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Mood Disorders in Young People With Acquired Brain Injury: An Integrated Model

PURPOSE/OBJECTIVE: Young people with paediatric acquired brain injury (pABI) are twice as likely to develop a mood disorder as their peers, frequently have significant unmet socio-emotional needs, and are at over double the risk of going on to use adult mental health services. Recent years have seen...

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Autores principales: Roberts, Henrietta, Ford, Tamsin J., Karl, Anke, Reynolds, Shirley, Limond, Jenny, Adlam, Anna-Lynne R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218558/
https://www.ncbi.nlm.nih.gov/pubmed/35754774
http://dx.doi.org/10.3389/fnhum.2022.835897
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author Roberts, Henrietta
Ford, Tamsin J.
Karl, Anke
Reynolds, Shirley
Limond, Jenny
Adlam, Anna-Lynne R.
author_facet Roberts, Henrietta
Ford, Tamsin J.
Karl, Anke
Reynolds, Shirley
Limond, Jenny
Adlam, Anna-Lynne R.
author_sort Roberts, Henrietta
collection PubMed
description PURPOSE/OBJECTIVE: Young people with paediatric acquired brain injury (pABI) are twice as likely to develop a mood disorder as their peers, frequently have significant unmet socio-emotional needs, and are at over double the risk of going on to use adult mental health services. Recent years have seen significant advances in the development of interventions for young people with mood disorders. However, evidence-based approaches to mood disorders in pABI are lacking and surprisingly little work has evaluated clinical and neuro-developmental models of mood disorders in this population. METHOD: We review the literature regarding key mechanisms hypothesised to account for the increased vulnerability to mood disorders in pABI: First, we summarise the direct neurocognitive consequences of pABI, considering the key areas of the brain implicated in vulnerability to mood disorders within a neurodevelopmental framework. Second, we outline five key factors that contribute to the heightened prevalence of mood disorders in young people following ABI. Finally, we synthesise these, integrating neuro-cognitive, developmental and systemic factors to guide clinical formulation. RESULTS AND IMPLICATIONS: We present a framework that synthesises the key mechanisms identified in our review, namely the direct effects of pABI, neurocognitive and neuroendocrine factors implicated in mood and anxiety disorders, maladaptive neuroplasticity and trauma, structural and systemic factors, and psychological adjustment and developmental context. This framework is the first attempt to provide integrated guidance on the multiple factors that contribute to elevated life-long risk of mood disorders following pABI.
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spelling pubmed-92185582022-06-24 Mood Disorders in Young People With Acquired Brain Injury: An Integrated Model Roberts, Henrietta Ford, Tamsin J. Karl, Anke Reynolds, Shirley Limond, Jenny Adlam, Anna-Lynne R. Front Hum Neurosci Neuroscience PURPOSE/OBJECTIVE: Young people with paediatric acquired brain injury (pABI) are twice as likely to develop a mood disorder as their peers, frequently have significant unmet socio-emotional needs, and are at over double the risk of going on to use adult mental health services. Recent years have seen significant advances in the development of interventions for young people with mood disorders. However, evidence-based approaches to mood disorders in pABI are lacking and surprisingly little work has evaluated clinical and neuro-developmental models of mood disorders in this population. METHOD: We review the literature regarding key mechanisms hypothesised to account for the increased vulnerability to mood disorders in pABI: First, we summarise the direct neurocognitive consequences of pABI, considering the key areas of the brain implicated in vulnerability to mood disorders within a neurodevelopmental framework. Second, we outline five key factors that contribute to the heightened prevalence of mood disorders in young people following ABI. Finally, we synthesise these, integrating neuro-cognitive, developmental and systemic factors to guide clinical formulation. RESULTS AND IMPLICATIONS: We present a framework that synthesises the key mechanisms identified in our review, namely the direct effects of pABI, neurocognitive and neuroendocrine factors implicated in mood and anxiety disorders, maladaptive neuroplasticity and trauma, structural and systemic factors, and psychological adjustment and developmental context. This framework is the first attempt to provide integrated guidance on the multiple factors that contribute to elevated life-long risk of mood disorders following pABI. Frontiers Media S.A. 2022-06-09 /pmc/articles/PMC9218558/ /pubmed/35754774 http://dx.doi.org/10.3389/fnhum.2022.835897 Text en Copyright © 2022 Roberts, Ford, Karl, Reynolds, Limond and Adlam. https://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) and the copyright owner(s) 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
Roberts, Henrietta
Ford, Tamsin J.
Karl, Anke
Reynolds, Shirley
Limond, Jenny
Adlam, Anna-Lynne R.
Mood Disorders in Young People With Acquired Brain Injury: An Integrated Model
title Mood Disorders in Young People With Acquired Brain Injury: An Integrated Model
title_full Mood Disorders in Young People With Acquired Brain Injury: An Integrated Model
title_fullStr Mood Disorders in Young People With Acquired Brain Injury: An Integrated Model
title_full_unstemmed Mood Disorders in Young People With Acquired Brain Injury: An Integrated Model
title_short Mood Disorders in Young People With Acquired Brain Injury: An Integrated Model
title_sort mood disorders in young people with acquired brain injury: an integrated model
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218558/
https://www.ncbi.nlm.nih.gov/pubmed/35754774
http://dx.doi.org/10.3389/fnhum.2022.835897
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