and its association with chronic hepatitis C virus infection in Saudi Arabia |
title_sort | variations in depdc5 gene and its association with chronic hepatitis c virus infection in saudi arabia |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4311515/ https://www.ncbi.nlm.nih.gov/pubmed/25551790 http://dx.doi.org/10.1186/s12879-014-0632-y |
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