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Diabetologia. 2015 Oct;58(10):2317-23. doi: 10.1007/s00125-015-3672-y. Epub 2015 Jul 3.

Islet autoantibody phenotypes and incidence in children at increased risk for type 1 diabetes.

Author information

1
Institute of Diabetes Research, Helmholtz Zentrum München and Forschergruppe Diabetes, Klinikum rechts der Isar, Technische Universität München, Ingolstaedter Landstr. 1, 85764, Neuherberg, Germany.
2
Forschergruppe Diabetes e.V., Neuherberg, Germany.
3
Center for Regenerative Therapies Dresden, Faculty of Medicine, Technische Universität, Dresden, Germany.
4
Paul Langerhans Institute of the Helmholtz Zentrum München at University Clinic Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
5
Institute of Diabetes and Obesity, Helmholtz Zentrum München, Neuherberg, Germany.
6
Institute of Diabetes Research, Helmholtz Zentrum München and Forschergruppe Diabetes, Klinikum rechts der Isar, Technische Universität München, Ingolstaedter Landstr. 1, 85764, Neuherberg, Germany. anette-g.ziegler@helmholtz-muenchen.de.
7
Forschergruppe Diabetes e.V., Neuherberg, Germany. anette-g.ziegler@helmholtz-muenchen.de.

Abstract

AIMS/HYPOTHESIS:

Autoantibodies that precede type 1 diabetes frequently develop in early childhood and target distinct beta cell proteins. The aim of this study was to determine the heterogeneity of islet autoantibody development and fate.

METHODS:

The ages of development of insulin autoantibodies (IAA) and GAD autoantibodies (GADA), followed by multiple islet autoantibodies and progression to diabetes were examined in 2,441 children participating in two German birth cohorts.

RESULTS:

In 218 children who developed islet autoantibodies, the first islet autoantibody-positive sample was characterised by single IAA in 80 (37%), multiple islet autoantibodies in 68 (31%) and single GADA in 63 (29%) children. Of the children who were single antibody positive at seroconversion, 35 (44%) IAA-positive and 15 (24%) GADA-positive children developed multiple islet autoantibodies. Single persistent antibodies had heterogeneous affinities; GADA were also heterogeneous in their binding to N-terminally truncated GAD65 and in an ELISA. Progression to diabetes occurred in >50% of children within 10 years in all groups that developed multiple islet autoantibodies and in 44% of children with persistent single high-affinity IAA or persistent single GADA that were positive in both a radiobinding assay and ELISA. The earliest autoantibody development was seen in children with single IAA that progressed to multiple islet autoantibodies or in those with persistent high-affinity single IAA, with a sharp peak in incidence observed at age 9 months. The peak incidence occurred at age 2 years for children who underwent seroconversion directly to multiple islet autoantibodies and at 5 years for children who first seroconverted to GADA and subsequently developed other autoantibodies. Seroconversion to low-affinity IAA or persistent single GADA occurred at a low incidence after the age of 9 months.

CONCLUSIONS/INTERPRETATION:

Children of different ages have differing susceptibilities to autoimmunisation against specific beta cell autoantigens.

KEYWORDS:

Incidence; Islet autoantibodies; Type 1 diabetes

PMID:
26138334
DOI:
10.1007/s00125-015-3672-y
[Indexed for MEDLINE]

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