Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/16677
Title: Associations between systemic bone mineral density and early knee cartilage changes in middle-aged adults without clinical knee disease: a prospective cohort study
Austin Authors: Teichtahl, Andrew J;Wang, Yuanyuan;Wluka, Anita E;Strauss, Boyd J;Proietto, Joseph ;Dixon, John B;Jones, Graeme;Cicuttini, Flavia M
Affiliation: Department of Epidemiology and Preventive Medicine, School of Public Health and Preventive Medicine, Monash University, Alfred Hospital, Melbourne, Victoria, Australia
Menzies Research Institute,Tasmania, Hobart, Tasmania, Australia
Baker IDI Heart and Diabetes Institute, Commercial Road, Melbourne, Victoria, Australia
Department of Medicine, Monash University, Melbourne, Victoria, Australia
Department of Medicine, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australia
Issue Date: 18-May-2017
Date: 2017-05-18
Publication information: Arthritis Research & Therapy 2017; 19(1): 98
Abstract: BACKGROUND: Osteoarthritis has a high prevalence in people with high bone mineral density (BMD). Nevertheless, whether high systemic BMD predates early structural features of knee osteoarthritis is unclear. This study examined the association between systemic BMD and knee cartilage defect progression and cartilage volume loss in middle-aged people without clinical knee disease. METHODS: Adults (n = 153) aged 25-60 years had total body, lumbar spine, and total hip BMD assessed by dual-energy X-ray absorptiometry at baseline (2005-2008), and tibial cartilage volume and tibiofemoral cartilage defects assessed by magnetic resonance imaging at baseline and follow up (2008-2010). RESULTS: Higher spine BMD was associated with increased risk for progression of medial (OR = 1.45, 95% CI 1.10, 1.91) and lateral (OR = 1.30, 95% CI 1.00, 1.67) tibiofemoral cartilage defects. Total hip BMD was also positively associated with the progression of medial (OR = 1.63, 95% CI 1.10, 2.41) and lateral (OR = 1.53, 95% CI 1.08, 2.18) tibiofemoral cartilage defects. Greater total body, spine, and total hip BMD were associated with increased rate of lateral tibial cartilage volume loss (for every 1 g/10 cm2 increase in total body BMD: B = 0.44%, 95% CI 0.17%, 0.71%; spine BMD: 0.17%, 95% CI 0.04%, 0.30%; total hip BMD: 0.29%, 95% CI 0.13%, 0.45%), with no significant associations for medial tibial cartilage volume loss. CONCLUSION: In middle-aged people without clinical knee disease, higher systemic BMD was associated with increased early knee cartilage damage. Further work is needed to clarify the effect of systemic BMD at different stages of the pathway from health through to disease in knee osteoarthritis, as new therapies targeting bone are developed for the management of knee osteoarthritis.
URI: https://ahro.austin.org.au/austinjspui/handle/1/16677
DOI: 10.1186/s13075-017-1314-0
Journal: Arthritis Research & Therapy
PubMed URL: https://pubmed.ncbi.nlm.nih.gov/28521839
Type: Journal Article
Subjects: Bone mineral density
Cartilage defects
Cartilage volume
Knee
Osteoarthritis
Appears in Collections:Journal articles

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