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Erschienen in: Journal of Translational Medicine 1/2010

Open Access 01.11.2010 | Poster presentation

Predictors of chronicity and the discriminative value of the new ACR/EULAR rheumatoid arthritis classification criteria in an untreated polyarthritis cohort with less than 6 weeks of disease duration

verfasst von: A F Mourão, H Canhão, R A Moura, R Cascão, P Weinmann, A Rodrigues, J Pereira, C Resende, S Capela, J A Pereira da Silva, J E Fonseca

Erschienen in: Journal of Translational Medicine | Sonderheft 1/2010

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A F Mourão, H Canhão contributed equally to this work.

Aims

1. To find predictors of progression to RA in a cohort of patients with a very recent onset polyarthritis. 2. To test the performance of the new ACR/EULAR criteria for the classification of RA in this population.

Patients

Patients with polyarthritis with less than 6 weeks of duration were enrolled during a period of 4 years. They were not exposed previously to corticosteroids or DMARDs. All patients were prospectively followed-up in order to establish a definitive clinical diagnosis. A protocol was applied, including demographic and clinical data, and a blood sample was collected to assess ESR, RF and ACPA levels, before any treatment was started.

Results

Thirty-seven patients were included. During the follow up most of the patients evolved into RA (57%). The median age of the patients of the RA-group was similar to the median age of the non-RA group (median (IQR) 47 (31-58.5) vs 43 (34-69) years, p=0.74). At the initial visit the DAS 28 in the RA group was significantly higher than in the non-RA group, as well as the VAS and the number of swollen joints. The ESR values did not differ significantly between RA and non-RA groups (Table 1).
Table 1
Baseline differences between patients who latter evolved into RA (RA-group), comparing to who did not (non-RA group).
Parameter
RA
Non-RA
p-value
DAS28
6.2 (4.9-7.3)
4.8 (3.8-5.9)
0.016*
VAS
60 (50-89.5)
46 (30-60)
0.045*
Swollen joints
8 (3-20)
2 (0-9.7)
0.042*
Tender joints
10 (3-20)
5.5 (2-17.7)
0.202
Total involved joints
12 (8-18)
10.5 (3.5-18)
0.380
CRP
2.74 (1.7-4.3)
2.1 (0.1-4.8)
0.810
ESR
37 (26.5-63.5)
25 (19.5-60)
0.419
HAQ
1.9 (1-2)
0.87 (0.25-1)
0.020*
*p-value <0.05; DAS28: Disease Activity Score 28; VAS: Visual Analogue Scale; ESR: Erythrocyte sedimentation rate; HAQ: Health Assessment Questionnaire; RA: Rheumatoid arthritis. Values are expressed as median and interquartile range: median (IQR).
Among the 21 RA patients, 21 were evaluated for RF and 17 for ACPA in the first visit. Of these, 45% presented RF and 37.5% presented ACPA. RF and ACPA were not detectable in any of the patients who did not evolve to RA.
According to the new criteria for the classification of RA, the mean total score of the RA group at baseline was significantly higher than the non-RA group (median (IQR) 6 (4.5-8) vs 4.5 (2.2-6), p=0,007). Interestingly, the highest score reached in the non-RA patients was 6 points, the cut-off point to classify patients as having RA.

Conclusion

In our cohort a high DAS28 score, a high number of swollen joints, a low functional status and the presence of RF or ACPA are associated with the future evolution into RA. The new ACR/EULAR criteria for the classification of RA seem to identify the majority of patients that will evolve to RA.
Open AccessThis article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution 2.0 International License (https://​creativecommons.​org/​licenses/​by/​2.​0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Titel
Predictors of chronicity and the discriminative value of the new ACR/EULAR rheumatoid arthritis classification criteria in an untreated polyarthritis cohort with less than 6 weeks of disease duration
verfasst von
A F Mourão
H Canhão
R A Moura
R Cascão
P Weinmann
A Rodrigues
J Pereira
C Resende
S Capela
J A Pereira da Silva
J E Fonseca
Publikationsdatum
01.11.2010
Verlag
BioMed Central
Erschienen in
Journal of Translational Medicine / Ausgabe Sonderheft 1/2010
Elektronische ISSN: 1479-5876
DOI
https://doi.org/10.1186/1479-5876-8-S1-P65

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