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Erschienen in: Diabetologia 2/2017

04.11.2016 | Article

Peptide serum markers in islet autoantibody-positive children

verfasst von: Christine von Toerne, Michael Laimighofer, Peter Achenbach, Andreas Beyerlein, Tonia de las Heras Gala, Jan Krumsiek, Fabian J. Theis, Anette G. Ziegler, Stefanie M. Hauck

Erschienen in: Diabetologia | Ausgabe 2/2017

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Abstract

Aims/hypothesis

We sought to identify minimal sets of serum peptide signatures as markers for islet autoimmunity and predictors of progression rates to clinical type 1 diabetes in a case–control study.

Methods

A double cross-validation approach was applied to first prioritise peptides from a shotgun proteomic approach in 45 islet autoantibody-positive and -negative children from the BABYDIAB/BABYDIET birth cohorts. Targeted proteomics for 82 discriminating peptides were then applied to samples from another 140 children from these cohorts.

Results

A total of 41 peptides (26 proteins) enriched for the functional category lipid metabolism were significantly different between islet autoantibody-positive and autoantibody-negative children. Two peptides (from apolipoprotein M and apolipoprotein C-IV) were sufficient to discriminate autoantibody-positive from autoantibody-negative children. Hepatocyte growth factor activator, complement factor H, ceruloplasmin and age predicted progression time to type 1 diabetes with a significant improvement compared with age alone.

Conclusion/interpretation

Distinct peptide signatures indicate islet autoimmunity prior to the clinical manifestation of type 1 diabetes and enable refined staging of the presymptomatic disease period.
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Metadaten
Titel
Peptide serum markers in islet autoantibody-positive children
verfasst von
Christine von Toerne
Michael Laimighofer
Peter Achenbach
Andreas Beyerlein
Tonia de las Heras Gala
Jan Krumsiek
Fabian J. Theis
Anette G. Ziegler
Stefanie M. Hauck
Publikationsdatum
04.11.2016
Verlag
Springer Berlin Heidelberg
Erschienen in
Diabetologia / Ausgabe 2/2017
Print ISSN: 0012-186X
Elektronische ISSN: 1432-0428
DOI
https://doi.org/10.1007/s00125-016-4150-x

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