Exploring the disparity between inflammation and disability in the 10-year outcomes of people with rheumatoid arthritis.


Journal

Rheumatology (Oxford, England)
ISSN: 1462-0332
Titre abrégé: Rheumatology (Oxford)
Pays: England
ID NLM: 100883501

Informations de publication

Date de publication:
28 11 2022
Historique:
received: 07 01 2022
accepted: 25 02 2022
pubmed: 12 3 2022
medline: 2 12 2022
entrez: 11 3 2022
Statut: ppublish

Résumé

To identify groups of people with RA with different disability trajectories over 10 years, despite comparable levels of inflammation. Data for this analysis came from three European prospective cohort studies of people with RA [Norfolk Arthritis Register (NOAR), Early RA Network (ERAN), Étude et Suivi des Polyarthrites Indifférenciées Récentes (ESPOIR)]. Participants were assessed regularly over 8 (ERAN) to 10 (NOAR/ESPOIR) years. Inclusion criteria were: recruited after 1 January 2000, <24 months baseline symptom duration, and disability (HAQ) and inflammation [two-component DAS28 (DAS28-2C)] recorded at baseline and at one other follow-up. People in each cohort also completed patient-reported outcome measures at each assessment (pain, fatigue, depressive symptoms). Group-based trajectory models were used to identify distinct groups of people with similar HAQ and DAS28-2C trajectories over follow-up. This analysis included 2500 people with RA (NOAR: 1000, ESPOIR: 766, ERAN: 734). ESPOIR included more women and the participants were younger [mean (standard deviation) age: NOAR: 57.1 (14.6), ESPOIR: 47.6 (12.5), ERAN: 56.8 (13.8); women: NOAR: 63.9%, ESPOIR: 76.9%, ERAN: 69.1%). Within each cohort, two pairs of trajectories following the hypothesized pattern (comparable DAS28-2Cs but different HAQs) were identified. Higher pain, fatigue and depressive symptoms were associated with increased odds of being in the high HAQ trajectories. Excess disability is persistent in RA. Controlling inflammation may not be sufficient to alleviate disability in all people with RA, and effective pain, fatigue and mood management may be needed in some groups to improve long-term function.

Identifiants

pubmed: 35274696
pii: 6547046
doi: 10.1093/rheumatology/keac137
pmc: PMC9707289
doi:

Substances chimiques

Antirheumatic Agents 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

4687-4701

Subventions

Organisme : Versus Arthritis
ID : 21229
Pays : United Kingdom
Organisme : Medical Research Council
Pays : United Kingdom
Organisme : Versus Arthritis
ID : 21755
Pays : United Kingdom
Organisme : Department of Health
Pays : United Kingdom

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of the British Society for Rheumatology.

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Auteurs

James M Gwinnutt (JM)

Centre for Epidemiology Versus Arthritis, Division of Musculoskeletal and Dermatological Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester.

Sam Norton (S)

Health Psychology Section, Institute of Psychiatry, Psychology and Neuroscience.
Centre for Rheumatic Diseases, Department of Inflammation Biology, Faculty of Life Sciences and Medicine, King's College London, London.

Kimme L Hyrich (KL)

Centre for Epidemiology Versus Arthritis, Division of Musculoskeletal and Dermatological Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester.
NIHR Manchester Biomedical Research Centre, Manchester University NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK.

Mark Lunt (M)

Centre for Epidemiology Versus Arthritis, Division of Musculoskeletal and Dermatological Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester.

Nathalie Rincheval (N)

Laboratory of Biostatistics and Epidemiology, University of Montpellier, Montpellier.

Adeline Ruyssen-Witrand (A)

Centre de Rhumatologie, Hôpital Purpan.
Faculté de Médecine, Université Toulouse III, Paul Sabatier University, Inserm UMR1027, Toulouse.

Bruno Fautrel (B)

Department of Rheumatology, Sorbonne University-Assistance Publique Hôpitaux de Paris, Pitie Salpetriere Hospital.
PEPITES team, Pierre Louis Institute of Epidemiology and Public Health, INSERM UMRS 1136, Paris, France.

Daniel F McWilliams (DF)

Pain Centre Versus Arthritis, University of Nottingham.
NIHR Nottingham Biomedical Research Centre, Nottingham.

David A Walsh (DA)

Pain Centre Versus Arthritis, University of Nottingham.
NIHR Nottingham Biomedical Research Centre, Nottingham.
Department of Rheumatology, Sherwood Forest Hospitals NHS Foundation Trust, Sutton in Ashfield.

Elena Nikiphorou (E)

Centre for Rheumatic Diseases, Department of Inflammation Biology, Faculty of Life Sciences and Medicine, King's College London, London.
Rheumatology Department, King's College Hospital.

Patrick D W Kiely (PDW)

Department of Rheumatology, St George's University Hospitals NHS Foundation Trust.
Institute of Medical and Biomedical Education, St George's University of London, London.

Adam Young (A)

Centre for Health Services and Clinical Research, Life and Medical Sciences, University of Hertfordshire, Hatfield.

Jacqueline R Chipping (JR)

Norwich Medical School, University of East Anglia.
Rheumatology Department, Norfolk and Norwich University Hospitals NHS Trust, Norwich, UK.

Alex MacGregor (A)

Norwich Medical School, University of East Anglia.
Rheumatology Department, Norfolk and Norwich University Hospitals NHS Trust, Norwich, UK.

Suzanne M M Verstappen (SMM)

Centre for Epidemiology Versus Arthritis, Division of Musculoskeletal and Dermatological Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester.
NIHR Manchester Biomedical Research Centre, Manchester University NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK.

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