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The prognostic value of baseline erosions in undifferentiated arthritis

INTRODUCTION: Undifferentiated arthritis (UA) has a variable disease course; 40 to 50% of UA patients remit spontaneously, while 30% develop rheumatoid arthritis (RA). Identifying the UA patients who will develop RA is essential to initiate early disease-modifying anti-rheumatic drug (DMARD) therapy...

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Autores principales: Thabet, Mohamed M, Huizinga, Thomas WJ, van der Heijde, Désirée M, van der Helm-van Mil, Annette HM
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2787272/
https://www.ncbi.nlm.nih.gov/pubmed/19832979
http://dx.doi.org/10.1186/ar2832
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author Thabet, Mohamed M
Huizinga, Thomas WJ
van der Heijde, Désirée M
van der Helm-van Mil, Annette HM
author_facet Thabet, Mohamed M
Huizinga, Thomas WJ
van der Heijde, Désirée M
van der Helm-van Mil, Annette HM
author_sort Thabet, Mohamed M
collection PubMed
description INTRODUCTION: Undifferentiated arthritis (UA) has a variable disease course; 40 to 50% of UA patients remit spontaneously, while 30% develop rheumatoid arthritis (RA). Identifying the UA patients who will develop RA is essential to initiate early disease-modifying anti-rheumatic drug (DMARD) therapy. Although the presence of bone erosions at baseline is predictive for a severe destructive disease course in RA, the prognostic importance of erosive joints for disease outcome in UA is unknown. This study evaluates the predictive value of erosive joints for the disease outcome in UA as measured by RA development and disease persistency. METHODS: Baseline hands and feet radiographs of 518 UA patients were evaluated for erosions using a clinical definition as well as the Sharp/van der Heijde method. After 1 year follow-up, patients were re-assessed for the fulfilment of the 1987 ACR classification criteria for RA. Disease persistency was defined as the absence of sustained remission during all available follow-up (mean 8 ± 3 years). RESULTS: At baseline, 28.6% of UA patients had erosive joints. Presence of ≥2 erosive joints showed a positive predictive value for RA development of 53% and for persistent disease of 68%. Patients with erosions that did not develop RA were less often anticyclic citrullinated peptide antibody (ACPA)+ve, rheumatoid factor (RF)+ve and had lower C-reactive protein (CRP), erythrocytic sedimentation rate (ESR) and number of swollen joints compared to those who developed RA. Feet erosions are equally predictive compared to erosions at hands. CONCLUSIONS: Presence of ≥2 erosive joints at baseline in UA patients gives a risk for RA development of 53% and for persistent disease of 68%, indicating that erosions in UA are not always predictive for unfavorable disease outcomes.
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spelling pubmed-27872722009-12-02 The prognostic value of baseline erosions in undifferentiated arthritis Thabet, Mohamed M Huizinga, Thomas WJ van der Heijde, Désirée M van der Helm-van Mil, Annette HM Arthritis Res Ther Research article INTRODUCTION: Undifferentiated arthritis (UA) has a variable disease course; 40 to 50% of UA patients remit spontaneously, while 30% develop rheumatoid arthritis (RA). Identifying the UA patients who will develop RA is essential to initiate early disease-modifying anti-rheumatic drug (DMARD) therapy. Although the presence of bone erosions at baseline is predictive for a severe destructive disease course in RA, the prognostic importance of erosive joints for disease outcome in UA is unknown. This study evaluates the predictive value of erosive joints for the disease outcome in UA as measured by RA development and disease persistency. METHODS: Baseline hands and feet radiographs of 518 UA patients were evaluated for erosions using a clinical definition as well as the Sharp/van der Heijde method. After 1 year follow-up, patients were re-assessed for the fulfilment of the 1987 ACR classification criteria for RA. Disease persistency was defined as the absence of sustained remission during all available follow-up (mean 8 ± 3 years). RESULTS: At baseline, 28.6% of UA patients had erosive joints. Presence of ≥2 erosive joints showed a positive predictive value for RA development of 53% and for persistent disease of 68%. Patients with erosions that did not develop RA were less often anticyclic citrullinated peptide antibody (ACPA)+ve, rheumatoid factor (RF)+ve and had lower C-reactive protein (CRP), erythrocytic sedimentation rate (ESR) and number of swollen joints compared to those who developed RA. Feet erosions are equally predictive compared to erosions at hands. CONCLUSIONS: Presence of ≥2 erosive joints at baseline in UA patients gives a risk for RA development of 53% and for persistent disease of 68%, indicating that erosions in UA are not always predictive for unfavorable disease outcomes. BioMed Central 2009 2009-10-15 /pmc/articles/PMC2787272/ /pubmed/19832979 http://dx.doi.org/10.1186/ar2832 Text en Copyright ©2009 Thabet et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research article
Thabet, Mohamed M
Huizinga, Thomas WJ
van der Heijde, Désirée M
van der Helm-van Mil, Annette HM
The prognostic value of baseline erosions in undifferentiated arthritis
title The prognostic value of baseline erosions in undifferentiated arthritis
title_full The prognostic value of baseline erosions in undifferentiated arthritis
title_fullStr The prognostic value of baseline erosions in undifferentiated arthritis
title_full_unstemmed The prognostic value of baseline erosions in undifferentiated arthritis
title_short The prognostic value of baseline erosions in undifferentiated arthritis
title_sort prognostic value of baseline erosions in undifferentiated arthritis
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2787272/
https://www.ncbi.nlm.nih.gov/pubmed/19832979
http://dx.doi.org/10.1186/ar2832
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