Gorus F K, Sodoyez J C, Pipeleers D G, Keymeulen B, Foriers A, Van Schravendijk C F
Department of Metabolism and Endocrinology, Vrije Universiteit Brussel, Belgium.
Diabetologia. 1992 Nov;35(11):1080-6. doi: 10.1007/BF02221685.
A radiobinding assay for the detection of autoantibodies against islet amyloid polypeptide was developed, analytically validated, and--in parallel with a similar assay for the detection of autoantibodies against insulin--applied to sera from recent-onset Type 1 (insulin-dependent) diabetic patients and from age- and sex-matched control subjects. There was no difference in islet amyloid polypeptide autoantibody titres between patient groups and matched control subjects, nor within subject groups according to age. At onset of Type 1 diabetes, elevated islet amyloid polypeptide-autoantibody levels (> 97th percentile of control subjects) were only detected in 1 of 30 patients aged 0-19 years and in 2 of 35 patients aged 20-39 years. By contrast, insulin autoantibodies were frequently demonstrated, in particular at onset of diabetes under age 20 (0-19 years: 18 of 30 patients; 20-39 years: 10 of 35 patients; p < 0.01 vs matched control subjects). Islet amyloid polypeptide autoantibodies were not detectable in 3 insulinoma patients nor in 37 patients (aged 33-70 years) with Type 2 diabetes (vs 1 of 40 in matched control subjects). In positive serum, adsorption onto protein A-Sepharose removed islet amyloid polypeptide binding activity, hereby confirming its antibody nature. In conclusion, Type 1 diabetes is associated with an age-dependent autoantibody reaction against insulin but not against islet amyloid polypeptide. Conditions associated with amyloid deposition in islets (Type 2 diabetes, insulinoma and ageing) do not favour the formation of autoantibodies against islet amyloid polypeptide.
我们开发了一种用于检测抗胰岛淀粉样多肽自身抗体的放射结合测定法,并进行了分析验证,同时将其与一种类似的用于检测抗胰岛素自身抗体的测定法一起应用于近期发病的1型(胰岛素依赖型)糖尿病患者以及年龄和性别匹配的对照受试者的血清中。患者组与匹配的对照受试者之间,以及根据年龄划分的受试者组内部,胰岛淀粉样多肽自身抗体滴度均无差异。在1型糖尿病发病时,仅在30名0至19岁的患者中的1名以及35名20至39岁的患者中的2名中检测到胰岛淀粉样多肽自身抗体水平升高(>对照受试者的第97百分位数)。相比之下,胰岛素自身抗体则经常出现,尤其是在20岁以下糖尿病发病时(0至19岁:30名患者中的18名;20至39岁:35名患者中的10名;与匹配的对照受试者相比,p<0.01)。在3名胰岛素瘤患者以及37名2型糖尿病患者(年龄33至70岁)中均未检测到胰岛淀粉样多肽自身抗体(与之相比,匹配的对照受试者中40名中有1名检测到)。在阳性血清中,与蛋白A-琼脂糖珠吸附可去除胰岛淀粉样多肽结合活性,从而证实其抗体性质。总之,1型糖尿病与针对胰岛素而非胰岛淀粉样多肽的年龄依赖性自身抗体反应相关。与胰岛淀粉样沉积相关的疾病(2型糖尿病、胰岛素瘤和衰老)不利于抗胰岛淀粉样多肽自身抗体的形成。