Associations between joint space narrowing and molecular markers of collagen and proteoglycan turnover in patients with knee osteoarthritis

• Published in: Journal of rheumatology 2006-06, Vol.33 (6), p.1147-1151
• Main Authors: MAZZUCA, Steven A, POOLE, A. Robin, BRANDT, Kenneth D, KATZ, Barry P, LANE, Kathleen A, LOBANOK, Tatiana
• Format: Article
• Language: English
• Subjects: Anti-Bacterial Agents - therapeutic use; Biological and medical sciences; Biomarkers - blood; Collagen - blood; Disease Progression; Diseases of the osteoarticular system; Doxycycline - therapeutic use; Female; Humans; Knee Dislocation - diagnostic imaging; Knee Dislocation - metabolism; Knee Dislocation - pathology; Knee Joint - pathology; Medical sciences; Middle Aged; Miscellaneous. Osteoarticular involvement in other diseases; Obesity; Osteoarthritis; Osteoarthritis, Knee - blood; Osteoarthritis, Knee - drug therapy; Osteoarthritis, Knee - pathology; Proteoglycans - blood; Radiography; Weight-Bearing
• ISSN: 0315-162X; 1499-2752

OBJECTIVE: We examined whether plasma concentrations of biomarkers of the collagenase cleavage of type II collagen (C2C), types I and II collagens (C1,2C), type II collagen synthesis (CPII), proteoglycan aggrecan turnover (CS846), and the ratio C2C:CPII would distinguish subjects with progressive radiographic osteoarthritis (OA) from those with stable disease. METHODS: Subjects were 120 obese middle-aged women with unilateral knee OA who participated in a 30-month clinical trial of structure modification with doxycycline, in which a standardized semiflexed anteroposterior view of the knee was obtained at baseline, 16 months, and 30 months. Subjects were selected from a larger sample to permit a priori comparisons between 60 OA progressors and 60 nonprogressors, as defined by joint space narrowing (JSN) in the medial tibiofemoral compartment. Each group contained 30 subjects who exhibited clinically significant increases in knee pain over 30 months and 30 who did not. Plasma samples were obtained every 6 months for determination of C2C, CPII, CS846, and C1,2C. RESULTS: None of the biomarkers was a significant predictor of progression of JSN. Over the interval from baseline to 16 months, the mean and the maximum of the intercurrent CS846 values were significantly associated with JSN (i.e., 0.12-0.14 mm of JSN per SD decrease in mean or maximum CS846; p < 0.01). The mean of serial CS846 levels was related to JSN also during the interval between months 16 and 30. CONCLUSION: Markers of type II collagen synthesis/degradation and of proteoglycan aggrecan turnover were not predictive of JSN in knee OA in this pilot study. However, serial concentrations of proteoglycan aggrecan epitope CS846 were associated with JSN during both the intervals studied.