Brown Adipose Tissue as Nutrient Buffer Through Diet Induced Thermogenesis (BANDIT)
Brown Adipose Tissue, Metabolic Disease
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
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
Experimental
Experimental
BAT positive
BAT negative
Maximal activated supraclavicular BAT SUVmean >1,5 g/ml-
Maximal activated supraclavicular BAT SUVmean <1,5 g/ml