Cb. Sanjeevi et al., ANALYSIS OF HLA-DQA1 AND HLA-DQB1 GENES IN MEXICAN-AMERICANS WITH INSULIN-DEPENDENT DIABETES-MELLITUS, Tissue antigens, 42(2), 1993, pp. 72-77
Mexican American patients (n = 35) with insulin-dependent diabetes mel
litus (IDDM) and control subjects (n = 39) were HLA-DQA and DQB typed
by the polymerase chain reaction technique combined with allele-specif
ic oligonucleotide probes. Either DQB10302 or DQB1*0201 was present a
mong 91% (32/35) of the patients compared to 67% (26/39) of controls.
Either DQA10501 or DQA1*0301 was present in all patients (100% or 35/
35) compared to 29/39 (74%) (OR 12.06 Pc < 0.05) of controls. All four
of these genes, in cis or trans, were present in 15/35 (43%) of the p
atients compared to 3/39 (8%) of controls (OR 9.0; Pc < 0.01). The pre
sence of one or more non-susceptibility alleles showed a dose-related
decrease in relative risk. Presence of aspartic acid (Asp) at position
57 of the DQ beta chain did not confer protection and non-Asp homozyg
ozity did not confer susceptibility to IDDM in this ethnic group. In c
onclusion, susceptibility to IDDM in Mexican Americans is associated w
ith particular DQA and DQB combinations, illustrates dose-dependent pa
rameters and contradicts the critical residue hypothesis.