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Cold Induced Futile Cycles In White Adipose Tissue (Metabol)

K

Kantonsspital Baden

Status

Completed

Conditions

Metabolism Disorder

Treatments

Diagnostic Test: 13C-Glucose injection
Other: External cooling
Diagnostic Test: FDG PET/CT

Study type

Interventional

Funder types

Other

Identifiers

NCT04614116
Cold exposure of WAT

Details and patient eligibility

About

Investigation of futile cycles in white adipose tissue under cold conditions for thermogenesis using two substitutes for glucose metabolism (18F-FDG and 13C-Glucose).

Full description

Thermogenesis is defined as a process, which generates heat by the depletion of energy-rich molecules. Evolutionary, it is an essential process that allows the survival at lower temperatures. Since the discovery of brown adipose tissue (BAT) it is believed that this part of the adipose tissue can dissipate energy for heat thanks to the uncoupling protein 1 (UCP1). Since energy expenditure is increased as a consequence of thermogenesis, pharmacological induction of this pathway presents an interesting therapeutic target to counter obesity. However, recent investigations indicate that white adipose tissue (WAT) is much more versatile and probably essentially indispensable for thermogenesis.

To investigate the mechanism of this futile cycle in WAT we plan to investigate the glucose metabolism in 24 healthy volunteers with 2 exams (one with and one without external cooling) with two substitutes for glucose. We will use 18F-FDG to quantify the glucose influx into WAT using dynamic PET/CT scans and 13C-Glucose to analyze the downstream metabolites.

Enrollment

24 patients

Sex

Male

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Informed Consent as documented by signature
  • Healthy participants, as determined by screening assessments and Principal Investigator's judgment
  • Health status is defined by the absence of evidence of any active or chronic disease following a medical and surgical history, basic physical examination and blood test

Exclusion criteria

  • any clinically relevant history or the presence of e.g. respiratory, renal, hepatic, gastrointestinal, hematological, lymphatic, neurological, cardiovascular, psychiatric, metabolic disease, etc.
  • Intake of the following medications: Insulin, oral antidiabetic drugs, GLP-1-agonists, Corticosteroids, Sympathomimetic and Sympatholytic drug, Beta-Blocker, Statins.
  • BMI > 35 kg/m2
  • Resting pulse rate > 70 bpm, resting blood pressure > 130/90 mmHg.
  • Serum creatinine > 145 µmol/L
  • ASAT> 75 U/L and ALAT > 75 U/L
  • γ GT > 100 UI/L and total bilirubin > 30 µmol/l
  • Glucose > 7.1 mmol/L
  • HbA1c > 46 mmol/mol (>6.4%)
  • Intake of anticoagulants or inhibitors of platelet aggregation (e.g. Aspirin, clopidogrel).
  • Known tendency to form keloids (hypertrophic scar tissue)
  • 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,
  • Participation in another study with investigational drug within the 30 days preceding and during the present study
  • Participation in another study involving ionizing radiation in the same year
  • Previous enrolment into the current study,
  • Enrolment of the investigator, his/her family members, employees and other dependent persons

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

24 participants in 2 patient groups

Biopsy without cold induction
Other group
Description:
Participants will undergo a fat biopsy after the first scan, without cooling
Treatment:
Diagnostic Test: 13C-Glucose injection
Diagnostic Test: FDG PET/CT
Biopsy with cold induction
Other group
Description:
Participants will undergo a fat biopsy after the second scan, with cooling
Treatment:
Other: External cooling
Diagnostic Test: 13C-Glucose injection
Diagnostic Test: FDG PET/CT

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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