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The importance of a multidimensional approach to the preclinical study of major depressive disorder and apathy
Both the neuropsychiatric syndrome of apathy and major depressive disorder comprise a heterogenous cluster of symptoms which span multiple behavioural domains. Despite this heterogeneity, there is a tendency in the preclinical literature to conclude a MDD or apathy-like phenotype from a single dimen...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9788393/ https://www.ncbi.nlm.nih.gov/pubmed/36413089 http://dx.doi.org/10.1042/ETLS20220004 |
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author | Jackson, Megan G. Robinson, Emma S. J. |
author_facet | Jackson, Megan G. Robinson, Emma S. J. |
author_sort | Jackson, Megan G. |
collection | PubMed |
description | Both the neuropsychiatric syndrome of apathy and major depressive disorder comprise a heterogenous cluster of symptoms which span multiple behavioural domains. Despite this heterogeneity, there is a tendency in the preclinical literature to conclude a MDD or apathy-like phenotype from a single dimensional behavioural task used in isolation, which may lead to inaccurate phenotypic interpretation. This is significant, as apathy and major depressive disorder are clinically distinct with different underlying mechanisms and treatment approaches. At the clinical level, apathy and major depressive disorder can be dissociated in the negative valence (loss) domain of the Research Domain Criteria. Symptoms of MDD in the negative valence (loss) domain can include an exaggerated response to emotionally salient stimuli and low mood, while in contrast apathy is characterised by an emotionally blunted state. In this article, we highlight how using a single dimensional approach can limit psychiatric model interpretation. We discuss how integrating behavioural findings from both the positive and negative (loss) valence domains of the Research Domain Criteria can benefit interpretation of findings. We focus particularly on behaviours relating to the negative valence (loss) domain, which may be used to distinguish between apathy and major depressive disorder at the preclinical level. Finally, we consider how future approaches using home cage monitoring may offer a new opportunity to detect distinct behavioural profiles and benefit the overall translatability of findings. |
format | Online Article Text |
id | pubmed-9788393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97883932023-01-06 The importance of a multidimensional approach to the preclinical study of major depressive disorder and apathy Jackson, Megan G. Robinson, Emma S. J. Emerg Top Life Sci Review Articles Both the neuropsychiatric syndrome of apathy and major depressive disorder comprise a heterogenous cluster of symptoms which span multiple behavioural domains. Despite this heterogeneity, there is a tendency in the preclinical literature to conclude a MDD or apathy-like phenotype from a single dimensional behavioural task used in isolation, which may lead to inaccurate phenotypic interpretation. This is significant, as apathy and major depressive disorder are clinically distinct with different underlying mechanisms and treatment approaches. At the clinical level, apathy and major depressive disorder can be dissociated in the negative valence (loss) domain of the Research Domain Criteria. Symptoms of MDD in the negative valence (loss) domain can include an exaggerated response to emotionally salient stimuli and low mood, while in contrast apathy is characterised by an emotionally blunted state. In this article, we highlight how using a single dimensional approach can limit psychiatric model interpretation. We discuss how integrating behavioural findings from both the positive and negative (loss) valence domains of the Research Domain Criteria can benefit interpretation of findings. We focus particularly on behaviours relating to the negative valence (loss) domain, which may be used to distinguish between apathy and major depressive disorder at the preclinical level. Finally, we consider how future approaches using home cage monitoring may offer a new opportunity to detect distinct behavioural profiles and benefit the overall translatability of findings. Portland Press Ltd. 2022-11-22 /pmc/articles/PMC9788393/ /pubmed/36413089 http://dx.doi.org/10.1042/ETLS20220004 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and the Royal Society of Biology and distributed under the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) . Open access for this article was enabled by the participation of University of Bristol in an all-inclusive Read & Publish agreement with Portland Press and the Biochemical Society under a transformative agreement with JISC. |
spellingShingle | Review Articles Jackson, Megan G. Robinson, Emma S. J. The importance of a multidimensional approach to the preclinical study of major depressive disorder and apathy |
title | The importance of a multidimensional approach to the preclinical study of major depressive disorder and apathy |
title_full | The importance of a multidimensional approach to the preclinical study of major depressive disorder and apathy |
title_fullStr | The importance of a multidimensional approach to the preclinical study of major depressive disorder and apathy |
title_full_unstemmed | The importance of a multidimensional approach to the preclinical study of major depressive disorder and apathy |
title_short | The importance of a multidimensional approach to the preclinical study of major depressive disorder and apathy |
title_sort | importance of a multidimensional approach to the preclinical study of major depressive disorder and apathy |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9788393/ https://www.ncbi.nlm.nih.gov/pubmed/36413089 http://dx.doi.org/10.1042/ETLS20220004 |
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