Elliott R B, Pilcher C C
Department of Paediatrics, School of Medicine, Auckland, New Zealand.
J Autoimmun. 1994 Dec;7(6):881-8. doi: 10.1006/jaut.1994.1072.
The majority of children who develop Type 1 diabetes under the age of 10-years-old show islet cell antibodies at levels of 40 or more units. Those who have lower levels (10- < 40) usually have co-existent insulin autoantibodies. Of these children 85% have these criteria. When these criteria were applied to large groups of similarly aged children who were either first degree relatives of a type 1 diabetic or had no such family history, 3.8% and 0.38% respectively showed these criteria. The observed sensitivity of these characteristics in identifying children who develop diabetes in the subsequent 5 years is 79% for both groups. The calculated expected incidence of disease in the subsequent 10 years for these two groups is 2.15% and 0.215% respectively. This model of autoantibody prediction of diabetes in children thus applies equally well in terms of sensitivity and specificity to those with and without a family history of diabetes.
大多数在10岁前患1型糖尿病的儿童,其胰岛细胞抗体水平达到40个单位或更高。抗体水平较低(10 - <40)的儿童通常同时存在胰岛素自身抗体。这些儿童中有85%符合这些标准。当将这些标准应用于大量年龄相仿、要么是1型糖尿病患者的一级亲属、要么没有此类家族病史的儿童群体时,两组分别有3.8%和0.38%符合这些标准。在识别随后5年内患糖尿病的儿童方面,这些特征的观察到的敏感性在两组中均为79%。计算得出这两组在随后10年的预期发病率分别为2.15%和0.215%。因此,这种用于预测儿童糖尿病的自身抗体模型,在敏感性和特异性方面,对有糖尿病家族史和无糖尿病家族史的儿童同样适用。