4.7 Article

Serum bile acid response to oral glucose is attenuated in patients with early type 2 diabetes and correlates with 2-hour plasma glucose in individuals without diabetes

Journal

DIABETES OBESITY & METABOLISM
Volume 24, Issue 6, Pages 1132-1142

Publisher

WILEY
DOI: 10.1111/dom.14683

Keywords

bile acids; fibroblast growth factor-19; glucagon-like peptide-1; postprandial glycaemia; type 2 diabetes

Funding

  1. University of Adelaide, as part of the Wiley The University of Adelaide agreement via the Council of Australian University Librarians
  2. WOA Institution: The University of Adelaide
  3. Blended DEAL: CAUL [2022]

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This study found that the serum bile acid response to a 75-g oral glucose load is attenuated in patients with 'early' type 2 diabetes, while in individuals without diabetes it correlates with 2-hour plasma glucose levels.
Aim To determine the serum bile acid (BA) response to 75-g oral glucose in individuals without diabetes, and whether this is attenuated in patients with 'early' type 2 diabetes (T2D) and related to the glycaemic response at 2 hours in either group. Methods Forty newly diagnosed, treatment-naive Han Chinese T2D subjects and 40 age-, gender-, and body mass index-matched controls without T2D ingested a 75-g glucose drink after an overnight fast. Plasma glucose and serum concentrations of total and individual BAs, fibroblast growth factor-19 (FGF-19), total glucagon-like peptide-1 (GLP-1), and insulin, were measured before and 2 hours after oral glucose. Results Fasting total BA levels were higher in T2D than control subjects (P < .05). At 2 hours, the BA profile exhibited a shift from baseline in both groups, with increases in conjugated BAs and/or decreases in unconjugated BAs. There were increases in total BA and FGF-19 levels in control (both P < .05), but not T2D, subjects. Plasma glucose concentrations at 2 hours related inversely to serum total BA levels in control subjects (r = -0.42, P = .006). Total GLP-1 and the insulin/glucose ratio were increased at 2 hours in both groups, and the magnitude of the increase was greater in control subjects. Conclusions The serum BA response to a 75-g oral glucose load is attenuated in patients with 'early' T2D, as is the secretion of FGF-19 and GLP-1, while in individuals without T2D it correlates with 2-hour plasma glucose levels. These observations support a role for BAs in the regulation of postprandial glucose metabolism.

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