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Towards formal models of psychopathological traits that explain symptom trajectories

BACKGROUND: A dominant methodology in contemporary clinical neuroscience is the use of dimensional self-report questionnaires to measure features such as psychological traits (e.g., trait anxiety) and states (e.g., depressed mood). These dimensions are then mapped to biological measures and computat...

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Autores principales: Sharp, Paul B., Miller, Gregory A., Dolan, Raymond J., Eldar, Eran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7520959/
https://www.ncbi.nlm.nih.gov/pubmed/32981516
http://dx.doi.org/10.1186/s12916-020-01725-4
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author Sharp, Paul B.
Miller, Gregory A.
Dolan, Raymond J.
Eldar, Eran
author_facet Sharp, Paul B.
Miller, Gregory A.
Dolan, Raymond J.
Eldar, Eran
author_sort Sharp, Paul B.
collection PubMed
description BACKGROUND: A dominant methodology in contemporary clinical neuroscience is the use of dimensional self-report questionnaires to measure features such as psychological traits (e.g., trait anxiety) and states (e.g., depressed mood). These dimensions are then mapped to biological measures and computational parameters. Researchers pursuing this approach tend to equate a symptom inventory score (plus noise) with some latent psychological trait. MAIN TEXT: We argue this approach implies weak, tacit, models of traits that provide fixed predictions of individual symptoms, and thus cannot account for symptom trajectories within individuals. This problem persists because (1) researchers are not familiarized with formal models that relate internal traits to within-subject symptom variation and (2) rely on an assumption that trait self-report inventories accurately indicate latent traits. To address these concerns, we offer a computational model of trait depression that demonstrates how parameters instantiating a given trait remain stable while manifest symptom expression varies predictably. We simulate patterns of mood variation from both the computational model and the standard self-report model and describe how to quantify the relative validity of each model using a Bayesian procedure. CONCLUSIONS: Ultimately, we would urge a tempering of a reliance on self-report inventories and recommend a shift towards developing mechanistic trait models that can explain within-subject symptom dynamics.
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spelling pubmed-75209592020-09-30 Towards formal models of psychopathological traits that explain symptom trajectories Sharp, Paul B. Miller, Gregory A. Dolan, Raymond J. Eldar, Eran BMC Med Opinion BACKGROUND: A dominant methodology in contemporary clinical neuroscience is the use of dimensional self-report questionnaires to measure features such as psychological traits (e.g., trait anxiety) and states (e.g., depressed mood). These dimensions are then mapped to biological measures and computational parameters. Researchers pursuing this approach tend to equate a symptom inventory score (plus noise) with some latent psychological trait. MAIN TEXT: We argue this approach implies weak, tacit, models of traits that provide fixed predictions of individual symptoms, and thus cannot account for symptom trajectories within individuals. This problem persists because (1) researchers are not familiarized with formal models that relate internal traits to within-subject symptom variation and (2) rely on an assumption that trait self-report inventories accurately indicate latent traits. To address these concerns, we offer a computational model of trait depression that demonstrates how parameters instantiating a given trait remain stable while manifest symptom expression varies predictably. We simulate patterns of mood variation from both the computational model and the standard self-report model and describe how to quantify the relative validity of each model using a Bayesian procedure. CONCLUSIONS: Ultimately, we would urge a tempering of a reliance on self-report inventories and recommend a shift towards developing mechanistic trait models that can explain within-subject symptom dynamics. BioMed Central 2020-09-28 /pmc/articles/PMC7520959/ /pubmed/32981516 http://dx.doi.org/10.1186/s12916-020-01725-4 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Opinion
Sharp, Paul B.
Miller, Gregory A.
Dolan, Raymond J.
Eldar, Eran
Towards formal models of psychopathological traits that explain symptom trajectories
title Towards formal models of psychopathological traits that explain symptom trajectories
title_full Towards formal models of psychopathological traits that explain symptom trajectories
title_fullStr Towards formal models of psychopathological traits that explain symptom trajectories
title_full_unstemmed Towards formal models of psychopathological traits that explain symptom trajectories
title_short Towards formal models of psychopathological traits that explain symptom trajectories
title_sort towards formal models of psychopathological traits that explain symptom trajectories
topic Opinion
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7520959/
https://www.ncbi.nlm.nih.gov/pubmed/32981516
http://dx.doi.org/10.1186/s12916-020-01725-4
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