Disequilibrium linkage between the polymorphism in exons 2, 3 and 4 of the MICA gene and HLA-B antigen of patient with ankylosing spondylitis.
- Author:
Hong SU
1
;
Bao-long WANG
;
Xiu-jun ZHANG
;
Jia-hu HAO
;
Qin XIAO
;
Dong-qing YE
Author Information
- Publication Type:Journal Article
- MeSH: Alleles; Exons; genetics; Gene Frequency; Genotype; HLA-B Antigens; genetics; HLA-B27 Antigen; genetics; Histocompatibility Antigens Class I; genetics; Humans; Linkage Disequilibrium; genetics; Polymerase Chain Reaction; Polymorphism, Genetic; genetics; Spondylitis, Ankylosing; genetics
- From: Chinese Journal of Medical Genetics 2006;23(4):446-448
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the association between the exons 2 to 4 of the MICA gene and ankylosing spondylitis (AS).
METHODSBy PCR-SSOP, DNA samples from 56 AS patients and 112 random healthy individuals, as normal control were genotyped to analyse the polymorphism in exons 2, 3, 4 of the MICA alleles.
RESULTSMICA*008 was dominant in MICA allele,accounted for 32.14% and 30.36% in AS patients and normal controls respectively. The frequency of MICA*007 was significantly increased in AS patients, when compared with normal controls (chi-square=10.18, P<0.05, RR=2.50). No difference was found in the other MICA alleles. The haplotype analysis revealed that there were the strong linkage disequilibrium between MICA and HLA-B of AS patients, and normal controls. There was a difference in MICA*007-B27 between two groups (chi-square=18.46, P<0.05, RR=7.47). Both HLA-B27 and MICA*007 were strongly associated with AS. Stratified analysis showed that HLA-B27 was significantly relative to AS,while it was not found between MICA*007 and AS.
CONCLUSIONThe increased frequency of MICA alleles may be due to its strong linkage disequilibrium with HLA-B27.
