The Role of Brown Adipose Tissue in Triglyceride Clearance in People
NCT ID: NCT02786251
Last Updated: 2022-03-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
29 participants
INTERVENTIONAL
2016-05-31
2019-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
NONE
Study Groups
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BAT+
Individuals with significant amounts of BAT (\>20 ml)
Cold exposure
During cold exposure intervention, we will use an individualized cold exposure protocol above the individual shivering threshold of each participant using liquid condition garments and a temperature controlled room.
Exposure to thermoneutral conditions
For the thermoneutral conditions intervention, subjects will be exposed to thermoneutral conditions (\~26-28°C).
BAT-
Individuals with no/minimal amounts of BAT (\<20 ml)
Cold exposure
During cold exposure intervention, we will use an individualized cold exposure protocol above the individual shivering threshold of each participant using liquid condition garments and a temperature controlled room.
Exposure to thermoneutral conditions
For the thermoneutral conditions intervention, subjects will be exposed to thermoneutral conditions (\~26-28°C).
Interventions
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Cold exposure
During cold exposure intervention, we will use an individualized cold exposure protocol above the individual shivering threshold of each participant using liquid condition garments and a temperature controlled room.
Exposure to thermoneutral conditions
For the thermoneutral conditions intervention, subjects will be exposed to thermoneutral conditions (\~26-28°C).
Eligibility Criteria
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Inclusion Criteria
* BMI 25.0-35.0 kg/m²
Exclusion Criteria
* Previous bariatric surgery or gastrointestinal surgery
* Structured exercise \>2 days/week for ≥35 min of intense exercise (e.g., jogging, activity that causes heavy breathing and sweating) or ≥150 min per week of moderate intensity exercise (e.g., brisk walking)
* Unstable weight (\>5% change during the last 2 months before entering the study)
* Significant organ system dysfunction (e.g., diabetes requiring medications, severe pulmonary, disorders of the gastrointestinal tract, kidney or cardiovascular disease)
* Current cancer or cancer that has been in remission for \<5 years
* Conditions that render subject unable to complete all testing procedures (e.g., severe ambulatory impairments, limb amputations, or metal implants that interfere with imaging procedures; coagulation disorders)
* Use of medications that are judged by the investigators to affect the study outcome measures or increase the risk of study procedures (e.g., anticoagulants) and that cannot be temporarily discontinued for this study
* Smoke cigarettes or use of illegal drugs
* Consumption of \>14 units of alcohol (e.g., glass of wine or bottle of beer) per week
* Pregnant or lactating
* Persons who are not able to grant voluntary informed consent
* Persons who are unable or unwilling to follow the study protocol or who, for any reason, the research team considers not an appropriate candidate for this study, including non-compliance with screening appointments or study visits
21 Years
65 Years
FEMALE
Yes
Sponsors
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Washington University School of Medicine
OTHER
Responsible Party
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Principal Investigators
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Maria Chondronikola, PhD, RDN
Role: PRINCIPAL_INVESTIGATOR
University of California, Davis
Locations
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Washington University School of Medicine
St Louis, Missouri, United States
Countries
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References
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Chondronikola M, Yoshino J, Ramaswamy R, Giardina JD, Laforest R, Wahl RL, Patterson BW, Mittendorfer B, Klein S. Very-low-density lipoprotein triglyceride and free fatty acid plasma kinetics in women with high or low brown adipose tissue volume and overweight/obesity. Cell Rep Med. 2024 Jan 16;5(1):101370. doi: 10.1016/j.xcrm.2023.101370.
Other Identifiers
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201602059
Identifier Type: -
Identifier Source: org_study_id
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