ICA and GAD65 autoantibody profiles and HLA-DR and DQ analysis were pe
rformed on 43 Black juvenile onset IDDM patients and 34 unrelated Blac
k controls from Tennessee, USA. 75% of patients were positive for GAD6
5 autoantibodies but only 53% had ICA; 39% both ICA and GAD65 antibodi
es. The strongest HLA association was with the DR3 haplotype DRB103 D
QA10501 DQB1*0201 (63% of patients v 12% of controls RR = 13.0, p < 0
.00002). DRB104 DQA1*0301 DQB1*0302, associated with IDDM in Caucasia
ns but rare in Negroids, occurred in 27% of patients and 6% of control
s (RR = 5.9, p < 0.04). All patients carried DQB10302 or DQB1*0201. D
QB10602 was significantly reduced in patients (2.4% v 41%, RR = 0.036
, p < 0.008) and DRB11501 was absent in patients (0% v 35%). The freq
uency of GAD65 autoantibodies in Black American IDDM patients is compa
rable to that in Caucasians; however ICA positivity is reduced. GAD65
antibodies may therefore be a more sensitive serological test to ident
ify individuals in the Black American general population for markers a
ssociated with increased risk of developing IDDM. Current screening me
thods for predicting preclinical IDDM in Caucasians relies on a combin
ation of immune and HLA markers of IDDM; studies of these markers in t
he Black Americans will make it possible to extend these options to ad
ditional genetically diverse populations.