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Single Nucleotide Polymorphisms of Cytokine Genes are Associated with Fibrosis of the Intrahepatic Bile Duct Wall in Human Clonorchiasis.

Authors :
Byung-Suk Chung
Jeong-Keun Lee
Min-Ho Choi
Myoung Hee Park
Dongil Choi
Sung-Tae Hong
Source :
Korean Journal of Parasitology; Jun2009, Vol. 47 Issue 2, p145-151, 7p, 5 Charts
Publication Year :
2009

Abstract

This study examined the association of cytokine gene polymorphisms with intrahepatic bile duct wall fibrosis in human clonorchiasis. A total of 240 residents in Heilongjiang, China underwent ultrasonography, blood sampling, and stool examination. Single nucleotide polymorphism (SNP) sites for IFN-γ (+874 T/A), IL-10 (-1,082 G/A, -819 C/T, -592 C/ A), TNF-α (-308 G/A), and TGF-β1 (codon 10 T/C, codon 25 G/C) genes were observed with the TaqMan allelic discrimination assay. No significant correlation was observed between individual cytokine gene polymorphisms and intrahepatic duct dilatation (IHDD). Among individuals with clonorchiasis of moderate intensity, the incidence of IHDD was high in those with IFN-γ intermediate-producing genotype, +874AT (80.0%, P = 0.177), and in those with TNF-α low- producing genotype, -308GG (63.0%, P = 0.148). According to the combination of IFN-γ and TNF-α genotypes, the risks for IHDD could be stratified into high (intermediate-producing IFN-γ and low producing TNF-α), moderate, and low (low-producing IFN-γ and high producing TNF-α,) risk groups. The incidence of IHDD was significantly different among these groups (P= 0.022); 88.9% (odds ratio, OR = 24.0) in high, 56.5% (OR = 3.9) in moderate, and 25.0% (OR = 1) in low risk groups. SNP of IFN-γ and TNF-α, genes may contribute to the modulation of fibrosis in the intrahepatic bile duct wall in clonorchiasis patients. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00234001
Volume :
47
Issue :
2
Database :
Supplemental Index
Journal :
Korean Journal of Parasitology
Publication Type :
Academic Journal
Accession number :
43157809
Full Text :
https://doi.org/10.3347/kjp.2009.47.2.145