Recovery of the incretin effect in type 2 diabetic patients after biliopancreatic diversion

Research output: Contribution to journalJournal articleResearchpeer-review

  • Fernanda S. Novaes
  • Ana C.J. Vasques
  • José C. Pareja
  • Knop, Filip Krag
  • Andrea Tura
  • Élinton A. Chaim
  • Bruno Geloneze

Context: Bariatric surgery often results in remission of the diabetic state in obese patients. Increased incretin effect seems to play an important role in the glycemic improvements after Rouxen-Y gastric bypass, but the impact of biliopancreatic diversion (BPD) remains unexplored. Objective: The objective was to elucidate the effect of BPD on the incretin effect and its interplay with beta-cell function and insulin sensitivity (IS) in obese subjects with type 2 diabetes (T2DM). Design, Setting and Patients: Twenty-three women were studied: a control group of 13 lean, normal glucose-tolerant women (lean NGT) studied once and 10 obese patients with T2DM studied before, 1 and 12 months after BPD. Intervention: The ObeseT2DM group underwent BPD. Main Outcome Measures: The main outcome measure was the change in incretin effect as measured by the isoglycemic intravenous glucose infusion test. Secondary outcomes encompassed IS and beta-cell function. Results: At baseline, the incretin effect was lower in obese T2DM compared to lean NGT (P < .05). One month after BPD, the incretin effect was not changed, but at 12 months it reached the level of the lean NGT group (P > .05). IS improved (P < .05) 1 month after BPD and at 12 months it resembled the levels of the lean NGT group. Insulin secretory rate and beta-cell glucose sensitivity increased after BPD and achieved levels similar to lean NGT group 1 month after BPD and even higher levels at 12 months (P < .05). Conclusions: BPD has no acute impact on the reduced incretin effect, but 12 months after surgery the incretin effect normalizes alongside normalization of glucose control, IS and beta-cell function.

Original languageEnglish
JournalJournal of Clinical Endocrinology and Metabolism
Volume100
Issue number5
Pages (from-to)1984-1988
Number of pages5
ISSN0021-972X
DOIs
Publication statusPublished - 1 May 2015

Bibliographical note

Publisher Copyright:
Copyright © 2015 by the Endocrine Society.

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