Association between knee magnetic resonance imaging markers and knee symptoms over 6–9 years in young adults

Author:

Singh Ambrish1ORCID,Venn Alison1,Blizzard Leigh1,March Lyn23,Eckstein Felix456,Jones Graeme1ORCID,Wirth Wolfgang456,Cicuttini Flavia7,Ding Changhai178ORCID,Antony Benny1

Affiliation:

1. Menzies Institute for Medical Research, University of Tasmania , Hobart, TS, Australia

2. Institute of Bone and Joint Research, Kolling Institute of Medical Research, University of Sydney , Sydney, NSW, Australia

3. Florance and Cope Professorial Rheumatology Department, University of Sydney Royal North Shore Hospital, St Leonards , Sydney, NSW, Australia

4. Chondrometrics GmbH , Ainring, Germany

5. Department of Imaging and Functional Musculoskeletal Research, Institute of Anatomy & Cell Biology, Paracelsus Medical University Salzburg & Nuremberg , Salzburg, Austria

6. Ludwig Boltzmann Institute for Arthritis and Rehabilitation, Paracelsus Medical University , Salzburg, Austria

7. Department of Epidemiology and Preventive Medicine, Monash University , Melbourne, VIC, Australia

8. Clinical Research Centre, Zhujiang Hospital, Southern Medical University , Guangzhou, China

Abstract

Abstract Objectives To describe associations between MRI markers with knee symptoms in young adults. Methods Knee symptoms were assessed using the WOMAC scale during the Childhood Determinants of Adult Health Knee Cartilage study (CDAH-knee; 2008–2010) and at the 6- to 9-year follow-up (CDAH-3; 2014–2019). Knee MRI scans obtained at baseline were assessed for morphological markers (cartilage volume, cartilage thickness, subchondral bone area) and structural abnormalities [cartilage defects and bone marrow lesions (BMLs)]. Univariable and multivariable (age, sex, BMI adjusted) zero-inflated Poisson (ZIP) regression models were used for analysis. Results The participants’ mean age in CDAH-knee and CDAH-3 were 34.95 (s.d. 2.72) and 43.27 (s.d. 3.28) years, with 49% and 48% females, respectively. Cross-sectionally, there was a weak but significant negative association between medial femorotibial compartment (MFTC) [ratio of the mean (RoM) 0.99971084 (95% CI 0.9995525, 0.99986921), P < 0.001], lateral femorotibial compartment (LFTC) [RoM 0.99982602 (95% CI 0.99969915, 0.9999529), P = 0.007] and patellar cartilage volume [RoM 0.99981722 (95% CI 0.99965326, 0.9999811), P = 0.029] with knee symptoms. Similarly, there was a negative association between patellar cartilage volume [RoM 0.99975523 (95% CI 0.99961427, 0.99989621), P = 0.014], MFTC cartilage thickness [RoM 0.72090775 (95% CI 0.59481806, 0.87372596), P = 0.001] and knee symptoms assessed after 6–9 years. The total bone area was negatively associated with knee symptoms at baseline [RoM 0.9210485 (95% CI 0.8939677, 0.9489496), P < 0.001] and 6–9 years [RoM 0.9588811 (95% CI 0.9313379, 0.9872388), P = 0.005]. The cartilage defects and BMLs were associated with greater knee symptoms at baseline and 6–9 years. Conclusion BMLs and cartilage defects were positively associated with knee symptoms, whereas cartilage volume and thickness at MFTC and total bone area were weakly and negatively associated with knee symptoms. These results suggest that the quantitative and semiquantitative MRI markers can be explored as a marker of clinical progression of OA in young adults.

Funder

International Graduate Research Scholarship

University of Tasmania

National Health and Medical Research Council of Australia

National Health and Medical Research Council

Research Enhancement

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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