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Predictors of Change in Bodily Pain in Early Rheumatoid Arthritis: An Inception Cohort Study

OBJECTIVE: To investigate possible predictors for lack of pain improvement after 1 year of treatment for early rheumatoid arthritis (RA). METHODS: The Early Rheumatoid Arthritis Network (ERAN) database was used for analysis of baseline and 1-year pain data. The ERAN is a hospital-based inception coh...

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Autores principales: McWilliams, Daniel F, Zhang, Weiya, Mansell, Josephine S, Kiely, Patrick D W, Young, Adam, Walsh, David A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3770924/
https://www.ncbi.nlm.nih.gov/pubmed/22556121
http://dx.doi.org/10.1002/acr.21723
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author McWilliams, Daniel F
Zhang, Weiya
Mansell, Josephine S
Kiely, Patrick D W
Young, Adam
Walsh, David A
author_facet McWilliams, Daniel F
Zhang, Weiya
Mansell, Josephine S
Kiely, Patrick D W
Young, Adam
Walsh, David A
author_sort McWilliams, Daniel F
collection PubMed
description OBJECTIVE: To investigate possible predictors for lack of pain improvement after 1 year of treatment for early rheumatoid arthritis (RA). METHODS: The Early Rheumatoid Arthritis Network (ERAN) database was used for analysis of baseline and 1-year pain data. The ERAN is a hospital-based inception cohort of 1,189 people. Short Form 36 questionnaire bodily pain scores were used to calculate change in pain at 1 year as the outcome. The proportion of the Disease Activity Score in 28 joints (DAS28) attributable to patient-reported components (joint tenderness and visual analog scale score; DAS28-P) at baseline was derived as a predictor. Predictors of less improvement in pain were investigated using adjusted odds ratios (OR(adj)) generated by logistic regression, adjusting for 14 additional clinical and demographic covariates. RESULTS: Greater pain at baseline was associated with sex, high DAS28, worse mental health, and smoking. Most patients with early RA reported incomplete improvement in bodily pain after 1 year. The DAS28-P index did not significantly change in the patients whose disease remained active. Less improvement in pain was predicted by female sex (OR(adj) 3.41, 95% confidence interval [95% CI] 1.35–8.64) and a high DAS28-P index at baseline (OR(adj) for tertiles 2.09, 95% CI 1.24–3.55). Other conventional RA risk factors did not predict pain changes. CONCLUSION: The factors most likely to predict less improvement in pain in early RA are female sex and a high DAS28-P index. A high DAS28-P index may reflect greater contributions of noninflammatory factors, such as central sensitization, to pain. Strategies in addition to inflammatory disease suppression may be required to adequately treat pain.
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spelling pubmed-37709242013-09-13 Predictors of Change in Bodily Pain in Early Rheumatoid Arthritis: An Inception Cohort Study McWilliams, Daniel F Zhang, Weiya Mansell, Josephine S Kiely, Patrick D W Young, Adam Walsh, David A Arthritis Care Res (Hoboken) Rheumatoid Arthritis OBJECTIVE: To investigate possible predictors for lack of pain improvement after 1 year of treatment for early rheumatoid arthritis (RA). METHODS: The Early Rheumatoid Arthritis Network (ERAN) database was used for analysis of baseline and 1-year pain data. The ERAN is a hospital-based inception cohort of 1,189 people. Short Form 36 questionnaire bodily pain scores were used to calculate change in pain at 1 year as the outcome. The proportion of the Disease Activity Score in 28 joints (DAS28) attributable to patient-reported components (joint tenderness and visual analog scale score; DAS28-P) at baseline was derived as a predictor. Predictors of less improvement in pain were investigated using adjusted odds ratios (OR(adj)) generated by logistic regression, adjusting for 14 additional clinical and demographic covariates. RESULTS: Greater pain at baseline was associated with sex, high DAS28, worse mental health, and smoking. Most patients with early RA reported incomplete improvement in bodily pain after 1 year. The DAS28-P index did not significantly change in the patients whose disease remained active. Less improvement in pain was predicted by female sex (OR(adj) 3.41, 95% confidence interval [95% CI] 1.35–8.64) and a high DAS28-P index at baseline (OR(adj) for tertiles 2.09, 95% CI 1.24–3.55). Other conventional RA risk factors did not predict pain changes. CONCLUSION: The factors most likely to predict less improvement in pain in early RA are female sex and a high DAS28-P index. A high DAS28-P index may reflect greater contributions of noninflammatory factors, such as central sensitization, to pain. Strategies in addition to inflammatory disease suppression may be required to adequately treat pain. John Wiley & Sons, Inc. 2012-10 2012-09-28 /pmc/articles/PMC3770924/ /pubmed/22556121 http://dx.doi.org/10.1002/acr.21723 Text en Copyright © 2012 by the American College of Rheumatology http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Rheumatoid Arthritis
McWilliams, Daniel F
Zhang, Weiya
Mansell, Josephine S
Kiely, Patrick D W
Young, Adam
Walsh, David A
Predictors of Change in Bodily Pain in Early Rheumatoid Arthritis: An Inception Cohort Study
title Predictors of Change in Bodily Pain in Early Rheumatoid Arthritis: An Inception Cohort Study
title_full Predictors of Change in Bodily Pain in Early Rheumatoid Arthritis: An Inception Cohort Study
title_fullStr Predictors of Change in Bodily Pain in Early Rheumatoid Arthritis: An Inception Cohort Study
title_full_unstemmed Predictors of Change in Bodily Pain in Early Rheumatoid Arthritis: An Inception Cohort Study
title_short Predictors of Change in Bodily Pain in Early Rheumatoid Arthritis: An Inception Cohort Study
title_sort predictors of change in bodily pain in early rheumatoid arthritis: an inception cohort study
topic Rheumatoid Arthritis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3770924/
https://www.ncbi.nlm.nih.gov/pubmed/22556121
http://dx.doi.org/10.1002/acr.21723
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