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Published online before print December 20, 2002, 10.1148/radiol.2262012190
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(Radiology 2003;226:373-381.)
© RSNA, 2003


Musculoskeletal Imaging

Osteoarthritis: MR Imaging Findings in Different Stages of Disease and Correlation with Clinical Findings1

Thomas M. Link, MD, Lynne S. Steinbach, MD, Srinka Ghosh, MS, Michael Ries, MD, Ying Lu, PhD, Nancy Lane, MD and Sharmila Majumdar, PhD

1 From the Departments of Radiology (T.M.L., L.S.S., S.G., Y.L., S.M.), Orthopedic Surgery (M.R.), and Medicine (N.L.), University of California, San Francisco. Received January 22, 2002; revision requested March 20; revision received April 30; accepted June 25. Supported by National Institutes of Health grants RO1-AR46905 and RO1-AG17762. Address correspondence to T.M.L., Department of Radiology, Technische Universitaet Muenchen, Ismaninger Str 22, 81675 Munich, Germany (e-mail: tmlink@roe.med.tu-muenchen.de).


    ABSTRACT
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
PURPOSE: To determine whether knee pain, stiffness, and limited function in patients with different stages of osteoarthritis correlate with the degree of disease assessed on magnetic resonance (MR) images and radiographs.

MATERIALS AND METHODS: Radiographs in 50 patients with varying degrees of osteoarthritis of the knee were assessed by using the the Western Ontario and McMaster University (WOMAC) osteoarthritis index and the Kellgren-Lawrence (KL) scale. MR images were obtained and analyzed by two readers for cartilage lesions, bone marrow edema pattern, and ligamentous and meniscal lesions.

RESULTS: Thirteen of 16 knees with a KL score of 4 showed full-thickness cartilage lesions and bone marrow edema pattern. Cruciate ligament tears were found in five of 12 knees with a KL score of 3 and in nine of 16 knees with a KL score of 4. While the KL score correlated significantly (P < .05) with the grade of cartilage lesions, and a substantially higher percentage of lesions with higher KL scores were found on MR images, the correlations between MR imaging findings and KL score versus clinical findings were not significant (P > .05). Significant differences between WOMAC scores were found only for the grades of cartilage lesions (P < .05).

CONCLUSION: Cartilage lesions, bone marrow edema pattern, and meniscal and ligamentous lesions were frequently demonstrated on MR images in patients with advanced osteoarthritis. Clinical findings showed no significant correlations with KL score and extent of findings at MR imaging.

© RSNA, 2003

Index terms: Arthritis, degenerative, 452.4851, 452.711 • Cartilage, MR, 4521.121412, 4521.121415 • Knee, arthritis, 452.4851, 452.711 • Knee, ligaments, menisci, and cartilage, 452.4851 • Knee, MR, 4521.121412, 4521.121415


    INTRODUCTION
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
It is well known from results of previous studies that osteoarthritis leads to progressive cartilage loss, and a number of techniques have been developed to assess cartilage qualitatively (13) and to quantify cartilage volume (47). Apart from cartilage loss, however, a number of other findings are frequently associated with osteoarthritis, such as bone marrow edema pattern and synovial and ligamentous lesions (811). These lesions, in addition to cartilage loss, also have a substantial influence on the progression of disease and loss of clinical function.

Radiography is still standard for assessment of the progression of osteoarthritis, and the Kellgren-Lawrence (KL) scale (12,13) is used most frequently by clinicians. The KL scale was also adopted by the World Health Organization as the reference standard for cross-sectional and longitudinal epidemiologic studies. As yet, however, it is not well known what abnormalities to expect at magnetic resonance (MR) imaging at different stages of disease and whether MR imaging may be useful as an additional diagnostic tool, given a specific grade of osteoarthritis.

In addition, since pain, stiffness, and limited function are the most clinically important problems in patients with osteoarthritis, it is important to correlate these symptoms with abnormal MR imaging and radiographic findings. Clinical scores for osteoarthritis have been developed to measure relevant patient outcome in drug trials. One of the most well established scores is the Western Ontario and McMaster University (WOMAC) osteoarthritis index, a multidimensional health status instrument (14,15) that quantifies pain, stiffness, and limited function in patients with osteoarthritis of the knee and hip.

The purpose of this study was to analyze findings on MR images of the knee obtained at different stages of osteoarthritis and to determine whether pain, stiffness, and limited function correlate with the degree of disease assessed on MR images and radiographs.


    MATERIALS AND METHODS
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Patients and Clinical Assessment
Fifty consecutive patients with various degrees of osteoarthritis of the knee who were referred for MR imaging were recruited for this study. Patients with a history of trauma, previous surgery, or inflammatory arthritis were excluded. Patients with clinically suspected osteoarthritis of the knee were recruited and included in the study when typical radiographic signs of osteoarthritis (ie, osteophytes, subchondral sclerosis, and joint space narrowing) were demonstrated. The mean age of the patients (30 women and 20 men; age range, 43–81 years) was 63.7 years ± 11.5 (SD). Informed consent was obtained from all patients after the nature of the examinations had been fully explained. All examinations were performed in accordance with the rules and regulations of the local human research committee.

All patients were examined clinically, and WOMAC scores (14) were determined. The WOMAC system was developed to quantify symptoms related to osteoarthritis and to assess relevant patient outcome in drug trials. This well-established clinical grading system quantifies the degree of pain, functional impairment, and stiffness in patients with osteoarthritis.

The patients were interviewed by an orthopedic surgeon (M.R.), and questions concerning the amount of knee pain and stiffness the patients were currently experiencing were answered by using a five-point scale (none, slight, moderate, severe, and extreme). In addition, patients answered questions to assess physical function—that is, the ability to move around and take care of themselves. These questions focused on the ability of the patients to perform such functions as descending and ascending stairs, standing, walking, rising from bed, and going shopping. On the basis of the answers to these questions, the overall WOMAC scores were determined. The scores varied from 0 (no pain, stiffness, or functional impairment) to 500 (extreme pain, stiffness, and functional impairment).

Imaging
In all patients, radiographs of the knee were obtained in lateral and anteroposterior planes. In addition, a sunrise view of the patellofemoral joint was obtained. MR imaging of the knee was performed with a 1.5-T MR imager (Signa; GE Medical Systems, Waukesha, Wis) by using a bilateral dual phased-array coil (USA Instruments, Cleveland, Ohio) for signal reception. Since patients with symptomatic knees were examined by using a fairly long acquisition protocol, reduction of motion artifacts and accuracy of patient and coil positioning were optimized by positioning the knee flexed (30°–35°) on a dedicated holder (machined in-house, 152° angle). Patients were immobilized by using hook-and- loop straps.

The MR imaging protocol included five pulse sequences. The first was a sagittal high-spatial-resolution volumetric fat-suppressed spoiled gradient-echo sequence. Imaging parameters were as follows: 30/8 (repetition time msec/echo time msec), flip angle of 30°, matrix of 512 x 256, field of view of 12 cm, one signal acquired, and acquisition time of 9 minutes 31 seconds with 64 sections. The in-plane spatial resolution was 0.234 x 0.234 mm2, and the section thickness was 2 mm.

The second and third sequences were coronal and sagittal, respectively, T2-weighted fat-suppressed fast spin-echo sequences with 3,000/70, echo train length of eight, matrix of 256 x 192, field of view of 14 cm, one signal acquired, bandwidth of 16 kHz, acquisition time of 2 minutes 36 seconds, and section thickness of 4 mm.

The fourth and fifth sequences were coronal and sagittal, respectively, T1-weighted spin-echo sequences with 500/9, matrix of 256 x 192, field of view of 14 cm, one signal acquired, bandwidth of 16 kHz, acquisition time of 3 minutes 28 seconds, and section thickness of 4 mm.

Image Analysis
All radiographs and MR images were analyzed by two radiologists (L.S.S., T.M.L.) in consensus without knowledge of patient age or sex. To obviate recall bias, MR images and radiographs were analyzed separately in random order. The radiographic findings were scored according to the KL scale, which is a standard radiologic grading system for osteoarthritis (12,13). Features considered evidence of osteoarthritis were osteophytes in the joint margins, narrowing of joint spaces, and subchondral sclerosis. On the basis of these features, the following KL scores were defined (Fig 1): 0, no features of osteoarthritis; 1, doubtful osteoarthritis, with minute osteophytes of doubtful importance; 2, minimal osteoarthritis, with definite osteophytes but unimpaired joint space; 3, moderate osteoarthritis, with osteophytes and moderate diminution of joint space; and 4, severe osteoarthritis, with greatly impaired joint space and sclerosis of subchondral bone.



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Figure 1. Anteroposterior (top) and lateral (bottom) radiographs of knees with KL scores of 1-4. A, Knee with a KL score of 1 with minimal osteophytes at the medial femoral condyle (arrowhead in anteroposterior view) and the patellar joint surface (arrowhead in lateral view) and sharpening of the medial tibial spine (arrow). B, Knee with a KL score of 2 with small but definite osteophytes (arrows) but unimpaired joint space (anteroposterior view). C, Knee with a KL score of 3 with moderately impaired joint space (arrow) and osteophytes (arrowheads). D, Knee with a KL score of 4 with substantially impaired joint space (arrow), severe osteophytes (white arrowheads), and sclerosis of subchondral bone (black arrowhead).

 
During assessment of MR images, the readers were blinded to KL and WOMAC scores and patient age. The MR images were analyzed by means of consensus concerning cartilage lesions, joint effusion, popliteal cysts, ligaments, and menisci. Additional features included reactive bone marrow changes, osteophytes, subchondral cysts, and loose bodies. Six compartments were defined: the medial and lateral femoral condyle, the femoral trochlea, the medial and lateral tibia, and the patella.

Cartilage lesions were graded in a manner analogous to the Noyes and Stabler (16) classification, which was modified for MR imaging by Recht et al (3): Grade I lesions were defined as having areas of inhomogeneous signal intensity on high-spatial-resolution spoiled gradient-echo images; grade IIa lesions, as cartilage defects that involved less than half of the articular cartilage thickness; grade IIb lesions, as cartilage defects involving more than half of the cartilage but less than full thickness; and grade III lesions, as cartilage defects exposing the bone.

Bone marrow edema pattern was defined as diffuse subchondral low signal intensity on T1-weighted images and high signal intensity on T2-weighted images. Edema pattern was mild when it was less than 1 cm in diameter in the long axis on fat-suppressed T2-weighted images. It was moderate when its diameter was 1–2 cm and severe when its diameter was larger than 2 cm in the long axis. Osteophytes were classified as mild when they were located in the joint margins and were less than 0.5 cm in diameter when measured from the base to the tip on T1-weighted images; when osteophytes were larger than 0.5 cm in diameter, they were defined as severe.

For correlation with KL and WOMAC scores, the most advanced cartilage lesions and the most severe bone marrow edema patterns or other findings in the individual joint were used. Meniscal lesions included meniscal tears and intrasubstance degeneration. Meniscal tears ranged from minor tears that did not change the shape of the menisci to severe tears in which the meniscus was substantially deformed and torn or it could no longer be depicted. Intrasubstance degeneration was defined as signal intensity changes of the meniscus without tears. Cruciate ligament tears were diagnosed when the ligament was interrupted by abnormal signal intensity on T2-weighted images, had abnormal alignment, or was completely absent. Pathologic changes of the collateral ligaments included edematous changes, such as collateral ligament sprains and tears.

Data Analysis
Contingency table analysis was performed when the data were either nominal or ordinal. These results were presented in crosstabs tables. A {chi}2 or Fisher exact test was used to examine the associations. Since the values showed an abnormal distribution, the medians and interquartile ranges (IQRs) of the WOMAC scores were determined for the KL scores and the individual abnormalities on MR images, such as cartilage defects and bone marrow edema pattern. The significance of differences between the groups was calculated by using a Wilcoxon rank sum test at the .05 significance level. Spearman correlations between the scores were determined. All statistical computations were processed by using Statview 4.1 software (Abacus, Berkeley, Calif), JMP software (SAS Institute, Cary, NC), and S-plus software (Insightful, Seattle, Wash).


    RESULTS
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
KL Scores versus MR Imaging Findings
According to the KL scale, 10 patients had a score of 1 (median age, 57 years; IQR, 51–71 years; six women and four men), 11 patients had a score of 2 (median age, 60 years; IQR, 50–74 years; seven women and four men), 13 patients had a score of 3 (median age, 68 years; IQR, 48–74 years; seven women and six men), and 16 patients had a score of 4 (median age, 66 years; IQR, 62–74 years; 10 women and six men). Except for the age differences in the groups with KL scores of 1 and 4 (P = .047), age and sex differences between these groups were not significant (P > .05).

Cartilage lesions were found on MR images in 43 of 50 knees (Table 1). All knees without cartilage lesions except for one were given a KL score of 1 or 2. The grade of cartilage lesions increased with increasing KL scores (r = 0.55, P < .01). Thirteen of 16 knees with a KL score of 4 showed full-thickness cartilage lesions. Figure 2 depicts cartilage lesions with different KL scores.


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TABLE 1. Cartilage Defects at Various Stages of Osteoarthritis in 50 Patients

 


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Figure 2. Sagittal MR images with representative findings in knees with KL scores of 1-4. A and B depict two knees with a KL score of 1. A, Fat-suppressed spoiled gradient-echo 30/8 image with a 30° flip angle depicts cartilage thinning (arrow) of less than 50% at the femur. B, T1-weighted spin-echo 500/9 image shows mild osteophytes (arrows) at the femur. C and D depict two knees with a KL score of 2. C, Fat-suppressed spoiled gradient-echo 30/8 image with a 30° flip angle shows inhomogeneous signal intensity of the femoral condyle cartilage (grade I) and cartilage thinning of less (grade IIa, arrow) and more (grade IIb, patella) than 50%. In addition, severe joint effusion (arrowhead) is shown. D, T1-weighted spin-echo 500/9 image depicts a torn posterior horn of the lateral meniscus (arrow) and severe cartilage thinning (arrowhead) in the femoropatellar joint. E and F depict two knees with a KL score of 3. E, Fat-suppressed spoiled gradient-echo 30/8 image with a 30° flip angle shows a grade IIb lesion (arrow) of the posterior femoral condyle cartilage and a grade III lesion (arrowhead) of the tibia. F, Fat-suppressed T2-weighted fast spin-echo 3,000/70 image depicts bone marrow edema (arrowheads) of the femur and the tibia anteriorly, as well as joint effusion (arrow). G and H depict two knees with a KL score of 4. G, Fat-suppressed spoiled gradient-echo 30/8 image with a 30° flip angle shows a grade III cartilage lesion (arrow) of the femur and the tibia, while the femoropatellar joint appears normal. H, Fat-suppressed T2-weighted fast spin-echo 3,000/70 image depicts severe bone marrow edema (arrowheads) in the femur and the tibia and destruction of the posterior horn of the medial meniscus (straight arrow). Joint effusion (curved arrow), which extends into a popliteal cyst, is demonstrated.

 
Bone marrow edema was depicted in 30 of 50 knees (Table 2). While only seven of the 21 knees with a KL score of 1 or 2 had bone marrow edema pattern, 13 of the 16 knees with a KL score of 4 showed bone marrow edema pattern. Figure 2 shows fat-suppressed T2-weighted images with bone marrow edema pattern in knees with KL scores of 3 and 4. A significant increase in bone marrow edema pattern with increase in KL score was observed (P < .05).


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TABLE 2. Bone Marrow Edema at Various Stages of Osteoarthritis in 50 Patients

 
Popliteal and osteochondral cysts, as well as more severe and central osteophytes (Fig 3), were found more frequently (P < .01) in the advanced stages of osteoarthritis (Table 3). Joint effusion was also found more frequently (P < .01) in patients with advanced osteoarthritis (Table 4, Fig 2). Meniscal lesions were found in all but four knees (two with a KL score of 1, one with a KL score of 2, and one with a KL score of 3) (Table 4, Fig 2). Intrasubstance degeneration was found in only four knees with a KL score of 1 or 2. All knees with a KL score of 4 had severe meniscal lesions—that is, complex tears with deformity or severe destruction. Ligamentous lesions were also found in a higher percentage of knees with advanced osteoarthritis (P < .05), which affected either the anterior cruciate ligament in 14 patients (nine of 14 [64%] tears were found in knees with a KL score of 4) or the collateral ligaments in seven patients (four of seven [58%] lesions were found in knees with a KL score of 4) (Table 4, Fig 4).



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Figure 3. Sagittal fat-suppressed spoiled gradient-echo 30/8 MR image with a 30° flip angle demonstrates a central osteophyte (arrow) in a patient with advanced osteoarthritis with cartilage defects (arrowhead) at the femur and tibia and osteophytes at the patella.

 

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TABLE 3. Osteophytes and Subchondral and Popliteal Cysts at Various Stages of Osteoarthritis in 50 Patients

 

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TABLE 4. Abnormalities at Various Stages of Osteoarthritis in 50 Patients

 


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Figure 4. Ligamentous and meniscal lesions in patients with advanced osteoarthritis. A, Sagittal T1-weighted spin-echo 500/9 MR image. The anterior cruciate ligament is absent (arrow) as a sign of severe degenerative changes, suggestive of a tear. B, Coronal fat-suppressed T2-weighted fast spin-echo 3,000/70 image shows destruction of the medial meniscus (arrowhead) and medial collateral ligament sprain with a tear (arrow).

 
All anterior cruciate ligament tears were found in knees with a KL score of 3 or 4, while none of the knees with a KL score of 1 or 2 showed tears. Collateral ligamentous lesions, on the other hand, were found in two knees with a KL score of 1 or 2. All of the collateral ligamentous lesions were found in the compartment that was most severely affected by osteoarthritis, which was located medially in five knees. Three loose bodies were found, two of which were in knees with a KL score of 4 (Table 4).

WOMAC Scores versus KL Scores and MR Imaging Findings
WOMAC scores were determined for pain (median, 115.5; IQR, 48–200), stiffness (median, 119; IQR, 44–200), and function (median, 173.5; IQR, 100–272). There was no significant correlation between WOMAC scores for pain and stiffness versus age, but there was a moderate correlation between WOMAC scores for function and age (r = 0.38, P < .05). Significant differences between men and women were not found.

While the KL score correlated well with the extent of MR imaging findings in the knee, the correlations between MR imaging and clinical findings were limited. Correlations between WOMAC and KL scores were not significant. While the WOMAC pain score tended to be lower in knees with a KL score of 1, the stiffness score was higher in knees with a KL score of 4 compared with those in knees with other scores (Table 5). Differences between the individual groups, however, were not significant (P > .05). The function score showed no significant differences between the groups. Figure 5 shows radiographic and MR imaging findings in a patient with high WOMAC scores and a KL score of 2, and Figure 6 shows findings in a patient with low WOMAC scores and a KL score of 4.


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TABLE 5. Clinical Findings at Various Stages of Osteoarthritis in 50 Patients

 


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Figure 5. MR imaging findings in a 73-year-old woman with high WOMAC scores (median scores: pain, 140; stiffness, 150; function, 206) and minor findings of osteoarthritis on corresponding radiographs (KL score of 2). A, Anteroposterior radiograph shows minor changes of osteoarthritis, including mild osteophytes (arrowheads). B, Sagittal fat-suppressed spoiled gradient-echo 30/8 MR image with a 30° flip angle depicts grade IIa cartilage defects at the femur but grade IIb lesions (arrow) at the tibia. C, Sagittal fat-suppressed T2-weighted 3,000/70 MR image shows joint effusion but no bone marrow edema pattern.

 


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Figure 6. MR imaging findings in a 74-year-old man with low WOMAC scores (median scores: pain, 20; stiffness, 50; function, 35) and advanced osteoarthritis depicted on corresponding radiographs and MR images (KL score of 4). A, Anteroposterior radiograph shows advanced signs of osteoarthritis with medial joint space narrowing, osteophytes, and subchondral sclerosis. B, Sagittal fat-suppressed spoiled gradient-echo 30/8 MR image with a 30° flip angle shows grade III cartilage lesions (arrows) at the femur and the tibia. C, Sagittal T1-weighted spin-echo 500/9 MR image depicts subchondral cystic changes (arrow), osteophytes, destruction of the medial meniscus (white arrowheads), and joint effusion (black arrowhead).

 
For cartilage lesions assessed on MR images, the highest WOMAC scores for pain, stiffness, and function were found in patients with less than 50% cartilage loss (grade IIa); however, this patient group was fairly small (n = 5) (Table 6). The lowest WOMAC scores for pain and function were found in patients without cartilage lesions; the lowest scores for stiffness, however, were found in patients with more than 50% cartilage loss and full-thickness lesions (grades IIb and III). Differences between group IIa and the other groups and between group 0 (no cartilage lesions) and groups IIb and III were statistically significant (P < .05) for pain and function but not for stiffness. When comparing WOMAC scores for patients without cartilage lesions (pain: median, 60; IQR, 28–80) and those with lesions (pain: median, 134; IQR, 86.5–210), significant differences were found for pain and function (P < .05) but not for stiffness. No significant differences in WOMAC scores were found for patients without cartilage lesions or for patients with low-grade cartilage lesions (groups 0, I, and IIa; median score for pain, 80; IQR, 28–295) versus those with high-grade lesions (groups IIb and III; median score for pain, 120; IQR, 86.25–200) (P > .05).


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TABLE 6. Clinical Findings at Various Stages of Cartilage Abnormality as Assessed on MR Images in 50 Patients

 
Bone marrow edema pattern grades and WOMAC scores showed no significant correlations. The differences of the WOMAC scores between the edema grades (no edema, mild edema, moderate edema, or severe edema) were also not significant (P > .05) (Table 7).


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TABLE 7. Clinical Findings at Various Stages of Bone Marrow Edema as Assessed on MR Images in 50 Patients

 
The WOMAC pain score was higher in patients with joint effusion (n = 38; median, 120; IQR, 86–200) than in those without joint effusion (n = 12; median, 55; IQR, 31–120.5), but differences were not significant (P > .05). Differences were also not significant for patients with popliteal cysts (n = 16; median, 115.5; IQR, 90.25–218) versus those without cysts (n = 34; median, 100; IQR, 41–200) (P > .05) or for patients with mild osteophytes (n = 23; median, 150; IQR, 79.5–241.75) versus those with severe osteophytes (n = 27; median, 111; IQR, 60.5–180) (P > .05). Patients with central osteophytes had significantly higher WOMAC stiffness scores (n = 14; median, 177; IQR, 24.5–312.5) than did those without central osteophytes (n = 36; median, 100; IQR, 33–150) (P < .05), but WOMAC pain and function scores showed no significant differences between patients with central osteophytes (pain: median, 150; IQR, 70.25–238.75) and patients without central osteophytes (pain: median, 111; IQR, 45.5–180) (P > .05). Patients with subchondral cysts did not have significantly higher WOMAC pain scores (n = 22; median, 140; IQR, 50–220) than those of patients without cysts (n = 28; median, 100; IQR, 45.75–160) (P > .05).

Median WOMAC pain and stiffness scores were higher in patients with meniscal tears (n = 42; pain: median, 120; IQR, 80–200) than in those without meniscal tears (n = 8; median, 83; IQR, 41–242.75); however, differences were not significant (P > .05). WOMAC pain scores were also not significant (P > .05) between patients with anterior cruciate ligament tears (n = 14; median, 110; IQR, 85–180) and patients without tears (n = 36; median, 127; IQR, 43.25–215). WOMAC pain and stiffness scores tended to be higher in patients with collateral ligamentous lesions (n = 7; median, 150; IQR, 100–200) than in those without lesions (n = 43; median, 77.5; 26.5–153), but again, these differences were not significant (P > .05).


    DISCUSSION
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
The results of this study show a significant relationship between the radiographic stages of osteoarthritis and the extent of associated MR imaging findings, including cartilage defects, bone marrow changes, and meniscal and ligamentous lesions; however, except for cartilage lesions, the clinical findings as assessed with the WOMAC scores were not significantly associated with the radiographic and MR imaging findings.

Although our findings appear difficult to comprehend initially, they are not completely surprising. In a recent study by Hannan et al (17), similar results were reported in an analysis of the cross-sectional data of the National Health and Nutrition Examination Survey, or NHANES I, with regard to three indicators of osteoarthritis of the knee: radiographic signs of osteoarthritis, self-reported knee pain, and a self-reported diagnosis of arthritis by a physician. These authors classified osteoarthritis in a manner analogous to the KL scale and found disease with a KL score of 2–4 in only 319 of the 6,880 (3.7%) patients enrolled in the study. Only 47% of this subset of patients reported knee pain, and only 61% were told by their physician that they had osteoarthritis. However, knee pain was reported by 1,004 of the 6,880 (14.6%) patients enrolled in their study, and only 15% of patients had osteoarthritis with a KL score of 2–4 on the basis of radiographic assessment, but 59% reported having a diagnosis of osteoarthritis assigned by a physician. Similar results were published by Meding et al (18), who analyzed 1,888 patients undergoing 2,759 knee arthroplasties and found that the degree of osteoarthritis as assessed on preoperative radiographs was independent of pain.

On the other hand, results of several studies (1921) showed that radiographic features of osteoarthritis of the knee were significantly associated with pain. Lethbridge-Cejku et al (19) examined patients who reported ever having knee pain or having current knee pain and found that pain, as reported, was associated with definite radiographic osteoarthritis (KL score >= 2); this pain definition, however, appears relatively vague. Since most of the patients in our study actually had (minor or major) pain (n = 47), and the degree of pain was not scored in most of those previous studies, these results are difficult to compare.

In our study, we used a well-established clinical scale (14,15) and correlated the calculated scores not only with radiographic signs but also with a number of typical MR imaging features of osteoarthritis (8,11). Investigators in most previous studies correlated radiographic signs of osteoarthritis and clinical findings, but again, these clinical findings were frequently not well defined or graded.

In contrast to KL scores, scores derived from cartilage findings at MR imaging were significantly associated with WOMAC scores. WOMAC pain and function scores were significantly lower in patients without cartilage defects than in those with cartilage defects. An interesting finding was the high WOMAC scores in the patients with grade IIa cartilage lesions; it may be hypothesized that clinical symptoms are most substantial at the onset of osteoarthritis, when cartilage defects occur. As cartilage damage progressed, a trend toward lower WOMAC pain and stiffness scores was shown in the present cross-sectional study, which may potentially be explained by the knee becoming more accustomed to the cartilage damage. The function score, however, stayed on a relatively high level.

In the present study, knee pain, function, and stiffness scores were not significantly associated with the presence or the amount of bone marrow edema. These findings are in contrast to results of a previous study by Felson et al (9). In their cross-sectional study, 401 patients with radiographically diagnosed osteoarthritis were analyzed; 351 had knee pain, and 50 had no knee pain. Seventy-eight percent of the patients with knee pain had bone marrow lesions, and 30% of those without knee pain had bone marrow lesions. Still, there is a substantial overlap. Since only three patients in our study had no knee pain, and two of these had no bone marrow edema, the comparison of the results of our study with those of Felson et al (9) is limited. As in our study, however, those authors showed that in patients with pain, severity of pain and bone marrow lesions were not associated.

Hill et al (10) showed that knee pain and the presence and amount of joint effusion on MR images were significantly associated. In a study population of 381 subjects with radiographically determined osteoarthritis and pain, as well as in 52 patients with signs of osteoarthritis but no pain, severe or moderate joint effusion was present in 55% of patients with pain but in only 16% of patients without pain. Distributions of popliteal cysts in patients with and patients without pain, however, were similar. In our study, neither the presence nor the amount of joint effusion or the presence of popliteal cysts was significantly associated with the clinical findings. However, there was a trend toward higher pain scores in patients with joint effusion.

The comparison of clinical, radiographic, and MR imaging findings in osteoarthritis may appear to be of more interest for the rheumatologist or orthopedic surgeon than for the radiologist. However, the radiologist must be aware of these associated findings when evaluating MR images, since the clinician will use the report and the MR images for therapeutic decision making. Even in a relatively advanced stage of osteoarthritis, a patient can be relatively free of symptoms, in which case, surgery may not be indicated.

Many osseous, cartilage, and ligamentous derangements are associated with osteoarthritis. One of the most eminent signs of osteoarthritis on MR images is changes in the hyaline cartilage. In our study, all knees with a KL grade of 4 showed advanced cartilage defects (groups IIb and III). Only seven of 50 knees showed no cartilage lesions. Fifteen of 21 knees with a KL grade of 1 or 2 showed cartilage lesions. These findings are in agreement with those in other studies concerning the sensitivity of MR imaging in the diagnosis of hyaline cartilage lesions as an early marker in osteoarthritis (2225). In our study, the grading of cartilage defects also correlated best with clinical findings.

A number of studies have been performed to improve the imaging of hyaline cartilage, including the application of optimized sequences, such as driven equilibrium (26), high-spatial-resolution techniques (27,28), T2 maps at 3 T (1), and contrast material–enhanced techniques (2). In the present study, we used a high-spatial-resolution fat-suppressed spoiled gradient-echo sequence for cartilage imaging, which is a standard sequence and is well suited to depict surface defects of cartilage (3,24,29) but may have limitations in depicting the cartilage structure. This may explain the small number of grade I cartilage lesions diagnosed in our study.

With the development of more sophisticated techniques for cartilage repair in osteoarthritis, such as new articular cartilage replacement techniques, including chondrocyte transplantation, improved osteochondral transplantation, chondroprotective agents, and cartilage growth stimulating factors (25,30), optimized MR imaging for diagnosis and therapy planning in osteoarthritis and for monitoring of these interventions is of growing importance.

In addition to cartilage lesions, another important finding in osteoarthritis is bone marrow edema. In our study, 13 of 16 knees with a KL score of 4 but only three of 10 knees with a KL score of 1 showed bone marrow edema pattern. Other investigators (9,11) also reported bone marrow edema pattern in advanced osteoarthritis. Zanetti et al (11) correlated bone marrow edema pattern and histologic findings in 16 patients with advanced osteoarthritis who underwent total knee replacement. At histologic examination, however, most of the areas with bone marrow edema pattern consisted of normal bone marrow, and only 11% of the analyzed areas showed bone marrow necrosis; 8%, abnormal trabeculae; 4%, bone marrow edema; 4%, bone marrow fibrosis; and 2%, bone marrow bleeding. Studies performed to classify prevalence and degree of bone marrow edema according to osteoarthritis stage, to our knowledge, have not yet been performed.

As shown by results of other studies (8,10), in addition to cartilage lesions and bone marrow edema, meniscal lesions, joint effusion, and popliteal cysts are associated with osteoarthritis. While Fernandez-Madrid et al (8) found meniscal degeneration and tears in 52% of 52 patients with a clinical and radiologic diagnosis of osteoarthritis, 92% (46 of 50) of patients in our study showed meniscal lesions, and 84% (42 of 50) showed meniscal tears. All of the knees with a KL score of 3 or 4 showed meniscal tears in our study. Joint effusion was found in 60% of patients in the study of Fernandez-Madrid et al (8) versus 76% in our study population.

Additional MR findings in osteoarthritis described in the literature include synovial thickening, subarticular cysts, bone attrition (flattening and depression), and central osteophytes (10,22,31,32). McCauley et al (32) analyzed MR images of the knee in 193 patients and found 35 central osteophytes in 29 patients. These patients were older and had more cartilage defects and osteophytes. As in that study, all except one of our patients with central osteophytes had grade IIb or III cartilage lesions. Central osteophytes were found most frequently in osteoarthritis with a KL score of 4.

In our study, we also demonstrated a large number of ligamentous lesions (anterior cruciate ligament tears and collateral ligament sprains or tears) associated with advanced osteoarthritis. Since none of these patients had a history of trauma that would explain an anterior cruciate ligament tear, a degenerative cause is most likely. Collateral ligament sprains were located at the most severely damaged joint compartment (mostly medially) and may be explained by stress due to altered biomechanical loading of the knee.

Potential limitations of the present study are that a relatively small number of patients were examined in each group and that arthroscopy to confirm the presence or absence of a meniscal tear, cartilage defect, or ligament injury was not performed.

In conclusion, results of the present study show that a number of osseous, cartilaginous, synovial, ligamentous, and meniscal lesions depicted on MR images are associated with osteoarthritis and that the extent of these lesions correlates with radiographically determined KL scores. However, radiologists should be aware that these findings do not correlate with clinical findings (represented by the WOMAC scores in our study). Radiographic KL scores and clinical WOMAC scores were not associated, while among the MR imaging findings, only cartilage lesions were significantly associated with clinical findings.


    ACKNOWLEDGMENTS
 
We thank Cynthia Frazier, research associate, for her support with data acquisition and management.


    FOOTNOTES
 
Abbreviations: IQR = interquartile range, KL = Kellgren-Lawrence, WOMAC = Western Ontario and McMaster University

Author contributions: Guarantors of integrity of entire study, T.M.L., S.M., L.S.S.; study concepts and design, T.M.L., S.M., L.S.S.; literature research, T.M.L., S.G.; clinical studies, M.R., N.L., T.M.L., L.S.S.; data acquisition, T.M.L., L.S.S., S.G.; data analysis/interpretation, T.M.L., L.S.S., S.G., Y.L., S.M.; statistical analysis, Y.L., T.M.L., S.G.; manuscript preparation, T.M.L., S.M.; manuscript definition of intellectual content, editing, and revision/review, T.M.L., L.S.S., S.M., Y.L.; manuscript final version approval, T.M.L., L.S.S., S.M.


    REFERENCES
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 

  1. Mosher TJ, Dardzinski BJ, Smith MB. Human articular cartilage: influence of aging and early symptomatic degeneration on the spatial variation of T2—preliminary findings at 3 T. Radiology 2000; 214:259-266.[Abstract/Free Full Text]
  2. Trattnig S, Mlynarik V, Breitenseher M, et al. MRI visualization of proteoglycan depletion in articular cartilage via intravenous administration of Gd-DTPA. Magn Reson Imaging 1999; 17:577-583.[CrossRef][Medline]
  3. Recht MP, Piraino DW, Paletta GA, Schils JP, Belhobek GH. Accuracy of fat-suppressed three-dimensional spoiled gradient-echo FLASH MR imaging in the detection of patellofemoral articular cartilage abnormalities. Radiology 1996; 198:209-212.[Abstract/Free Full Text]
  4. Peterfy CG, van Dijke CF, Janzen DL, et al. Quantification of articular cartilage in the knee with pulse saturation transfer subtraction and fat-suppressed MR imaging: optimization and validation. Radiology 1994; 192:485-491.[Abstract/Free Full Text]
  5. Peterfy CG, van Dijke CF, Lu Y, et al. Quantification of the volume of articular cartilage in the metacarpophalangeal joints of the hand: accuracy and precision of three-dimensional MR imaging. AJR Am J Roentgenol 1995; 165:371-375.[Abstract/Free Full Text]
  6. Hohe J, Faber S, Stammberger T, Reiser M, Englmeier K, Eckstein F. A technique for 3D in vivo quantification of proton density and magnetization transfer coefficients of knee joint cartilage. Osteoarthritis Cartilage 2000; 8:426-433.[CrossRef][Medline]
  7. Hyhlik-Durr A, Faber S, Burgkart R, et al. Precision of tibial cartilage morphometry with a coronal water-excitation MR sequence. Eur Radiol 2000; 10:297-303.[CrossRef][Medline]
  8. Fernandez-Madrid F, Karvonen RL, Teitge RA, Miller PR, Negendank WG. MR features of osteoarthritis of the knee. Magn Reson Imaging 1994; 12:703-709.[CrossRef][Medline]
  9. Felson DT, Chaisson CE, Hill CL, et al. The association of bone marrow lesions with pain in knee osteoarthritis. Ann Intern Med 2001; 134:541-549.[Abstract/Free Full Text]
  10. Hill CL, Gale DG, Chaisson CE, et al. Knee effusions, popliteal cysts, and synovial thickening: association with knee pain in osteoarthritis. J Rheumatol 2001; 28:1330-1337.[Medline]
  11. 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.[Abstract/Free Full Text]
  12. Kellgren J, Lawrence J. Radiological assessment of osteoarthritis. Ann Rheum Dis 1957; 16:494-501.
  13. Hart D, Spector T. Assessment of changes in joint tissues in patients treated with a disease-modifying osteoarthritis drug (DMOAD): monitoring outcomes In: Osteoarthritis. Oxford, England: Oxford University Press, 1998; 450-458.
  14. Bellamy N, Buchanan WW, Goldsmith CH, Campbell J, Stitt LW. Validation study of WOMAC: a health status instrument for measuring clinically important patient relevant outcomes to antirheumatic drug therapy in patients with osteoarthritis of the hip or knee. J Rheumatol 1988; 15:1833-1840.[Medline]
  15. Creamer P, Lethbridge-Cejku M, Hochberg MC. Determinants of pain severity in knee osteoarthritis: effect of demographic and psychosocial variables using 3 pain measures. J Rheumatol 1999; 26:1785-1792.[Medline]
  16. Noyes FR, Stabler CL. A system for grading articular cartilage lesions at arthroscopy. Am J Sports Med 1989; 17:505-513.[Abstract/Free Full Text]
  17. Hannan MT, Felson DT, Pincus T. Analysis of discordance between radiographic changes and knee pain in osteoarthritis of the knee. J Rheumatol 2000; 27:1513-1517.[Medline]
  18. Meding JB, Ritter MA, Faris PM, Keating EM, Harris W. Does the preoperative radiographic degree of osteoarthritis correlate to the results in primary total knee arthroplasty? J Arthroplasty 2001; 16:13-16.
  19. Lethbridge-Cejku M, Scott WW, Reichle R, et al. Association of radiographic features of osteoarthritis of the knee with knee pain: data from the Baltimore Longitudinal Study of Aging. Arthritis Care Res 1995; 8:182-188.[Medline]
  20. Boegard T, Rudling O, Petersson IF, Jonsson K. Correlation between radiographically diagnosed osteophytes and magnetic resonance detected cartilage defects in the tibiofemoral joint. Ann Rheum Dis 1998; 57:401-407.[Abstract/Free Full Text]
  21. Boegard T, Rudling O, Petersson IF, Jonsson K. Correlation between radiographically diagnosed osteophytes and magnetic resonance detected cartilage defects in the patellofemoral joint. Ann Rheum Dis 1998; 57:395-400.[Abstract/Free Full Text]
  22. Boegard TL, Rudling O, Pettersson IF, Jonsson K. Magnetic resonance imaging in the knee in chronic knee pain. A 2-year follow-up. Osteoarthritis Cartilage 2001; 9:473-480.
  23. Kawahara Y, Uetani M, Nakahara N, et al. Fast spin-echo MR of the articular cartilage in the osteoarthrotic knee: correlation of MR and arthroscopic findings. Acta Radiol 1998; 39:120-125.[Medline]
  24. Uhl M, Allmann KH, Tauer U, et al. Comparison of MR sequences in quantifying in vitro cartilage degeneration in osteoarthritis of the knee. Br J Radiol 1998; 71:291-296.[Abstract]
  25. Waldschmidt JG, Braunstein EM, Buckwalter KA. Magnetic resonance imaging of osteoarthritis. Rheum Dis Clin North Am 1999; 25:451-465.[CrossRef][Medline]
  26. Hargreaves BA, Gold GE, Lang PK, et al. MR imaging of articular cartilage using driven equilibrium. Magn Reson Med 1999; 42:695-703.[CrossRef][Medline]
  27. Rubenstein JD, Li JG, Majumdar S, Henkelman RM. Image resolution and signal-to-noise ratio requirements for MR imaging of degenerative cartilage. AJR Am J Roentgenol 1997; 169:1089-1096.[Abstract/Free Full Text]
  28. Link TM, Majumdar S, Peterfy C, et al. High resolution MRI of small joints: impact of spatial resolution on diagnostic performance and SNR. Magn Reson Imaging 1998; 16:147-155.[CrossRef][Medline]
  29. Peterfy CG, Genant HK. Emerging applications of magnetic resonance imaging in the evaluation of articular cartilage. Radiol Clin North Am 1996; 34:195-213.[Medline]
  30. McCauley TR, Disler DG. Magnetic resonance imaging of articular cartilage of the knee. J Am Acad Orthop Surg 2001; 9:2-8.[Abstract/Free Full Text]
  31. Fernandez-Madrid F, Karvonen RL, Teitge RA, Miller PR, An T, Negendank WG. Synovial thickening detected by MR imaging in osteoarthritis of the knee confirmed by biopsy as synovitis. Magn Reson Imaging 1995; 13:177-183.[CrossRef][Medline]
  32. McCauley TR, Kornaat PR, Jee WH. Central osteophytes in the knee: prevalence and association with cartilage defects on MR imaging. AJR Am J Roentgenol 2001; 176:359-364.[Abstract/Free Full Text]



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