Adaptive thermogenesis with weight loss in humans

• Published in: Obesity (Silver Spring, Md.) Vol. 21; no. 2; pp. 218 - 228
• Main Authors: Müller, M.J., Bosy‐Westphal, A.
• Format: Journal Article
• Language: English
• Published: Hoboken, USA John Wiley & Sons, Inc 01.02.2013; Blackwell Publishing Ltd
• Subjects: Adaptation; Adipose Tissue, Brown - metabolism; Body Composition; Body Weight; Diet; Energy Intake; Energy Metabolism - physiology; Food; Humans; Leptin - blood; Metabolism; Musculoskeletal system; Obesity; Physiology; Rest - physiology; Sympathetic Nervous System - metabolism; Thermogenesis; Weight control; Weight Loss - physiology; Minnesota
• ISSN: 1930-7381; 1930-739X; 1930-739X
• DOI: 10.1002/oby.20027

Adaptive thermogenesis (AT) with weight loss refers to underfeeding‐associated fall in resting and non‐resting energy expenditure (REE, non‐REE); this is independent of body weight and body composition. In humans, the existence of AT was inconsistently shown and its clinical significance has been questioned. Objectives: Discrepant findings are mainly due to different definitions of AT, the use of various and nonstandardized study protocols, and the limits of accuracy of methods to assess energy expenditure. With controlled underfeeding, AT takes more than 2 wk to develop. AT accounts to an average of 0.5 MJ (or 120 kcal) with a considerable between subject variance. Design and Methods: Low‐sympathetic nervous system activity, 3,5,3′‐tri‐iodothyronine (T3) and leptin are likely to add to AT; however, the kinetic changes of their plasma levels with underfeeding differ from the time course of AT and controlled intervention studies substituting and titrating these hormones are rare in humans. AT in response to underfeeding is independent of thermogenesis in response to either diet or cold. Although fat‐free mass (FFM) and, thus, liver, and skeletal muscle are considered as major sites of AT, cold‐induced nonshivering thermogenesis relates to the metabolism of brown adipose tissue (BAT). In humans, diet‐induced thermogenesis is related to postprandial substrate metabolism of FFM with a questionable role of BAT. Obviously, the REE component of AT differs from and its non‐REE component with respect to organ contribution as well as mechanisms. Thus, AT cannot be considered as unique. Conclusions: AT should be characterized based on individual components of daily energy expenditure, detailed body composition analyses, and mathematical modeling. The biological basis of AT as well as the influences of age, sex, obesity, stress, and inflammation remain to be established in humans.