Association of Bone Marrow Lesions with Knee Structures and Risk Factors for Bone Marrow Lesions in the Knees of Clinically Healthy, Community-Based Adults

https://doi.org/10.1016/j.semarthrit.2007.01.008Get rights and content

Objectives

Subchondral bone marrow lesions (BML) are involved in pain and progression of knee osteoarthritis (OA). Little is known about their role in the knee in those without clinical OA. Our aim was to examine the prevalence and risk factors for BML, and their relationship with other knee structures in community-based adults without clinical OA.

Methods

Two hundred ninety-seven healthy subjects without knee pain or injury were recruited from an existing community-based cohort recruited at baseline in 1990-1994. Subjects with a single magnetic resonance imaging (MRI) of their dominant knee at follow-up were studied in 2003-2004. BML, cartilage defects, cartilage volume, and bone area of the knee were assessed using MRI.

Results

Thirty-nine subjects (13%) had evidence of BML. BML were associated with the presence of cartilage defects in the medial (odds ratio (OR) 1.80, P = 0.004) and lateral (OR 1.45, P = 0.04) tibiofemoral compartments, but not cartilage volume. BML were positively associated with total tibial bone area (OR 1.22, P = 0.02). Increasing age (OR 1.10, P < 0.001), male gender (OR 3.86, P = 0.01), and increasing body height (OR 1.07, P = 0.03) were independently associated with BML in the total tibiofemoral compartment.

Conclusions

BML are present in the knees of community-based adults without clinical OA and are strongly associated with tibiofemoral cartilage defects. Risk factors for BML were age, male gender, and body height. Longitudinal studies will be needed to clarify the role of BML in structural change of the knee and how this relates to the pathogenesis of symptomatic knee OA.

Section snippets

Subjects

This study was conducted within the Melbourne Collaborative Cohort Study (MCCS), which is a prospective cohort study of 41,528 community-based people (24,479 women), aged 40 to 69 years at recruitment, which occurred between 1990 and 1994, with the aim of examining the role of lifestyle factors in the risk of cancer and heart disease (9). Participants for this current study were recruited from the MCCS. As our intent was to investigate subjects with no clinical knee OA as defined by the

Results

Two hundred ninety-seven participants, 63% women, aged 58.0 ± 5.5 years with BMI 25.2 ± 3.8 kg/m2, took part in this study (Table 1). There were no significant differences between this population and the original MCCS population which has the following profile: 61% women, aged 57.8 ± 3.0 years, and BMI 25.7 ± 3.8 kg/m2. Thirty-nine (13.1%) subjects had BML in the subchondral bone of the knee: 14 males and 25 females. Five subjects had lesions in both medial and lateral compartments.

The

Discussion

In this study of community-based adults without clinical OA, BML were present in 13% of subjects. BML prevalence was similar in the lateral and medial tibiofemoral compartments, although there was an inverse relationship between BML in the 2 compartments. Large BML were positively associated with cartilage defects in both the medial and lateral compartments but not cartilage volume. Large BML were also positively associated with tibial plateau bone area in total tibiofemoral compartment.

Acknowledgments

The Melbourne Collaborative Cohort Study recruitment was funded by VicHealth and The Cancer Council of Victoria. We especially thank the study participants who made this study possible.

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    The authors have no conflict of interest to disclose.

    This study was funded by a program grant from the National Health and Medical Research Council (NHMRC; 209057) and was further supported by infrastructure provided by The Cancer Council of Victoria. We acknowledge the NHMRC (Project Grant 334150), Colonial Foundation, and Shepherd Foundation for support. Dr. Wang is the recipient of an NHMRC PhD Scholarship. Dr. Wluka is the recipient of an NHMRC Public Health (Australia) Fellowship (317840) and corecipient of the Cottrell Fellowship, Royal Australasian College of Physicians.

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