Pancreas Islet Cell-Specific Antibody Detection by ELISA

Author:

Van Aelst Sophie1,Gillard Pieter2ORCID,Weets Ilse3,Dillaerts Doreen4,Billen Jaak5,Mathieu Chantal2ORCID,Bossuyt Xavier45

Affiliation:

1. Department of Laboratory Medicine, Heilig-Hart Hospital Lier, Lier, Belgium

2. Department of Endocrinology, University Hospitals Leuven, Leuven, Belgium

3. Department of Clinical Chemistry and Radioimmunology, Brussels Free University, Elsene, Brussels, Belgium

4. Department of Microbiology and Immunology, KU Leuven—University of Leuven, Leuven, Belgium

5. Department of Laboratory Medicine, University Hospitals Leuven, Leuven, Belgium

Abstract

Abstract Background Islet cell-specific autoantibodies are useful to classify diabetes. The aim of this study was to evaluate the performance of commercially available ELISAs to detect autoantibodies to glutamic acid decarboxylase 65-kDa isoform (GADA), tyrosine phosphatase-related islet antigen 2 (IA-2A), zinc transporter protein 8 (ZnT8A), and insulin (IAA). The performance of ELISA was compared to the performance of RIA. Methods We retrospectively identified 76 newly diagnosed type 1 diabetes mellitus patients (median age 27 years, female/male: 0.65) and 131 disease controls (median age 45 years, female/male: 0.60). The ELISAs were from Medipan. RIAs were in-house methods from the Belgian Diabetes Registry or from Medipan or DIASource. Results Sensitivity and specificity of ELISA were, respectively, 97% and 97% for GADA, 61% and 99% for IA-2A, 1% and 96% for IAA, and 70% and 98% for ZnT8A. The likelihood ratio for type 1 diabetes increased with increasing antibody levels for GADA, IA-2A, and ZnT8A measured by ELISA. The positive predictive value of double positivity for either GADA, IA-2A, or ZnT8A was 100%. Conclusions The ELISAs to detect GADA, IA-2A, and ZnT8A have good performance characteristics. Combining autoantibody assays and taking into account antibody levels improves the interpretation of autoantibody testing.

Funder

Novo Nordisk

Sanofi and ActoBio Therapeutics

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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