Brown Fat Clinical Trial
Official title:
Efficacy of Pharmacological Stimulation of Brown and White Fat in Lean and Obese Young Adults
To determine whether pharmacological stimulation of supraclavicular Brown Adipose Tissue
(BAT or "Brown Fat") and subcutaneous White Adipose Tissue (WAT) using an FDA-approved beta3
agonist is as effective in increasing oxidative metabolism in BAT and WAT as is the exposure
to cold, the investigators will assess the efficacy of an FDA approved beta3 agonist
Mirabegron (trade name Myrbetriq, Astellas Pharma, Inc.) for increasing oxidative metabolism
in supraclavicular BAT and subcutaneous WAT in lean and obese young adults.
The investigators anticipate that both methods to stimulate supraclavicular BAT and
subcutaneous WAT will result in similar 18F-labeled fluoro-deoxyglucose (FDG) tracer uptake
on positron emission tomography (PET) images as well as oxidative metabolism. This would
demonstrate that pharmacological stimulation of BAT is effective and could lead to further,
more detailed clinical trials in obese subjects.
Obesity and diabetes have increased to epidemic proportions in the US and in many other
countries. In addition, the comorbidities of these metabolic diseases, such as
cardiovascular disease, cancer, osteoarthritis are placing a huge burden on the health and
health care system of the United States. Finding new avenues for human therapeutics is thus
a critical challenge. Brown adipose tissue (BAT or "Brown Fat") functions to dissipate
stored chemical energy in the form of heat and serves to defend mammals from hypothermia and
obesity.
It is now firmly established that humans have functional BAT that can be activated by mild
cold stress and imaged by 18F-labeled fluoro-deoxyglucose (FDG) PET imaging. Moreover, it is
now understood that there are two distinct types of brown fat cells: the "classical" brown
fat (most common in supraclavicular fat depots) that form developmentally from a muscle-like
myf5-positive lineage and brown fat cells that can appear in white adipose tissue (WAT)
depots upon prolonged exposure to cold or beta-adrenergic signaling. These latter cells
originate from a myf5-negative lineage and are referred to as beige cells. Recent data
suggests that most adult humans might have both brown and beige fat cells that are inactive
but could be activated via the adrenergic system. Once activated, thermogenesis in these
cells could affect the body's energy balance and might be instrumental in weight management.
Although adrenergic activation using cold exposure has been shown to be highly effective in
activating both brown and beige fat cells, it is difficult to implement in daily routine and
there is a need for other, more practical, interventions. Mirabegron (trade name Myrbetriq,
Astellas Pharma, Inc.) is a drug for the treatment of overactive bladder which was FDA
approved in July of 2012. Mirabegron activates the beta3 adrenergic receptor in the detrusor
muscle in the bladder, which leads to muscle relaxation and an increase in bladder capacity.
There are reports of increased BAT FDG uptake following MIrabegron administration in both
rodents and recently in humans. Because pharmacological stimulation of brown/beige fat cells
might increase daily energy expenditure, this might represent a novel mechanism for weight
management and eventually a new avenue for the treatment for obesity.
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Status | Clinical Trial | Phase | |
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Completed |
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