Genetic polymorphism at codon 10 of the transforming growth factor-beta1 gene in patients with alcoholic liver cirrhosis.
10.3350/kjhep.2011.17.1.37
- Author:
Jong Joon LEE
1
;
Soo Kyung PARK
;
Oh Sang KWON
;
In Sik WON
;
Dong Kyu KIM
;
Young Kul JUNG
;
Yang Suh KU
;
Yun Soo KIM
;
Duck Joo CHOI
;
Ju Hyun KIM
Author Information
1. Department of Internal Medicine, Gachon University of Medicine and Science, Incheon, Korea. osshsjuj@yahoo.co.kr
- Publication Type:Original Article ; Controlled Clinical Trial
- Keywords:
Transforming growth factor beta1;
Alcoholic liver cirrhosis;
Genetic polymorphism
- MeSH:
Aged;
Alcohol Drinking;
Codon;
Female;
Genotype;
Heterozygote;
Homozygote;
Humans;
Liver Cirrhosis, Alcoholic/*genetics/pathology;
Male;
Middle Aged;
*Polymorphism, Genetic;
Transforming Growth Factor beta1/*genetics/metabolism
- From:The Korean Journal of Hepatology
2011;17(1):37-43
- CountryRepublic of Korea
- Language:English
-
Abstract:
BACKGROUND/AIMS: Transforming growth factor beta1 (TGF-beta1) is a key cytokine in the production of extracellular matrix. A genetic polymorphism at codon 10 of the TGF-beta1 gene is associated with liver fibrosis. We investigated the effect of genetic polymorphisms at codon 10 on the development of alcoholic liver cirrhosis (ALC). METHODS: In total, 119 controls and 182 patients with ALC, were enrolled in the study. Clinical and laboratory data including total lifetime alcohol intake were collected at enrollment. The genotype at codon 10 was determined for each patient by single-strand conformation polymorphism. RESULTS: There were three types of genetic polymorphism at codon 10: homozygous proline (P/P), heterozygous proline/leucine (P/L), and homozygous leucine (L/L). Among the controls, the proportions of P/P, P/L, and L/L were 26.1%, 44.5%, and 29.4%, respectively in the ALC group, these proportions were 23.1%, 43.4%, and 33.5%, respectively. The genotype distribution did not differ between the controls and the ALC group. In the ALC group, age, total lifetime alcohol intake, and distribution of Child-Pugh class did not differ with the genotype. Of the male patients with ALC (n=164), the proportions of P/P, P/L, and L/L were 20.1%, 44.5%, and 35.4%, respectively the genotype distribution did not differ between the male controls and the male ALC patients. CONCLUSIONS: The genotype at codon 10 in TGF-beta1 does not appear to influence the development of ALC. Further study is needed to investigate other genetic factors that influence the development of ALC in patients with chronic alcohol intake.
