Role of Human Brown Fat in Obesity, Metabolism and Cardiovascular Disease: Strategies to Turn Up the Heat

Prog Cardiovasc Dis. 2018 Jul-Aug;61(2):232-245. doi: 10.1016/j.pcad.2018.07.002. Epub 2018 Jul 4.

Abstract

Human brown adipose tissue (BAT) was re-discovered in 2009 by several independent groups, who showed that it is present and active in adults, as judged from the profound uptake of the glucose analogue radiotracer 18F-fluorodeoxyglucose in positron-emission tomography and computed tomography scan analysis after cold exposure. A potential clinical implication of activating BAT relates to its high metabolic activity and its potential role in stimulating energy expenditure (i.e. resting energy expenditure, meal-induced thermogenesis, and cold-induced thermogenesis), which makes it an attractive target to reduce adiposity. Moreover, due to its ability to oxidise glucose and lipids, BAT activation may also potentially exert beneficial metabolic and cardiovascular effects through reducing glucose and lipid levels, respectively. This review describes the potential role of human BAT in the prevention and treatment of obesity, metabolism, and cardiovascular disease focusing on its impact on energy expenditure and management of body fat accumulation as well as on glucose and lipid metabolism. This article also summarises the strategies that are currently being studied to activate human BAT.

Keywords: (18)F-fluorodeoxyglucose; Browning; Cold exposure; Computed tomography; Dietary compounds; Energy balance; Exercise; Pharmacological agents; Positron-emission tomography.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adipose Tissue, Brown / metabolism*
  • Adipose Tissue, Brown / physiopathology
  • Adiposity
  • Cardiovascular Diseases / epidemiology
  • Cardiovascular Diseases / metabolism*
  • Cardiovascular Diseases / physiopathology
  • Cardiovascular Diseases / therapy
  • Energy Metabolism*
  • Glucose / metabolism
  • Humans
  • Lipid Metabolism
  • Obesity / epidemiology
  • Obesity / metabolism*
  • Obesity / physiopathology
  • Obesity / therapy
  • Risk Factors
  • Thermogenesis*

Substances

  • Glucose