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DOI 10.1007/s00125-018-4599-x

Медицинская библиотека · Diabetologia · 2018

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

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

СтатьяНаблюдательное исследованиеПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

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, p = 1.1 × 10-4). 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% (p = 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.

Для цитирования: 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. Metabolomics insights into early type 2 diabetes pathogenesis and detection in individuals with normal fasting glucose.. Diabetologia. 2018. DOI: 10.1007/s00125-018-4599-x.

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