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Serum Proteomes Distinguish Children Developing Type 1 Diabetes in a Cohort With HLA-Conferred Susceptibility
Author(s) -
Robert Moulder,
Santosh D. Bhosale,
Timo Erkkilä,
Essi Laajala,
Jussi Salmi,
Elizabeth V. Nguyen,
Henna Kallionpää,
Juha Mykkänen,
Mari Vähä-Mäkilä,
Heikki Hyöty,
Riitta Veijola,
Jorma Ilonen,
Tuula Simell,
Jorma Toppari,
Mikael Knip,
David R. Goodlett,
Harri Lähdesmäki,
Olli Simell,
Riitta Lahesmaa
Publication year - 2015
Publication title -
diabetes
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.219
H-Index - 330
eISSN - 1939-327X
pISSN - 0012-1797
DOI - 10.2337/db14-0983
Subject(s) - autoantibody , type 1 diabetes , seroconversion , human leukocyte antigen , proteome , cohort , diabetes mellitus , immunology , medicine , disease , biology , antibody , bioinformatics , endocrinology , antigen
We determined longitudinal serum proteomics profiles from children with HLA-conferred diabetes susceptibility to identify changes that could be detected before seroconversion and positivity for disease-associated autoantibodies. Comparisons were made between children who seroconverted and progressed to type 1 diabetes (progressors) and those who remained autoantibody negative, matched by age, sex, sample periodicity, and risk group. The samples represented the prediabetic period and ranged from the age of 3 months to 12 years. After immunoaffinity depletion of the most abundant serum proteins, isobaric tags for relative and absolute quantification were used for sample labeling. Quantitative proteomic profiles were then measured for 13 case-control pairs by high-performance liquid chromatography-tandem mass spectrometry (LC-MS/MS). Additionally, a label-free LC-MS/MS approach was used to analyze depleted sera from six case-control pairs. Importantly, differences in abundance of a set of proteins were consistently detected before the appearance of autoantibodies in the progressors. Based on top-scoring pairs analysis, classification of such progressors was observed with a high success rate. Overall, the data provide a reference of temporal changes in the serum proteome in healthy children and children progressing to type 1 diabetes, including new protein candidates, the levels of which change before clinical diagnosis.

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