- Research article
- Open Access
Development of bone marrow lesions is associated with adverse effects on knee cartilage while resolution is associated with improvement - a potential target for prevention of knee osteoarthritis: a longitudinal study
Arthritis Research & Therapy volume 12, Article number: R10 (2010)
To examine the relationship between development or resolution of bone marrow lesions (BMLs) and knee cartilage properties in a 2 year prospective study of asymptomatic middle-aged adults.
271 adults recruited from the Melbourne Collaborative Cohort Study, underwent a magnetic resonance imaging scan (MRI) of their dominant knee at baseline and again approximately 2 years later. Cartilage volume, cartilage defects and BMLs were determined at both time points.
Among 234 subjects free of BMLs at baseline, 33 developed BMLs over 2 years. The incidence of BMLs was associated with progression of tibiofemoral cartilage defects (OR 2.63 (95% CI 0.93, 7.44), P = 0.07 for medial compartment; OR 3.13 (95% CI 1.01, 9.68), P = 0.048 for lateral compartment). Among 37 subjects with BMLs at baseline, 17 resolved. Resolution of BMLs was associated with reduced annual loss of medial tibial cartilage volume (regression coefficient -35.9 (95%CI -65, -6.82), P = 0.02) and a trend for reduced progression of medial tibiofemoral cartilage defects (OR 0.2 (95% CI 0.04, 1.09), P = 0.06).
In this cohort study of asymptomatic middle-aged adults the development of new BMLs was associated with progressive knee cartilage pathology while resolution of BMLs prevalent at baseline was associated with reduced progression of cartilage pathology. Further work examining the relationship between changes and BML and cartilage may provide another important target for the prevention of knee osteoarthritis.
There is increasing interest in the role of bone marrow lesions (BMLs), detected by magnetic resonance imaging (MRI), in the pathogenesis of knee osteoarthritis (OA) [1, 2]. Histological examination of BMLs in knees has reported that they may represent areas of osteonecrosis, oedema, trabecular abnormalities and bony remodeling . BMLs are present in both symptomatic [4–7] and asymptomatic populations [8, 9]. Although BMLs are found to be extremely common in OA populations and, once present, are unlikely to resolve [7, 10, 11], in asymptomatic populations they tend to have a more fluctuating course . BMLs have most commonly been described in relation to mechanical factors such as trauma [13–16], knee malalignment , and increased body weight . However, more recently systemic factors such as osteo-protective medications  and nutritional factors [19, 20] have been reported to affect the risk of BMLs.
Very little is known about the relation between BMLs and other changes in knee structures in asymptomatic, clinically healthy populations. Most previous studies have focussed on symptomatic populations with established knee OA [6, 10, 11, 21], where BMLs are associated with knee symptoms [4, 21–25] and progression of structural changes including joint space narrowing , loss of cartilage [6, 26] and increased prevalence and severity of cartilage defects [23, 27]. More recently in an asymptomatic population, the presence of BMLs at baseline was shown to be associated with longitudinal progression of cartilage defects and loss of cartilage volume  suggesting that BMLs also have a pathogenic role in pre-clinical OA.
The significance of development or resolution of prevalent BMLs has only recently been examined in populations with, or at high risk of, knee OA [6, 7, 29]. In two of these studies, the majority of BMLs persisted so both could only examine the effect of change in size of the BMLs, had limited ability to examine incident BMLs, and had no power to investigate resolution [6, 7]. In contrast, for participants of the Multi-centre Osteoarthritis Study (MOST) who either had or were at high risk of OA, approximately 40% of BMLs completely resolved and about one-third of cartilage locations developed new BMLs over 30 months, but no significant association between resolution of BMLs and change in cartilage was seen. In addition, the presence, resolution and progression of the BMLs was observed simultaneously within the same knee suggesting that complete resolution of all BMLs in a knee occurred less frequently. Worsening of BMLs and development of new BMLs was associated with increased cartilage loss compared with where BMLs remained stable ; however, no comparison between knees with incident BMLs and knees that remained free of BMLs was made. Recently, we have shown for asymptomatic populations that BMLs fluctuate with about 50% resolving and about 14% of people developing new ones over two years [12, 30]. Thus, the aim of this study was to examine the relation between incident BMLs and the resolution of BMLs prevalent at baseline and change in knee cartilage over two years in a cohort of asymptomatic middle-aged adults.
Materials and methods
The study was conducted within the Melbourne Collaborative Cohort Study, a prospective cohort study of 41,528 people, assembled to examine the role of lifestyle and genetic factors in the risk of cancer and chronic diseases in Melbourne, Australia . Participants for the current study were recruited from this cohort in 2003-04 if they were aged between 50 and 79 years without any of the following exclusion criteria: a clinical diagnosis of knee OA as defined by American College of Rheumatology criteria ; knee pain lasting for more than 24 hours in the past five years; a previous knee injury requiring non-weight bearing treatment for more than 24 hours or surgery (including arthroscopy); a history of any form of arthritis diagnosed by a medical practitioner or a contraindication to MRI, as previously described . The study was approved by The Cancer Council Victoria's Human Research Ethics Committee and the Standing Committee on Ethics in Research Involving Humans of Monash University, Melbourne. All participants gave written informed consent.
Height (cm) was measured using a stadiometer with shoes removed at baseline (1990-94). Weight (kg) was measured with bulky clothing removed at the time of MRI. Body mass index (BMI) was calculated from these data (weight (kg)/height2 (m2)).
MRI and the measurement of BMLs, cartilage volume and defects
An MRI of the dominant knee (defined as the lower limb from which the subject stepped off from when initiating gait) for each participant was performed between October 2003 and December 2004 and approximately two years later, as described on a 1.5-T whole body MR unit (Philips, Medical Systems, Eindhoven, the Netherlands) using a commercial transmit-receive extremity coil . The following sequences and parameters were used: fat suppressed, gradient recall acquisition in the steady state, three dimensional T1-weighted (58 msec/12 msec/55°, repetition time/echo time/flip angle), one signal average, slice thickness 1.5 mm, field of view 16 cm and matrix 512 × 512 scans. In addition, a coronal T2-weighted fat-saturated acquisition, (3500 to 3800 msec/20/80 msec/90°, repetition time/echo time/flip angle), two signal averages, echo train length of 10, with a slice thickness of 3.0 mm, a 1.0 inter slice gap, 1 excitation, a field of view of 13 cm, and a matrix of 256 × 192 pixels was also obtained .
Assessment of BMLs
BMLs were defined as areas of ill-defined increased signal intensity adjacent to subcortical bone present in either the medial or lateral, distal femur or proximal tibia assessed of coronal T2-weighted fat-saturated images . Two trained observers (MD and AW), who were blinded to patient characteristics, as well as sequence of images, together assessed the presence of lesions for each subject. The presence or absence of a BML was determined as previously described . Two trained observers, who were blinded to patient characteristics, as well as sequence of images, together assessed the presence of lesions for each subject. The presence or absence of a BML was determined as previously described [17, 28]. Briefly, a lesion was defined as present if it appeared on two or more adjacent slices underlying the cartilage plate. A BML was defined as 'incident' if it was present at follow up in the knees without BMLs at baseline. A BML was defined as 'resolved' if it was present at baseline but disappeared at follow up. A BML was classified as 'persistent' if it was present in the same location on both the baseline and follow-up scans. The reproducibility for determination of the BMLs was assessed using 60 randomly selected knee MRIs (κ value 0.88, P < 0.001).
Measurement of cartilage volume
The volumes of individual cartilage plates (medial and lateral tibia) were measured from the total volume by manually drawing disarticulation contours around the cartilage boundaries on each section on a workstation as described . The coefficients of variation for the medial and lateral tibial cartilage volume measures were 3.4% and 2.0% respectively [35, 36]. Annual change in cartilage volume was calculated as follow up cartilage volume subtracted from initial cartilage volume then divided by the period of time between MRI scans, as described .
Assessment of cartilage defects
Cartilage defects were graded on the sagittal T1-weighted MR images with a classification system as previously described [37–39], in the medial and lateral tibial and femoral cartilages. Cartilage defects were graded as follows: grade 0, normal cartilage; grade 1, focal blistering and intracartilaginous low-signal intensity area with an intact surface and bottom; grade 2, irregularities on the surface or bottom and loss of thickness of less than 50%; grade 3, deep ulceration with loss of thickness of more than 50%; grade 4, full-thickness cartilage wear with exposure of subchondral bone. A cartilage defect also had to be present in at least two consecutive slices. The baseline and follow-up cartilage defects were graded in duplicate (the cartilage defects were re-graded one month later), unpaired and blinded to the sequence. The defect scores at medial tibiofemoral (0-8) and lateral tibiofemoral (0-8) compartments were used in the study. Intra-observer reliability (expressed as intraclass correlation coefficient, ICC) was 0.90 for the medial tibiofemoral compartment and 0.89 for the lateral tibiofemoral compartment . Change in cartilage defects in a compartment was classified as to whether or not they progressed (i.e. increase in cartilage defect score), regressed (i.e. reduction in cartilage defect score) or remained stable (i.e. no change in cartilage defect score).
All variables were assessed for normality by visually inspecting histograms. Baseline characteristics for the 271 subjects who completed both MRI scans were tabulated. Linear regression was used to examine the compartment specific relation between having an incident or resolved BML and annual change in cartilage volume. Logistic regression was used to determine the compartment specific odds of cartilage defect progression versus regression/stability in relation to if a person had an incident BML or a resolved BML over two years. Potential confounders of age, gender, BMI, and tibial plateau area for annual change in cartilage volume were included in multivariate analyses. A P value less than 0.05 (two-tailed) was regarded as statistically significant. All analyses were performed using the SPSS statistical package (version 15.0.0, SPSS, Cary, NC, USA).
Two hundred and seventy-one (90%) of the originally recruited 297 participants completed both MRI scans at baseline and approximately two years later. Reasons for loss to follow up included: death (3), withdrawal for health reasons (4), withdrawal of consent (10), ineligible for follow up (pacemakers) (4), and inability to be contacted (5). The only significant difference between those who completed follow up and those who were lost to follow up was that those lost to follow up were slightly heavier (P = 0.01). Of the 271 participants, 234 (86%) did not have a BML in their knee at baseline. Over the two-year study period, 33 (14%) developed a BML in their knee. Of the 37 (14%) participants who had a BML in their knee at baseline, 20 (54%) persisted and 17 (46%) resolved over the two-year study period. The characteristics of the participants are presented in Table 1.
Relation between incident BMLs and tibiofemoral cartilage properties
The associations between developing an incident BML and annual change in cartilage volume and progression of tibiofemoral cartilage defects are presented in Table 2. Within the medial compartment developing an incident BML was not associated with annual change in medial cartilage volume, but a trend for incidence of medial BMLs being associated with progression of medial tibiofemoral cartilage defects was observed (odds ratio (OR) = 2.63, 95% confidence interval (CI) = 0.93 to 7.44, P = 0.07). A similar finding was seen in the lateral compartment. Although incidence of lateral BMLs was not associated with annual change in lateral cartilage volume, having an incident lateral BML was associated with a 3.13 fold (95% CI = 1.01 to 9.68, P = 0.05) increased odds of having lateral tibiofemoral defects progress. Figure 1 shows MRI images of knee that developed an incident BML over the two-year period and the worsening of a tibial defect located above the incident BML.
Relation between resolved BMLs and tibiofemoral cartilage properties
The compartment specific associations between having a BML resolve compared with it persisting over two years and annual change in cartilage volume and progression of tibiofemoral defects are presented in Table 3. Having a medial BML resolve over the study period was associated with a trend for reduced annual loss in medial tibial cartilage volume (regression coefficient = -28.7 μl, 95% CI = -58.11 to 0.68, P = 0.05) in univariate analyses. After adjusting for potential confounders this relation became significant (regression coefficient = -35.9 μl, 95% CI = -65 to -6.82, P = 0.02). A trend for resolution of medial BMLs and reduced likelihood of progression of medial tibiofemoral defects was also observed in both univariate (OR = 0.23, 95% CI = 0.05 to 1.08, P = 0.06) and multivariate analyses (OR = 0.2, 95% CI = 0.04 to 1.09, P = 0.06). No relation between the resolution of lateral BMLs and annual change in lateral cartilage volume or progression of lateral tibiofemoral defects was seen.
In this cohort of asymptomatic middle-aged adults, the development of new BMLs in knees free of BMLs at baseline was associated with the progression of tibiofemoral cartilage defects over two years. In contrast, the resolution of BMLs was associated with reduced loss of medial tibial cartilage volume and a trend towards reduced progression of tibiofemoral cartilage defects.
The relation between incident BMLs and change in cartilage has only recently been examined . Among elderly participants with or at high risk of knee OA, development of new BMLs was associated with a worsening cartilage score as assessed using the WORMS (Whole organ MRI score) scale compared with knees where a BML remained stable; however, a comparison of cartilage loss with knees that remained BML free was not performed . Although we did not show a relation between incident BMLs and change in cartilage volume, there was progression of cartilage defects. This may be due to the relative short duration of two years of follow up; in a pain-free population, people are likely to have slower cartilage loss, and also due to the fact that cartilage defects are an earlier and independent marker of cartilage pathology . We have shown that cartilage defects are present in asymptomatic people with no clinical or radiological OA and to be predictors of cartilage loss in healthy people  and those with OA , independent of initial cartilage volume. Thus, it may be that the relation we have observed between incident BMLs and cartilage defects reflects early cartilage pathology and longer duration of follow up may be needed in order to observe subsequent cartilage volume loss.
In this asymptomatic population we found that the resolution of BMLs over two years was associated with beneficial effects on cartilage as evidenced by reduced loss of tibial cartilage volume and a trend towards reduced progression of tibiofemoral cartilage defects, suggesting this is not simply due to cartilage swelling. Our results are supported by recent observations in OA populations [6, 7, 29]. For subjects with OA, an increase in size of BML was shown to be associated with increasing C-terminal cross-linking telopeptide of collagen type II levels  and increased cartilage loss [7, 29]. To our knowledge only one study, the MOST, has examined cartilage changes in knees where BMLs resolved; however, no significant association was observed between resolution of BMLs and change in cartilage . This may, at least in part, be due to the mixed nature of the MOST population because the purpose of the MOST was to examine a population at high risk of OA. In the MOST population, approximately 12% had symptomatic OA, approximately 24% had symptoms and about one-third had a Kellgren Lawrence score greater than or equal to two and past injury and surgery were not excluded. Therefore, the joints of these participants may already be further along the pathological pathway of structural change from the normal joint to one with OA, where the factors culminating in a BML, and acting on the whole knee, are established. In this situation, the reduction in change of cartilage associated with the resolution of BMLs may be lessened. In contrast, our population was asymptomatic and participants with prior injury or knee surgery were excluded.
There is growing evidence to suggest that BMLs have an important role in the pathogenesis of knee OA. They are common and persistent in symptomatic OA where they are associated with pain and progression of OA [4, 6, 17, 21–26]. Although less common in asymptomatic people, BMLs are also associated with progressive knee cartilage pathology [28, 42]. In this asymptomatic population with no clinical OA, the development of new BMLs was associated with adverse effects on knee cartilage, while resolution of BMLs was associated with improvement in cartilage. Although it has been suggested that BMLs are largely due to adverse biomechanical factors, we, and other investigators, have shown that systemic factors also affect the risk of BMLs [18, 20, 43]. It may be that in the observed relation between BMLs and cartilage, factors contributing to the development of BMLs have resulted in impairment of the supply of nutrients and oxygen to the overlying cartilage plate, which may also reduce the strength of the bony support of articular cartilage [44, 45]. Our data also suggest that this is reversible because resolution of BMLs was associated with reduction in cartilage defects and cartilage loss. Thus identifying factors that reduce the incidence of BMLs and increase their resolution may offer therapeutic targets in the prevention of knee OA.
This study has a number of potential limitations. Firstly, it examined a healthy asymptomatic population selected on the criteria of no knee pain or injury and therefore, the results are not generalisable to symptomatic populations or people who have injured their knees. On the other hand, the findings from our study can be generalised to populations that may be targeted for primary prevention or early treatment of knee OA. Second, we did not obtain radiographs of the knees, so some subjects may have had asymptomatic radiographic OA. However, we used the American College of Rheumatology clinical criteria of OA  to determine the status of knees, and individuals with significant knee injury in the past, pain at baseline, knee surgery or medical diagnosis of any other type of arthritis were excluded. Due to the small number of persistent BMLs we were unable to examine change in BML size. The small number of BMLs may have also reduced our power to detect significant associations and may explain the trends reported. In this study we did not assess knee alignment, which has been shown to be associated with the presence of BMLs . If malalignment were to be a major determinant of BMLs, we would not expect it to change significantly in a healthy asymptomatic population over a period of only two years, so would expect it to underestimate the relations we observed.
In this cohort study of asymptomatic middle-aged adults the development of new BMLs was associated with progressive knee cartilage pathology, while resolution of BMLs prevalent at baseline was associated with reduced progression of cartilage pathology. Further work examining the relation between changes and BML and cartilage may provide another important target for the prevention of knee OA.
body mass index
bone marrow lesion
C-terminal crosslinking telopeptide of collagen type II
Multi-centre Osteoarthritis Study
magnetic resonance imaging
Sharma L, Song J, Felson DT, Cahue S, Shamiyeh E, Dunlop DD: The role of knee alignment in disease progression and functional decline in knee osteoarthritis. JAMA. 2001, 286: 188-195. 10.1001/jama.286.2.188.
Felson DT, Niu J, Guermazi A, Roemer F, Aliabadi P, Clancy M, Torner J, Lewis CE, Nevitt MC: Correlation of the development of knee pain with enlarging bone marrow lesions on magnetic resonance imaging. Arthritis Rheum. 2007, 56: 2986-2992. 10.1002/art.22851.
Zanetti M, Bruder E, Romero J, Hodler J: Bone marrow edema pattern in osteoarthritic knees: correlation between MR imaging and histologic findings. Radiology. 2000, 215: 835-840.
Felson DT, Chaisson CE, Hill CL, Totterman SMS, Gale E, Skinner KM, Kazis L, Gale DR: The association of bone marrow lesions with pain in knee osteoarthritis. Ann Intern Med. 2001, 134: 541-549.
Link TM, Steinbach LS, Ghosh S, Ries M, Lu Y, Lane N, Majumdar S: MR imaging findings in different stages of disease and correlation with clinical findings. Radiology. 2003, 226: 373-381. 10.1148/radiol.2262012190.
Garnero P, Peterfy C, Zaim S, Schoenharting M: Bone marrow abnormalities on magnetic resonance imaging are associated with type II collagen degradation in knee osteoarthritis. Arthritis Rheum. 2005, 52: 2822-2829. 10.1002/art.21366.
Hunter DJ, Zhang Y, Niu J, Goggins J, Amin S, LaValley MP, Guermazi A, Genant H, Gale D, Felson DT: Increase in bone marrow lesions associated with cartilage loss: a longitudinal magnetic resonance imaging study of knee osteoarthritis. Arthritis Rheum. 2006, 54: 1529-1535. 10.1002/art.21789.
Guymer E, Baranyay F, Wluka AE, Hanna F, Bell RJ, Davis SR, Wang Y, Cicuttini FM: A study of the prevalence and associations of subchondral bone marrow lesions in the knees of healthy middle-aged women. Osteoarthritis Cartilage. 2007, 15: 1437-1442. 10.1016/j.joca.2007.04.010.
Baranyay FJ, Wang Y, Wluka AE, English DR, Giles GG, Sullivan RO, FM C: Association of bone marrow lesions with knee structures and risk factors for bone marrow lesions in the knees of clinically healthy, community-based adults. Semin Arthritis Rheum. 2007, 37: 112-118. 10.1016/j.semarthrit.2007.01.008.
Kornaat PR, Kloppenburg M, Sharma R, Botha-Scheepers SA, Hellio Le Graverand M-P, Coene LNJEM, Bloem JL, Watt I: Bone marrow edema-like lesions change in volume in the majority of patients with osteoarthritis: associations with clinical features. Eur Radiol. 2007, 17: 3073-3078. 10.1007/s00330-007-0711-1.
Boegard T, Rudling O, Petersson IF, Jonnson K: Magnetic resonance imaging of the knee in chronic knee pain: a 2 year follow-up. Osteoarthritis Cartilage. 2001, 9: 473-480. 10.1053/joca.2001.0414.
Berry PA, Davies-Tuck ML, Wluka AE, Hanna FS, Bell RJ, Davis SR, Adams J, FM C: The natural history of bone marrow lesions in community-based middle-aged women without clinical knee osteoarthritis. Semin Arthritis Rheum. 2009, 39: 213-217. 10.1016/j.semarthrit.2008.05.003.
Vincken PWJ, ter Braak BPM, van Erkel AR, Coerkamp EG, Mallens WMC, JL B: Clinical consequences of bone bruise around the knee. Eur Radiol. 2006, 16: 97-107. 10.1007/s00330-005-2735-8.
Costa-Paz M, Muscolo L, Ayerza M, Makino A, Aponte-Tinao L: Magnetic resonance imaging follow up study of bone bruises associated with anterior cruciate ligament ruptures. Arthroscopy. 2001, 17: 445-449.
Palmer WE, Levine SM, Dupuy DE: Knee and shoulder fractures: association of fracture detection and marrow edema on MR images with mechanism of injury. Radiology. 1997, 204: 395-401.
Mink JH, Duetsch AL: Occult cartilage and bone injuries of the knee: Detection, classification and assessment with MR imaging. Radiology. 1989, 170: 823-829.
Felson DT, McLaughlin S, Goggins J, LaValley MP, Gale E, Totterman S, Li W, Hill C, Gale D: Bone marrow edema and its relation to progression of knee osteoarthritis. Ann Intern Med. 2003, 139: 330-336.
Carbone LD, Nevitt MC, Wildy K, Barrow KD, Harris F, Felson DT, Peterfy C, Visser M, Harris TB, Wang BWE, SB K: The relationship of antiresorptive drug use to structural findings and symptoms of knee osteoarthritis. Arthritis Rheum. 2004, 50: 3516-3525. 10.1002/art.20627.
Wang Y, Wluka AE, Hodge AM, English DR, Giles GG, O'Sullivan R, Cicuttini FM: Effect of fatty acids on bone marrow lesions and cartilage in healthy, middle-aged subjects without clinical knee osteoarthritis. Osteoarthritis Cartilage. 2008, 16: 579-583. 10.1016/j.joca.2007.09.007.
Wang Y, Hodge AM, Wluka AE, English DR, Giles FG, O'Sullivan R, Forbes A, Cicuttini FM: Effect of antioxidants on knee cartilage and bone in healthy, middle-aged subjects: a cross sectional study. Arthritis Res Ther. 2007, 9: R66-10.1186/ar2225.
Felson DT, Niu J, Roemer F, Aliabadi P, Clancy M, Torner J, Lewis CE, Nevitt MC: Correlation of the development of knee pain with enlarging bone marrow lesion on magnetic resonance imaging. Arthritis Rheum. 2007, 56: 2986-2992. 10.1002/art.22851.
Lo GH, Hunter DJ, Zhang Y, McLennan CE, LaValley MP, Kiel DP, McLean RR, Genant HK, Guermazi A, Felson DT: Bone marrow lesions in the knee are associated with increased local bone density. Arthritis Rheum. 2005, 52: 2814-2821. 10.1002/art.21290.
Sowers MF, Hayes C, Jamadar D, Capul D, Lachance L, Jannausch M: Magnetic resonance-detected subchondral bone marrow and cartilage defect characteristics associated with pain and x-ray defined knee osteoarthritis. Osteoarthritis Cartilage. 2003, 11: 387-393. 10.1016/S1063-4584(03)00080-3.
Zhai G, Blizzard L, Srikanth V, Ding C, Cooley H, Cicuttini FM, Jones G: Correlates of knee pain in older adults: Tasmanian older adult cohort study. Arthritis Rheum. 2006, 55: 264-271. 10.1002/art.21835.
Torres L, Dunlop DD, Peterfy C, Guermazzi A, Prasad P, Hayes KW, Song J, Cahue S, Chang A, Marshall M, Sharma L: The relationship between specific tissue lesions and pain severity in persons with knee osteoarthritis. Osteoarthritis Cartilage. 2006, 14: 1033-1040. 10.1016/j.joca.2006.03.015.
Phan CM, Link TM, Blumenkrantz G, Dunn TC, Ries MD, Steinbach LS, Majumdar S: MR imaging findings in the follow up of patients with different stages of knee osteoarthritis and the correlation with clinical symptoms. Eur Radiol. 2006, 16: 608-618. 10.1007/s00330-005-0004-5.
Kijowski R, Stanton P, Fine J, De Smet A: Subchondral bone marrow edema in patients with degeneration of the articular cartilage of the knee joint. Radiology. 2006, 238: 943-949. 10.1148/radiol.2382050122.
Wluka AE, Hanna FS, Davies-Tuck M, Wang Y, Bell RJ, Davis SR, Adams J, Cicuttini FM: Bone marrow lesions predict increase in knee cartilage defects and loss of cartilage volume in middle-aged women without knee pain over 2 years. Ann Rheum Dis. 2009, 68: 850-855. 10.1136/ard.2008.092221.
Roemer FW, Guermazi A, Javaid MK, Lynch JA, Niu J, Zhang Y, Felson DT, Lewis CE, Torner J, Nevitt MC: Change in MRI-detected subchondral bone marrow lesions is associated with cartilage loss - the MOST study a longitudinal multicenter study of knee osteoarthritis. Ann Rheum Dis. 2009, 68: 1461-1465. 10.1136/ard.2008.096834.
Davies-Tuck ML, Wluka AE, Wang Y, English DR, Giles GG, Cicuttini FM: The natural history of bone marrow lesions in community based adults with no clinical knee osteoarthritis. Ann Rheum Dis. 2009, 68: 904-908. 10.1136/ard.2008.092973.
Giles GG, English DR: The Melbourne Collaborative Cohort Study. IARC Sci Publ. 2002, 156: 69-70.
Altman R, Asch E, Bloch D, Bole G, Borenstein D, Brandt K, Christy W, Cooke TD, Greenwald R, Hochberg M: Development of criteria for the classification and reporting of osteoarthritis. Classification of osteoarthritis of the knee. Diagnostic and Therapeutic Criteria Committee of the American Rheumatism Association. Arthritis Rheum. 1986, 29: 1039-1049. 10.1002/art.1780290816.
Wang Y, Wluka AE, English DR, Teichtahl AJ, Giles GG, O'Sullivan R, Cicuttini FM: Body composition and knee cartilage properties in healthy, community-based adults. Ann Rheum Dis. 2007, 66: 1244-1248. 10.1136/ard.2006.064352.
McAlindon TE, Watt I, McCrae F, Goddard P, Dieppe PA: Magnetic resonance imaging in osteoarthritis of the knee: correlation with radiographic and scintigraphic findings. Ann Rheum Dis. 1991, 50: 14-19. 10.1136/ard.50.1.14.
Wluka AE, Stuckey S, Snaddon J, Cicuttini FM: The determinants of change in tibial cartilage volume in osteoarthritic knees. Arthritis Rheum. 2002, 46: 2065-2072. 10.1002/art.10460.
Wluka AE, Wolfe F, Stuckey SL, Cicuttini FM: How does tibial cartilage volume relate to symptoms in subjects with knee osteoarthritis?. Ann Rheum Dis. 2004, 63: 264-268. 10.1136/ard/2003.007666.
Wluka AE, Ding C, Jones G, Cicuttini FM: The clinical correlates of articular cartilage defects in symptomatic knee osteoarthritis: a prospective study. Rheumatology (Oxford). 2005, 44: 1311-1316. 10.1093/rheumatology/kei018.
Cicuttini FM, Ding C, Wluka AE, Davis SR, Ebeling PR, Jones G: Association of cartilage defects with loss of knee cartilage in healthy, middle-age adults: a prospective study. Arthritis Rheum. 2005, 52: 2033-2039. 10.1002/art.21148.
Ding C, Cicuttini F, Scott F, Boon C, Jones G: Association of prevalent and incident knee cartilage defects with loss of tibial and patellar cartilage: a longitudinal study. Arthritis Rheum. 2005, 52: 3918-3927. 10.1002/art.21474.
Ding C, Garnero P, Cicuttini FM, Scott F, Cooley H, Jones G: Knee cartilage defects: association with early radiographic osteoarthritis, decreased cartilage volume, increased joint surface area, and type II collagen breakdown. Osteoarthritis Cartilage. 2005, 13: 198-205. 10.1016/j.joca.2004.11.007.
Cicuttini FM, Ding C, Wluka AE, Davis SR, Ebeling PR, Jones G: Association of cartilage defects with loss of knee cartilage in healthy, middle-age adults: a prospective study. Arthritis Rheum. 2005, 52: 2033-2039. 10.1002/art.21148.
Hanna FS, Bell RJ, Cicuttini FM, SL D, Wluka AE, Davis SR: High sensitivity C-reactive protein is associated with lower tibial cartilage volume but not lower patella cartilage volume in healthy women at midlife. Arthritis Res Ther. 2008, 10: R27-10.1186/ar2380.
Wang Y, Wluka AE, Hodge AM, English DR, Giles GG, O'Sullivan R, Cicuttini FM: Effect of fatty acids on bone marrow lesions and cartilage in healthy, middle-aged subjects without clinical knee osteoarthritis. Osteoarthritis Cartilage. 2008, 16: 579-583.
Findlay DM: Vascular pathology and osteoarthritis. Rheumatology (Oxford). 2007, 46: 1763-1768. 10.1093/rheumatology/kem191.
Winet H, Hsieh A, Bao JY: Approaches to study of ischemia in bone. J Biomed Mater Res. 1998, 43: 410-421. 10.1002/(SICI)1097-4636(199824)43:4<410::AID-JBM8>3.0.CO;2-B.
We would especially like to thank the study participants who made this study possible. The Melbourne Collaborative Cohort Study recruitment was funded by VicHealth and The Cancer Council of Victoria. 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 would like to acknowledge the NHMRC (project grant 334150) and Colonial Foundation. Drs Wluka and Wang are the recipients of NHMRC Public Health Fellowships (317840 and 465142, respectively). Ms Davies-Tuck is the recipient of Australian Post-graduate Award PhD Scholarship.
The authors declare that they have no competing interests.
FC, AW, DE, GG and RO were all involved in the design and implementation of the study including data collection and measurement. MD, AE, AF, YY and FC were involved in the analysis and interpretation of the data. All authors were involved in the manuscript preparation.
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
About this article
Cite this article
Davies-Tuck, M.L., Wluka, A.E., Forbes, A. et al. Development of bone marrow lesions is associated with adverse effects on knee cartilage while resolution is associated with improvement - a potential target for prevention of knee osteoarthritis: a longitudinal study. Arthritis Res Ther 12, R10 (2010). https://doi.org/10.1186/ar2911
- Cartilage Defect
- Cartilage Loss
- Cartilage Volume
- Bone Marrow Lesion
- Knee Cartilage