The British Journal of Rheumatology, Vol 37, 95-97, Copyright © 1998 by British Society for Rheumatology
F Takeuchi, H Nabeta, GH Hong, S Kuwata, K Tanimoto and K Ito
Associations between polymorphisms of DMA and DMB alleles and systemic
lupus erythematosus (SLE) were studied in 51 Japanese SLE patients and 77
normal subjects by the polymerase chain reaction-restriction fragment
length polymorphism (PCR-RFLP) method. Phenotype frequencies of DMB*0101
tended to increase in SLE, but the difference was not significant (76.5% vs
70.1% in controls). The phenotype frequency of DMB*0103 was decreased in
the SLE group, but the difference was not significant (49.0% vs 53.2%).
Furthermore, there was no evidence of any association of either DMA or DMB
alleles with HLA-DRB1*1501. The phenotype frequency of DMB*0101 was higher
in the SLE group with anti- double-stranded DNA antibody (a-dsDNA) than in
the SLE group without a- dsDNA, but the difference was not significant (P =
0.045, corrected P not significant). No other DMA or DMB alleles showed any
associations in various immunological subgroups of SLE. These data suggest
that neither the DMA nor the DMB gene determines susceptibility to SLE in
Japanese.
ORIGINAL PAPERS
Polymorphisms of DMA and DMB genes in Japanese systemic lupus erythematosus
Department of Medicine and Physical Therapy, Faculty of Medicine, University of Tokyo, Japan.
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