骨关节炎是一种多关节疾病。是吗?

M.A. van den Berg , E. Panfilov , J.H. Krijthe , R. Agricola , A. Tiulpin
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引用次数: 0

摘要

oa经常影响髋关节和膝关节;然而,大多数预后研究单独评估这些关节。鉴于它们之间的生物力学和系统联系,这种关节特异性的关注可能会忽略疾病进展的重要模式。更好地了解髋关节和膝关节骨性关节炎的进展可以支持更准确的预测模型和治疗策略的发展。目的:确定与单独的OA进展相比,髋关节和膝关节合并OA进展是否表现出不同的表型。方法:本研究使用了OAI数据,其中包括年龄在45-79岁之间有患膝关节OA风险的参与者的数据。该数据集包括基线和48个月随访时获得的双侧膝关节后前位x线片和标准化负重骨盆前位x线片。人工测量膝关节最小JSW (mJSW),自动测量髋关节最小JSW。骨性关节炎进展定义为任意髋关节JSN≥0.5 mm或任意膝关节JSN≥0.7 mm。在48个月的随访中,四个关节中任何一个没有JSN的参与者被排除在外。选择的参与者被分类为孤立(髋关节或膝关节)或合并(髋关节和膝关节)进展。采用结合临床和结构基线特征的逻辑回归模型来探讨联合进展与孤立进展的关系。根据KLG和改良的Croft分级,将4个关节的基线放射学OA (ROA)状态分为无ROA(0)、早期ROA(1)和明确ROA(2)。调整比值比(aOR)及其95%置信区间,使用10,000次迭代的bootstrapping估计,并评估模型的拟合优度。结果纳入的1190名ROA进展的参与者(平均年龄61.5±8.8岁;Bmi 29.1±4.5;女性占55.1%),合并ROA进展281例(23.6%)。我们描述性地回顾了髋关节和膝关节ROA基线分级的共同发生情况(表1)。在该人群中观察到的相对较小的合并进展患病率阻止了在我们的模型中包括这些ROA状态相互作用效应。logistic模型比仅截距模型(似然比检验,p <;0.0001),可接受的拟合优度(Hosmer-Lemeshow检验,p = 0.40)。与孤立患者相比,一些基线特征与合并进展的几率更高相关,包括年龄较大、女性、右膝内翻、髋关节mJSW较高以及左髋关节有明确的ROA(图1)。有趣的是,右髋关节有ROA或左膝外翻会降低合并进展的几率。结论:我们的研究结果表明,髋关节和膝关节骨性关节炎的进展可能代表一种具有可识别特征的独特临床表型。虽然模型显示了统计上显著的关联,并证明了足够的拟合,但这些结果应谨慎解释。需要更大、更多样化的数据集来进一步验证这些发现,并研究多关节骨关节炎进展的异质性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
OSTEOARTHRITIS IS A MULTI-JOINT DISEASE. OR IS IT?

INTRODUCTION

OA frequently affects both the hip and knee joints; however, most prognostic studies evaluate these joints in isolation. Given the biomechanical and systemic connections between them, this joint-specific focus may overlook important patterns of disease progression. A better understanding of combined hip and knee OA progression could support the development of more accurate prediction models and treatment strategies.

OBJECTIVE

To determine whether combined hip and knee OA progression exhibits a distinct phenotype compared to isolated OA progression.

METHODS

This study used the OAI data, which comprises data from participants aged 45–79 years at risk of developing knee OA. The dataset features bilateral posteroanterior knee radiographs and standardized weight-bearing anteroposterior pelvic radiographs obtained at the baseline and 48-month follow-up visits. Minimal JSW (mJSW) was measured manually for knees and automatically for hips. OA progression was defined as JSN of ≥0.5 mm in either hip or ≥0.7 mm in either knee. Participants with no JSN in any of the four joints at the 48-month follow-up were excluded. The selected participants were classified as having isolated (either hip or knee) or combined (both hip and knee) progression. A logistic regression model incorporating clinical and structural baseline features was used to explore associations with combined progression compared to isolated progression. Baseline radiographic OA (ROA) status of each of the four joints was classified as no ROA (0), early ROA (1) and definite ROA (2) based on the KLG and modified Croft grades. Adjusted odds ratios (aOR) and their 95% confidence intervals, estimated using bootstrapping with 10,000 iterations, and the goodness-of-fit of the model were assessed.

RESULTS

Among the 1,190 included participants with any ROA progression (mean age 61.5 ± 8.8 years; BMI 29.1 ± 4.5; 55.1% female), 281 (23.6%) showed combined ROA progression. The co-occurrence of baseline hip and knee ROA grades was reviewed descriptively (Table 1). The observed relatively small prevalence of combined progression in this population prevented including these ROA status interaction effects within our model. The logistic model showed improved fit over an intercept-only model (likelihood ratio test, p < 0.0001), and acceptable goodness-of-fit (Hosmer-Lemeshow test, p = 0.40). Several baseline features were associated with higher odds of combined progression compared to isolated, including older age, female sex, varus knee alignment in the right knee, higher mJSW in the hip, and having definite ROA in the left hip (Figure 1). Interestingly, having ROA in the right hip or valgus knee alignment in the left knee would decrease the odds of combined progression.

CONCLUSION

Our findings suggest that combined hip and knee OA progression may represent a distinct clinical phenotype with identifiable characteristics. While the model showed statistically significant associations and demonstrated adequate fit, these results should be interpreted cautiously. Larger and more diverse datasets are needed to further validate these findings and investigate the heterogeneity of multi-joint OA progression.
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Osteoarthritis imaging
Osteoarthritis imaging Radiology and Imaging
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