Weetman A P, Zhang L, Webb S, Shine B
Department of Medicine, University of Cambridge Clinical School, Addenbrooke's Hospital, UK.
Clin Endocrinol (Oxf). 1990 Jul;33(1):65-71. doi: 10.1111/j.1365-2265.1990.tb00466.x.
We have tested the possible association of HLA-DQB and HLA-DPB alleles with Graves' thyrotoxicosis, with or without severe ophthalmopathy, by polymerase chain amplification of genomic DNA and allele-specific oligonucleotide probing. There was no significantly abnormal distribution of DQB alleles compared to 50 control subjects except for a reduced prevalence of DQw 3.1 in the Graves' patients with severe ophthalmopathy (X2 = 6.23, P less than 0.02). HLA-DPB 2.1/8 was found in only 1 of 40 of these patients compared with 15 of the controls (X2 = 11.49, P less than 0.001). Ten of 48 patients with Graves' disease but without clinically significant eye involvement were HLA-DPB 2.1/8 positive, not significantly different from controls, but significantly different from the ophthalmopathy group (X2 = 6.70, P less than 0.01). The other DPB alleles in both groups of Graves' disease patients were the same as controls. These results suggest that HLA-DPB 2.1/8 may confer a protective effect in Graves' disease with respect to ophthalmopathy.
我们通过对基因组DNA进行聚合酶链反应扩增及等位基因特异性寡核苷酸探针杂交,检测了HLA - DQB和HLA - DPB等位基因与伴有或不伴有严重眼病的格雷夫斯甲状腺毒症之间可能存在的关联。与50名对照受试者相比,除了患有严重眼病的格雷夫斯病患者中DQw 3.1的患病率降低外(X2 = 6.23,P小于0.02),DQB等位基因的分布没有明显异常。在这些患者中的40例中只有1例发现HLA - DPB 2.1/8,而对照组中有15例(X2 = 11.49,P小于0.001)。48例患有格雷夫斯病但无明显眼部受累的患者中有10例HLA - DPB 2.1/8呈阳性,与对照组无显著差异,但与眼病组有显著差异(X2 = 6.70,P小于0.01)。两组格雷夫斯病患者中的其他DPB等位基因与对照组相同。这些结果表明,HLA - DPB 2.1/8可能在格雷夫斯病眼病方面具有保护作用。