4.7 Article

Roux-en-Y Gastric Bypass Surgery Has Unique Effects on Postprandial FGF21 but Not FGF19 Secretion

Journal

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
Volume 102, Issue 10, Pages 3858-3864

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1210/jc.2017-01295

Keywords

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Funding

  1. National Institutes of Health [DK101578, DK56341, DK20579, P30DK092950, UL1-RR-024992, UL1-TR-000448, TR-000450]
  2. Atkins Foundation Philanthropic Trust
  3. Pershing Square Foundation

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Context: Fibroblast growth factor (FGF)19 and FGF21 are secreted by the intestine and liver in response to macronutrient intake. Intestinal resection and reconstruction via bariatric surgery may alter their regulation. Objective: We tested the hypothesis that weight loss induced by Roux-en-Y gastric bypass (RYGB) surgery, but not matched weight loss induced by laparoscopic adjustable gastric banding (LAGB), increases postprandial plasma FGF19 and FGF21 concentrations. Design: Glucose kinetics and plasma FGF19 and FGF21 responses to mixed meal ingestion and to glucose-insulin infusion during a hyperinsulinemic-euglycemic clamp procedure, with stable isotope tracer methods, were evaluated in 28 adults with obesity before and after 20% weight loss induced by RYGB (n = 16) or LAGB (n = 12). Results: LAGB- and RYGB-induced weight loss increased postprandial plasma FGF19 concentrations (P < 0.05). However, weight loss after RYGB, but not LAGB, increased postprandial plasma FGF21 concentrations (1875 +/- 330 to 2976 +/- 682 vs 2150 +/- 310 and 1572 +/- 265 pg/mL x 6 hours, respectively). The increase in plasma FGF21 occurred similar to 2 hours after the peak in delivery of ingested glucose into systemic circulation. Glucose-insulin infusion increased plasma FGF21, but not FGF19, concentrations. The increase in plasma FGF21 during glucose-insulin infusion was greater after than before weight loss in both surgery groups without a difference between groups, whereas plasma FGF19 was not affected by either procedure. Conclusions: RYGB-induced weight loss has unique effects on postprandial FGF21 metabolism, presumably due to rapid delivery of ingested macronutrients to the small intestine and delivery of glucose to the liver.

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