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In an attempt to improve the diagnostic value of measuring antibodies to islet cell cytoplasmic antigen, coded sera were distributed to 38 laboratories and results were returned for analysis. Comparison between laboratories revealed that results for some individual sera differed by up to nine doubling dilutions and even within laboratories duplicate samples could differ by six doubling dilutions. By including dilutions of sera it was possible to draw a standard curve for each laboratory and this revealed major variations in shape, slope and intercept. However, using each laboratory's standard curve and converting results to units, a substantial improvement was obtained. The approach described improves standardisation and will permit laboratories to identify poor precision and/or any systematic change in assay performance.

Type

Journal article

Journal

J Immunol Methods

Publication Date

21/01/1988

Volume

106

Pages

83 - 88

Keywords

Animals, Autoantibodies, Child, Diabetes Mellitus, Type 1, Fluorescent Antibody Technique, Haplorhini, Humans, International Cooperation, Islets of Langerhans, Reference Standards, Reference Values, Statistics as Topic