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Analysis of IL28B Variants in an Egyptian Population Defines the 20 Kilobases Minimal Region Involved in Spontaneous Clearance of Hepatitis C Virus

Spontaneous clearance of hepatitis C virus (HCV) occurs in ∼30% of acute infections. Host genetics play a major role in HCV clearance, with a strong effect of single nucleotide polymorphisms (SNPs) of the IL28B gene already found in different populations, mostly infected with viral genotypes 1 and 3...

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Autores principales: Pedergnana, Vincent, Abdel-Hamid, Mohamed, Guergnon, Julien, Mohsen, Amira, Le Fouler, Lénaïg, Theodorou, Ioannis, Mohamed, Mostafa Kamal, Fontanet, Arnaud, Plancoulaine, Sabine, Abel, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3375300/
https://www.ncbi.nlm.nih.gov/pubmed/22719902
http://dx.doi.org/10.1371/journal.pone.0038578
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author Pedergnana, Vincent
Abdel-Hamid, Mohamed
Guergnon, Julien
Mohsen, Amira
Le Fouler, Lénaïg
Theodorou, Ioannis
Mohamed, Mostafa Kamal
Fontanet, Arnaud
Plancoulaine, Sabine
Abel, Laurent
author_facet Pedergnana, Vincent
Abdel-Hamid, Mohamed
Guergnon, Julien
Mohsen, Amira
Le Fouler, Lénaïg
Theodorou, Ioannis
Mohamed, Mostafa Kamal
Fontanet, Arnaud
Plancoulaine, Sabine
Abel, Laurent
author_sort Pedergnana, Vincent
collection PubMed
description Spontaneous clearance of hepatitis C virus (HCV) occurs in ∼30% of acute infections. Host genetics play a major role in HCV clearance, with a strong effect of single nucleotide polymorphisms (SNPs) of the IL28B gene already found in different populations, mostly infected with viral genotypes 1 and 3. Egypt has the highest prevalence of HCV infection in the world, which is mostly due to viral genotype 4. We investigated the role of several IL28B SNPs in HCV spontaneous clearance in an Egyptian population. We selected nine SNPs within the IL28B genomic region covering the linkage disequilibrium (LD) block known to be associated with HCV clearance in European populations. These SNPs were genotyped in 261 HCV-infected Egyptian subjects (130 with spontaneous clearance and 131 with chronic infection). The most associated SNPs were rs12979860 (P = 1.6×10(−7)) and the non-synonymous IL28B SNP, rs8103142 (P = 1.6×10(−7)). Interestingly, three SNPs at the two bounds of the region were monomorphic, reducing the size of the LD block in which the causal variants are potentially located to ∼20 kilobases. HCV clearance in Egypt was associated with a region of IL28B smaller than that identified in European populations, and involved the non-synonymous IL28B SNP, rs8103142.
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spelling pubmed-33753002012-06-20 Analysis of IL28B Variants in an Egyptian Population Defines the 20 Kilobases Minimal Region Involved in Spontaneous Clearance of Hepatitis C Virus Pedergnana, Vincent Abdel-Hamid, Mohamed Guergnon, Julien Mohsen, Amira Le Fouler, Lénaïg Theodorou, Ioannis Mohamed, Mostafa Kamal Fontanet, Arnaud Plancoulaine, Sabine Abel, Laurent PLoS One Research Article Spontaneous clearance of hepatitis C virus (HCV) occurs in ∼30% of acute infections. Host genetics play a major role in HCV clearance, with a strong effect of single nucleotide polymorphisms (SNPs) of the IL28B gene already found in different populations, mostly infected with viral genotypes 1 and 3. Egypt has the highest prevalence of HCV infection in the world, which is mostly due to viral genotype 4. We investigated the role of several IL28B SNPs in HCV spontaneous clearance in an Egyptian population. We selected nine SNPs within the IL28B genomic region covering the linkage disequilibrium (LD) block known to be associated with HCV clearance in European populations. These SNPs were genotyped in 261 HCV-infected Egyptian subjects (130 with spontaneous clearance and 131 with chronic infection). The most associated SNPs were rs12979860 (P = 1.6×10(−7)) and the non-synonymous IL28B SNP, rs8103142 (P = 1.6×10(−7)). Interestingly, three SNPs at the two bounds of the region were monomorphic, reducing the size of the LD block in which the causal variants are potentially located to ∼20 kilobases. HCV clearance in Egypt was associated with a region of IL28B smaller than that identified in European populations, and involved the non-synonymous IL28B SNP, rs8103142. Public Library of Science 2012-06-14 /pmc/articles/PMC3375300/ /pubmed/22719902 http://dx.doi.org/10.1371/journal.pone.0038578 Text en Pedergnana et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Pedergnana, Vincent
Abdel-Hamid, Mohamed
Guergnon, Julien
Mohsen, Amira
Le Fouler, Lénaïg
Theodorou, Ioannis
Mohamed, Mostafa Kamal
Fontanet, Arnaud
Plancoulaine, Sabine
Abel, Laurent
Analysis of IL28B Variants in an Egyptian Population Defines the 20 Kilobases Minimal Region Involved in Spontaneous Clearance of Hepatitis C Virus
title Analysis of IL28B Variants in an Egyptian Population Defines the 20 Kilobases Minimal Region Involved in Spontaneous Clearance of Hepatitis C Virus
title_full Analysis of IL28B Variants in an Egyptian Population Defines the 20 Kilobases Minimal Region Involved in Spontaneous Clearance of Hepatitis C Virus
title_fullStr Analysis of IL28B Variants in an Egyptian Population Defines the 20 Kilobases Minimal Region Involved in Spontaneous Clearance of Hepatitis C Virus
title_full_unstemmed Analysis of IL28B Variants in an Egyptian Population Defines the 20 Kilobases Minimal Region Involved in Spontaneous Clearance of Hepatitis C Virus
title_short Analysis of IL28B Variants in an Egyptian Population Defines the 20 Kilobases Minimal Region Involved in Spontaneous Clearance of Hepatitis C Virus
title_sort analysis of il28b variants in an egyptian population defines the 20 kilobases minimal region involved in spontaneous clearance of hepatitis c virus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3375300/
https://www.ncbi.nlm.nih.gov/pubmed/22719902
http://dx.doi.org/10.1371/journal.pone.0038578
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