Literature DB >> 30658176

Discrete Trajectories of Resolving and Persistent Pain in People With Rheumatoid Arthritis Despite Undergoing Treatment for Inflammation: Results From Three UK Cohorts.

Daniel F McWilliams1, Olivia Dawson2, Adam Young3, Patrick D W Kiely4, Eamonn Ferguson5, David A Walsh6.   

Abstract

Rheumatoid arthritis (RA) is an example of human chronic inflammatory pain. Modern treatments suppress inflammation, yet pain remains a major problem for many people with RA. We hypothesized that discrete RA subgroups might display favorable or unfavorable pain trajectories when receiving treatment, and that baseline characteristics will predict trajectory allocation. Growth mixture modelling was used to identify discrete trajectories of Short Form-36 bodily pain scores during 3 years in 3 RA cohorts (Early RA Network (n = 683), British Society for Rheumatology Biologics Register Biologics (n = 7,090) and nonbiologics (n = 1,720) cohorts. Logistic regression compared baseline predictor variables between trajectories. The role of inflammation was examined in a subgroup analysis of people with normal levels of inflammatory markers after 3 years. The mean Short Form-36 bodily pain scores in each cohort improved but remained throughout 3 years of follow-up of >1 standard deviation worse than the UK general population average. Discrete persistent pain (59-79% of cohort participants) and resolving pain (19-27%) trajectories were identified in each cohort. In Early RA Network, a third trajectory displaying persistently low pain (23%) was also identified. In people with normal levels of inflammatory markers after 3 years, 65% were found to follow a persistent pain trajectory. When trajectories were compared, greater disability (adjusted odds ratio = 2.3-2.5 per unit baseline Health Assessment Questionnaire score) and smoking history (adjusted odds ratio = 1.6-1.8) were risk factors for persistent pain trajectories in each cohort. In conclusion, distinct trajectories indicate patient subgroups with very different pain prognosis during treatment for RA. Inflammation does not fully explain the pain trajectories, and noninflammatory factors as well as acute phase response predict which trajectory an individual will follow. Targeted treatments additional to those which suppress inflammation might reduce the long-term burden of arthritis pain. PERSPECTIVE: Immunosuppression decreases inflammation in RA, but pain outcomes are less favorable. Discrete persistent and resolving pain trajectories were identified after treatment, both in early and established RA. Smoking and greater disability at baseline predicted persistent pain. Identifying patient subgroups with a poor pain prognosis could enable adjunctive treatment to improve outcomes.
Copyright © 2019 the American Pain Society. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Rheumatoid arthritis; cohort; inflammation; pain; trajectory

Year:  2019        PMID: 30658176     DOI: 10.1016/j.jpain.2019.01.001

Source DB:  PubMed          Journal:  J Pain        ISSN: 1526-5900            Impact factor:   5.820


  8 in total

1.  Depression as a major determinant of PASS (Patient's Acceptable Symptoms State) in rheumatoid arthritis: a cross-sectional study in Brazilian patients.

Authors:  Paulo Henrique Stocker; Marcos Henrique Jasper; Bárbara Kahlow; Renato Nisihara; Thelma Skare
Journal:  Rev Assoc Med Bras (1992)       Date:  2022-08       Impact factor: 1.712

2.  Comparison of chronic widespread pain prevalence with different criteria in two cohorts of rheumatoid arthritis.

Authors:  M Aronsson; S Bergman; E Lindqvist; M L E Andersson
Journal:  Clin Rheumatol       Date:  2021-11-23       Impact factor: 2.980

Review 3.  Smoking, alcohol consumption and disease-specific outcomes in rheumatic and musculoskeletal diseases (RMDs): systematic reviews informing the 2021 EULAR recommendations for lifestyle improvements in people with RMDs.

Authors:  Maud Wieczorek; James Martin Gwinnutt; Maxime Ransay-Colle; Suzanne Mm Verstappen; Francis Guillemin; Andra Balanescu; Heike Bischoff-Ferrari; Annelies Boonen; Giulio Cavalli; Savia de Souza; Annette de Thurah; Thomas Ernst Dorner; Rikke Helene Moe; Polina Putrik; Javier Rodríguez-Carrio; Lucía Silva-Fernández; Tanja A Stamm; Karen Walker-Bone; Joep Welling; Mirjana Zlatkovic-Svenda
Journal:  RMD Open       Date:  2022-03

4.  Predictors of unacceptable pain with and without low inflammation over 5 years in early rheumatoid arthritis-an inception cohort study.

Authors:  Anna Eberhard; Stefan Bergman; Thomas Mandl; Tor Olofsson; Maria Rydholm; Lennart Jacobsson; Carl Turesson
Journal:  Arthritis Res Ther       Date:  2021-06-14       Impact factor: 5.156

5.  Investigating musculoskeletal health and wellbeing; a cohort study protocol.

Authors:  Bonnie Millar; Daniel F McWilliams; Abhishek Abhishek; Kehinde Akin-Akinyosoye; Dorothee P Auer; Victoria Chapman; Michael Doherty; Eamonn Ferguson; John R F Gladman; Paul Greenhaff; Joanne Stocks; Ana M Valdes; David A Walsh
Journal:  BMC Musculoskelet Disord       Date:  2020-03-21       Impact factor: 2.362

6.  Fatigue in early rheumatoid arthritis: data from the Early Rheumatoid Arthritis Network.

Authors:  Onosi Sylvia Ifesemen; Daniel Frederick McWilliams; Sam Norton; Patrick D W Kiely; Adam Young; David Andrew Walsh
Journal:  Rheumatology (Oxford)       Date:  2022-08-30       Impact factor: 7.046

7.  Central Aspects of Pain in Rheumatoid Arthritis (CAP-RA): protocol for a prospective observational study.

Authors:  Onosi S Ifesemen; Daniel F McWilliams; Eamonn Ferguson; Richard Wakefield; Kehinde Akin-Akinyosoye; Deborah Wilson; Dorothy Platts; Susan Ledbury; David A Walsh
Journal:  BMC Rheumatol       Date:  2021-06-24

8.  Socio-demographic determinants in the evolution of pain in inflammatory rheumatic diseases: results from ESPOIR and DESIR cohorts.

Authors:  Sushmithadev Kumaradev; Christian Roux; Jérémie Sellam; Serge Perrot; Thao Pham; Aline Dugravot; Anna Molto
Journal:  Rheumatology (Oxford)       Date:  2022-04-11       Impact factor: 7.580

  8 in total

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