HLA-DRB1*08, DRB1*03/DRB3*0101, and DRB3*0202 are susceptibility genes for Graves' disease in North American Caucasians, whereas DRB1*07 is protective

被引:72
作者
Chen, QY
Huang, W
She, JX
Baxter, F
Volpe, R
Maclaren, NK
机构
[1] Res Inst Children, Harahan, LA 70123 USA
[2] Louisiana State Univ, Med Ctr, Dept Pediat, New Orleans, LA 70112 USA
[3] Childrens Hosp, New Orleans, LA 70112 USA
[4] Univ Florida, Coll Med, Dept Pathol & Lab Med, Gainesville, FL 32610 USA
[5] Univ Toronto, Dept Med, Div Endocrinol, Toronto, ON, Canada
关键词
D O I
10.1210/jc.84.9.3182
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Graves' disease is known to be HLA-D associated; however, the primary loci involved remain unclear. We examined HLA genotypes of DRB1 and DQB1 plus DRB3 subtypes using PCR-based sequence-specific priming in two groups of North American (Gainesville, FL; and Toronto, Canada) Caucasian patients with Graves' disease. We stratified patients into those with either early age at onset (<20 yr; 13.1 +/- 4.8 yr; n = 30) and later age at onset of disease (38.8 +/- 9.7 yr; n = 62) and compared the results to 192 normal controls. As expected, we found that DRB1*03 was associated with Graves' disease, but at a higher odds ratios for early-onset than later-onset patients (3.7 vs. 2.2). The frequency of DRB1*08 was also increased in both groups of patients, but significantly so only in patients with early-onset Graves' (P = 0.001; chi(2) = 10.8). DRB3 was highly associated with Graves' in both groups of patients (P = 0.009; chi(2) = 6.83 and P = 0.0015; chi(2) = 10.1, respectively); however, the subtypes of DRB3 revealed differential susceptibilities. Whereas the frequencies of both DRB3*0101 and DRB3*0202 were increased over the entire cohort, that of DRB3*0301 was not. Significant P values were found for DRB3*0101 in patients with early-onset and for DRB3*0202 in patients with later onset of Graves' disease. When the haplotypes of DRB1*03-DRB3 of all subtypes were removed for analysis (all DRB1*03 positive also had DRB3*0101), the frequency of DRB3*0202 remained significantly higher in the patients with later onset of Graves' disease than in controls (P = 0.0043; chi(2) = 8.13), but DRB3 was no longer positively associated with the early-onset group. In addition, we found that DRB1*07 was negatively associated with both groups of patients (P = 0.024; chi(2) = 5.10 and P = 0.0085; chi(2) = 6.93). These data suggest that DRB3*0202 is more likely to be the primary susceptible locus than DRB1*03 for patients with later onset of Graves' disease.
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页码:3182 / 3186
页数:5
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