膝关节骨关节炎纵向探索性研究中髌下脂肪垫形态的综合比较分析:对其作为独立预后标志作用的新认识

IF 4.9 2区 医学 Q1 Medicine
Jean-Pierre Pelletier, Patrice Paiement, François Abram, Marc Dorais, Jean-Pierre Raynauld, Johanne Martel-Pelletier
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引用次数: 0

摘要

没有既定的标志物可以有效地将膝骨关节炎(OA)患者表型划分为亚组。髌下脂肪垫(IPFP)形态学数据可以预测疾病症状,结构变化和膝关节置换术(KR)是稀疏和相互矛盾的。这项为期96个月的纵向探索性研究旨在确定哪些IPFP形态特征是针对这些结果最有效的独立预后标志物。这项纵向研究分析了来自骨关节炎倡议(OAI)进展队列的1075个目标膝关节(每个参与者一个膝关节)。结构变化包括软骨、骨髓病变(BMLs)和关节积液量,使用自动定量磁共振成像系统(MRI)进行评估。使用MRI结合新开发的全自动神经元驱动技术评估IPFP总体和信号(高和低)强度体积和区域。使用WOMAC评分对症状进行评估。KR的数据来自OAI数据库。在基线和12、24、48和96个月收集数据,并使用重复测量混合模型(MMRM)或ANCOVA进行分析。基线特征为轻度至中度膝关节炎。随着时间的推移,疾病症状(WOMAC)、软骨体积、IPFP总体和低信号体积、最大和低信号区域均下降(均p≤0.001)。关节积液和高信号体积和面积增加(p≤0.001)。包涵处IPFP形态与软骨体积(低信号和高信号体积,48、96个月,p≤0.04)、BML体积(整体体积,48个月,p=0.05;高信号面积,12个月,p≤0.04),积液量(低信号48个月,高信号96个月,p≤0.05)。纳入时,较小的IPFP大小(低于中位数)与96个月的累积KR相关(总体和低信号体积,p≤0.04,最大面积,p=0.05)。这项利用全自动技术的纵向探索性研究强调,i) IPFP体积(全局和两个信号)在预测OA的长期结构变化方面优于面积指标,ii) IPFP体积和面积较小与KR需求减少有关。这些发现为IPFP形态作为膝关节OA预后预测生物标志物的有用性提供了新的见解,为膝关节OA患者分层提供了一种新的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comprehensive comparative analysis of infrapatellar fat pad morphologies in a longitudinal knee osteoarthritis exploratory study: new insights into its role as an independent prognostic marker
No established markers can effectively phenotype knee osteoarthritis (OA) patients into subgroups. Infrapatellar fat pad (IPFP) morphology data that can forecast disease symptoms, structural changes, and knee replacement (KR) are sparse and conflicting. This 96-month longitudinal exploratory study aimed to identify which IPFP morphological features were the most effective independent prognostic markers against these outcomes. This longitudinal study analyzed 1075 target knees (one knee per participant) from the Osteoarthritis Initiative (OAI) progression cohort. Structural changes include cartilage, bone marrow lesions (BMLs), and joint effusion volumes assessed using automated and quantitative magnetic resonance imaging systems (MRI). The IPFP global and signal (hyper- and hypo-) intensity volumes and areas were assessed using MRI combined with a newly developed, fully automated neuron-driven technology. Symptoms were evaluated using WOMAC scores. Data on KR was obtained from the OAI database. Data were collected at baseline and 12, 24, 48 and 96 months and analyzed using a mixed model for repeated measures (MMRM) or ANCOVA. The baseline characteristics were mild to moderate knee OA. Over time, disease symptoms (WOMAC), cartilage volume, IPFP global and hypointense signal volumes, and maximal and hypointense signal areas decreased (all p≤0.001). Joint effusion and hyperintense signal volume and area increased (both p≤0.001). Associations were found between IPFP morphologies at inclusion and changes in cartilage volume (hypointense and hyperintense volumes, 48, 96 months, p≤0.04), BML volume (global volume 48 months, p=0.05; hyperintense area, 12 months, p≤0.04), and effusion volume (hypointense volume 48 months and hyperintense volume 96 months, p≤0.05). At inclusion, smaller IPFP sizes (below median) were associated with cumulative KR at 96 months (global and hypointense volumes, p≤0.04 and maximum area, p=0.05). This longitudinal exploratory study, leveraging a fully automated technology, highlights that i) IPFP volume (global and both signals) is superior to area metrics in predicting long-term structural changes in OA, and ii) smaller IPFP volume and area are linked with reduced need for KR. These findings provide new insights into the usefulness of IPFP morphology as a predictive biomarker of knee OA outcomes, offering a new approach to stratifying knee OA patients.
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来源期刊
CiteScore
8.60
自引率
2.00%
发文量
261
审稿时长
14 weeks
期刊介绍: Established in 1999, Arthritis Research and Therapy is an international, open access, peer-reviewed journal, publishing original articles in the area of musculoskeletal research and therapy as well as, reviews, commentaries and reports. A major focus of the journal is on the immunologic processes leading to inflammation, damage and repair as they relate to autoimmune rheumatic and musculoskeletal conditions, and which inform the translation of this knowledge into advances in clinical care. Original basic, translational and clinical research is considered for publication along with results of early and late phase therapeutic trials, especially as they pertain to the underpinning science that informs clinical observations in interventional studies.
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