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A Review of Hypothalamic-Pituitary-Adrenal Axis Function in Chronic Fatigue Syndrome

Hypothalamic-pituitary-adrenal (HPA) axis dysfunction has been found in a high proportion of chronic fatigue syndrome (CFS) patients and includes enhanced corticosteroid-induced negative feedback, basal hypocortisolism, attenuated diurnal variation, and a reduced responsivity to challenge. A putativ...

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Detalles Bibliográficos
Autores principales: Tomas, Cara, Newton, Julia, Watson, Stuart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4045534/
https://www.ncbi.nlm.nih.gov/pubmed/24959566
http://dx.doi.org/10.1155/2013/784520
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author Tomas, Cara
Newton, Julia
Watson, Stuart
author_facet Tomas, Cara
Newton, Julia
Watson, Stuart
author_sort Tomas, Cara
collection PubMed
description Hypothalamic-pituitary-adrenal (HPA) axis dysfunction has been found in a high proportion of chronic fatigue syndrome (CFS) patients and includes enhanced corticosteroid-induced negative feedback, basal hypocortisolism, attenuated diurnal variation, and a reduced responsivity to challenge. A putative causal role for genetic profile, childhood trauma, and oxidative stress has been considered. In addition, the impact of gender is demonstrated by the increased frequency of HPA axis dysregulation in females. Despite the temporal relationship, it is not yet established whether the endocrine dysregulation is causal, consequent, or an epiphenomenon of the disorder. Nonetheless, given the interindividual variation in the effectiveness of existing biological and psychological treatments, the need for novel treatment strategies such as those which target the HPA axis is clear.
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spelling pubmed-40455342014-06-23 A Review of Hypothalamic-Pituitary-Adrenal Axis Function in Chronic Fatigue Syndrome Tomas, Cara Newton, Julia Watson, Stuart ISRN Neurosci Review Article Hypothalamic-pituitary-adrenal (HPA) axis dysfunction has been found in a high proportion of chronic fatigue syndrome (CFS) patients and includes enhanced corticosteroid-induced negative feedback, basal hypocortisolism, attenuated diurnal variation, and a reduced responsivity to challenge. A putative causal role for genetic profile, childhood trauma, and oxidative stress has been considered. In addition, the impact of gender is demonstrated by the increased frequency of HPA axis dysregulation in females. Despite the temporal relationship, it is not yet established whether the endocrine dysregulation is causal, consequent, or an epiphenomenon of the disorder. Nonetheless, given the interindividual variation in the effectiveness of existing biological and psychological treatments, the need for novel treatment strategies such as those which target the HPA axis is clear. Hindawi Publishing Corporation 2013-09-30 /pmc/articles/PMC4045534/ /pubmed/24959566 http://dx.doi.org/10.1155/2013/784520 Text en Copyright © 2013 Cara Tomas et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Tomas, Cara
Newton, Julia
Watson, Stuart
A Review of Hypothalamic-Pituitary-Adrenal Axis Function in Chronic Fatigue Syndrome
title A Review of Hypothalamic-Pituitary-Adrenal Axis Function in Chronic Fatigue Syndrome
title_full A Review of Hypothalamic-Pituitary-Adrenal Axis Function in Chronic Fatigue Syndrome
title_fullStr A Review of Hypothalamic-Pituitary-Adrenal Axis Function in Chronic Fatigue Syndrome
title_full_unstemmed A Review of Hypothalamic-Pituitary-Adrenal Axis Function in Chronic Fatigue Syndrome
title_short A Review of Hypothalamic-Pituitary-Adrenal Axis Function in Chronic Fatigue Syndrome
title_sort review of hypothalamic-pituitary-adrenal axis function in chronic fatigue syndrome
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4045534/
https://www.ncbi.nlm.nih.gov/pubmed/24959566
http://dx.doi.org/10.1155/2013/784520
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