Synovial Fluid Cytokines, Chemokines and MMP Levels in Osteoarthritis Patients with Knee Pain Display a Profile Similar to Many Rheumatoid Arthritis Patients

被引:19
|
作者
Meehan, Richard T. [1 ]
Regan, Elizabeth A. [1 ]
Hoffman, Eric D. [1 ]
Wolf, Molly L. [1 ]
Gill, Mary T. [1 ]
Crooks, James L. [1 ,2 ]
Parmar, Prashant J. [3 ]
Scheuring, Richard A. [4 ]
Hill, John C. [5 ]
Pacheco, Karin A. [1 ]
Knight, Vijaya [6 ]
机构
[1] Natl Jewish Hlth, Dept Med Immunol Labs & Bioinformat, Denver, CO 80206 USA
[2] CU Anschutz Sch Med, Colorado Sch Publ Hlth, Aurora, CO 80045 USA
[3] St Joseph Hosp, Natl Jewish Hlth, Dept Internal Med, Denver, CO 80218 USA
[4] NASA, Flight Med, Johnson Space Ctr, Houston, TX 77058 USA
[5] Univ Colorado, Dept Orthoped Surg, CU Sports Med, Denver, CO 80222 USA
[6] Childrens Hosp, Immunol Dept, Denver, CO 80045 USA
关键词
synovial fluid; biomarkers; cytokines; osteoarthritis; DISEASE-ACTIVITY; BIOMARKERS; ASSOCIATION; MEDICINE; UTILITY; DRUGS;
D O I
10.3390/jcm10215027
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: There are currently no effective disease-modifying drugs to prevent cartilage loss in osteoarthritis and synovial fluid is a potentially valuable source of biomarkers to understand the pathogenesis of different types of arthritis and identify drug responsiveness. The aim of this study was to compare the differences between SF cytokines and other proteins in patients with OA (n = 21) to those with RA (n = 27) and normal knees (n = 3). Methods: SF was obtained using ultrasound (US) guidance and an external pneumatic compression device. RA patients were categorized as active (n = 20) or controlled (n = 7) based upon SF white blood cell counts (> or < 300 cells/mm(3)). Samples were cryopreserved and analyzed by multiplex fluorescent bead assays (Luminex). Between-group differences of 16 separate biomarker proteins were identified using ANOVA on log10-transformed concentrations with p values adjusted for multiple testing. Results: Only six biomarkers were significantly higher in SF from active RA compared to OA-TNF-alpha, IL-1-beta IL-7, MMP-1, MMP-2, and MMP-3. Only MMP-8 levels in RA patients correlated with SF WBC counts (p < 0.0001). Among OA patients, simultaneous SF IL-4, IL-6, IL-8, and IL-15 levels were higher than serum levels, whereas MMP-8, MMP-9, and IL-18 levels were higher in serum (p < 0.05). Conclusion: These results support the growing evidence that OA patients have a pro-inflammatory/catabolic SF environment. SF biomarker analysis using multiplex testing and US guidance may distinguish OA phenotypes and identify treatment options based upon targeted inflammatory pathways similar to patients with RA.
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页数:14
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