膝关节超声诊断骨关节炎的共同变异模式:机器学习方法。

Sahar Sawani, Liubov Arbeeva, Katherine A Yates, Carolina Alvarez, Todd A Schwartz, Serena Savage-Guin, Jordan B Renner, Catherine J Bakewell, Minna J Kohler, Janice Lin, Jonathan Samuels, Amanda E Nelson
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引用次数: 0

摘要

目的:利用一种新的机器学习方法,基于人口统计学和临床变量、症状和超声(US)特征来识别膝骨关节炎(KOA)的表型。设计:约翰斯顿县健康研究参与者提供人口统计学、症状和功能评估以及关节x线片,这些数据被转化为临床数据块。得到标准化的膝关节US, US特征组成第二个数据块。基于角度的联合和个体变异解释(AJIVE)算法用于识别共享和个体变异模式。我们将重点放在共享结构上,以探索美国特征和非美国临床数据在总体上是如何变化的,以及在放射学KOA (rKOA)的子集中。结果:该分析包括861名参与者(平均年龄55岁,平均BMI 33 kg/m2);335例(39%)有rKOA。AJIVE确定了共享变异的两个组成部分(SC1和SC2)。BMI较高、年龄较大、症状和结局评分较差的美国患者出现SC1相关骨赘和软骨损伤。SC2将积液和滑膜炎的存在联系起来,但较少的软骨损伤与较好的身体功能和较低的BMI相关。rKOA患者也有类似的情况。结论:我们确定了两个共同的变异方向,这可能代表不同的KOA表型。第一个符合先前的KOA研究,将骨赘和软骨损伤的存在与更严重的症状和功能联系起来。第二种可能代表KOA的炎症亚型,有更多的积液和滑膜炎,但较少的骨赘病和软骨损伤。这些临床可行的表型应在未来的研究中得到证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Patterns of Shared Variation in Knee Ultrasound for Osteoarthritis: A Machine Learning Approach.

Objective: To identify phenotypes of knee osteoarthritis (KOA) based on demographic and clinical variables, symptoms, and ultrasound (US) features using a novel machine learning approach.

Design: Johnston County Health Study participants provided demographics, symptomatic and functional assessments, and joint radiographs, which were transformed into the clinical data block. Standardized knee US were obtained, and US features composed the second data block. The Angle-based Joint and Individual Variation Explained (AJIVE) algorithm was used to identify shared and individual modes of variation. We focused on shared structure to explore how US features and non-US clinical data vary together overall, and in the subset with radiographic KOA (rKOA).

Results: This analysis included 861 participants (mean age 55 years, mean BMI 33 kg/m2); 335 (39%) had rKOA. AJIVE identified two components of shared variation (SC1 and SC2). SC1 associated osteophytes and cartilage damage on US with higher BMI, older age, and worse symptoms and outcome scores. SC2 correlated the presence of effusion and synovitis but less cartilage damage on US with better physical function and lower BMI. A similar pattern was seen in those with rKOA.

Conclusions: We identified two shared directions of variation which may represent distinct phenotypes of KOA. The first fits with prior KOA studies linking presence of osteophytes and cartilage damage to worse symptoms and function. The second may represent an inflammatory subtype of KOA, with greater effusion and synovitis but less osteophytosis and cartilage damage. These clinically feasible phenotypes should be confirmed in future studies.

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Osteoarthritis imaging
Osteoarthritis imaging Radiology and Imaging
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