Predictive and concurrent validity of cartilage thickness change as a marker of knee osteoarthritis progression: data from the Osteoarthritis Initiative

被引:45
作者
Wirth, W. [1 ,2 ]
Hunter, D. J. [3 ,4 ]
Nevitt, M. C. [5 ]
Sharma, L. [6 ]
Kwoh, C. K. [7 ]
Ladel, C. [8 ]
Eckstein, F. [1 ,2 ]
机构
[1] Paracelsus Med Univ Salzburg & Nuremberg, Inst Anat, Salzburg, Austria
[2] Chondrometrics GmbH, Ainring, Germany
[3] Univ Sydney, Royal North Shore Hosp, Dept Rheumatol, Sydney, NSW, Australia
[4] Univ Sydney, Kolling Inst, Inst Bone & Joint Res, Sydney, NSW, Australia
[5] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
[6] Northwestern Univ, Chicago, IL 60611 USA
[7] Univ Arizona, Arthrit Ctr, Div Rheumatol, Tucson, AZ USA
[8] Merck KGaA, Darmstadt, Germany
基金
美国国家卫生研究院;
关键词
Cartilage thickness; MRI; Osteoarthritis; Progression; OA BIOMARKERS CONSORTIUM; REPLACEMENT; FOUNDATION; VALIDATION; COHORT; RATES; FNIH; PAIN; MRI;
D O I
10.1016/j.joca.2017.08.005
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Objective: To investigate the predictive and concurrent validity of magnetic resonance imaging (MRI)-based cartilage thickness change between baseline (BL) and year-two (Y2) follow-up (predictive validity) and between Y2 and Y4 follow-up (concurrent validity) for symptomatic and radiographic knee osteoarthritis (OA) progression during Y2 -> Y4. Methods: 777 knees from 777 Osteoarthritis Initiative (OAI) participants (age: 61.3 +/- 9.0 years, BMI: 30.1 +/- 4.8 kg/m(2)) with Kellgren Lawrence (KL) grade 1-3 at Y2 (visit before progression interval) had cartilage thickness measurements from 3T MRI at BL, Y2 (n = 777), and Y4 (n = 708). Analysis of covariance and logistic regression were used to assess the association of pain progression (>= 9 WOMAC units [scale 0-100], n = 205/572 with/without progression) and radiographic progression (>= 0.7 mm minimum joint space width (mJSW) loss, n = 166/611 with/without progression) between Y2 and Y4 with preceding (BL -> Y2) and concurrent (Y2 -> Y4) change in central medial femorotibial (cMFTC) compartment cartilage thickness. Results: Symptomatic progression was associated with concurrent (Y2 -> Y4: - 305 +/- 470 mu m vs - 155 +/- 346 mu m, Odds ratios (OR) = 1.5 [1.2, 1.7]) but not with preceding cartilage thickness loss in cMFTC (- 150 +/- 276 mu m vs - 151 +/- 299 mu m, OR = 0.9 95% CI: [0.8, 1.1]). Radiographic progression, in contrast, was significantly associated with both concurrent (- 542 +/- 550 mu m vs - 98 +/- 255 mu m, OR = 3.4 [2.6, 4.3]) and preceding cMFTC thickness loss (- 229 +/- 355 mu m vs - 130 +/- 270 mu m, OR = 1.3 [1.1, 1.5]). Conclusions: These results extend previous reports that did not discern predictive vs concurrent associations of cartilage thickness loss with OA progression. The observed predictive and concurrent validity of cartilage thickness loss for radiographic progression and observed concurrent validity for symptomatic progression provide an important step in qualifying cartilage thickness loss as a biomarker of knee OA progression. (C) 2017 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:2063 / 2071
页数:9
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