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Proteomic and metabolomic signatures in prediabetes progressing to diabetes or reversing to normoglycemia within 1 Year.
Diabetes Care 48, 405-415 (2025)
OBJECTIVE: Progression of prediabetes to type 2 diabetes has been associated with β-cell dysfunction, whereas its remission to normoglycemia has been related to improvement of insulin sensitivity. To understand the mechanisms and identify potential biomarkers related to prediabetes trajectories, we compared the proteomics and metabolomics profile of people with prediabetes progressing to diabetes or reversing to normoglycemia within 1 year. RESEARCH DESIGN AND METHODS: The fasting plasma concentrations of 1,389 proteins and the fasting, 30-min, and 120-min post-oral glucose tolerance test (OGTT) plasma concentrations of 152 metabolites were measured in up to 134 individuals with new-onset diabetes, prediabetes, or normal glucose tolerance. For 108 participants, the analysis was repeated with samples from 1 year before, when all had prediabetes. RESULTS: The plasma concentrations of 14 proteins were higher in diabetes compared with normoglycemia in a population with prediabetes 1 year before, and they correlated with indices of insulin sensitivity. Higher levels of dicarbonyl/L-xylulose reductase and glutathione S-transferase A3 in the prediabetic state were associated with an increased risk of diabetes 1 year later. Pathway analysis pointed toward differences in immune response between diabetes and normoglycemia that were already recognizable in the prediabetic state 1 year prior at baseline. The area under the curve during OGTT of the concentrations of IDL particles, IDL apolipoprotein B, and IDL cholesterol was higher in new-onset diabetes compared with normoglycemia. The concentration of glutamate increased in prediabetes progressing to diabetes. CONCLUSIONS: We identify new candidates associated with the progression of prediabetes to diabetes or its remission to normoglycemia. Pathways regulating the immune response are related to prediabetes trajectories.
Impact Factor
Scopus SNIP
Altmetric
16.600
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Anmerkungen
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Publikationstyp
Artikel: Journalartikel
Dokumenttyp
Wissenschaftlicher Artikel
Schlagwörter
Apolipoprotein-a-ii; Type-2; Profiles; Risk; Bond
Sprache
englisch
Veröffentlichungsjahr
2025
HGF-Berichtsjahr
2025
ISSN (print) / ISBN
0149-5992
e-ISSN
1935-5548
Zeitschrift
Diabetes Care
Quellenangaben
Band: 48,
Heft: 3,
Seiten: 405-415
Verlag
American Diabetes Association
Verlagsort
Alexandria, Va.
Begutachtungsstatus
Peer reviewed
Institut(e)
Institute of Pancreatic Islet Research (IPI)
Institute of Diabetes Research and Metabolic Diseases (IDM)
Institute of Diabetes Research and Metabolic Diseases (IDM)
POF Topic(s)
90000 - German Center for Diabetes Research
Forschungsfeld(er)
Helmholtz Diabetes Center
PSP-Element(e)
G-502600-012
G-502600-004
G-502400-001
G-502600-008
G-502600-001
G-502600-007
G-502600-004
G-502400-001
G-502600-008
G-502600-001
G-502600-007
Förderungen
German Ministry of Research and Education - Bundesministerium für Bildung und Foschung (BMBF) - Deutsches Zentrum für Diabetesforschung (DZD e.V.)
Deutsche Diabetes Gesellschaft (DDG)
Deutsche Foschungsgemeinschaft (DFG)
German Center of Diabetes Research (DZD e.V.), German Ministry of Research and Education
Deutsche Diabetes Gesellschaft (DDG)
Deutsche Foschungsgemeinschaft (DFG)
German Center of Diabetes Research (DZD e.V.), German Ministry of Research and Education
WOS ID
001434800100038
Scopus ID
85219498548
PubMed ID
39746149
Erfassungsdatum
2025-03-21