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Model-Based Therapeutic Correction of Hypothalamic-Pituitary-Adrenal Axis Dysfunction

The hypothalamic-pituitary-adrenal (HPA) axis is a major system maintaining body homeostasis by regulating the neuroendocrine and sympathetic nervous systems as well modulating immune function. Recent work has shown that the complex dynamics of this system accommodate several stable steady states, o...

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Detalles Bibliográficos
Autores principales: Ben-Zvi, Amos, Vernon, Suzanne D., Broderick, Gordon
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2613527/
https://www.ncbi.nlm.nih.gov/pubmed/19165314
http://dx.doi.org/10.1371/journal.pcbi.1000273
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author Ben-Zvi, Amos
Vernon, Suzanne D.
Broderick, Gordon
author_facet Ben-Zvi, Amos
Vernon, Suzanne D.
Broderick, Gordon
author_sort Ben-Zvi, Amos
collection PubMed
description The hypothalamic-pituitary-adrenal (HPA) axis is a major system maintaining body homeostasis by regulating the neuroendocrine and sympathetic nervous systems as well modulating immune function. Recent work has shown that the complex dynamics of this system accommodate several stable steady states, one of which corresponds to the hypocortisol state observed in patients with chronic fatigue syndrome (CFS). At present these dynamics are not formally considered in the development of treatment strategies. Here we use model-based predictive control (MPC) methodology to estimate robust treatment courses for displacing the HPA axis from an abnormal hypocortisol steady state back to a healthy cortisol level. This approach was applied to a recent model of HPA axis dynamics incorporating glucocorticoid receptor kinetics. A candidate treatment that displays robust properties in the face of significant biological variability and measurement uncertainty requires that cortisol be further suppressed for a short period until adrenocorticotropic hormone levels exceed 30% of baseline. Treatment may then be discontinued, and the HPA axis will naturally progress to a stable attractor defined by normal hormone levels. Suppression of biologically available cortisol may be achieved through the use of binding proteins such as CBG and certain metabolizing enzymes, thus offering possible avenues for deployment in a clinical setting. Treatment strategies can therefore be designed that maximally exploit system dynamics to provide a robust response to treatment and ensure a positive outcome over a wide range of conditions. Perhaps most importantly, a treatment course involving further reduction in cortisol, even transient, is quite counterintuitive and challenges the conventional strategy of supplementing cortisol levels, an approach based on steady-state reasoning.
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spelling pubmed-26135272009-01-23 Model-Based Therapeutic Correction of Hypothalamic-Pituitary-Adrenal Axis Dysfunction Ben-Zvi, Amos Vernon, Suzanne D. Broderick, Gordon PLoS Comput Biol Research Article The hypothalamic-pituitary-adrenal (HPA) axis is a major system maintaining body homeostasis by regulating the neuroendocrine and sympathetic nervous systems as well modulating immune function. Recent work has shown that the complex dynamics of this system accommodate several stable steady states, one of which corresponds to the hypocortisol state observed in patients with chronic fatigue syndrome (CFS). At present these dynamics are not formally considered in the development of treatment strategies. Here we use model-based predictive control (MPC) methodology to estimate robust treatment courses for displacing the HPA axis from an abnormal hypocortisol steady state back to a healthy cortisol level. This approach was applied to a recent model of HPA axis dynamics incorporating glucocorticoid receptor kinetics. A candidate treatment that displays robust properties in the face of significant biological variability and measurement uncertainty requires that cortisol be further suppressed for a short period until adrenocorticotropic hormone levels exceed 30% of baseline. Treatment may then be discontinued, and the HPA axis will naturally progress to a stable attractor defined by normal hormone levels. Suppression of biologically available cortisol may be achieved through the use of binding proteins such as CBG and certain metabolizing enzymes, thus offering possible avenues for deployment in a clinical setting. Treatment strategies can therefore be designed that maximally exploit system dynamics to provide a robust response to treatment and ensure a positive outcome over a wide range of conditions. Perhaps most importantly, a treatment course involving further reduction in cortisol, even transient, is quite counterintuitive and challenges the conventional strategy of supplementing cortisol levels, an approach based on steady-state reasoning. Public Library of Science 2009-01-23 /pmc/articles/PMC2613527/ /pubmed/19165314 http://dx.doi.org/10.1371/journal.pcbi.1000273 Text en Ben-Zvi et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ben-Zvi, Amos
Vernon, Suzanne D.
Broderick, Gordon
Model-Based Therapeutic Correction of Hypothalamic-Pituitary-Adrenal Axis Dysfunction
title Model-Based Therapeutic Correction of Hypothalamic-Pituitary-Adrenal Axis Dysfunction
title_full Model-Based Therapeutic Correction of Hypothalamic-Pituitary-Adrenal Axis Dysfunction
title_fullStr Model-Based Therapeutic Correction of Hypothalamic-Pituitary-Adrenal Axis Dysfunction
title_full_unstemmed Model-Based Therapeutic Correction of Hypothalamic-Pituitary-Adrenal Axis Dysfunction
title_short Model-Based Therapeutic Correction of Hypothalamic-Pituitary-Adrenal Axis Dysfunction
title_sort model-based therapeutic correction of hypothalamic-pituitary-adrenal axis dysfunction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2613527/
https://www.ncbi.nlm.nih.gov/pubmed/19165314
http://dx.doi.org/10.1371/journal.pcbi.1000273
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