4.7 Article

Co-localisation of non-cartilaginous articular pathology increases risk of cartilage loss in the tibiofemoral joint-the MOST study

Journal

ANNALS OF THE RHEUMATIC DISEASES
Volume 72, Issue 6, Pages 942-948

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/annrheumdis-2012-201810

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Funding

  1. National Institutes of Health from the National Institute of Aging [U01-AG-18947, U01-AG-18832, U01-AG-19069, U01-AG-18820]
  2. Facet Solutions
  3. Genzyme
  4. Stryker
  5. Merck Serono
  6. Novartis
  7. Astra Zeneca
  8. National Institutes of Health

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Purpose To assess risk of cartilage loss in the tibiofemoral joint in relation to baseline damage severity, and to analyse the association of nearby pathologic findings on the risk of subsequent cartilage loss. Methods The Multicenter Osteoarthritis Study is a longitudinal study of individuals with or at high risk for knee osteoarthritis. MRI examinations were assessed according to the Whole Organ MRI Score. Included were all knees with available baseline and 30 months MRIs. Ordinal logistic regression was used to estimate risk of cartilage loss in each subregion in relation to the number of associated articular features including bone marrow lesions, meniscal damage and extrusion and also in regard to baseline damage severity, respectively. Results 13 524 subregions of 1365 knees were included. 3777 (27.9%) subregions exhibited prevalent cartilage damage at baseline and 1119 (8.3%) subregions showed cartilage loss at 30-month follow-up. Risk of cartilage loss was increased for subregions with associated features (OR 2.53, 95% CI 2.03 to 3.15 for one, 4.32 95% CI 3.42 to 5.47 for two and 5.30 95% CI 3.95 to 7.12 for three associated features; p for trend <0.0001). Subregions with prevalent cartilage damage showed increased risk for further cartilage loss compared to subregions with intact cartilage at baseline with small superficial defects exhibiting highest risk. Conclusions Risk of cartilage loss is increased for subregions with associated pathology and further increased when more than one type of associated feature is present. In addition, prevalent cartilage damage increases risk for subsequent cartilage loss.

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