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Effect of Bile Acids on GLP-1 Secretion

Not Applicable
Completed
Conditions
Type 2 Diabetes
Obesity
Interventions
Registration Number
NCT01666223
Lead Sponsor
University Hospital, Gentofte, Copenhagen
Brief Summary

The purpose of this study is to describe the physiological, pathophysiological and potentially therapeutic implications of bile-induced glucagon-like peptide-1 (GLP-1) secretion in human glucose homeostasis.

Detailed Description

The investigators hypothesize that even modest increments in endogenous GLP-1 secretion will elicit important antidiabetic effects of GLP-1. To evaluate whether bile acids have such effects, the investigators plan to perform intraduodenal infusion of two different bile acids and placebo.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
20
Inclusion Criteria
  • danish caucasian ethnicity
  • normal haemoglobin
  • BMI > 25 kg/m2
  • HbA1c < 9%
  • informed consent
Exclusion Criteria
  • liver disease(ALT and AST > upper reference limit)
  • gastrointestinal disease
  • liver and biliary tract disease
  • nephropathy (serum creatinine > 150 μM, and/or albuminuria)
  • treatment with insulin, glp-1 analogues and/ or DPP-4 inhibitors
  • treatment with medicine that can not be paused for 12 hours
  • previous abdominal surgery eg. cholecystectomy
  • BMI < 18,5 kg/m2 or > 35 kg/m2

Healthy Volunteers

Inclusion Criteria:

  • danish caucasian ethnicity
  • normal haemoglobin
  • HbA1c < 6,0 (American Diabetes Association guidelines)
  • informed consent

Exclusion Criteria:

  • liver disease(ALT and AST > upper reference limit)
  • gastrointestinal disease
  • liver and biliary tract disease
  • nephropathy (serum creatinine > 150 μM, and/or albuminuria)
  • treatment with medicine that can not be paused for 12 hours
  • previous abdominal surgery eg. cholecystectomy
  • BMI < 18,5 kg/m2 or > 35 kg/m2
  • first degree relatives diagnosed with diabetes
  • previously diagnosed with diabetes, or treated with antidiabetic agents

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Colesevelam + chenodeoxycholic acidColesevelam 3750 mg + chenodeoxycholic acid 1250 mg-
Placebosaline-
ColesevelamColesevelam-
Chenodeoxycholic acidChenodeoxycholic Acid-
Primary Outcome Measures
NameTimeMethod
Change in GLP-1At baseline, and at 5, 10, 20, 30, 40, 50, 60, 75, 90, 105, 120, 150 and 180 minutes
Secondary Outcome Measures
NameTimeMethod
Change in peptide YY (PYY)At baseline, and at 5, 10, 20, 30, 40, 50, 60, 75, 90, 105, 120, 150 and 180 minutes
Change in oxyntomodulinAt baseline, and at 5, 10, 20, 30, 40, 50, 60, 75, 90, 105, 120, 150 and 180 minutes
Change in bile acidsAt baseline, and at 5, 10, 20, 30, 40, 50, 60, 75, 90, 105, 120, 150 and 180 minutes
Change in gastrinAt baseline, and at 5, 10, 20, 30, 40, 50, 60, 75, 90, 105, 120, 150 and 180 minutes
Change in CCKAt baseline, and at 5, 10, 20, 30, 40, 50, 60, 75, 90, 105, 120, 150 and 180 minutes
Change in appetite, satiety and prospective food consumptionAt baseline, and 30, 60, 90, 120 and 180 minutes

Evaluated by Visual Analog Scale (VAS)

Change in gallbladder volume-30, 0 (baseline), 30, 60, 120 og 180 minutes

Evaluated by ultrasound

Change in basal metabolic rateAt -30, 60 og 150 minutes

Evaluated by indirect calorimetry

Change in bile acid compositionAt -30, 0, 30, 60, 120 og 180 minutes

Evaluated by duodenal aspiration

Change in insulinAt baseline, and at 5, 10, 20, 30, 40, 50, 60, 75, 90, 105, 120, 150 and 180 minutes
Change in C-peptideAt baseline, and at 5, 10, 20, 30, 40, 50, 60, 75, 90, 105, 120, 150 and 180 minutes
Change in glucagonAt baseline, and at 5, 10, 20, 30, 40, 50, 60, 75, 90, 105, 120, 150 and 180 minutes
Change in glucagon-like-peptide 2 (GLP-2)At baseline, and at 5, 10, 20, 30, 40, 50, 60, 75, 90, 105, 120, 150 and 180 minutes
Change in glucose-dependent insulinotropic polypeptide (GIP)At baseline, and at 5, 10, 20, 30, 40, 50, 60, 75, 90, 105, 120, 150 and 180 minutes

Trial Locations

Locations (1)

Diabetes Research Division, Department of Internal Medicine, Gentofte Hospital, University of Copenhagen

🇩🇰

Hellerup, Copenhagen, Denmark

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