Biochemical, clinical, demographic and imaging biomarkers for disease progression in knee osteoarthritis

Author:

Liem Yulia1,Judge Andrew2,Li Yunfei1,Sharif Mohammed1ORCID

Affiliation:

1. Translational Health Sciences, Bristol Medical School, University of Bristol, Level 2 Learning & Research Building, Southmead Hospital, Bristol, BS10 5NB, UK

2. Musculoskeletal Research Unit, Bristol Medical School, University of Bristol, Level 1 Learning & Research Building, Southmead Hospital, BS10 5NB, UK

Abstract

Aim: To identify prognostic biomarker(s) for knee osteoarthritis (OA) in the Osteoarthritis Initiative (OAI) cohort. Methods: Multilevel regression was used to determine the association between baseline biomarkers and change in biomarkers from baseline to 24 months with clinical and radiographic OA progression over 48 months of follow-up. Results: Higher values of baseline urinary CTXII were consistently associated with an increased risk of OA disease progression outcomes: Kellgren & Lawrence grade (odds ratio [OR]: 1.15, 95% CI: 1.03–1.28); medial joint space narrowing (OR: 1.06, 95% CI: 1.02–1.10); lateral osteophytes (OR: 1.05, 95% CI: 1.01–1.10); joint space width (regression coefficient: -0.005, 95% CI: -0.008–0.001); and Western Ontario and McMaster Universities Arthritis Index pain scores (OR: 1.02, 95% CI: 1.01–1.04). Changes in serum PIIANP and serum COMP over 24 months were associated with clinical disease progression. Conclusion: Urinary CTXII showed stronger associations with radiographic OA and appears to be a reliable prognostic marker, while changes in other biomarkers were found in early symptomatic OA, supporting the phasic nature of OA.

Funder

Higher Education Funding Council for England

Joint China Scholarship Council-University of Bristol Scholarship Scheme

Versus Arthritis

Publisher

Future Medicine Ltd

Subject

Biochemistry (medical),Clinical Biochemistry,Drug Discovery

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