Cortisol, obesity, and the metabolic syndrome: A cross‐sectional study of obese subjects and review of the literature

Objective: Circulating cortisol and psychosocial stress may contribute to the pathogenesis of obesity and metabolic syndrome (MS). To evaluate these relationships, a cross‐sectional study of 369 overweight and obese subjects and 60 healthy volunteers was performed and reviewed the previous literatur...

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Published inObesity (Silver Spring, Md.) Vol. 21; no. 1; pp. E105 - E117
Main Authors Abraham, S.B., Rubino, D., Sinaii, N., Ramsey, S., Nieman, L.K.
Format Journal Article
LanguageEnglish
Published Hoboken, USA John Wiley & Sons, Inc 01.01.2013
Blackwell Publishing Ltd
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Summary:Objective: Circulating cortisol and psychosocial stress may contribute to the pathogenesis of obesity and metabolic syndrome (MS). To evaluate these relationships, a cross‐sectional study of 369 overweight and obese subjects and 60 healthy volunteers was performed and reviewed the previous literature. Design and Methods: Overweight and obese subjects had at least two other features of Cushing's syndrome. They underwent measurements representing cortisol dynamics (24 h urine cortisol excretion (UFC), bedtime salivary cortisol, 1 mg dexamethasone suppression test) and metabolic parameters (BMI, blood pressure (BP); fasting serum triglycerides, HDL, insulin, and glucose). Subjects also completed the Perceived Stress Scale (PSS). UFC, salivary cortisol, and weight from 60 healthy volunteers were analyzed. Results: No subject had Cushing's syndrome. UFC and dexamethasone responses were not associated with BMI or weight. However, salivary cortisol showed a trend to increase as BMI increased (P < 0.0001), and correlated with waist circumference (WC) in men (rs = 0.28, P = 0.02) and systolic BP in women (rs = 0.24, P = 0.0008). Post‐dexamethasone cortisol levels were weak to moderately correlated with fasting insulin (rs = −0.31, P = 0.01) and HOMA‐IR (rs = −0.31, P = 0.01) in men and systolic (rs = 0.18, P = 0.02) and diastolic BP (rs = 0.20, P = 0.009) in women. PSS results were higher in obese subjects than controls, but were not associated with cortisol or metabolic parameters. As expected, WC correlated with fasting insulin, HOMA‐IR, and systolic BP (adjusted for BMI and gender; P < 0.01). Literature showed inconsistent relationships between cortisol and metabolic parameters. Conclusion: Taken together, these data do not support a strong relationship between systemic cortisol or stress and obesity or MS.
Bibliography:National Institute of Child Health and Human Development, National Institutes of Health.
Disclosure
Funding agencies
The authors declare no conflict of interest.
Eunice Kennedy Shriver
This work was supported in part by the intramural program of The
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ISSN:1930-7381
1930-739X
1930-739X
DOI:10.1002/oby.20083