ADAM33 Polymorphisms Are Associated with Susceptibility to Systemic Lupus Erythematosus in a Korean Population.
- Author:
Ji Young KIM
1
;
Young KIM
;
Soo Cheon CHAE
;
Shin Seok LEE
;
Mi Kyoung LIM
;
Dong Huyk SHEEN
;
Hun Taeg CHUNG
;
Seung Cheol SHIM
Author Information
- Publication Type:Original Article
- Keywords: Disintegrin and metalloproteinase domain 33 protein; Systemic lupus erythematosus; Single nucleotide polymorphism
- MeSH: Haplotypes; Humans; Immunoglobulin M; Linkage Disequilibrium; Lupus Erythematosus, Systemic*; Odds Ratio; Polymorphism, Single Nucleotide; Real-Time Polymerase Chain Reaction
- From:Journal of Rheumatic Diseases 2016;23(2):88-95
- CountryRepublic of Korea
- Language:English
- Abstract: OBJECTIVE: The objective of this study is to assess whether genetic functional variants of disintegrin and metalloprotease 33 (ADAM33) are associated with susceptibility to systemic lupus erythematosus (SLE) in a Korean population. METHODS: We previously identified 48 single nucleotide polymorphisms (SNPs) in ADAM33. Six SNPs were selected with regard to the linkage disequilibrium pattern. An association study of ADAM33 was conducted in 190 patients with SLE and 469 control subjects. SNPs were genotyped using the TaqMan Real-time polymerase chain reaction method, and haplotype analyses of related variants were performed. RESULTS: All SNPs were in Hardy-Weinberg equilibrium. Significant associations were found between the ADAM33 polymorphisms and SLE at rs2787094 (adjusted odds ratio [OR] 1.88, 95% confidence interval [CI] 1.00 to 3.54; p<0.0001). The rs554743 polymorphism was associated with the presence of the immunoglobulin M anti-cardiolipin antibody (adjusted OR 0.29, 95% CI 0.10 to 0.83; p=0.021). CONCLUSION: ADAM33 polymorphisms were associated with susceptibility to SLE and development of clinical disease manifestations in a Korean population. Further study is warranted to clarify the role of ADAM33 in SLE pathogenesis.
