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Metabolomics insights into early type 2 diabetes pathogenesis and detection in individuals with normal fasting glucose.

Authors :
Merino, Jordi
Leong, Aaron
Liu, Ching-Ti
Porneala, Bianca
Walford, Geoffrey A.
von Grotthuss, Marcin
Wang, Thomas J.
Flannick, Jason
Dupuis, Josée
Levy, Daniel
Gerszten, Robert E.
Florez, Jose C.
Meigs, James B.
Source :
Diabetologia; Jun2018, Vol. 61 Issue 6, p1315-1324, 10p, 1 Diagram, 3 Charts, 2 Graphs
Publication Year :
2018

Abstract

Aims/hypothesis: Identifying the metabolite profile of individuals with normal fasting glucose (NFG [<5.55 mmol/l]) who progressed to type 2 diabetes may give novel insights into early type 2 diabetes disease interception and detection.Methods: We conducted a population-based prospective study among 1150 Framingham Heart Study Offspring cohort participants, age 40-65 years, with NFG. Plasma metabolites were profiled by LC-MS/MS. Penalised regression models were used to select measured metabolites for type 2 diabetes incidence classification (training dataset) and to internally validate the discriminatory capability of selected metabolites beyond conventional type 2 diabetes risk factors (testing dataset).Results: Over a follow-up period of 20 years, 95 individuals with NFG developed type 2 diabetes. Nineteen metabolites were selected repeatedly in the training dataset for type 2 diabetes incidence classification and were found to improve type 2 diabetes risk prediction beyond conventional type 2 diabetes risk factors (AUC was 0.81 for risk factors vs 0.90 for risk factors + metabolites, <italic>p</italic> = 1.1 × 10<superscript>−4</superscript>). Using pathway enrichment analysis, the nitrogen metabolism pathway, which includes three prioritised metabolites (glycine, taurine and phenylalanine), was significantly enriched for association with type 2 diabetes risk at the false discovery rate of 5% (<italic>p</italic> = 0.047). In adjusted Cox proportional hazard models, the type 2 diabetes risk per 1 SD increase in glycine, taurine and phenylalanine was 0.65 (95% CI 0.54, 0.78), 0.73 (95% CI 0.59, 0.9) and 1.35 (95% CI 1.11, 1.65), respectively. Mendelian randomisation demonstrated a similar relationship for type 2 diabetes risk per 1 SD genetically increased glycine (OR 0.89 [95% CI 0.8, 0.99]) and phenylalanine (OR 1.6 [95% CI 1.08, 2.4]).Conclusions/interpretation: In individuals with NFG, information from a discrete set of 19 metabolites improved prediction of type 2 diabetes beyond conventional risk factors. In addition, the nitrogen metabolism pathway and its components emerged as a potential effector of earliest stages of type 2 diabetes pathophysiology. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0012186X
Volume :
61
Issue :
6
Database :
Complementary Index
Journal :
Diabetologia
Publication Type :
Academic Journal
Accession number :
129492175
Full Text :
https://doi.org/10.1007/s00125-018-4599-x