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

Circulating cortisol and psychosocial stress may contribute to the pathogenesis of obesity and metabolic syndrome. To evaluate these relationships, we performed a cross-sectional study of 369 overweight and obese subjects and 60 healthy volunteers and reviewed the previous literature. Overweight and...

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Autores principales: Abraham, SB, Rubino, D, Sinaii, N, Ramsey, S, Nieman, LK
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602916/
https://www.ncbi.nlm.nih.gov/pubmed/23505190
http://dx.doi.org/10.1002/oby.20083
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author Abraham, SB
Rubino, D
Sinaii, N
Ramsey, S
Nieman, LK
author_facet Abraham, SB
Rubino, D
Sinaii, N
Ramsey, S
Nieman, LK
author_sort Abraham, SB
collection PubMed
description Circulating cortisol and psychosocial stress may contribute to the pathogenesis of obesity and metabolic syndrome. To evaluate these relationships, we performed a cross-sectional study of 369 overweight and obese subjects and 60 healthy volunteers and reviewed the previous literature. Overweight and obese subjects had at least two other features of Cushing’s syndrome. They underwent measurements representing cortisol dynamics (24h 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. 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 (r(s)=0.28, P=0.02) and systolic BP in women (r(s)=0.24, P =0.0008). Post-dexamethasone cortisol levels were weak to moderately correlated with fasting insulin (r(s)=− 0.31, P=0.01) and HOMA-IR (r(s)=−0.31, P=0.01) in men and systolic (r(s)=0.18, P= 0.02) and diastolic BP (r(s)=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. Taken together, these data do not support a strong relationship between systemic cortisol or stress and obesity or metabolic syndrome.
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spelling pubmed-36029162013-07-01 Cortisol, obesity and the metabolic syndrome: A cross-sectional study of obese subjects and review of the literature Abraham, SB Rubino, D Sinaii, N Ramsey, S Nieman, LK Obesity (Silver Spring) Article Circulating cortisol and psychosocial stress may contribute to the pathogenesis of obesity and metabolic syndrome. To evaluate these relationships, we performed a cross-sectional study of 369 overweight and obese subjects and 60 healthy volunteers and reviewed the previous literature. Overweight and obese subjects had at least two other features of Cushing’s syndrome. They underwent measurements representing cortisol dynamics (24h 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. 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 (r(s)=0.28, P=0.02) and systolic BP in women (r(s)=0.24, P =0.0008). Post-dexamethasone cortisol levels were weak to moderately correlated with fasting insulin (r(s)=− 0.31, P=0.01) and HOMA-IR (r(s)=−0.31, P=0.01) in men and systolic (r(s)=0.18, P= 0.02) and diastolic BP (r(s)=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. Taken together, these data do not support a strong relationship between systemic cortisol or stress and obesity or metabolic syndrome. 2013-01 /pmc/articles/PMC3602916/ /pubmed/23505190 http://dx.doi.org/10.1002/oby.20083 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Abraham, SB
Rubino, D
Sinaii, N
Ramsey, S
Nieman, LK
Cortisol, obesity and the metabolic syndrome: A cross-sectional study of obese subjects and review of the literature
title Cortisol, obesity and the metabolic syndrome: A cross-sectional study of obese subjects and review of the literature
title_full Cortisol, obesity and the metabolic syndrome: A cross-sectional study of obese subjects and review of the literature
title_fullStr Cortisol, obesity and the metabolic syndrome: A cross-sectional study of obese subjects and review of the literature
title_full_unstemmed Cortisol, obesity and the metabolic syndrome: A cross-sectional study of obese subjects and review of the literature
title_short Cortisol, obesity and the metabolic syndrome: A cross-sectional study of obese subjects and review of the literature
title_sort cortisol, obesity and the metabolic syndrome: a cross-sectional study of obese subjects and review of the literature
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602916/
https://www.ncbi.nlm.nih.gov/pubmed/23505190
http://dx.doi.org/10.1002/oby.20083
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