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Brown Adipose Tissue as Nutrient Buffer Through Diet Induced Thermogenesis (BANDIT)

Primary Purpose

Brown Adipose Tissue, Metabolic Disease

Status
Not yet recruiting
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Carbohydrate
Fat
Protein
Sponsored by
University Hospital, Basel, Switzerland
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Brown Adipose Tissue focused on measuring Diet induced thermogenesis, Cold exposure, Energy Expenditure

Eligibility Criteria

18 Years - 40 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: BMI 18.5 to 28 kg/m2 Able to give informed consent as documented by signature Exclusion Criteria: Concomitant medication other than prescription free analgesics (paracetamol and NSAID) and oral contraceptives Other clinically significant concomitant disease states (e.g., renal failure, hepatic dysfunction, cardiovascular disease, diabetes mellitus) Hyper- or hypothyroidism Smoker / habitual tobacco use Weight change of >5% within 3 months prior to inclusion Hypersensitivity to cold (e.g. Raynaud syndrome) Known or suspected non-compliance, drug or alcohol abuse Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc. of the participant Enrolment of the investigator, his/her family members, employees and other dependent persons Enrolment into another study using ionizing radiation within the previous 12 months Enrolment into another study including a pharmacological or nutritional intervention Pregnancy or lactation Lab parameters Serum-Creatinine: above 1.5x upper limit of normal (ULN) Glycated Hemoglobin (HbA1c): above 6.0% Random plasma glucose >11 mM

Sites / Locations

  • University Hospital Basel, Dept. of Endocrinology

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

BAT positive

BAT negative

Arm Description

Maximal activated supraclavicular BAT SUVmean >1,5 g/ml-

Maximal activated supraclavicular BAT SUVmean <1,5 g/ml

Outcomes

Primary Outcome Measures

AUC Glucose
Area under the curve (AUC) of glucose after the oral glucose load in participants with functional BAT as compared to participants without functional BAT

Secondary Outcome Measures

AUC Branched chain amino acids
AUC of BCAAs after protein load in in participants with functional BAT as compared to participants without functional BAT
AUC triglycerides
AUC of plasma triglycerides after lipid test meal in participants with functional BAT as compared to participants without functional BAT.
Diet induced thermogenesis
Diet-induced thermogenesis: AUC of EE above RMR in response to the respective macronutrient (carbohydrate, protein or fat). Measured by indirect calorimetry. The results for each macronutrient will be compared between the BAT positive and BAT negative participants.

Full Information

First Posted
October 5, 2023
Last Updated
October 5, 2023
Sponsor
University Hospital, Basel, Switzerland
Collaborators
ETH Zurich (Switzerland)
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1. Study Identification

Unique Protocol Identification Number
NCT06078345
Brief Title
Brown Adipose Tissue as Nutrient Buffer Through Diet Induced Thermogenesis
Acronym
BANDIT
Official Title
Brown Adipose Tissue as Nutrient Buffer Through Diet Induced Thermogenesis
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
October 12, 2023 (Anticipated)
Primary Completion Date
June 30, 2025 (Anticipated)
Study Completion Date
June 30, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Basel, Switzerland
Collaborators
ETH Zurich (Switzerland)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
To test the hypothesis that active BAT improves metabolic health by buffering postprandial metabolites plasma metabolites and energy expenditure will be compared in volunteers with and without active BAT. Both groups will receive test meals with protein, fat and carbohydrates separately, so that the individual impacts of these macronutrients on diet induced thermogenesis and the buffering function of BAT can be derived. BAT biopsies will be taken before and after the test meals for molecular analysis.
Detailed Description
In this prospective interventional study healthy individuals will be screened for presence of active BAT: Maximal BAT activity will be achieved by a mild cold stimulus over 2 hous and quantified by 18F-FDG-PET/CT 30 min after injection of 75 MBq of 18F-FDG. Individuals with FDG-PET positive BAT will be included as BAT-positive subjects (n=15) and individuals with absence of FDG-positive BAT will be included as BAT-negative subjects (n=15) and then take part in three study visits in random order. During the study visits participants will consume a standardized isocaloric liquid meal consisting of A) glucose (OGTT) B) fat and C) protein. Energy expenditure will be measured by indirect calorimetry before as well as hourly after the meal for 5 hours. Blood samples will be taken before and at 30 minute intervals after the meal for 5 hours for analysis of blood glucose, triglycerides, FAAs, representative amino acids, insulin and noradrenaline. Subjects will undergo ultrasound-guided biopsy of the supraclavicular fat depot in the fasting state and after one of the test meals so that biopsies from 5 individuals in each group after each test meal will be obtained.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brown Adipose Tissue, Metabolic Disease
Keywords
Diet induced thermogenesis, Cold exposure, Energy Expenditure

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Prospective interventional trial in healthy volunteers with random sequence of the three study interventions.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
BAT positive
Arm Type
Experimental
Arm Description
Maximal activated supraclavicular BAT SUVmean >1,5 g/ml-
Arm Title
BAT negative
Arm Type
Experimental
Arm Description
Maximal activated supraclavicular BAT SUVmean <1,5 g/ml
Intervention Type
Other
Intervention Name(s)
Carbohydrate
Intervention Description
400 Kcal glucose (100g oGTT)
Intervention Type
Other
Intervention Name(s)
Fat
Intervention Description
400 Kcal glucose rapeseed oil.
Intervention Type
Other
Intervention Name(s)
Protein
Intervention Description
400 Kcal Moltein PURE (111g)
Primary Outcome Measure Information:
Title
AUC Glucose
Description
Area under the curve (AUC) of glucose after the oral glucose load in participants with functional BAT as compared to participants without functional BAT
Time Frame
1h before and 5 hours after nutritional intervention
Secondary Outcome Measure Information:
Title
AUC Branched chain amino acids
Description
AUC of BCAAs after protein load in in participants with functional BAT as compared to participants without functional BAT
Time Frame
1h before and 5 hours after nutritional intervention
Title
AUC triglycerides
Description
AUC of plasma triglycerides after lipid test meal in participants with functional BAT as compared to participants without functional BAT.
Time Frame
1h before and 5 hours after nutritional intervention
Title
Diet induced thermogenesis
Description
Diet-induced thermogenesis: AUC of EE above RMR in response to the respective macronutrient (carbohydrate, protein or fat). Measured by indirect calorimetry. The results for each macronutrient will be compared between the BAT positive and BAT negative participants.
Time Frame
1h before and 5 hours after nutritional intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: BMI 18.5 to 28 kg/m2 Able to give informed consent as documented by signature Exclusion Criteria: Concomitant medication other than prescription free analgesics (paracetamol and NSAID) and oral contraceptives Other clinically significant concomitant disease states (e.g., renal failure, hepatic dysfunction, cardiovascular disease, diabetes mellitus) Hyper- or hypothyroidism Smoker / habitual tobacco use Weight change of >5% within 3 months prior to inclusion Hypersensitivity to cold (e.g. Raynaud syndrome) Known or suspected non-compliance, drug or alcohol abuse Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc. of the participant Enrolment of the investigator, his/her family members, employees and other dependent persons Enrolment into another study using ionizing radiation within the previous 12 months Enrolment into another study including a pharmacological or nutritional intervention Pregnancy or lactation Lab parameters Serum-Creatinine: above 1.5x upper limit of normal (ULN) Glycated Hemoglobin (HbA1c): above 6.0% Random plasma glucose >11 mM
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Matthias J Betz, MD
Phone
0041 61 556 56 54
Email
matthias.betz@usb.ch
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Matthias J Betz, MD
Organizational Affiliation
University Hospital, Basel, Switzerland
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Basel, Dept. of Endocrinology
City
Basel
Country
Switzerland

12. IPD Sharing Statement

Plan to Share IPD
No

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Brown Adipose Tissue as Nutrient Buffer Through Diet Induced Thermogenesis

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