4.7 Article

Postprandial Plasma Concentrations of Individual Bile Acids and FGF-19 in Patients With Type 2 Diabetes

期刊

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
卷 101, 期 8, 页码 3002-3009

出版社

ENDOCRINE SOC
DOI: 10.1210/jc.2016-1607

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  1. Department of Pharmaceutical Biosciences, Uppsala University, Uppsala, Sweden
  2. Department of Clinical Biochemistry at Rigshospitalet, Copenhagen, Denmark
  3. Novo Nordisk Foundation Center for Basic Metabolic Research, University of Copenhagen
  4. Dutch Diabetes Research Foundation
  5. NNF Center for Basic Metabolic Research [Holst Group] Funding Source: researchfish
  6. Novo Nordisk Fonden [NNF16OC0020224, NNF15OC0016230, NNF12OC1015904] Funding Source: researchfish

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Context: Bile acids regulate lipid and carbohydrate metabolism by interaction with membrane or intracellular proteins including the nuclear farnesoid X receptor (FXR). Postprandial activation of ileal FXR leads to secretion of fibroblast growth factor 19 (FGF-19), a gut hormone that may be implicated in postprandial glucose metabolism. Objective: To describe postprandial plasma concentrations of 12 individual bile acids and FGF-19 in patients with type 2 diabetes (T2D) and healthy controls. Design and Setting: Descriptive study, performed at the Center for Diabetes Research, Gentofte Hospital, Hellerup, Denmark. Participants: Fifteen patients with T2D and 15 healthy matched controls with normal glucose tolerance. Interventions: A 75-g oral glucose tolerance test and three isocaloric and isovolemic liquid meals with low, medium, and high fat content, respectively. Main Outcome Measures: Bile acid and FGF-19 concentrations. Results: Postprandial total bile acid concentrations increased with increasing meal fat content (P < .05), peaked after 1-2 hours, and were higher in T2D patients vs controls (oral glucose tolerance test, low and medium fat meals, P < .05; high fat meal, P = .30). Differences reflected mainly unconjugated and glycine-conjugated forms of deoxycholic acid (DCA) and to a lesser extent cholic acid (CA) and ursodeoxycholic acid (UDCA), whereas chenodeoxycholic acid (CDCA) concentrations were comparable in the two groups. FGF-19 concentrations tended to be lower in T2D patients vs controls, but differences were not statistically significant due to considerable variation. Conclusion: Postprandial plasma patterns of bile acids with FXR agonistic properties (CDCA, DCA, and CA) and FXR antagonistic properties (UDCA) in T2D patients support the notion of a T2D-bile acid-FGF-19 phenotype with possible pathophysiological implications.

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