The goal of this observational, non-interventional cohort study is to identify tests or markers in blood or knee fluid, or any genetic risk factors that might contribute to worsening or improvement of knee osteoarthritis. Males and females aged ≥18 with early-stage knee osteoarthritis, prior proven acute knee injury, or degenerative meniscal tear will be recruited at Imperial College Healthcare NHS Trust. Those with prior proven acute knee injury must be aged ≤ 50. A single knee per participant will be followed throughout the study; this will be referred to as ''affected knee'', identified at baseline. The study involves: 1. Samples collection: * From individuals recruited in-person: blood or buccal (cheek) swab and/or knee joint (synovial) fluid - this will be collected during routine NHS visit, if individuals undergo scheduled knee surgery or knee aspiration procedure (Knee aspiration is a procedure to remove excess fluid from the knee joint for diagnosis or treatment). * From individuals recruited remotely: saliva sample. 2. Clinical data collection at baseline: Participants will complete study Core Questionnaire Pack. These are questionnaires asking about their knee pain, function, and activity level. 3. Clinical data collection at yearly remote visits, through years 1-5: Participants will complete study Follow-Up Questionnaire Pack, asking about participants' knee pain, function, and activity level - same as at baseline, but additionally they will be asked about any knee surgeries on the affected knee, since their last study visit. 4. Imaging data collection at baseline and at Year 2 or Year 3 follow-up visit: If at baseline visit X-ray imaging is available as a part of usual NHS care, then participants will only be invited to attend one X-ray appointment at Year 2 or Year 3 follow-up visit. We expect to recruit up to 200 participants with approximately 100 participants having early-stage knee osteoarthritis or degenerative meniscal tear and the remaining participants having prior proven acute knee injury. Individuals will be able join the study for between 2-3 years. Follow up visits will last up to 5 years.
We are studying people who are in the early-stage of knee osteoarthritis or at risk of knee osteoarthritis. The current course of osteoarthritis is quite unpredictable. Early on symptoms (and structural changes) can get worse or can get better, but we don't know why. Current treatments are often reactive, meaning doctors wait until the disease is advanced before they do much. This study is designed to help us better predict this process.
Study Type
OBSERVATIONAL
Enrollment
200
Centre for Inflammatory Disease, 9th Floor, Commonwealth Building, Imperial College London, Department of Immunology and Inflammation, Hammersmith Campus, Du Cane Road, London
London, United Kingdom
Knee injury and Osteoarthritis Outcome Score (KOOS)
Collected via study questionnaires completed by participants.
Time frame: Baseline and 2 years
Tegner Activity Score (TAS)
Collected via study questionnaires completed by participants.
Time frame: Baseline and minimum at 2 years/maximum 5 years
Post enrolment surgical intervention data (arthroplasty)
Collected via study questionnaires completed by participants.
Time frame: Years 1-5
X-ray radiographs of the index knee
Evaluation of joint space narrowing in the tibio-femoral and patello-femoral joints, and the presence of osteophyte formation.
Time frame: Baseline and 2 years
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