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Methylglyoxal products in pre-symptomatic type 1 diabetes

INTRODUCTION: Progression 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 pr...

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Autores principales: Shuck, Sarah C., Achenbach, Peter, Roep, Bart O., Termini, John S., Hernandez-Castillo, Carlos, Winkler, Christiane, Weiss, Andreas, Ziegler, Anette-Gabriele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9892703/
https://www.ncbi.nlm.nih.gov/pubmed/36742390
http://dx.doi.org/10.3389/fendo.2023.1108910
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author Shuck, Sarah C.
Achenbach, Peter
Roep, Bart O.
Termini, John S.
Hernandez-Castillo, Carlos
Winkler, Christiane
Weiss, Andreas
Ziegler, Anette-Gabriele
author_facet Shuck, Sarah C.
Achenbach, Peter
Roep, Bart O.
Termini, John S.
Hernandez-Castillo, Carlos
Winkler, Christiane
Weiss, Andreas
Ziegler, Anette-Gabriele
author_sort Shuck, Sarah C.
collection PubMed
description INTRODUCTION: Progression 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. METHODS: We 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. RESULTS: We 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. DISCUSSION: MG-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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spelling pubmed-98927032023-02-03 Methylglyoxal products in pre-symptomatic type 1 diabetes Shuck, Sarah C. Achenbach, Peter Roep, Bart O. Termini, John S. Hernandez-Castillo, Carlos Winkler, Christiane Weiss, Andreas Ziegler, Anette-Gabriele Front Endocrinol (Lausanne) Endocrinology INTRODUCTION: Progression 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. METHODS: We 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. RESULTS: We 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. DISCUSSION: MG-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. Frontiers Media S.A. 2023-01-19 /pmc/articles/PMC9892703/ /pubmed/36742390 http://dx.doi.org/10.3389/fendo.2023.1108910 Text en Copyright © 2023 Shuck, Achenbach, Roep, Termini, Hernandez-Castillo, Winkler, Weiss and Ziegler https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Shuck, Sarah C.
Achenbach, Peter
Roep, Bart O.
Termini, John S.
Hernandez-Castillo, Carlos
Winkler, Christiane
Weiss, Andreas
Ziegler, Anette-Gabriele
Methylglyoxal products in pre-symptomatic type 1 diabetes
title Methylglyoxal products in pre-symptomatic type 1 diabetes
title_full Methylglyoxal products in pre-symptomatic type 1 diabetes
title_fullStr Methylglyoxal products in pre-symptomatic type 1 diabetes
title_full_unstemmed Methylglyoxal products in pre-symptomatic type 1 diabetes
title_short Methylglyoxal products in pre-symptomatic type 1 diabetes
title_sort methylglyoxal products in pre-symptomatic type 1 diabetes
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9892703/
https://www.ncbi.nlm.nih.gov/pubmed/36742390
http://dx.doi.org/10.3389/fendo.2023.1108910
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