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Investigating the Burden of Chronic Pain: An Inflammatory and Metabolic Composite
Background. Chronic pain is associated with increased morbidity and mortality, predominated by cardiovascular disease and cancer. Investigating related risk factor measures may elucidate the biological burden of chronic pain. Objectives. We hypothesized that chronic pain severity would be positively...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4909918/ https://www.ncbi.nlm.nih.gov/pubmed/27445627 http://dx.doi.org/10.1155/2016/7657329 |
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author | Sibille, Kimberly T. Steingrímsdóttir, Ólöf A. Fillingim, Roger B. Stubhaug, Audun Schirmer, Henrik Chen, Huaihou McEwen, Bruce S. Nielsen, Christopher S. |
author_facet | Sibille, Kimberly T. Steingrímsdóttir, Ólöf A. Fillingim, Roger B. Stubhaug, Audun Schirmer, Henrik Chen, Huaihou McEwen, Bruce S. Nielsen, Christopher S. |
author_sort | Sibille, Kimberly T. |
collection | PubMed |
description | Background. Chronic pain is associated with increased morbidity and mortality, predominated by cardiovascular disease and cancer. Investigating related risk factor measures may elucidate the biological burden of chronic pain. Objectives. We hypothesized that chronic pain severity would be positively associated with the risk factor composite. Methods. Data from 12,982 participants in the 6th Tromsø study were analyzed. Questionnaires included demographics, health behaviors, medical comorbidities, and chronic pain symptoms. The risk factor composite was comprised of body mass index, fibrinogen, C-reactive protein, and triglycerides. Chronic pain severity was characterized by frequency, intensity, time/duration, and total number of pain sites. Results. Individuals with chronic pain had a greater risk factor composite than individuals without chronic pain controlling for covariates and after excluding inflammation-related health conditions (p < 0.001). A significant “dose-response” relationship was demonstrated with pain severity (p < 0.001). In individuals with chronic pain, the risk factor composite varied by health behavior, exercise, lower levels and smoking, and higher levels. Discussion. The risk factor composite was higher in individuals with chronic pain, greater with increasing pain severity, and influenced by health behaviors. Conclusions. Identification of a biological composite sensitive to pain severity and adaptive/maladaptive behaviors would have significant clinical and research utility. |
format | Online Article Text |
id | pubmed-4909918 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-49099182016-06-23 Investigating the Burden of Chronic Pain: An Inflammatory and Metabolic Composite Sibille, Kimberly T. Steingrímsdóttir, Ólöf A. Fillingim, Roger B. Stubhaug, Audun Schirmer, Henrik Chen, Huaihou McEwen, Bruce S. Nielsen, Christopher S. Pain Res Manag Research Article Background. Chronic pain is associated with increased morbidity and mortality, predominated by cardiovascular disease and cancer. Investigating related risk factor measures may elucidate the biological burden of chronic pain. Objectives. We hypothesized that chronic pain severity would be positively associated with the risk factor composite. Methods. Data from 12,982 participants in the 6th Tromsø study were analyzed. Questionnaires included demographics, health behaviors, medical comorbidities, and chronic pain symptoms. The risk factor composite was comprised of body mass index, fibrinogen, C-reactive protein, and triglycerides. Chronic pain severity was characterized by frequency, intensity, time/duration, and total number of pain sites. Results. Individuals with chronic pain had a greater risk factor composite than individuals without chronic pain controlling for covariates and after excluding inflammation-related health conditions (p < 0.001). A significant “dose-response” relationship was demonstrated with pain severity (p < 0.001). In individuals with chronic pain, the risk factor composite varied by health behavior, exercise, lower levels and smoking, and higher levels. Discussion. The risk factor composite was higher in individuals with chronic pain, greater with increasing pain severity, and influenced by health behaviors. Conclusions. Identification of a biological composite sensitive to pain severity and adaptive/maladaptive behaviors would have significant clinical and research utility. Hindawi Publishing Corporation 2016 2016-06-02 /pmc/articles/PMC4909918/ /pubmed/27445627 http://dx.doi.org/10.1155/2016/7657329 Text en Copyright © 2016 Kimberly T. Sibille et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Sibille, Kimberly T. Steingrímsdóttir, Ólöf A. Fillingim, Roger B. Stubhaug, Audun Schirmer, Henrik Chen, Huaihou McEwen, Bruce S. Nielsen, Christopher S. Investigating the Burden of Chronic Pain: An Inflammatory and Metabolic Composite |
title | Investigating the Burden of Chronic Pain: An Inflammatory and Metabolic Composite |
title_full | Investigating the Burden of Chronic Pain: An Inflammatory and Metabolic Composite |
title_fullStr | Investigating the Burden of Chronic Pain: An Inflammatory and Metabolic Composite |
title_full_unstemmed | Investigating the Burden of Chronic Pain: An Inflammatory and Metabolic Composite |
title_short | Investigating the Burden of Chronic Pain: An Inflammatory and Metabolic Composite |
title_sort | investigating the burden of chronic pain: an inflammatory and metabolic composite |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4909918/ https://www.ncbi.nlm.nih.gov/pubmed/27445627 http://dx.doi.org/10.1155/2016/7657329 |
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