Effects of infliximab therapy on biological markers of synovium activity and cartilage breakdown in patients with rheumatoid arthritis

被引:27
作者
Marotte, H. [1 ]
Gineyts, E. [2 ,3 ]
Miossec, P. [1 ]
Delmas, P. D. [2 ,3 ]
机构
[1] Hop Edouard Herriot, Hosp Civils Lyon BioMerieux Res Unit Rheumatoid A, F-69437 Lyon, France
[2] Univ Lyon 1, F-69365 Lyon, France
[3] INSERM, Res Unit 831, F-69365 Lyon, France
关键词
GLUCOSYL-GALACTOSYL-PYRIDINOLINE; NECROSIS-FACTOR-ALPHA; BASE-LINE LEVELS; PROGRESSION; ASSOCIATION; DAMAGE; BONE; METHOTREXATE; DEGRADATION;
D O I
10.1136/ard.2008.096057
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Defining the remission criteria of rheumatoid arthritis ( RA) remains a critical issue. Markers of synovium activity, urinary glucosyl-galactosyl-pyridinoline (Glc-Gal-PYD) and of cartilage destruction, urinary C-terminal crosslinking telopeptide of type II collagen (CTX-II) have been shown to reflect disease activity and joint damage progression in RA. Methods: The prospective study cohort comprised 66 RA patients treated with infliximab and methotrexate and 76 healthy controls. Measurements of urinary Glc-Gal-PYD and CTX-II were performed at baseline and at 1 year of infliximab therapy. Results: At baseline, urinary Glc-Gal-PYD and CTX-II levels were increased in patients with RA and correlated with modified Sharp scores and progression of joint damage. Patients with more progressive joint destruction had higher Glc-Gly-PYD and CTX-II baseline levels. Conclusion: These markers reflected bone erosion evolution and might be useful for treatment monitoring and evaluation of RA. Markers remained high even in clinical responders after infliximab, suggesting persistence of synovitis.
引用
收藏
页码:1197 / 1200
页数:4
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