Characterization of patients with diabetes who were incidentally found to be glutamic acid decarboxylase autoantibody‐positive by bridging‐type enzyme‐linked immunosorbent assay

Abstract This study aimed to characterize diabetic patients incidentally found to be positive for glutamic acid decarboxylase autoantibodies (GADA) in general practice. Using bridging‐type enzyme‐linked immunosorbent assay, we screened 1,040 patients with phenotypic type 2 diabetes for GADA, finding...

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Main Authors: Eiji Kawasaki, Takahiro Fukuyama, Aira Uchida, Yoko Sagara, Hidekazu Tamai, Yuko Nakano, Masayuki Tojikubo, Yuji Hiromatsu, Nobuhiko Koga
Format: Article
Language:English
Published: Wiley 2020-11-01
Series:Journal of Diabetes Investigation
Subjects:
Online Access:https://doi.org/10.1111/jdi.13307
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spelling doaj-cda2fb21e4d24c82a6dcb44c219f78bb2021-05-02T21:48:54ZengWileyJournal of Diabetes Investigation2040-11162040-11242020-11-011161507151010.1111/jdi.13307Characterization of patients with diabetes who were incidentally found to be glutamic acid decarboxylase autoantibody‐positive by bridging‐type enzyme‐linked immunosorbent assayEiji Kawasaki0Takahiro Fukuyama1Aira Uchida2Yoko Sagara3Hidekazu Tamai4Yuko Nakano5Masayuki Tojikubo6Yuji Hiromatsu7Nobuhiko Koga8Department of Diabetes and Endocrinology Shin‐Koga Hospital Kurume JapanDepartment of Diabetes and Endocrinology Shin‐Koga Hospital Kurume JapanDepartment of Diabetes and Endocrinology Shin‐Koga Hospital Kurume JapanDepartment of Diabetes and Endocrinology Shin‐Koga Hospital Kurume JapanDepartment of Diabetes and Endocrinology Shin‐Koga Hospital Kurume JapanDepartment of Diabetes and Endocrinology Shin‐Koga Hospital Kurume JapanDepartment of Diabetes and Endocrinology Shin‐Koga Hospital Kurume JapanDepartment of Diabetes and Endocrinology Shin‐Koga Hospital Kurume JapanDepartment of Diabetes and Endocrinology Shin‐Koga Hospital Kurume JapanAbstract This study aimed to characterize diabetic patients incidentally found to be positive for glutamic acid decarboxylase autoantibodies (GADA) in general practice. Using bridging‐type enzyme‐linked immunosorbent assay, we screened 1,040 patients with phenotypic type 2 diabetes for GADA, finding 25 (2.4%) to be positive. However, on retesting, with a median interval of 19 days, 44% of GADA‐positive patients turned negative (Disappearing Group). The mean age at diabetes onset was significantly higher (P < 0.05) and GADA titers at first determination were significantly lower (P < 0.001) in the Disappearing Group compared with the Persistent Positive Group. On initial screening, all patients in the Disappearing Group had GADA titers of <6.5 U/mL. The current study showed that a portion of phenotypic type 2 diabetic patients incidentally identified as GADA‐positive were falsely positive, and that to avoid the misclassification, remeasurement of GADA is essential in cases showing very low titers.https://doi.org/10.1111/jdi.13307AutoantibodyFalse positiveSlowly‐progressive type 1 diabetes
collection DOAJ
language English
format Article
sources DOAJ
author Eiji Kawasaki
Takahiro Fukuyama
Aira Uchida
Yoko Sagara
Hidekazu Tamai
Yuko Nakano
Masayuki Tojikubo
Yuji Hiromatsu
Nobuhiko Koga
spellingShingle Eiji Kawasaki
Takahiro Fukuyama
Aira Uchida
Yoko Sagara
Hidekazu Tamai
Yuko Nakano
Masayuki Tojikubo
Yuji Hiromatsu
Nobuhiko Koga
Characterization of patients with diabetes who were incidentally found to be glutamic acid decarboxylase autoantibody‐positive by bridging‐type enzyme‐linked immunosorbent assay
Journal of Diabetes Investigation
Autoantibody
False positive
Slowly‐progressive type 1 diabetes
author_facet Eiji Kawasaki
Takahiro Fukuyama
Aira Uchida
Yoko Sagara
Hidekazu Tamai
Yuko Nakano
Masayuki Tojikubo
Yuji Hiromatsu
Nobuhiko Koga
author_sort Eiji Kawasaki
title Characterization of patients with diabetes who were incidentally found to be glutamic acid decarboxylase autoantibody‐positive by bridging‐type enzyme‐linked immunosorbent assay
title_short Characterization of patients with diabetes who were incidentally found to be glutamic acid decarboxylase autoantibody‐positive by bridging‐type enzyme‐linked immunosorbent assay
title_full Characterization of patients with diabetes who were incidentally found to be glutamic acid decarboxylase autoantibody‐positive by bridging‐type enzyme‐linked immunosorbent assay
title_fullStr Characterization of patients with diabetes who were incidentally found to be glutamic acid decarboxylase autoantibody‐positive by bridging‐type enzyme‐linked immunosorbent assay
title_full_unstemmed Characterization of patients with diabetes who were incidentally found to be glutamic acid decarboxylase autoantibody‐positive by bridging‐type enzyme‐linked immunosorbent assay
title_sort characterization of patients with diabetes who were incidentally found to be glutamic acid decarboxylase autoantibody‐positive by bridging‐type enzyme‐linked immunosorbent assay
publisher Wiley
series Journal of Diabetes Investigation
issn 2040-1116
2040-1124
publishDate 2020-11-01
description Abstract This study aimed to characterize diabetic patients incidentally found to be positive for glutamic acid decarboxylase autoantibodies (GADA) in general practice. Using bridging‐type enzyme‐linked immunosorbent assay, we screened 1,040 patients with phenotypic type 2 diabetes for GADA, finding 25 (2.4%) to be positive. However, on retesting, with a median interval of 19 days, 44% of GADA‐positive patients turned negative (Disappearing Group). The mean age at diabetes onset was significantly higher (P < 0.05) and GADA titers at first determination were significantly lower (P < 0.001) in the Disappearing Group compared with the Persistent Positive Group. On initial screening, all patients in the Disappearing Group had GADA titers of <6.5 U/mL. The current study showed that a portion of phenotypic type 2 diabetic patients incidentally identified as GADA‐positive were falsely positive, and that to avoid the misclassification, remeasurement of GADA is essential in cases showing very low titers.
topic Autoantibody
False positive
Slowly‐progressive type 1 diabetes
url https://doi.org/10.1111/jdi.13307
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