Document Detail


Carriage of the EGF rs4444903 A>G functional polymorphism associates with disease progression in chronic HBV infection.
MedLine Citation:
PMID:  22236006     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Because epidermal growth factor (EGF) up-regulation is characteristic of the cirrhotic liver, we hypothesised that the EGF rs4444903 A > G functional polymorphism might be associated with a worse disease course in patients with chronic HBV infection. To verify this hypothesis, 170 HBV-positive patients (125 males) with a median age of 52 years were studied. Sixty-two of these patients were followed longitudinally for a median time of 21 years. Genotyping for the EGF rs4444903 A > G polymorphism was performed by the polymerase chain reaction-based restriction fragment length polymorphism assay. In the cross-sectional study, the EGF rs4444903 A > G polymorphism genotypic frequencies significantly differed between transplant patients (A/A = 20·4%, A/G = 52·3%, G/G = 27·3%) and HBsAg+ carriers (active and inactive: A/A = 35·7%, A/G = 47·6%, G/G = 16·7%, P = 0·036 for the linear trend). In the longitudinal study, the EGF rs4444903 A > G polymorphism was found to be an independent predictor of cirrhosis development (O.R. 7·73, 95% C.I. 1·21-49·5, P = 0·007). Three groups of patients were identified: A/A female homozygotes (n = 9), A/A male homozygotes (n = 13) and carriers of the G allele of either gender (n = 40). Cirrhosis did not occur among A/A females (n = 0/9), seldom occurred among A/A males (n = 2/13) and reached the highest frequency among G/* patients (n = 13/40, P = 0·026). In conclusion, the EGF rs4444903 A > G polymorphism appears to be associated with an unfavourable disease course of chronic HBV infection and cirrhosis development. This effect might be modulated, at least in part, by the gender of the patient.
Authors:
S Cmet; C Fabris; G Fattovich; E Falleti; D Bitetto; A Cussigh; E Fontanini; E Fornasiere; M Pirisi; P Toniutto
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Clinical and experimental immunology     Volume:  167     ISSN:  1365-2249     ISO Abbreviation:  Clin. Exp. Immunol.     Publication Date:  2012 Feb 
Date Detail:
Created Date:  2012-01-12     Completed Date:  2012-03-05     Revised Date:  2013-06-26    
Medline Journal Info:
Nlm Unique ID:  0057202     Medline TA:  Clin Exp Immunol     Country:  England    
Other Details:
Languages:  eng     Pagination:  296-302     Citation Subset:  IM    
Copyright Information:
© 2012 The Authors. Clinical and Experimental Immunology © 2012 British Society for Immunology.
Affiliation:
Laboratory Medicine, Department of Medical Sciences, Clinical and Experimental, University of Udine, Udine, Italy.
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MeSH Terms
Descriptor/Qualifier:
5' Untranslated Regions / genetics*
Adolescent
Adult
Aged
Aged, 80 and over
Alleles
Cross-Sectional Studies
Disease Progression
Epidermal Growth Factor / genetics*
Female
Gene Frequency
Genetic Predisposition to Disease
Genotype
Hepatitis B, Chronic / complications,  genetics*
Humans
Liver Cirrhosis / etiology,  genetics*
Male
Middle Aged
Polymorphism, Single Nucleotide*
Retrospective Studies
Sex Factors
Young Adult
Chemical
Reg. No./Substance:
0/5' Untranslated Regions; 62229-50-9/Epidermal Growth Factor
Comments/Corrections

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