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Allostatic Self-efficacy: A Metacognitive Theory of Dyshomeostasis-Induced Fatigue and Depression

This paper outlines a hierarchical Bayesian framework for interoception, homeostatic/allostatic control, and meta-cognition that connects fatigue and depression to the experience of chronic dyshomeostasis. Specifically, viewing interoception as the inversion of a generative model of viscerosensory i...

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Autores principales: Stephan, Klaas E., Manjaly, Zina M., Mathys, Christoph D., Weber, Lilian A. E., Paliwal, Saee, Gard, Tim, Tittgemeyer, Marc, Fleming, Stephen M., Haker, Helene, Seth, Anil K., Petzschner, Frederike H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5108808/
https://www.ncbi.nlm.nih.gov/pubmed/27895566
http://dx.doi.org/10.3389/fnhum.2016.00550
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author Stephan, Klaas E.
Manjaly, Zina M.
Mathys, Christoph D.
Weber, Lilian A. E.
Paliwal, Saee
Gard, Tim
Tittgemeyer, Marc
Fleming, Stephen M.
Haker, Helene
Seth, Anil K.
Petzschner, Frederike H.
author_facet Stephan, Klaas E.
Manjaly, Zina M.
Mathys, Christoph D.
Weber, Lilian A. E.
Paliwal, Saee
Gard, Tim
Tittgemeyer, Marc
Fleming, Stephen M.
Haker, Helene
Seth, Anil K.
Petzschner, Frederike H.
author_sort Stephan, Klaas E.
collection PubMed
description This paper outlines a hierarchical Bayesian framework for interoception, homeostatic/allostatic control, and meta-cognition that connects fatigue and depression to the experience of chronic dyshomeostasis. Specifically, viewing interoception as the inversion of a generative model of viscerosensory inputs allows for a formal definition of dyshomeostasis (as chronically enhanced surprise about bodily signals, or, equivalently, low evidence for the brain's model of bodily states) and allostasis (as a change in prior beliefs or predictions which define setpoints for homeostatic reflex arcs). Critically, we propose that the performance of interoceptive-allostatic circuitry is monitored by a metacognitive layer that updates beliefs about the brain's capacity to successfully regulate bodily states (allostatic self-efficacy). In this framework, fatigue and depression can be understood as sequential responses to the interoceptive experience of dyshomeostasis and the ensuing metacognitive diagnosis of low allostatic self-efficacy. While fatigue might represent an early response with adaptive value (cf. sickness behavior), the experience of chronic dyshomeostasis may trigger a generalized belief of low self-efficacy and lack of control (cf. learned helplessness), resulting in depression. This perspective implies alternative pathophysiological mechanisms that are reflected by differential abnormalities in the effective connectivity of circuits for interoception and allostasis. We discuss suitably extended models of effective connectivity that could distinguish these connectivity patterns in individual patients and may help inform differential diagnosis of fatigue and depression in the future.
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spelling pubmed-51088082016-11-28 Allostatic Self-efficacy: A Metacognitive Theory of Dyshomeostasis-Induced Fatigue and Depression Stephan, Klaas E. Manjaly, Zina M. Mathys, Christoph D. Weber, Lilian A. E. Paliwal, Saee Gard, Tim Tittgemeyer, Marc Fleming, Stephen M. Haker, Helene Seth, Anil K. Petzschner, Frederike H. Front Hum Neurosci Neuroscience This paper outlines a hierarchical Bayesian framework for interoception, homeostatic/allostatic control, and meta-cognition that connects fatigue and depression to the experience of chronic dyshomeostasis. Specifically, viewing interoception as the inversion of a generative model of viscerosensory inputs allows for a formal definition of dyshomeostasis (as chronically enhanced surprise about bodily signals, or, equivalently, low evidence for the brain's model of bodily states) and allostasis (as a change in prior beliefs or predictions which define setpoints for homeostatic reflex arcs). Critically, we propose that the performance of interoceptive-allostatic circuitry is monitored by a metacognitive layer that updates beliefs about the brain's capacity to successfully regulate bodily states (allostatic self-efficacy). In this framework, fatigue and depression can be understood as sequential responses to the interoceptive experience of dyshomeostasis and the ensuing metacognitive diagnosis of low allostatic self-efficacy. While fatigue might represent an early response with adaptive value (cf. sickness behavior), the experience of chronic dyshomeostasis may trigger a generalized belief of low self-efficacy and lack of control (cf. learned helplessness), resulting in depression. This perspective implies alternative pathophysiological mechanisms that are reflected by differential abnormalities in the effective connectivity of circuits for interoception and allostasis. We discuss suitably extended models of effective connectivity that could distinguish these connectivity patterns in individual patients and may help inform differential diagnosis of fatigue and depression in the future. Frontiers Media S.A. 2016-11-15 /pmc/articles/PMC5108808/ /pubmed/27895566 http://dx.doi.org/10.3389/fnhum.2016.00550 Text en Copyright © 2016 Stephan, Manjaly, Mathys, Weber, Paliwal, Gard, Tittgemeyer, Fleming, Haker, Seth and Petzschner. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Stephan, Klaas E.
Manjaly, Zina M.
Mathys, Christoph D.
Weber, Lilian A. E.
Paliwal, Saee
Gard, Tim
Tittgemeyer, Marc
Fleming, Stephen M.
Haker, Helene
Seth, Anil K.
Petzschner, Frederike H.
Allostatic Self-efficacy: A Metacognitive Theory of Dyshomeostasis-Induced Fatigue and Depression
title Allostatic Self-efficacy: A Metacognitive Theory of Dyshomeostasis-Induced Fatigue and Depression
title_full Allostatic Self-efficacy: A Metacognitive Theory of Dyshomeostasis-Induced Fatigue and Depression
title_fullStr Allostatic Self-efficacy: A Metacognitive Theory of Dyshomeostasis-Induced Fatigue and Depression
title_full_unstemmed Allostatic Self-efficacy: A Metacognitive Theory of Dyshomeostasis-Induced Fatigue and Depression
title_short Allostatic Self-efficacy: A Metacognitive Theory of Dyshomeostasis-Induced Fatigue and Depression
title_sort allostatic self-efficacy: a metacognitive theory of dyshomeostasis-induced fatigue and depression
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5108808/
https://www.ncbi.nlm.nih.gov/pubmed/27895566
http://dx.doi.org/10.3389/fnhum.2016.00550
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