Predicting arthritis outcomes-what can be learned from the Leiden Early Arthritis Clinic?

被引:238
作者
de Rooy, Diederik P. C. [1 ]
van der Linden, Michael P. M. [1 ]
Knevel, Rachel [1 ]
Huizinga, Tom W. J. [1 ]
van der Helm-van Mil, Annette H. M. [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Rheumatol, NL-2300 RC Leiden, Netherlands
关键词
Radiological damage; Erosions; Early arthritis; Undifferentiated arthritis; Rheumatoid arthritis; Prediction; Outcome; Risk factors; Disease persistency; Remission; CYCLIC CITRULLINATED PEPTIDE; EARLY RHEUMATOID-ARTHRITIS; RADIOGRAPHIC PROGRESSION; UNDIFFERENTIATED ARTHRITIS; JOINT DESTRUCTION; DOUBLE-BLIND; METHOTREXATE; INFLAMMATION; TISSUE; RULE;
D O I
10.1093/rheumatology/keq230
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Methods. A total of 570 UA patients and 676 RA patients included in the Leiden Early Arthritis Clinic cohort were studied for baseline characteristics. The disease outcomes studied were fulfilment of the 1987 ACR-RA criteria and arthritis persistence in UA patients and the rate of radiological joint destruction and achieving sustained DMARD-free remission in RA patients. Results. Predictive factors for fulfilment of the 1987 ACR-RA criteria and for persistent arthritis in UA were largely similar. Risk factors for a severe rate of joint destruction were: older age (P < 0.001); male gender (P < 0.001); longer symptom duration at first visit (P = 0.048), involvement of lower extremities (P < 0.001); BMI (P < 0.001); high acute phase reactants, presence of IgM-RF (P < 0.001); anti-CCP2 antibodies (P < 0.001); anti-modified citrullinated vimentin antibodies (P < 0.001) and HLA-DRB1 shared epitope alleles (P = 0.001). A high BMI was associated with a lower rate of joint destruction but with a higher risk of disease persistence. The proportion of variance in joint destruction explained was 32% Conclusion. Predictors for RA development, previously used to develop a prediction rule in UA patients, are largely similar to predictors for arthritis persistency. Only part of the joint destruction level in RA is explained by the currently known risk factors. New factors need to be identified in order to guide pharmaceutical intervention at the level of individual RA patients.
引用
收藏
页码:93 / 100
页数:8
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