Detection of Brown Adipose Tissue by Magnetic Resonance Imaging

  • STATUS
    Recruiting
  • End date
    Oct 23, 2021
  • participants needed
    40
  • sponsor
    University of North Carolina, Chapel Hill
Updated on 23 January 2021
fats

Summary

The primary goal of this study is to assess the accuracy of conventional fat fraction proton MRI for the detection of Brown Adipose Tissue (BAT) in healthy subjects using 18F-2-fluoro-2-deoxy-D-glucosefluorodeoxyglucose -PET as gold standard.

In this pilot study, MRI and PET imaging of BAT of healthy adult volunteers will be performed on a combined PET/MRI scanner under mild cold condition.

Description

In the fight against obesity, brown adipose tissue (BAT) is considered to be the newest target. The hypothesis is that this tissue is partially responsible for the imbalance between energy intake and energy expenditure that keeps lean people lean and obese people obese.

The detection of this tissue in adult humans represents an unmet need. BAT is difficult to detect and measurements of tissue fat fraction performed by magnetic resonance imaging have been proposed as a mean to differentiate the highly hydrated brown fat from the less hydrated white adipose tissue and from muscle.

To this end, the objective of this study is to assess the accuracy of magnetic resonance fat fraction measurements for the detection of BAT volume in adult humans, while using FDG-PET as gold standard.

For this study subjects will undergo a combined MRI/PET scan. The scans will be done during stimulation of thermogenic activity by mild cold exposure.

Details
Condition adiposity, Obesity
Clinical Study IdentifierNCT02237872
SponsorUniversity of North Carolina, Chapel Hill
Last Modified on23 January 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Is your age greater than or equal to 18 yrs?
Gender: Male or Female
Do you have Obesity?
Do you have any of these conditions: Obesity or adiposity?
Each subject must be fully informed and have signed consent
BMI < 34
Normal neurological and psychological development / able to give consent
Willingness to participate in this study

Exclusion Criteria

Subjects less than 18 years of age
Severe claustrophobia
Women who are pregnant, nursing an infant or planning to become pregnant in the next 30 days
People who have a condition that makes MRI unsafe for them (for example, cardiac pacemaker, epicardial pacemaker leads, cochlear implants, metal aneurysm clip, iron filings in your eyes or metal halo devices)
Have had radiation therapy or chemotherapy in the 2 months prior to PET scan
Subjects are taking medications that may interfere with BAT detection
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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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