Sequence of joint tissue inflammation during rheumatoid arthritis development

被引:16
|
作者
ten Brinck, R. M. [1 ]
van Steenbergen, H. W. [1 ]
van der Helm-van Mil, A. H. M. [1 ,2 ]
机构
[1] Leiden Univ, Med Ctr, Dept Rheumatol R C1, POB 9600, NL-2300 RC Leiden, Netherlands
[2] Erasmus MC, Dept Rheumatol, Rotterdam, Netherlands
基金
欧洲研究理事会;
关键词
Rheumatoid arthritis; Inflammation; Imaging; BONE-MARROW EDEMA; ENHANCED MRI; TENOSYNOVITIS; PATHOGENESIS; EROSIONS; STIR;
D O I
10.1186/s13075-018-1756-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Subclinical joint inflammation in patients with arthralgia is predictive for progression to rheumatoid arthritis (RA). However, the time course of progression for bone marrow edema (osteitis), synovitis, and/or tenosynovitis is unsettled. This longitudinal study assessed the course of magnetic resonance imaging (MRI)-detected subclinical joint inflammation during progression to RA. Methods: Patients that progressed from clinically suspect arthralgia (CSA) to RA underwent 1.5-T MRI of the metacarpophalangeal (MCP), wrist, and metatarsophalangeal (MTP) joints at presentation with arthralgia and at first identification of synovitis assessed through physical examination (n = 31). MRIs were evaluated for osteitis, synovitis, tenosynovitis, and erosions by two readers, blinded for clinical data and order in time. To estimate changes in MRI scores between the asymptomatic state and CSA onset, scores of MRI features at CSA baseline were compared with scores from age-matched symptom-free persons. Results: At presentation with CSA, synovitis and tenosynovitis scores were higher than scores from age-matched symptom-free persons (p = 0.004 and p = 0.001, respectively). Anti-citrullinated protein antibody (ACPA)-positive arthralgia patients also had increased osteitis scores (p = 0.04). Median duration between presentation with arthralgia and RA development was 17weeks. During progression to RA, synovitis and osteitis increased significantly (p = 0.001 and p = 0.036, respectively) in contrast to tenosynovitis and erosion scores. This pattern was similar in both ACPA subsets, although statistical significance was reached for synovitis and osteitis in ACPA-negative but not ACPA-positive RA. Conclusion: Increased tenosynovitis and synovitis scores at CSA onset and the increase in synovitis and osteitis during progression to RA suggest an outside-in' temporal relationship of arthritis development, in particular for ACPA-negative RA. For ACPA-positive RA, further studies are needed.
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页数:8
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