OBJECTIVE: To study the influence of DMA and DMB genes on susceptibility to
Rheumatoid Arthritis (RA). METHODS: HLA-DRB1, DMA and DMB polymorphisms we
re defined by PCR SSOP in 203 European Mediterranean RA patients and 181 un
related healthy controls. RESULTS: No significant difference in the phenoty
pe frequencies of DMA and DMB alleles was observed between patients and con
trols. We found decreased frequencies of DMA*0102 and DMB*0104 in patients
but this did not reach significance. These decreased frequencies could be d
ue to a positive linkage disequilibrium with DRB1*0701, an allele which is
underrepresented in RA patients. In stratified analysis with RA susceptibil
ity Epitope positive (SE) DRB1 alleles, there was no significant difference
in DMA and DMB phenotype frequencies between SE/SE, SE/X, and X/X patients
versus controls. Among SE/X subjects, no significant difference in DM dist
ribution frequencies was observed in DRB1*0101/X, 0102/X, 0401/X, 0404/X an
d 0405/X groups. CONCLUSION: DMA and DMB poly morphism does not seem to inf
luence susceptibility to develop RA. Differences in DMA phenotype frequenci
es between patients and controls are secondary to linkage disequilibrium wi
th DRB1 alleles. Human Immunology 60, 245-249 (1999). (C) American Society
for Histocompatibility and Immunogenetics, 1999. Published by Elsevier Scie
nce Inc.