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Evaluation of clinical and inflammatory profile in opioid addiction patients with comorbid pain: results from a multicenter investigation

BACKGROUND: Chronic pain is the most commonly reported comorbidity among patients with opioid addiction receiving methadone maintenance treatment (MMT), with an estimated prevalence ranging between 30% and 55%. Evidence suggests that patients with comorbid pain are at high risk for poor treatment re...

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Autores principales: Dennis, Brittany B, Samaan, M Constantine, Bawor, Monica, Paul, James, Plater, Carolyn, Pare, Guillaume, Worster, Andrew, Varenbut, Michael, Daiter, Jeff, Marsh, David C, Desai, Dipika, Thabane, Lehana, Samaan, Zainab
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4242695/
https://www.ncbi.nlm.nih.gov/pubmed/25429222
http://dx.doi.org/10.2147/NDT.S72785
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author Dennis, Brittany B
Samaan, M Constantine
Bawor, Monica
Paul, James
Plater, Carolyn
Pare, Guillaume
Worster, Andrew
Varenbut, Michael
Daiter, Jeff
Marsh, David C
Desai, Dipika
Thabane, Lehana
Samaan, Zainab
author_facet Dennis, Brittany B
Samaan, M Constantine
Bawor, Monica
Paul, James
Plater, Carolyn
Pare, Guillaume
Worster, Andrew
Varenbut, Michael
Daiter, Jeff
Marsh, David C
Desai, Dipika
Thabane, Lehana
Samaan, Zainab
author_sort Dennis, Brittany B
collection PubMed
description BACKGROUND: Chronic pain is the most commonly reported comorbidity among patients with opioid addiction receiving methadone maintenance treatment (MMT), with an estimated prevalence ranging between 30% and 55%. Evidence suggests that patients with comorbid pain are at high risk for poor treatment response, including continued illicit substance use. Due to the important relationship between the presence of pain and illicit substance abuse within the MMT setting, it is imperative that we target our efforts toward understanding the characteristics of this patient population. METHODS: The primary objective of this study was to explore the clinical and inflammatory profile of MMT patients reporting comorbid pain. This multicenter study enrolled patients (n=235) on MMT for the treatment of opioid dependence. Clinical history and blood and urine data were collected. Blood samples were obtained for estimating the serum levels of inflammatory markers (tumor necrosis factor [TNF]-α, interleukin-1 receptor antagonist [IL-1ra], IL-6, IL-8, IL-10, interferon [IFN]-γ and chemokine (C–C motif) ligand 2 [CCL2]). The study objectives were addressed using a descriptive statistical summary and a multivariable logistic regression model constructed in STATA version 12. RESULTS: Among the participants eligible for inclusion (n=235), serum IFN-γ level and substance abuse behavior proved to be important delineating characteristics for the detection of comorbid pain. Analysis of inflammatory profile showed IFN-γ to be significantly elevated among patients reporting comorbid pain (odds ratio [OR]: 2.02; 95% confidence interval [CI]: 1.17, 3.50; P=0.01). Patients reporting comorbid pain were also found to have an increase in positive opioid urine screens (OR: 1.02; 95% CI: 1.00, 1.03; P=0.01), indicating an increase in illicit opioid consumption. CONCLUSION: MMT patients with comorbid pain were shown to have elevated IFN-γ and higher rates of continued opioid abuse. The ability to objectively distinguish between patients with comorbid pain may help to both improve the prediction of poor responders to MMT as well as identify treatment approaches such as anti-inflammatory medications as safe alternatives for MMT patients with comorbid pain.
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spelling pubmed-42426952014-11-26 Evaluation of clinical and inflammatory profile in opioid addiction patients with comorbid pain: results from a multicenter investigation Dennis, Brittany B Samaan, M Constantine Bawor, Monica Paul, James Plater, Carolyn Pare, Guillaume Worster, Andrew Varenbut, Michael Daiter, Jeff Marsh, David C Desai, Dipika Thabane, Lehana Samaan, Zainab Neuropsychiatr Dis Treat Original Research BACKGROUND: Chronic pain is the most commonly reported comorbidity among patients with opioid addiction receiving methadone maintenance treatment (MMT), with an estimated prevalence ranging between 30% and 55%. Evidence suggests that patients with comorbid pain are at high risk for poor treatment response, including continued illicit substance use. Due to the important relationship between the presence of pain and illicit substance abuse within the MMT setting, it is imperative that we target our efforts toward understanding the characteristics of this patient population. METHODS: The primary objective of this study was to explore the clinical and inflammatory profile of MMT patients reporting comorbid pain. This multicenter study enrolled patients (n=235) on MMT for the treatment of opioid dependence. Clinical history and blood and urine data were collected. Blood samples were obtained for estimating the serum levels of inflammatory markers (tumor necrosis factor [TNF]-α, interleukin-1 receptor antagonist [IL-1ra], IL-6, IL-8, IL-10, interferon [IFN]-γ and chemokine (C–C motif) ligand 2 [CCL2]). The study objectives were addressed using a descriptive statistical summary and a multivariable logistic regression model constructed in STATA version 12. RESULTS: Among the participants eligible for inclusion (n=235), serum IFN-γ level and substance abuse behavior proved to be important delineating characteristics for the detection of comorbid pain. Analysis of inflammatory profile showed IFN-γ to be significantly elevated among patients reporting comorbid pain (odds ratio [OR]: 2.02; 95% confidence interval [CI]: 1.17, 3.50; P=0.01). Patients reporting comorbid pain were also found to have an increase in positive opioid urine screens (OR: 1.02; 95% CI: 1.00, 1.03; P=0.01), indicating an increase in illicit opioid consumption. CONCLUSION: MMT patients with comorbid pain were shown to have elevated IFN-γ and higher rates of continued opioid abuse. The ability to objectively distinguish between patients with comorbid pain may help to both improve the prediction of poor responders to MMT as well as identify treatment approaches such as anti-inflammatory medications as safe alternatives for MMT patients with comorbid pain. Dove Medical Press 2014-11-19 /pmc/articles/PMC4242695/ /pubmed/25429222 http://dx.doi.org/10.2147/NDT.S72785 Text en © 2014 Dennis et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Dennis, Brittany B
Samaan, M Constantine
Bawor, Monica
Paul, James
Plater, Carolyn
Pare, Guillaume
Worster, Andrew
Varenbut, Michael
Daiter, Jeff
Marsh, David C
Desai, Dipika
Thabane, Lehana
Samaan, Zainab
Evaluation of clinical and inflammatory profile in opioid addiction patients with comorbid pain: results from a multicenter investigation
title Evaluation of clinical and inflammatory profile in opioid addiction patients with comorbid pain: results from a multicenter investigation
title_full Evaluation of clinical and inflammatory profile in opioid addiction patients with comorbid pain: results from a multicenter investigation
title_fullStr Evaluation of clinical and inflammatory profile in opioid addiction patients with comorbid pain: results from a multicenter investigation
title_full_unstemmed Evaluation of clinical and inflammatory profile in opioid addiction patients with comorbid pain: results from a multicenter investigation
title_short Evaluation of clinical and inflammatory profile in opioid addiction patients with comorbid pain: results from a multicenter investigation
title_sort evaluation of clinical and inflammatory profile in opioid addiction patients with comorbid pain: results from a multicenter investigation
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4242695/
https://www.ncbi.nlm.nih.gov/pubmed/25429222
http://dx.doi.org/10.2147/NDT.S72785
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