Harkey Matthew S, Davis Julie E, Lu Bing, Price Lori Lyn, Eaton Charles B, Lo Grace H, Barbe Mary F, Ward Robert J, Zhang Ming, Liu Shao-Hsien, Lapane Kate L, MacKay James W, McAlindon Timothy E, Driban Jeffrey B
Division of Rheumatology, Allergy, and Immunology, Tufts Medical Center, Boston, Massachusetts.
Department of Quantitative Health Sciences, University of Massachusetts Medical School, Worcester, Massachusetts.
Clin Anat. 2019 Apr;32(3):369-378. doi: 10.1002/ca.23321. Epub 2018 Dec 26.
We compared the spatial distribution of tibiofemoral cartilage change between individuals who will develop accelerated knee osteoarthritis (KOA) versus typical onset of KOA prior to the development of radiographic KOA. We conducted a longitudinal case-control analysis of 129 individuals from the Osteoarthritis Initiative. We assessed the percent change in tibiofemoral cartilage on magnetic resonance images at 36 informative locations from 2 to 1 year prior to the development of accelerated (n = 44) versus typical KOA (n = 40). We defined cartilage change in the accelerated and typical KOA groups at 36 informative locations based on thresholds of cartilage percent change in a no KOA group (n = 45). We described the spatial patterns of cartilage change in the accelerated KOA and typical KOA groups and performed a logistic regression to determine if diffuse cartilage change (predictor; at least half of the tibiofemoral regions demonstrating change in multiple informative locations) was associated with KOA group (outcome). There was a non-significant trend that individuals with diffuse tibiofemoral cartilage change were 2.2 times more likely to develop accelerated knee OA when compared with individuals who develop typical knee OA (OR [95% CI] = 2.2 [0.90-5.14]. Adults with accelerated or typical KOA demonstrate heterogeneity in spatial distribution of cartilage thinning and thickening. These results provide preliminary evidence of a different spatial pattern of cartilage change between individuals who will develop accelerated versus typical KOA. These data suggest there may be different mechanisms driving the early structural disease progression between accelerated versus typical KOA. Clin. Anat. 32:369-378, 2019. © 2018 Wiley Periodicals, Inc.
我们比较了将发展为膝关节骨性关节炎(KOA)加速进展型的个体与在影像学KOA出现之前KOA典型发病个体之间胫股关节软骨变化的空间分布。我们对来自骨关节炎倡议组织的129名个体进行了纵向病例对照分析。我们在加速进展型KOA(n = 44)与典型KOA(n = 40)出现前2至1年,评估了磁共振图像上36个信息丰富位置的胫股关节软骨百分比变化。我们根据无KOA组(n = 45)的软骨百分比变化阈值,定义了加速进展型和典型KOA组中36个信息丰富位置的软骨变化。我们描述了加速进展型KOA组和典型KOA组软骨变化的空间模式,并进行了逻辑回归分析,以确定弥漫性软骨变化(预测因素;胫股关节区域至少一半在多个信息丰富位置显示变化)是否与KOA组(结果)相关。与发生典型膝关节OA的个体相比,胫股关节软骨弥漫性变化的个体发生膝关节OA加速进展的可能性高2.2倍,这一趋势无统计学意义(OR [95% CI] = 2.2 [0.90 - 5.14])。加速进展型或典型KOA的成年人在软骨变薄和增厚的空间分布上表现出异质性。这些结果为将发展为加速进展型与典型KOA的个体之间软骨变化的不同空间模式提供了初步证据。这些数据表明,加速进展型与典型KOA之间早期结构疾病进展的驱动机制可能不同。《临床解剖学》32:369 - 378,2019年。© 2018威利期刊公司
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