K.C. Vickers and S. Varma shear second authorship.
Article first published online: 20 JUN 2013
Copyright © 2013 The Obesity Society
Volume 21, Issue 5, pages 960–967, May 2013
How to Cite
Pavlatou, M. G., Vickers, K. C., Varma, S., Malek, R., Sampson, M., Remaley, A. T., Gold, P. W., Skarulis, M. C. and Kino, T. (2013), Circulating cortisol-associated signature of glucocorticoid-related gene expression in subcutaneous fat of obese subjects. Obesity, 21: 960–967. doi: 10.1002/oby.20073
Disclosure: The authors declared no conflict of interest.
Funding source: This study was funded by the Intramural Research Program of the Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Heart, Lung and Blood Institute, National Institute of Allergy and Inflammatory Diseases, National Institute of Diabetes and Digestive and Kidney Diseases and the National Institute of Mental Health, National Institutes of Health. We thank Drs. A.H. DeCherney, Program in Reproductive and Adult Endocrinology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, and G.P. Chrousos, 1st Department of Pediatrics, Athens University Medical School, for valuable discussion at the time of starting this study and for editing the manuscript, respectively. K.C.V. is supported by NIH NHLBI Intramural Research Program and NIH KHL113039A.
- Issue published online: 20 JUN 2013
- Article first published online: 20 JUN 2013
- Accepted manuscript online: 18 OCT 2012 01:00PM EST
- Manuscript Accepted: 3 SEP 2012
- Manuscript Received: 28 FEB 2012
- Intramural Research Program
- National Institute of Child Health and Human Development
- National Heart, Lung and Blood Institute
- National Institute of Allergy and Inflammatory Diseases
- National Institute of Diabetes and Digestive and Kidney Diseases
- National Institute of Mental Health
- National Institutes of Health
- NIH. Grant Number: KHL113039A
Serum cortisol concentrations fluctuate in a circadian fashion, and glucocorticoids exert strong effects on adipose tissue and induce obesity through the glucocorticoid receptor.
Design and Methods:
To examine the impact of physiologic levels of circulating cortisol on subcutaneous adipose tissue, 25 overweight and obese subjects were employed, and their serum levels of morning (AM) and evening (PM) cortisol, AM/PM cortisol ratios, and 24-h urinary-free cortisol (UFC) were compared with their clinical parameters, serum cytokine levels, and mRNA expression of 93 receptor action-regulating and 93 glucocorticoid-responsive genes in abdominal subcutaneous fat.
Results and Conclusions:
AM cortisol levels did not correlate with mRNA expression of the all genes examined, whereas PM cortisol levels, AM/PM cortisol ratios, and 24-h UFC were associated with distinct sets of these genes. Body mass index did not significantly correlate with the four cortisol parameters employed. These results suggest that physiologic levels of AM serum cortisol do not solely represent biological effects of circulating cortisol on the expression of glucocorticoid-related genes in subcutaneous adipose tissue, whereas PM levels, amplitude, and net amounts of the diurnally fluctuating serum cortisol have distinct effects. Through the genes identified in this study, glucocorticoids appear to influence intermediary metabolism, energy balance, inflammation, and local circadian rythmicity in subcutaneous fat. Our results may also explain in part the development of metabolic abnormality and obesity in subjects under stress or patients with melancholic/atypical depression who demonstrate elevated levels of PM serum cortisol.