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Delineating conditions and subtypes in chronic pain using neuroimaging

Differentiating subtypes of chronic pain still remains a challenge—both from a subjective and objective point of view. Personalized medicine is the current goal of modern medical care and is limited by the subjective nature of patient self-reporting of symptoms and behavioral evaluation. Physiology-...

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Autores principales: Holmes, Scott A., Upadhyay, Jaymin, Borsook, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6727994/
https://www.ncbi.nlm.nih.gov/pubmed/31579859
http://dx.doi.org/10.1097/PR9.0000000000000768
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author Holmes, Scott A.
Upadhyay, Jaymin
Borsook, David
author_facet Holmes, Scott A.
Upadhyay, Jaymin
Borsook, David
author_sort Holmes, Scott A.
collection PubMed
description Differentiating subtypes of chronic pain still remains a challenge—both from a subjective and objective point of view. Personalized medicine is the current goal of modern medical care and is limited by the subjective nature of patient self-reporting of symptoms and behavioral evaluation. Physiology-focused techniques such as genome and epigenetic analyses inform the delineation of pain groups; however, except under rare circumstances, they have diluted effects that again, share a common reliance on behavioral evaluation. The application of structural neuroimaging towards distinguishing pain subtypes is a growing field and may inform pain-group classification through the analysis of brain regions showing hypertrophic and atrophic changes in the presence of pain. Analytical techniques such as machine-learning classifiers have the capacity to process large volumes of data and delineate diagnostically relevant information from neuroimaging analysis. The issue of defining a “brain type” is an emerging field aimed at interpreting observed brain changes and delineating their clinical identity/significance. In this review, 2 chronic pain conditions (migraine and irritable bowel syndrome) with similar clinical phenotypes are compared in terms of their structural neuroimaging findings. Independent investigations are compared with findings from application of machine-learning algorithms. Findings are discussed in terms of differentiating patient subgroups using neuroimaging data in patients with chronic pain and how they may be applied towards defining a personalized pain signature that helps segregate patient subgroups (eg, migraine with and without aura, with or without nausea; irritable bowel syndrome vs other functional gastrointestinal disorders).
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spelling pubmed-67279942019-10-02 Delineating conditions and subtypes in chronic pain using neuroimaging Holmes, Scott A. Upadhyay, Jaymin Borsook, David Pain Rep Special Issue on Innovations and Controversies in Brain Imaging of Pain: Methods and Interpretations Differentiating subtypes of chronic pain still remains a challenge—both from a subjective and objective point of view. Personalized medicine is the current goal of modern medical care and is limited by the subjective nature of patient self-reporting of symptoms and behavioral evaluation. Physiology-focused techniques such as genome and epigenetic analyses inform the delineation of pain groups; however, except under rare circumstances, they have diluted effects that again, share a common reliance on behavioral evaluation. The application of structural neuroimaging towards distinguishing pain subtypes is a growing field and may inform pain-group classification through the analysis of brain regions showing hypertrophic and atrophic changes in the presence of pain. Analytical techniques such as machine-learning classifiers have the capacity to process large volumes of data and delineate diagnostically relevant information from neuroimaging analysis. The issue of defining a “brain type” is an emerging field aimed at interpreting observed brain changes and delineating their clinical identity/significance. In this review, 2 chronic pain conditions (migraine and irritable bowel syndrome) with similar clinical phenotypes are compared in terms of their structural neuroimaging findings. Independent investigations are compared with findings from application of machine-learning algorithms. Findings are discussed in terms of differentiating patient subgroups using neuroimaging data in patients with chronic pain and how they may be applied towards defining a personalized pain signature that helps segregate patient subgroups (eg, migraine with and without aura, with or without nausea; irritable bowel syndrome vs other functional gastrointestinal disorders). Wolters Kluwer 2019-08-07 /pmc/articles/PMC6727994/ /pubmed/31579859 http://dx.doi.org/10.1097/PR9.0000000000000768 Text en Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The International Association for the Study of Pain. This is an open access article distributed under the Creative Commons Attribution-NoDerivatives License 4.0 (CC BY-ND) (http://creativecommons.org/licenses/by-nd/4.0/) which allows for redistribution, commercial and non-commercial, as long as it is passed along unchanged and in whole, with credit to the author.
spellingShingle Special Issue on Innovations and Controversies in Brain Imaging of Pain: Methods and Interpretations
Holmes, Scott A.
Upadhyay, Jaymin
Borsook, David
Delineating conditions and subtypes in chronic pain using neuroimaging
title Delineating conditions and subtypes in chronic pain using neuroimaging
title_full Delineating conditions and subtypes in chronic pain using neuroimaging
title_fullStr Delineating conditions and subtypes in chronic pain using neuroimaging
title_full_unstemmed Delineating conditions and subtypes in chronic pain using neuroimaging
title_short Delineating conditions and subtypes in chronic pain using neuroimaging
title_sort delineating conditions and subtypes in chronic pain using neuroimaging
topic Special Issue on Innovations and Controversies in Brain Imaging of Pain: Methods and Interpretations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6727994/
https://www.ncbi.nlm.nih.gov/pubmed/31579859
http://dx.doi.org/10.1097/PR9.0000000000000768
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