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

OBJECTIVES: To identify groups of people with RA with different disability trajectories over 10 years, despite comparable levels of inflammation. METHODS: Data for this analysis came from three European prospective cohort studies of people with RA [Norfolk Arthritis Register (NOAR), Early RA Network...

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Autores principales: Gwinnutt, James M, Norton, Sam, Hyrich, Kimme L, Lunt, Mark, Combe, Bernard, Rincheval, Nathalie, Ruyssen-Witrand, Adeline, Fautrel, Bruno, McWilliams, Daniel F, Walsh, David A, Nikiphorou, Elena, Kiely, Patrick D W, Young, Adam, Chipping, Jacqueline R, MacGregor, Alex, Verstappen, Suzanne M M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9707289/
https://www.ncbi.nlm.nih.gov/pubmed/35274696
http://dx.doi.org/10.1093/rheumatology/keac137
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author Gwinnutt, James M
Norton, Sam
Hyrich, Kimme L
Lunt, Mark
Combe, Bernard
Rincheval, Nathalie
Ruyssen-Witrand, Adeline
Fautrel, Bruno
McWilliams, Daniel F
Walsh, David A
Nikiphorou, Elena
Kiely, Patrick D W
Young, Adam
Chipping, Jacqueline R
MacGregor, Alex
Verstappen, Suzanne M M
author_facet Gwinnutt, James M
Norton, Sam
Hyrich, Kimme L
Lunt, Mark
Combe, Bernard
Rincheval, Nathalie
Ruyssen-Witrand, Adeline
Fautrel, Bruno
McWilliams, Daniel F
Walsh, David A
Nikiphorou, Elena
Kiely, Patrick D W
Young, Adam
Chipping, Jacqueline R
MacGregor, Alex
Verstappen, Suzanne M M
author_sort Gwinnutt, James M
collection PubMed
description OBJECTIVES: To identify groups of people with RA with different disability trajectories over 10 years, despite comparable levels of inflammation. METHODS: 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. RESULTS: 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. CONCLUSION: 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.
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spelling pubmed-97072892022-11-30 Exploring the disparity between inflammation and disability in the 10-year outcomes of people with rheumatoid arthritis Gwinnutt, James M Norton, Sam Hyrich, Kimme L Lunt, Mark Combe, Bernard Rincheval, Nathalie Ruyssen-Witrand, Adeline Fautrel, Bruno McWilliams, Daniel F Walsh, David A Nikiphorou, Elena Kiely, Patrick D W Young, Adam Chipping, Jacqueline R MacGregor, Alex Verstappen, Suzanne M M Rheumatology (Oxford) Clinical Science OBJECTIVES: To identify groups of people with RA with different disability trajectories over 10 years, despite comparable levels of inflammation. METHODS: 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. RESULTS: 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. CONCLUSION: 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. Oxford University Press 2022-03-11 /pmc/articles/PMC9707289/ /pubmed/35274696 http://dx.doi.org/10.1093/rheumatology/keac137 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the British Society for Rheumatology. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Science
Gwinnutt, James M
Norton, Sam
Hyrich, Kimme L
Lunt, Mark
Combe, Bernard
Rincheval, Nathalie
Ruyssen-Witrand, Adeline
Fautrel, Bruno
McWilliams, Daniel F
Walsh, David A
Nikiphorou, Elena
Kiely, Patrick D W
Young, Adam
Chipping, Jacqueline R
MacGregor, Alex
Verstappen, Suzanne M M
Exploring the disparity between inflammation and disability in the 10-year outcomes of people with rheumatoid arthritis
title Exploring the disparity between inflammation and disability in the 10-year outcomes of people with rheumatoid arthritis
title_full Exploring the disparity between inflammation and disability in the 10-year outcomes of people with rheumatoid arthritis
title_fullStr Exploring the disparity between inflammation and disability in the 10-year outcomes of people with rheumatoid arthritis
title_full_unstemmed Exploring the disparity between inflammation and disability in the 10-year outcomes of people with rheumatoid arthritis
title_short Exploring the disparity between inflammation and disability in the 10-year outcomes of people with rheumatoid arthritis
title_sort exploring the disparity between inflammation and disability in the 10-year outcomes of people with rheumatoid arthritis
topic Clinical Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9707289/
https://www.ncbi.nlm.nih.gov/pubmed/35274696
http://dx.doi.org/10.1093/rheumatology/keac137
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