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Gender differences in PTSD severity and pain outcomes: baseline results from the LAMP trial

BACKGROUND: Post-traumatic stress disorder (PTSD) and chronic pain are highly prevalent comorbid conditions. Veterans dually burdened by PTSD and chronic pain experience more severe outcomes compared to either disorder alone. Few studies have enrolled enough women Veterans to test gender differences...

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Autores principales: Friedman, JK, Taylor, BC, Hagel Campbell, E, Allen, K, Bangerter, A, Branson, M, Bronfort, G, Calvert, C, Cross, LJS, Driscoll, M, Evans, R, Ferguson, JE, Haley, A, Hennessy, S, Meis, LA, Burgess, DJ
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10593051/
https://www.ncbi.nlm.nih.gov/pubmed/37873176
http://dx.doi.org/10.1101/2023.10.13.23296998
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author Friedman, JK
Taylor, BC
Hagel Campbell, E
Allen, K
Bangerter, A
Branson, M
Bronfort, G
Calvert, C
Cross, LJS
Driscoll, M
Evans, R
Ferguson, JE
Haley, A
Hennessy, S
Meis, LA
Burgess, DJ
author_facet Friedman, JK
Taylor, BC
Hagel Campbell, E
Allen, K
Bangerter, A
Branson, M
Bronfort, G
Calvert, C
Cross, LJS
Driscoll, M
Evans, R
Ferguson, JE
Haley, A
Hennessy, S
Meis, LA
Burgess, DJ
author_sort Friedman, JK
collection PubMed
description BACKGROUND: Post-traumatic stress disorder (PTSD) and chronic pain are highly prevalent comorbid conditions. Veterans dually burdened by PTSD and chronic pain experience more severe outcomes compared to either disorder alone. Few studies have enrolled enough women Veterans to test gender differences in pain outcomes [catastrophizing, intensity, interference] by the severity of PTSD. AIM: Examine gender differences in the association between PTSD symptoms and pain outcomes among Veterans enrolled in a chronic pain clinical trial. METHODS. Participants were 421 men and 386 women Veterans with chronic pain who provided complete data on PTSD symptoms and pain outcomes. We used hierarchical linear regression models to examine gender differences in pain outcomes by PTSD symptoms. RESULTS. Adjusted multivariable models indicated that PTSD symptoms were associated with higher levels of pain catastrophizing (0.57, 95% CI [0.51, 0.63]), pain intensity (0.30, 95% CI [0.24, 0.37]), and pain interference (0.46, 95% CI [0.39, 0.52]). No evidence suggesting differences in this association were found in either the crude or adjusted models (all interaction p-values<0.05). CONCLUSION: These findings may reflect the underlying mutual maintenance of these conditions whereby the sensation of pain could trigger PTSD symptoms, particularly if the trauma and pain are associated with the same event. Clinical implications and opportunities testing relevant treatments that may benefit both chronic pain and PTSD are discussed.
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spelling pubmed-105930512023-10-24 Gender differences in PTSD severity and pain outcomes: baseline results from the LAMP trial Friedman, JK Taylor, BC Hagel Campbell, E Allen, K Bangerter, A Branson, M Bronfort, G Calvert, C Cross, LJS Driscoll, M Evans, R Ferguson, JE Haley, A Hennessy, S Meis, LA Burgess, DJ medRxiv Article BACKGROUND: Post-traumatic stress disorder (PTSD) and chronic pain are highly prevalent comorbid conditions. Veterans dually burdened by PTSD and chronic pain experience more severe outcomes compared to either disorder alone. Few studies have enrolled enough women Veterans to test gender differences in pain outcomes [catastrophizing, intensity, interference] by the severity of PTSD. AIM: Examine gender differences in the association between PTSD symptoms and pain outcomes among Veterans enrolled in a chronic pain clinical trial. METHODS. Participants were 421 men and 386 women Veterans with chronic pain who provided complete data on PTSD symptoms and pain outcomes. We used hierarchical linear regression models to examine gender differences in pain outcomes by PTSD symptoms. RESULTS. Adjusted multivariable models indicated that PTSD symptoms were associated with higher levels of pain catastrophizing (0.57, 95% CI [0.51, 0.63]), pain intensity (0.30, 95% CI [0.24, 0.37]), and pain interference (0.46, 95% CI [0.39, 0.52]). No evidence suggesting differences in this association were found in either the crude or adjusted models (all interaction p-values<0.05). CONCLUSION: These findings may reflect the underlying mutual maintenance of these conditions whereby the sensation of pain could trigger PTSD symptoms, particularly if the trauma and pain are associated with the same event. Clinical implications and opportunities testing relevant treatments that may benefit both chronic pain and PTSD are discussed. Cold Spring Harbor Laboratory 2023-10-15 /pmc/articles/PMC10593051/ /pubmed/37873176 http://dx.doi.org/10.1101/2023.10.13.23296998 Text en https://creativecommons.org/publicdomain/zero/1.0/This article is a US Government work. It is not subject to copyright under 17 USC 105 and is also made available for use under a CC0 license (https://creativecommons.org/publicdomain/zero/1.0/) .
spellingShingle Article
Friedman, JK
Taylor, BC
Hagel Campbell, E
Allen, K
Bangerter, A
Branson, M
Bronfort, G
Calvert, C
Cross, LJS
Driscoll, M
Evans, R
Ferguson, JE
Haley, A
Hennessy, S
Meis, LA
Burgess, DJ
Gender differences in PTSD severity and pain outcomes: baseline results from the LAMP trial
title Gender differences in PTSD severity and pain outcomes: baseline results from the LAMP trial
title_full Gender differences in PTSD severity and pain outcomes: baseline results from the LAMP trial
title_fullStr Gender differences in PTSD severity and pain outcomes: baseline results from the LAMP trial
title_full_unstemmed Gender differences in PTSD severity and pain outcomes: baseline results from the LAMP trial
title_short Gender differences in PTSD severity and pain outcomes: baseline results from the LAMP trial
title_sort gender differences in ptsd severity and pain outcomes: baseline results from the lamp trial
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10593051/
https://www.ncbi.nlm.nih.gov/pubmed/37873176
http://dx.doi.org/10.1101/2023.10.13.23296998
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