Uchigata Y, Kuwata S, Tsushima T, Tokunaga K, Miyamoto M, Tsuchikawa K, Hirata Y, Juji T, Omori Y
Diabetes Center, Tokyo Women's Medical College, Japan.
J Clin Endocrinol Metab. 1993 Jul;77(1):249-54. doi: 10.1210/jcem.77.1.8325948.
The insulin autoimmune syndrome (IAS) is characterized by the following diagnostic criteria: severe spontaneous hypoglycemia without evidence of exogenous insulin administration, high levels of total serum immunoreactive insulin, and the presence of a high titer of antiinsulin antibody. Just before the onset of IAS, 13 of the 35 (37%) patients with IAS examined in this study had taken methimazole for the treatment of Graves' disease. To investigate the difference between the Graves' disease patients treated with methimazole who developed IAS and other IAS patients, HLA class II genes in both groups were analyzed by serological and DNA typing methods. All 13 patients with Graves' disease who developed IAS possessed a specific allelic combination, Bw62/Cw4/DR4 carrying DRB10406, whereas only 1 of 50 Graves' disease patients without IAS had Bw62/Cw4/DR4 (odds ratio, 891; P < 1 x 10(-10)) and carried not DRB10406 (odds ratio, 2727; P < 1 x 10(-10)), but DRB10405. Of the 22 IAS patients without Graves' disease, 13 had the combination Bw62/Cw4/DR4 carrying DRB10406 (odds ratio, 19.0; P < 0.07). Thus, it is highly likely that patients with Graves' disease develop IAS via treatment with methimazole when their Bw62/Cw4/DR4 carry DRB1*0406.
胰岛素自身免疫综合征(IAS)具有以下诊断标准:严重自发性低血糖且无外源性胰岛素使用证据、血清总免疫反应性胰岛素水平升高以及存在高滴度抗胰岛素抗体。在本研究中接受检查的35例IAS患者中,有13例(37%)在IAS发病前曾服用甲巯咪唑治疗格雷夫斯病。为了研究发生IAS的接受甲巯咪唑治疗的格雷夫斯病患者与其他IAS患者之间的差异,通过血清学和DNA分型方法分析了两组的HLA - II类基因。所有13例发生IAS的格雷夫斯病患者都拥有一种特定的等位基因组合,即携带DRB10406的Bw62/Cw4/DR4,而50例未发生IAS的格雷夫斯病患者中只有1例具有Bw62/Cw4/DR4(优势比,891;P < 1×10⁻¹⁰),且携带的不是DRB10406(优势比,2727;P < 1×10⁻¹⁰),而是DRB10405。在22例非格雷夫斯病的IAS患者中,有13例具有携带DRB10406的Bw62/Cw4/DR4组合(优势比,19.0;P < 0.07)。因此,携带DRB1*0406的Bw62/Cw4/DR4的格雷夫斯病患者经甲巯咪唑治疗后极有可能发生IAS。