Frontiers in Endocrinology (Jan 2023)

Methylglyoxal products in pre-symptomatic type 1 diabetes

  • Sarah C. Shuck,
  • Peter Achenbach,
  • Peter Achenbach,
  • Peter Achenbach,
  • Bart O. Roep,
  • John S. Termini,
  • Carlos Hernandez-Castillo,
  • Christiane Winkler,
  • Christiane Winkler,
  • Andreas Weiss,
  • Andreas Weiss,
  • Anette-Gabriele Ziegler,
  • Anette-Gabriele Ziegler,
  • Anette-Gabriele Ziegler

DOI
https://doi.org/10.3389/fendo.2023.1108910
Journal volume & issue
Vol. 14

Abstract

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IntroductionProgression to type 1 diabetes has emerged as a complex process with metabolic alterations proposed to be a significant driver of disease. Monitoring products of altered metabolism is a promising tool for determining the risk of type 1 diabetes progression and to supplement existing predictive biomarkers. Methylglyoxal (MG) is a reactive product produced from protein, lipid, and sugar metabolism, providing a more comprehensive measure of metabolic changes compared to hyperglycemia alone. MG forms covalent adducts on nucleic and amino acids, termed MG-advanced glycation end products (AGEs) that associate with type 1 diabetes.MethodsWe tested their ability to predict risk of disease and discriminate which individuals with autoimmunity will progress to type 1 diabetes. We measured serum MG-AGEs from 141 individuals without type 1 diabetes and 271 individuals with type 1 diabetes enrolled in the Fr1da cohort. Individuals with type 1 diabetes were at stages 1, 2, and 3.ResultsWe examined the association of MG-AGEs with type 1 diabetes. MG-AGEs did not correlate with HbA1c or differ between stages 1, 2, and 3 type 1 diabetes. Yet, RNA MG-AGEs were significantly associated with the rate of progression to stage 3 type 1 diabetes, with lower serum levels increasing risk of progression.DiscussionMG-AGEs were able to discriminate which individuals with autoantibodies would progress at a faster rate to stage 3 type 1 diabetes providing a potential new clinical biomarker for determining rate of disease progression and pointing to contributing metabolic pathways.

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