Effect of Bile Acid Sequestration on Postprandial GLP-1 Secretion, Glucose Homeostasis and Gut Microbiota

Type 2 Diabetes Clinical Trial

Official title:

Effect of Bile Acid Sequestration on Postprandial GLP-1 Secretion, Glucose Homeostasis and Gut Microbiota

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02061124
• Other study ID #: H-2-2013-148
• Status: Completed
• Phase: N/A
• First received: February 6, 2014
• Last updated: November 20, 2015
• Start date: February 2014
• Est. completion date: October 2015

Study information

• Verified date: November 2015
• Source: University Hospital, Gentofte, Copenhagen
• Contact: n/a
• Is FDA regulated: No
• Health authority: Denmark: The Regional Committee on Biomedical Research EthicsDenmark: National Board of HealthDenmark: Danish Dataprotection Agency
• Study type: Interventional

Clinical Trial Summary

Accumulating evidence suggests that bile acids and bacteria in our intestines may constitute essential components in the complex mechanisms regulating gut hormone secretion and glucose homeostasis. At the same time, bile acids and gut bacteria are interdependent. Thus, it is likely that modification of the enterohepatic circulation of bile acids can lead to changes in gut hormone secretion or gut bacteria composition and consequently affect glucose homeostasis.

The current study is a human interventional study with 7-day ingestion of a bile acid sequestrant or placebo, preceded and followed by meal tests and faecal sampling. The aim is to examine how (and if) bile acid sequestration can influence postprandial glucagon-like peptide-1 (GLP-1) secretion, gut microbiota and glucose homeostasis in patients with type 2 diabetes and healthy individuals. As a tool to sequester bile acids we will use sevelamer, a phosphate binding resin used in the treatment of hyperphosphataemia in adult patients with chronic kidney disease. Surprisingly, sevelamer was recently shown to improve glycaemic control in patients with chronic kidney disease and type 2 diabetes.

The investigators hypothesize that higher luminal concentrations of bile acids in the distal gut will elicit changes in the postprandial gut hormone secretion and gut bacteria composition. The current study will help to clarify this hypothesis and improve our general understanding of the association between bile acid circulation and signalling, gut hormone secretion, gut bacteria and glucose metabolism.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 50
• Est. completion date: October 2015
• Est. primary completion date: October 2015
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 35 Years to 80 Years

Eligibility

Inclusion Criteria:

Both groups

• Caucasian ethnicity

• Normal haemoglobin

• Age above 35 years and below 80 years

• Informed and written consent

• BMI > 23 kg/m2 and <35 kg/m2

Patients with type 2 diabetes

• Type 2 diabetes for at least 3 months

• Diagnosed according to the criteria of the World Health Organization (WHO)

Healthy Subjects

• Normal fasting plasma glucose (FPG) <6.5 mM and

• Normal glycated haemoglobin (HbA1c) <6.0 %

Exclusion Criteria:

Both groups

• Liver disease (alanine aminotransferase (ALAT) and/or serum aspartate aminotransferase (ASAT) >2 times normal values) or history of hepatobiliary disorder

• Gastrointestinal disease, previous intestinal resection, cholecystectomy or any major intra-abdominal surgery

• Hypo- or hyperphosphataemia

• Nephropathy (serum creatinine >150 µM and/or albuminuria

• Treatment with medicine that cannot be paused for 12 hours

• Intake of antibiotics six months prior to study

• Hypo- or hypercalcaemia

• Hypo- and hyperthyroidism

• Treatment with oral anticoagulants

• Active or recent malignant disease

• Any treatment or condition requiring acute or sub-acute medical or surgical intervention

• Lack of effective birth control in premenopausal women

• Positive pregnancy test on study days in premenopausal women

• Tobacco smoking

• Any condition considered incompatible with participation by the investigators

Patients with type 2 diabetes

• Treatment with insulin

• Treatment with incretin-based therapy

Healthy Subjects

• Diabetes or

• prediabetes (fasting plasma glucose levels >6.5 mM or HbA1c >6.0%)

• First-degree relatives with diabetes

Study Design

Allocation: Randomized, Endpoint Classification: Pharmacokinetics/Dynamics Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Basic Science

Related Conditions & MeSH terms

• Type 2 Diabetes

Intervention

Drug:
• Sevelamer 1600 mg TID for 7 days

• Placebo 1600 mg TID for 7 days

Locations

Country	Name	City	State
Denmark	Diabetes Research Division, Gentofte Hospital, Copenhagen	Hellerup

Sponsors (2)

Lead Sponsor	Collaborator
University Hospital, Gentofte, Copenhagen	Sanofi

Country where clinical trial is conducted

Denmark, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Blood analysis	Lipids	Fasting status on study days 1 and 7	No
Other	Blood analysis	Inflammatory and metabolic markers	Fasting status on study days 1 and 7	No
Other	Faecal samples	Gut microbiota composition	Prior to study days 1 and 7	No
Other	Blood analysis of paracetamol	Assessment of gastric emptying	-30 min to 240 min (ingestion of meal at 0 min) on study days 1 and 7	No
Other	Bodyweight		Fasting state on study days 1 and 7	No
Other	Indirect calorimetry	Basal metabolic rate	-30 min to 240 min (ingestion of meal at 0 min) on study days 1 and 7	No
Other	Ultrasound measurements	Gall bladder volume	-30 min to 240 min (ingestion of meal at 0 min) on study days 1 and 7	No
Other	Visual analog scale score	Appetite	-30 min to 240 min (ingestion of meal at 0 min) on study days 1 and 7	No
Primary	Incremental and total area under the Concentration-Time Curve (AUC 0-240 min)	Postprandial responses of glucagon-like peptide-1 (GLP-1)	-30, -15, 0, 10, 20, 30, 45, 60, 90, 120, 180, 240 min on study days 1 and 7 (meal tests start at 0 min)	No
Secondary	Incremental and total area under the Concentration-Time Curve (AUC 0-240 min)	Postprandial responses of various other gut hormones	-30, -15, 0, 10, 20, 30, 45, 60, 90, 120, 180, 240 min on study days 1 and 7 (meal tests start at 0 min)	No