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Clinical Trials/NCT02173834
NCT02173834
Completed
Not Applicable

Activation of Brown Adipose Tissue in Lean and Obese Men

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)1 site in 1 country20 target enrollmentMarch 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obesity
Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Enrollment
20
Locations
1
Primary Endpoint
Difference in sympathetic stimulation to BAT between lean and obese individuals
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

In this study the investigators aim to investigate whether the sympathetic stimulation of BAT, as assessed with a 123I-metaiodobenzylguanidine single-photon emission computed tomography computed tomography scan, differs between lean and obese individuals, as an explanation for the diminished metabolic brown adipose tissue activity in obese subjects.

The investigators hypothesis is that sympathetic nervous system activity in the obese is diminished as compared to their leaner counterparts as an explanation for the diminished metabolic brown adipose tissue activity in the obese.

Detailed Description

The sympathetic nervous system is the primary activator of Brown Adipose Tissue. Obese humans are known to have less metabolically active brown adipose tissue as compared to their leaner counterparts. The reason for this diminished metabolic brown adipose tissue activity is unknown. However, a lower sympathetic nervous system activation to brown adipose tissue in the obese might explain a diminished metabolic brown adipose tissue. Therefore, in this study, both the sympathetic nervous system activation to brown adipose tissue and the metabolic activity will be measured in lean and obese subjects. sympathetic nervous system activity will be measured using 123I-metaiodobenzylguanidine single-photon emission computed tomography scans, metabolic activity will be measured using 18F- fluorodeoxyglucose positron emission tomography CT scans.

Registry
clinicaltrials.gov
Start Date
March 2013
End Date
November 2013
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Responsible Party
Principal Investigator
Principal Investigator

F Holleman

MD, PhD

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Eligibility Criteria

Inclusion Criteria

  • Caucasian origin
  • Subjects should be able and willing to give informed consent
  • 18-40 years old
  • BMI range of 19-25 kg/m2 (lean study subjects) or 28-40 kg/m2 (obese study subjects)

Exclusion Criteria

  • Renal failure (creatinine\>135mmol/l)
  • Daily use of prescription medication

Outcomes

Primary Outcomes

Difference in sympathetic stimulation to BAT between lean and obese individuals

Time Frame: Participants will be followed for a mean duration of 2 weeks (the maximal time period between the two scans) The outcome measurements will be assessed when the last subject has been scanned approximately one year after starting the trial

Secondary Outcomes

  • Difference in correlation between sympathetic stimulation of BAT as assessed with 123I-MIBG SPECT scans and metabolic BAT activity as assessed with 18F-Fluorodeoxyglucose(FDG)- positron emission tomography(PET)-CT scan in lean and obese individuals(Participants will be followed for a mean duration of 2 weeks (the maximal time period between the two scans) The outcome measurements will be assessed when the last subject has been scanned approximately one year after starting the trial.)

Study Sites (1)

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