Clinical significance of the CCR5delta32 allele in hepatitis C.

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State: Public
Version: author
Serval ID
serval:BIB_11E09D3E99D4
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Clinical significance of the CCR5delta32 allele in hepatitis C.
Journal
Plos One
Author(s)
Morard I., Clément S., Calmy A., Mangia A., Cerny A., De Gottardi A., Gorgievski M., Heim M., Malinverni R., Moradpour D., Müllhaupt B., Semela D., Pascarella S., Bochud P.Y., Negro F.
Working group(s)
Swiss Hepatitis C Cohort Study Group
ISSN
1932-6203 (Electronic)
ISSN-L
1932-6203
Publication state
Published
Issued date
2014
Peer-reviewed
Oui
Volume
9
Number
9
Pages
e106424
Language
english
Notes
Publication types: Journal Article ; Multicenter Study ; Research Support, Non-U.S. Gov't
Publication Status: epublish
Abstract
BACKGROUND: The CCR5 receptor, expressed on Th1 cells, may influence clinical outcomes of HCV infection. We explored a possible link between a CCR5 32-base deletion (CCR5delta32), resulting in the expression of a non-functioning receptor, and clinical outcomes of HCV infection.
METHODS: CCR5 and HCV-related phenotypes were analysed in 1,290 chronically infected patients and 160 patients with spontaneous clearance.
RESULTS: Carriage of the CCR5delta32 allele was observed in 11% of spontaneous clearers compared to 17% of chronically infected patients (OR = 0.59, 95% CI interval 0.35-0.99, P = 0.047). Carriage of this allele also tended to be observed more frequently among patients with liver inflammation (19%) compared to those without inflammation (15%, OR = 1.38, 95% CI interval 0.99-1.95, P = 0.06). The CCR5delta32 was not associated with sustained virological response (P = 0.6), fibrosis stage (P = 0.8), or fibrosis progression rate (P = 0.4).
CONCLUSIONS: The CCR5delta32 allele appears to be associated with a decreased rate of spontaneous HCV eradication, but not with hepatitis progression or response to antiviral therapy.
Keywords
Alleles, Disease Progression, Female, Genotype, Hepacivirus/genetics, Hepatitis C/complications, Hepatitis C/diagnosis, Humans, Liver/metabolism, Liver/pathology, Male, Mutation, Patient Outcome Assessment, Phenotype, Receptors, CCR5/genetics
Pubmed
Web of science
Open Access
Yes
Create date
15/11/2014 10:53
Last modification date
20/08/2019 12:39
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