MHC associations with IDDM in the Korean population were studied to in
vestigate genetic susceptibility to this disorder. The frequencies of
HLA-DR3, -DR4 and -DR9 were significantly higher in diabetic patients.
However, the frequency of DR2 was significantly decreased in diabetic
patients. DQA10301 and DQA1*0501 were positively and DQA1+0102 and D
QA10201 negatively associated with IDDM. DQB1*0301 and DQB1*0601 were
negatively associated with IDDM. Heterodimers DQA10301-DQB1*0201, DQ
A10501-DQB1*0201 and DQA1*0501-DQB1*0302 were positively associated a
nd DQA10102-DQB1*0601 negatively associated with IDDM. The frequencie
s of DR3-DQA10301-DQB1*0201 and -DQA1*0501-DQB1*0201 were significant
ly higher in diabetic patients. The frequencies of DR4-DQA10301-DQB1*
0201 and DR9-DQA10301-DQB1*0303 were significantly higher in diabetic
patients, The presence of non-aspartic acid at position 57 of the DQ
beta-chain was not associated with susceptibility to IDDM. However, th
e frequency of Arg 52 homozygotes was significantly higher in diabetic
patients. These results suggest a role of the MHC molecule and also s
uggest racial differences in susceptibility to IDDM even within the As
ian populations.