Age‐Related Decrease in Cold‐Activated Brown Adipose Tissue and Accumulation of Body Fat in Healthy Humans

Brown adipose tissue (BAT) can be identified by 18F‐fluorodeoxyglucose (FDG)‐positron emission tomography (PET) combined with X‐ray computed tomography (CT) in adult humans. The objective of this study was to clarify the relationship between BAT and adiposity in healthy adult humans, particularly to test the idea that decreased BAT activity may be associated with body fat accumulation with age. One hundred and sixty‐two healthy volunteers aged 20–73 years (103 males and 59 females) underwent FDG‐PET/CT after 2‐h cold exposure at 19 °C with light clothing. Cold‐activated BAT was detected in 41% of the subjects (BAT‐positive). Compared with the BAT‐negative group, the BAT‐positive group was younger (P < 0.01) and showed a lower BMI (P < 0.01), body fat content (P < 0.01), and abdominal fat (P < 0.01). The incidence of cold‐activated BAT decreased with age (P < 0.01), being more than 50% in the twenties, but less than 10% in the fifties and sixties. The adiposity‐related parameters showed some sex differences, but increased with age in the BAT‐negative group (P < 0.01), while they remained unchanged from the twenties to forties in the BAT‐positive group, in both sexes. These results suggest that decreased BAT activity may be associated with accumulation of body fat with age.

[1]  L. Bukowiecki,et al.  Stimulatory effects of cold exposure and cold acclimation on glucose uptake in rat peripheral tissues. , 1990, The American journal of physiology.

[2]  Bruce M. Spiegelman,et al.  Towards a molecular understanding of adaptive thermogenesis , 2000, Nature.

[3]  L. Kozak Brown fat and the myth of diet-induced thermogenesis. , 2010, Cell metabolism.

[4]  Mami Matsushita,et al.  Brown Adipose Tissue, Whole‐Body Energy Expenditure, and Thermogenesis in Healthy Adult Men , 2011, Obesity.

[5]  Richard L Wahl,et al.  "USA-Fat": prevalence is related to ambient outdoor temperature-evaluation with 18F-FDG PET/CT. , 2003, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[6]  J. Seidell,et al.  Techniques for the measurement of visceral fat: a practical guide. , 1993, International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity.

[7]  M. Elia,et al.  Total energy expenditure in the elderly , 2000, European journal of clinical nutrition.

[8]  Y. Seino,et al.  Increased expression of glucose transporter GLUT-4 in brown adipose tissue of fasted rats after cold exposure. , 1993, The American journal of physiology.

[9]  M Florez-Duquet,et al.  Cold-induced thermoregulation and biological aging. , 1998, Physiological reviews.

[10]  M. Florez-Duquet,et al.  Cellular proliferation and UCP content in brown adipose tissue of cold-exposed aging Fischer 344 rats. , 1998, American journal of physiology. Regulatory, integrative and comparative physiology.

[11]  N. Stefan,et al.  Impact of Age on the Relationships of Brown Adipose Tissue With Sex and Adiposity in Humans , 2010, Diabetes.

[12]  M. Saito,et al.  Uncoupling protein 1 is necessary for norepinephrine-induced glucose utilization in brown adipose tissue. , 2005, Diabetes.

[13]  B. Horwitz,et al.  Influence of Age and Gender on Brown Adipose Tissue Norepinephrine Turnover , 1993, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[14]  M. Fulham,et al.  A critical appraisal of the prevalence and metabolic significance of brown adipose tissue in adult humans. , 2010, American journal of physiology. Endocrinology and metabolism.

[15]  Richard L Wahl,et al.  Uptake in supraclavicular area fat ("USA-Fat"): description on 18F-FDG PET/CT. , 2003, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[16]  Y. Wang,et al.  UCP1 deficiency increases susceptibility to diet‐induced obesity with age , 2005, Aging cell.

[17]  T. Bengtsson,et al.  Unexpected evidence for active brown adipose tissue in adult humans. , 2007, American journal of physiology. Endocrinology and metabolism.

[18]  W. D. van Marken Lichtenbelt,et al.  Cold-activated brown adipose tissue in healthy men. , 2009, The New England journal of medicine.

[19]  B. T. Engel,et al.  Aged C57BL/6J mice respond to cold with increased sympathetic nervous activity in interscapular brown adipose tissue. , 1993, Journal of gerontology.

[20]  Jan Nedergaard,et al.  Brown adipose tissue: function and physiological significance. , 2004, Physiological reviews.

[21]  J. Orava,et al.  Functional brown adipose tissue in healthy adults. , 2009, The New England journal of medicine.

[22]  E. Palmer,et al.  Identification and importance of brown adipose tissue in adult humans. , 2009, The New England journal of medicine.

[23]  M. St-Onge,et al.  Body composition changes with aging: the cause or the result of alterations in metabolic rate and macronutrient oxidation? , 2010, Nutrition.

[24]  Michael E. Symonds,et al.  Brown Adipose Tissue and Seasonal Variation in Humans , 2009, Diabetes.

[25]  J M Heaton,et al.  The distribution of brown adipose tissue in the human. , 1972, Journal of anatomy.

[26]  Jan Nedergaard,et al.  The presence of UCP1 demonstrates that metabolically active adipose tissue in the neck of adult humans truly represents brown adipose tissue , 2009, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.