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Bariatric Surgeries and Glucose Homeostasis During a Mixed Meal Test (BASMEAL)

I

Integrated University Hospital Trust of Verona

Status

Completed

Conditions

Obesity

Treatments

Procedure: laparoscopic adjustable gastric banding
Procedure: Roux-en-Y-gastric bypass
Other: diet treatment
Procedure: laparoscopic sleeve gastrectomy

Study type

Observational

Funder types

Other

Identifiers

NCT01767441
MGZenti MMT

Details and patient eligibility

About

Bariatric surgery can lead to improvement or even resolution of type 2 diabetes Mellitus (T2DM) with the spectrum of responses depending also on operation procedures. However, many mechanisms of metabolic action of different surgical techniques still are unclear.

The aim of this study is to provide a better understanding of the effects of three types of bariatric surgery (lap banding, gastric bypass and sleeve gastrectomy) on beta-cell function and incretin secretion. A mixed meal tolerance (MMT) test will be performed before and 1 and 12 months after surgery to assess beta cell adequacy and glucagon-like-peptide-1 (GLP1)/glucose-dependent insulinotropic polypeptide (GIP) bioavailability.

Full description

The effects of different kind of bariatric surgery on glucose homeostasis and its primary determinants (insulin sensitivity and secretion) may differ from one procedure to another. In spite being able to promote improvement/resolution of T2DM, many mechanisms of metabolic action of weight-loss surgery are still unclear. It has been hypothesized that changing the nutrient route through the gut may be a key factor in changing beta cell function and/or insulin sensitivity.

In this study a mixed meal test will be used to assess changes in glucose regulation, beta cell function and incretin bioavailability brought about by different bariatric surgeries in obese patients.

All participants will ingest a standardized mixed meal (163 Kcal; 57% carbohydrate, 33% fat, 22% prot) and will be monitored for 300 minutes thereafter.

Baseline (-20', -10', 0') blood samples will be collected to measure plasma glucose, insulin, C-peptide, incretins and the 13-Carbon-glucose/12-Carbon-glucose (13C-/12C-glucose) ratio (the last one by isotope ratio mass spectrometry).

At time 0', subjects will ingest a standardized mixed meal containing 30 g corn flour and 20 g cheese (parmesan) over 20 minutes. Plasma glucose, insulin, C-peptide, GLP1/GIP and the 13C-/12C-glucose ratio will be assessed at +10', +20', +30', +45', +60', +75', +90', +105', +120', +140', +160', +180', +200', +220', +240', +270', +300'.

Blood samples will be quickly spun at 1500 g at +4°C, plasma/serum will be collected and stored at -80°C.

The 13-Carbon content of maize starch is higher than most of non maize derived sugars. Thus, in individuals on maize and cane sugar free diets, the 13-Carbon/12-Carbon (13C/12C) maize starch ratio is higher (about 10:1000) than the 13C/12C ratio of endogenous glucose derived from glycogenolysis/gluconeogenesis. When these individuals ingest maize starch, the glucose molecules appearing in the systemic circulation which are derived from maize starch will display a 13C-/12C ratio which is identical to maize starch and higher than endogenous glucose. Thus, by measuring the time course of plasma 13C-/12C-glucose ratio, it will be possible to distinguish meal derived glucose from endogenous glucose output (glycogenolysis and gluconeogenesis).

This mixed meal test will be performed before and 1 and 12 months after bariatric surgery. The same tests with the same timing will be performed in a control group of obese patients not undergoing bariatric surgery, being treated with diet only.

Enrollment

16 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • BMI > 40 kg/m2.
  • BMI ≥ 35 kg/m2 and comorbidities.
  • No major organ disease unrelated to excess body weight.
  • Mentally able to understand the study and willingness to participate in the study

Exclusion criteria

  • BMI< 35 kg/m2.
  • pregnancy/lactation.
  • prior bariatric or gastrointestinal surgery. Malignancies; mental incapacity; unwillingness or language barriers precluding adequate understanding or cooperation

Trial design

16 participants in 4 patient groups

Roux-en-Y-gastric bypass
Description:
morbidly obese subjects undergoing gastric bypass surgery
Treatment:
Procedure: Roux-en-Y-gastric bypass
gastric banding
Description:
morbidly obese subjects undergoing laparoscopic adjustable gastric banding
Treatment:
Procedure: laparoscopic adjustable gastric banding
sleeve gastrectomy
Description:
morbidly obese subjects undergoing laparoscopic sleeve gastrectomy
Treatment:
Procedure: laparoscopic sleeve gastrectomy
control group
Description:
morbidly obese subjects not undergoing bariatric surgery, on diet treatment
Treatment:
Other: diet treatment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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