Stratification of type 1 diabetes risk on the basis of islet autoantibody characteristics

被引:210
作者
Achenbach, P
Warncke, K
Reiter, J
Naserke, HE
Williams, AJK
Bingley, PJ
Bonifacio, E
Ziegler, AG
机构
[1] Diabet Res Inst, D-80804 Munich, Germany
[2] Hosp Munchen Schwabing, Dept Med 3, D-80804 Munich, Germany
[3] Univ Bristol, Div Med, Bristol BS8 1TH, Avon, England
[4] San Raffaele Sci Inst, I-20132 Milan, Italy
关键词
D O I
10.2337/diabetes.53.2.384
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Family history of type 1 diabetes and autoantibodies to the islet antigens insulin (IAA), glutamate decarboxylase (GADA), and the protein tyrosine phosphatase-like protein IA-2 (IA-2A) are strong predictors of type 1 diabetes, but the rate of progression to diabetes in multiple islet autoantibody-positive relatives varies widely. We asked whether detailed characterization of islet autoantibodies that included determination of titer, epitope specificity, and IgG subclass would improve diabetes prediction in a large cohort of autoantibody-positive relatives. The study shows a strong association between risk and high titer, broad antibody responses to IA-2 and insulin. The highest risks were associated with high-titer IA-2A and IAA, IgG2, IgG3, and/or IgG4 subclass of IA-2A and IAA, and antibodies to the IA-2-related molecule IA-2beta. Using models based on these antibody characteristics, autoantibody-positive relatives can be classified into groups with risks of diabetes ranging from 7 to 89% within 5 years.
引用
收藏
页码:384 / 392
页数:9
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