Association between apolipoprotein E genotype, chronic liver disease, and hepatitis B virus.
10.3350/cmh.2012.18.3.295
- Author:
Seun Joo AHN
1
;
Dong Kyu KIM
;
Soon Sun KIM
;
Chang Bum BAE
;
Hyo Jung CHO
;
Han Gyeol KIM
;
Young Jip KIM
;
Joo Ho LEE
;
Hyo Jin LEE
;
Mi Yeon LEE
;
Kee Bum KIM
;
Jin Hee CHO
;
Sung Won CHO
;
Jae Youn CHEONG
Author Information
1. Department of Gastroenterology, Genomic Research Center for Gastroenterology, Ajou University School of Medicine, Suwon, Korea. jaeyoun620@gmail.com
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
Apolipoprotein E;
Hepatitis B virus;
Genotype;
Liver cirrhosis
- MeSH:
Adult;
Aged;
Aged, 80 and over;
Alleles;
Apolipoproteins E/*genetics/metabolism;
Carcinoma, Hepatocellular/*metabolism/pathology;
Case-Control Studies;
Child;
Chronic Disease;
Cohort Studies;
Female;
Gene Frequency;
Genotype;
Hepatitis B/complications/metabolism/virology;
Hepatitis B virus/*physiology;
Humans;
Liver Cirrhosis/etiology/*metabolism;
Liver Neoplasms/*metabolism/pathology;
Male;
Middle Aged;
Young Adult
- From:Clinical and Molecular Hepatology
2012;18(3):295-301
- CountryRepublic of Korea
- Language:English
-
Abstract:
BACKGROUND/AIMS: Apolipoprotein E (ApoE) plays an important role in regulating lipid and lipoprotein metabolism, and ApoE genotypes are known to affect plasma lipoprotein concentrations. We investigated whether ApoE genotype determines the disease outcome in hepatitis B virus (HBV)-infected individuals, and verified the association between ApoE genotype and the occurrence of hepatocellular carcinoma (HCC) in patients with chronic liver diseases of various etiologies. METHODS: This hospital-based, case-controlled study enrolled 156 subjects (47 healthy controls, 50 HBV-related liver cirrhosis patients, and 59 HCC patients). ApoE genotypes were determined using PCR-based ApoE genotyping kits. The biological significance of ApoE genotype was verified by measuring serum ApoE levels using an ELISA kits. RESULTS: The epsilon3 allele was the most common allele, with allele frequencies among the entire cohort of 5.8%, 84.3%, and 9.9% for the epsilon2, epsilon3, and epsilon4 alleles, respectively. Significantly more of those patients carrying the epsilon3/3 genotype had developed liver cirrhosis compared to the control subjects. Being an ApoE4 carrier was associated with a lower probability of developing liver cirrhosis. The allele frequencies and genotype distribution of ApoE did not differ significantly between the liver cirrhosis and HCC patients. The serum level of ApoE was significantly higher in patients with liver cirrhosis than in the healthy controls, but did not differ significantly with the ApoE genotype. CONCLUSIONS: The ApoE epsilon3/3 genotype frequency was higher in patients with HBV-associated liver cirrhosis than in the controls.
