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CO(2) reactivity as a biomarker of exposure-based therapy non-response: study protocol
BACKGROUND: Exposure-based therapy is an effective first-line treatment for anxiety-, obsessive–compulsive, and trauma- and stressor-related disorders; however, many patients do not improve, resulting in prolonged suffering and poorly used resources. Basic research on fear extinction may inform the...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9793569/ https://www.ncbi.nlm.nih.gov/pubmed/36575425 http://dx.doi.org/10.1186/s12888-022-04478-x |
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author | Smits, Jasper A. J. Monfils, Marie-H. Otto, Michael W. Telch, Michael J. Shumake, Jason Feinstein, Justin S. Khalsa, Sahib S. Cobb, Adam R. Parsons, E. Marie Long, Laura J. McSpadden, Bryan Johnson, David Greenberg, Alma |
author_facet | Smits, Jasper A. J. Monfils, Marie-H. Otto, Michael W. Telch, Michael J. Shumake, Jason Feinstein, Justin S. Khalsa, Sahib S. Cobb, Adam R. Parsons, E. Marie Long, Laura J. McSpadden, Bryan Johnson, David Greenberg, Alma |
author_sort | Smits, Jasper A. J. |
collection | PubMed |
description | BACKGROUND: Exposure-based therapy is an effective first-line treatment for anxiety-, obsessive–compulsive, and trauma- and stressor-related disorders; however, many patients do not improve, resulting in prolonged suffering and poorly used resources. Basic research on fear extinction may inform the development of a biomarker for the selection of exposure-based therapy. Growing evidence links orexin system activity to deficits in fear extinction and we have demonstrated that reactivity to an inhaled carbon dioxide (CO(2)) challenge—a safe, affordable, and easy-to-implement procedure—can serve as a proxy for orexin system activity and predicts fear extinction deficits in rodents. Building upon this basic research, the goal for the proposed study is to validate CO(2) reactivity as a biomarker of exposure-based therapy non-response. METHODS: We will assess CO(2) reactivity in 600 adults meeting criteria for one or more fear- or anxiety-related disorders prior to providing open exposure-based therapy. By incorporating CO(2) reactivity into a multivariate model predicting treatment non-response that also includes reactivity to hyperventilation as well as a number of related predictor variables, we will establish the mechanistic specificity and the additive predictive utility of the potential CO(2) reactivity biomarker. By developing models independently within two study sites (University of Texas at Austin and Boston University) and predicting the other site’s data, we will validate that the results are likely to generalize to future clinical samples. DISCUSSION: Representing a necessary stage in translating basic research, this investigation addresses an important public health issue by testing an accessible clinical assessment strategy that may lead to a more effective treatment selection (personalized medicine) for patients with anxiety- and fear-related disorders, and enhanced understanding of the mechanisms governing exposure-based therapy. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT05467683 (20/07/2022). |
format | Online Article Text |
id | pubmed-9793569 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97935692022-12-28 CO(2) reactivity as a biomarker of exposure-based therapy non-response: study protocol Smits, Jasper A. J. Monfils, Marie-H. Otto, Michael W. Telch, Michael J. Shumake, Jason Feinstein, Justin S. Khalsa, Sahib S. Cobb, Adam R. Parsons, E. Marie Long, Laura J. McSpadden, Bryan Johnson, David Greenberg, Alma BMC Psychiatry Study Protocol BACKGROUND: Exposure-based therapy is an effective first-line treatment for anxiety-, obsessive–compulsive, and trauma- and stressor-related disorders; however, many patients do not improve, resulting in prolonged suffering and poorly used resources. Basic research on fear extinction may inform the development of a biomarker for the selection of exposure-based therapy. Growing evidence links orexin system activity to deficits in fear extinction and we have demonstrated that reactivity to an inhaled carbon dioxide (CO(2)) challenge—a safe, affordable, and easy-to-implement procedure—can serve as a proxy for orexin system activity and predicts fear extinction deficits in rodents. Building upon this basic research, the goal for the proposed study is to validate CO(2) reactivity as a biomarker of exposure-based therapy non-response. METHODS: We will assess CO(2) reactivity in 600 adults meeting criteria for one or more fear- or anxiety-related disorders prior to providing open exposure-based therapy. By incorporating CO(2) reactivity into a multivariate model predicting treatment non-response that also includes reactivity to hyperventilation as well as a number of related predictor variables, we will establish the mechanistic specificity and the additive predictive utility of the potential CO(2) reactivity biomarker. By developing models independently within two study sites (University of Texas at Austin and Boston University) and predicting the other site’s data, we will validate that the results are likely to generalize to future clinical samples. DISCUSSION: Representing a necessary stage in translating basic research, this investigation addresses an important public health issue by testing an accessible clinical assessment strategy that may lead to a more effective treatment selection (personalized medicine) for patients with anxiety- and fear-related disorders, and enhanced understanding of the mechanisms governing exposure-based therapy. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT05467683 (20/07/2022). BioMed Central 2022-12-27 /pmc/articles/PMC9793569/ /pubmed/36575425 http://dx.doi.org/10.1186/s12888-022-04478-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 | Study Protocol Smits, Jasper A. J. Monfils, Marie-H. Otto, Michael W. Telch, Michael J. Shumake, Jason Feinstein, Justin S. Khalsa, Sahib S. Cobb, Adam R. Parsons, E. Marie Long, Laura J. McSpadden, Bryan Johnson, David Greenberg, Alma CO(2) reactivity as a biomarker of exposure-based therapy non-response: study protocol |
title | CO(2) reactivity as a biomarker of exposure-based therapy non-response: study protocol |
title_full | CO(2) reactivity as a biomarker of exposure-based therapy non-response: study protocol |
title_fullStr | CO(2) reactivity as a biomarker of exposure-based therapy non-response: study protocol |
title_full_unstemmed | CO(2) reactivity as a biomarker of exposure-based therapy non-response: study protocol |
title_short | CO(2) reactivity as a biomarker of exposure-based therapy non-response: study protocol |
title_sort | co(2) reactivity as a biomarker of exposure-based therapy non-response: study protocol |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9793569/ https://www.ncbi.nlm.nih.gov/pubmed/36575425 http://dx.doi.org/10.1186/s12888-022-04478-x |
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