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Controlled Clinical Trial
. 2019 Feb;42(2):311-317.
doi: 10.2337/dc18-1036. Epub 2018 Dec 6.

Insulin Clearance After Oral and Intravenous Glucose Following Gastric Bypass and Gastric Banding Weight Loss

Affiliations
Controlled Clinical Trial

Insulin Clearance After Oral and Intravenous Glucose Following Gastric Bypass and Gastric Banding Weight Loss

Ankit Shah et al. Diabetes Care. 2019 Feb.

Abstract

Objective: Hepatic insulin clearance is a significant regulator of glucose homestasis. We hypothesized that the improvement in insulin clearance rates (ICRs) under fasting conditions and in response to oral and intravenous (IV) glucose would improve similarly after Roux-en-Y gastric bypass (RYGB) and adjustable gastric banding (AGB) as a function of weight loss; the difference in ICR after oral and IV glucose stimulation will be enhanced after RYGB compared with AGB, an effect mediated by glucagon-like peptide 1 (GLP-1).

Research design and methods: In study 1, the ICR was calculated under fasting condition (F-ICR), after oral glucose (O-ICR), and after an isoglycemic IV glucose clamp (IV-ICR) in individuals from an established cohort with type 2 diabetes mellitus (T2DM) before, after 10% matched weight loss, and 1 year after either RYGB (n = 22) or AGB (n = 12). In study 2, O-ICR was studied in a separate cohort of individuals with T2DM (n = 22), before and 3 months after RYGB, with and without exendin(9-39) infusion.

Results: In study 1, age, BMI, T2DM duration and control, and ICR did not differ between RYGB and AGB preintervention. Weight loss at 1 year was two times greater after RYGB than after AGB (31.6 ± 5.9% vs. 16.6 ± 9.8%; P < 0.05). RYGB and AGB both significantly increased F-ICR, O-ICR, and IV-ICR at 1 year. ICR was inversely associated with insulinemia. The difference between IV-ICR and O-ICR was significantly greater after RYGB versus AGB. GLP-1 antagonism with exendin(9-39) led to an increase in O-ICR in subjects post-RYGB.

Conclusions: Weight loss increased ICR, an effect more pronounced after RYGB compared with AGB. Our data support a potential role for endogenous GLP-1 in the control of postprandial ICR after RYGB.

Trial registration: ClinicalTrials.gov NCT02287285.

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Figures

Figure 1
Figure 1
Change in fasting (A), oral (B), IV (C), and Δ (D) ICR before and after AGB or RYGB at presurgery (Pre), 10% matched weight loss, and 1 year postintervention. Mean ± SE. *P < 0.05 for paired Student t test vs. preintervention; $P < 0.05 for paired Student t test vs. 10% matched weight loss; #P < 0.05 for unpaired Student t test vs. AGB.
Figure 2
Figure 2
Changes in insulin clearance after 75-g OGTT (O-ICR) before (Pre) and 3 months after (3M) RYGB with saline (Sal) and EX9. Mean ± SE.

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