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Nottingham knee osteoarthritis risk prediction models
  1. Weiya Zhang1,
  2. Daniel F McWilliams1,
  3. Sarah L Ingham1,
  4. Sally A Doherty1,
  5. Stella Muthuri1,
  6. Kenneth R Muir2,
  7. Michael Doherty1
  1. 1Academic Rheumatology, University of Nottingham, Nottingham, UK
  2. 2Health Sciences Research Institute, University of Warwick, Coventry, UK
  1. Correspondence to Weiya Zhang, Academic Rheumatology, University of Nottingham, Clinical Sciences Building, City Hospital, Nottingham NG5 1PB, UK; weiya.zhang{at}nottingham.ac.uk

Abstract

Objectives (1) To develop risk prediction models for knee osteoarthritis (OA) and (2) to estimate the risk reduction that results from modification of potential risk factors.

Method This was a 12-year retrospective cohort study undertaken in the general population in Nottingham, UK. Baseline risk factors were collected by questionnaire. Incident radiographic knee OA was defined by Kellgren and Lawrence (KL) score ≥2. Incident symptomatic knee OA was defined by KL ≥2 plus knee pain. Progression of knee OA was defined by KL ≥1 grade increase from baseline. A logistic regression model was used for prediction. Calibration and discrimination of the models were tested in the Osteoarthritis Initiative (OAI) population and Genetics of Osteoarthritis and Lifestyle (GOAL) population. ORs of the models were compared with those obtained from meta-analysis of existing literature.

Results From a community sample of 424 people aged over 40, 3 risk prediction models were developed. These included incidence of radiographic knee OA, incidence of symptomatic knee OA and progression of knee OA. All models had good calibration and moderate discrimination power in OAI and GOAL. The ORs lied within the 95% CIs of the published studies. The risk reduction due to modifying obesity at the individual and the population levels were demonstrated.

Conclusions Risk prediction of knee OA based on the well established, common modifiable risk factors has been established. The models may be used to predict the risk of knee OA, and risk reduction due to preventing a specific risk factor.

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Footnotes

  • Competing interests None.

  • Ethics approval This study was conducted with the approval of the Nottingham University Hospitals NHS Trust and the Nottingham Research Ethics Committee.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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