Relationship between polymorphisms of vitamin D receptor gene and familial aggregation of HBsAg carriers.
- Author:
Jing SHAN
1
;
Lu WANG
;
Zhuo LI
;
Ying LIU
;
Ji-rong GAO
;
Yan-lei PANG
;
Jun-hong LI
;
Fu-min PANG
;
Xin-hui GUO
;
Hong-Zhi CHI
;
Chang-geng ZHANG
;
Hui LI
Author Information
- Publication Type:Journal Article
- MeSH: Case-Control Studies; Female; Gene Frequency; Genetic Predisposition to Disease; genetics; Haplotypes; Hepatitis B; genetics; Hepatitis B Surface Antigens; genetics; Humans; Male; Pedigree; Polymerase Chain Reaction; Polymorphism, Genetic; Receptors, Calcitriol; genetics
- From: Acta Academiae Medicinae Sinicae 2006;28(2):148-153
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo determine whether -Taq I T/C and -Fok I C/T polymorphisms of vitamin D receptor (VDR) gene are associated with the familial aggregation of hepatitis B virus (HBV) infection.
METHODSBased on a population-based case-control family design, 288 family members from 27 case families and 230 family members from 27 control families were recruited. VDR gene polymorphisms were analyzed. VDR-Taq I T/C and VDR-Fok I C/T polymorphisms were examined by polymerase chain reaction-restriction fragment length polymorphism.
RESULTSThe frequency of VDR-Taq I TT genotype in the case families was significantly higher than that in the control families (P < 0.05) , however, the frequency of VDR-Fok I CC genotype in the case families was significantly higher than that in the control families (P < 0.05). The frequency of family members carriying Taq I T-Fok I C haplotype in the case families was significantly higher than that in the control families (OR = 1.67, P < 0.05), however, the frequency of family members carrying Taq I C-Fok I T haplotype in the case families was significantly lower than that in the control families (OR = 0. 24, P < 0.05). The similar results were found in the familial biological kinship relatives with any HBV-infected makers.
CONCLUSIONVDR-Taq I and -Fok I gene polymorphisms are likely to play a substantial role in HBsAg familial aggregation.