Session Information
Session Type: Abstract Submissions (ACR)
Background/Purpose: The clinical significance of pre-radiographic MRI lesions in persons at risk for knee OA is unclear. Understanding whether such lesions are inconsequential or early disease will aid prevention and disease-modifying strategy design. We hypothesized, in persons at risk but without radiographic OA, that cartilage damage, bone marrow lesions (BML), meniscal tear (MT), and meniscal extrusion (ME) are each associated with 1) prevalent frequent knee symptoms and 2) incident persistent knee symptoms.
Methods: The Osteoarthritis Initiative is a cohort study of men and women age 45-79 years with or at increased risk to develop knee OA. 850 participants were bilateral K/L 0 at 12 months. In their 12-month right knee (left if right inadequate) MR images, we assessed cartilage, BML, MT, and ME using a modified MOAKS system, blinding readers to hypotheses and all other data. At baseline, of the 850, 578 were without frequent knee symptoms (knee symptoms or medication use for knee symptoms most days of a month in the past 12 months). Incident persistent knee symptoms were defined as frequent knee symptoms at 2 consecutive annual OAI visits. Multiple logistic regression models evaluated associations between each lesion and 1) prevalent frequent symptoms and 2) incident persistent symptoms by 60 months, adjusting for age, gender, BMI, knee injury, and knee surgery.
Results: As shown in Table 1, cartilage damage, BML, and ME were each associated with prevalent frequent knee symptoms. As shown in Table 2, cartilage damage and BML (particularly patellofemoral), and MT were each associated with incident persistent symptoms.
Conclusion: In persons at higher risk but without any evidence of radiographic knee OA, cartilage damage, BML, ME, and BMI were associated with prevalent frequent knee symptoms, and cartilage damage, BML, MT, and BMI with the new development of persistent symptoms by 5 years. These findings suggest that these lesions, in persons at higher risk for knee OA, are clinically significant and may represent early disease.
Table 1. Pre-radiographic MRI Lesions and Risk of Prevalent Frequent Knee Symptoms
n = 850 persons K/L 0 in both knees [mean age 59.6 years (8.8, SD), BMI 26.7 kg/m2 (4.2), 475 (55.9%) women].
(TF = tibiofemoral, PF = patellofemoral)
|
Number of knees (1 knee per person) |
Number of knees (row%) with frequent knee symptoms |
OR (95% CI) Unadjusted |
OR (95% CI) Adjusted for age, gender, BMI, previous knee injury, previous knee surgery |
Cartilage damage (TF or PF) |
642 |
178 (27.7%) |
1.81 (1.21, 2.69) |
1.75 (1.16, 2.63)* |
Cartilage damage (TF only) |
118 |
27 (22.9%) |
0.86 (0.54, 1.36) |
0.78 (0.49, 1.26)* |
Cartilage damage (PF only) |
257 |
64 (24.9%) |
0.98 (0.70, 1.37) |
0.95 (0.67, 1.35)* |
Cartilage damage (TF and PF) |
266 |
87 (32.7%) |
1.73 (1.26, 2.40) |
1.85 (1.32, 2.59)* |
No cartilage damage (TF or PF) |
208 |
36 (17.3%) |
reference |
reference |
|
|
|
|
|
BML (TF or PF) |
515 |
155 (30.1%) |
2.00 (1.42, 2.80) |
1.95 (1.38, 2.76)* |
BML (TF only) |
79 |
21 (26.6%) |
1.08 (0.64, 1.82) |
1.04 (0.60, 1.79)* |
BML (PF only) |
289 |
84 (29.1%) |
1.34 (0.98, 1.87) |
1.38 (0.99, 1.92)* |
BML (TF and PF) |
147 |
50 (34.0%) |
1.68 (1.15, 2.47) |
1.62 (1.09, 2.40)* |
No BML (TF or PF) |
335 |
59 (17.6%) |
reference |
reference |
|
|
|
|
|
MT |
180 |
51 (28.3%) |
1.22 (0.84, 1.77) |
1.22 (0.82, 1.81)* |
No MT |
670 |
163 (24.3%) |
reference |
reference |
|
|
|
|
|
ME |
117 |
39 (33.3%) |
1.58 (1.04, 2.41) |
1.67 (1.08, 2.59)* |
No ME |
733 |
175 (23.9%) |
reference |
reference |
* BMI also significant
Table 2. Pre-radiographic MRI Lesions and Risk of Incident Persistent Knee Symptoms
n = 578 persons K/L 0 in both knees and without frequent knee symptoms at baseline [mean age 59.3 years (9.0), BMI 26.6 kg/m2 (4.3), 324 (56.1%) women].
|
Number of knees (1 knee per person) |
Number of knees (row%) with incident persistent knee symptoms |
OR (95% CI) Unadjusted |
OR (95% CI) Adjusted for age, gender, BMI, previous knee injury, previous knee surgery |
Cartilage damage (TF or PF) |
423 |
86 (20.3%) |
1.94 (1.13, 3.35) |
1.72 (0.98, 3.02)* |
Cartilage damage (TF only) |
84 |
13 (15.5%) |
1.39 (0.65, 3.01) |
1.17 (0.51, 2.73)* |
Cartilage damage (PF only) |
178 |
38 (21.3%) |
2.07 (1.12, 3.80) |
1.98 (1.04, 3.75)* |
Cartilage damage (TF and PF) |
161 |
35 (21.7%) |
2.11 (1.14, 3.92) |
2.00 (1.04, 3.84) |
No cartilage damage (TF or PF) |
155 |
18 (11.6%) |
reference |
reference |
|
|
|
|
|
BML (TF or PF) |
337 |
75 (22.3%) |
2.09 (1.31, 3.33) |
1.90 (1.18, 3.06)* |
BML (TF only) |
48 |
9 (18.8%) |
1.69 (0.74, 3.84) |
1.42 (0.58, 3.45)** |
BML (PF only) |
197 |
43 (21.8%) |
2.04 (1.22, 3.42) |
1.82 (1.07, 3.08) |
BML (TF and PF) |
92 |
23 (25.0%) |
2.44 (1.32, 4.49) |
2.31 (1.24, 4.31) |
No BML (TF or PF) |
241 |
29 (12.0%) |
reference |
reference |
|
|
|
|
|
MT |
109 |
30 (27.5%) |
2.03 (1.24, 3.30) |
1.97 (1.17, 3.33)* |
No MT |
469 |
74 (15.8%) |
reference |
reference |
|
|
|
|
|
ME |
61 |
18 (29.5%) |
2.10 (1.16, 3.81) |
1.69 (0.90, 3.18)* |
No ME |
517 |
86 (16.6%) |
reference |
reference |
*BMI also significant
**Previous surgery also significant
Disclosure:
L. Sharma,
None;
J. S. Chmiel,
None;
O. Almagor,
None;
D. D. Dunlop,
None;
M. C. Hochberg,
Abbvie, Inc,
5,
Bioiberica SA,
5,
Eli Lilly and Company,
5,
Genentech, Inc,
5,
Iroko Pharmaceuticals, LLC,
5,
Merck, Inc,
5,
Novartis Pharma AG,
5,
Pfizer, Inc,
5,
Savient Pharmaceuticals,
5;
C. Eaton,
None;
C. K. Kwoh,
None;
R. D. Jackson,
NIH,
2;
J. M. Bathon,
None;
A. Guermazi,
Boston Imaging Core Lab,
1,
Merck Serono,
5,
Sanofi-Aventis Pharmaceutical,
5,
TissueGene,
5;
F. Roemer,
BICL, LLC,
1,
BICL, LLC,
3,
Merck-Serono,
5;
M. Crema,
BICL, LLC,
1,
BICL, LLC,
3;
W. J. Mysiw,
None;
M. C. Nevitt,
None.
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