Diabetes Antibody Standardization Program: First Proficiency Evaluation of Assays for Autoantibodies to Zinc Transporter 8

被引:87
|
作者
Lampasona, Vito [1 ]
Schlosser, Michael [2 ,3 ]
Mueller, Patricia W. [4 ]
Williams, Alistair J. K. [5 ]
Wenzlau, Janet M. [6 ]
Hutton, John C. [6 ]
Achenbach, Peter [7 ]
机构
[1] Ist Sci San Raffaele, Genom Unit Diag Human Pathol, Ctr Translat Genom & Bioinformat, I-20132 Milan, Italy
[2] Ernst Moritz Arndt Univ Greifswald, Dept Med Biochem & Mol Biol, Karlsburg, Germany
[3] Ernst Moritz Arndt Univ Greifswald, Inst Pathophysiol, Res Grp Predict Diagnost, Karlsburg, Germany
[4] Ctr Dis Control & Prevent, Natl Diabet Lab, Atlanta, GA USA
[5] Univ Bristol, Sch Clin Sci, Bristol, Avon, England
[6] Univ Colorado, Denver & Hlth Sci Ctr, Barbara Davis Ctr Childhood Diabet, Denver, CO 80202 USA
[7] German Res Ctr Environm Hlth, Helmholtz Ctr Munich, Diabet Res Inst, Neuherberg, Germany
关键词
CONCORDANCE CORRELATION-COEFFICIENT; GLUTAMIC-ACID DECARBOXYLASE; ISLET ANTIGEN-2; HIGH AGREEMENT; INSULIN; ONSET; IDENTIFICATION; SLC30A8; S1C30A8; ZNT-8;
D O I
10.1373/clinchem.2011.170662
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
BACKGROUND: Zinc transporter 8 (ZnT8) is a recently identified major autoantigen in type 1 diabetes, and autoantibodies to ZnT8 (ZnT8A) are new markers for disease prediction and diagnosis. Here we report the results of the first international proficiency evaluation of ZnT8A assays by the Diabetes Antibody Standardization Program (DASP). METHODS: After a pilot workshop in 2007, an expanded ZnT8A workshop was held in 2009, with 26 participating laboratories from 13 countries submitting results of 63 different assays. ZnT8A levels were measured in coded sera from 50 patients with newly diagnosed type 1 diabetes and 100 blood donor controls. Results were analyzed comparing area under the ROC curve (ROC-AUC), sensitivity adjusted to 95% specificity (AS95), concordance of sample ZnT8A positive or negative designation, and autoantibody levels. RESULTS: ZnT8A radio binding assays (RBAs) based on combined immunoprecipitation of the 2 most frequent ZnT8 COOH-terminal domain polymorphic variants showed a median ROC-AUC of 0.848 [interquartile range (IQR) 0.796-0.878] and a median AS95 of 70% (IQR 60%-72%). These RBAs were more sensitive than assays using as antigen either 1 ZnT8 variant only or chimeric constructs joining NH(2)- and COOH-terminal domains, assays based on immunoprecipitation and bioluminescent detection, or assays based on immunofluorescent staining of cells transfected with full-length antigen. CONCLUSIONS: The DASP workshop identified immunoprecipitation-based ZnT8A assays and antigen constructs that achieved both a high degree of sensitivity and specificity and were suitable for more widespread clinical application. (C) 2011 American Association for Clinical Chemistry
引用
收藏
页码:1693 / 1702
页数:10
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