PAIN AND STRUCTURAL OA PHENOTYPES: A POLL OF ATTENDEES AT THE OARSI 2024 IMAGING DISCUSSION GROUP SESSION

M.P. Jansen , F. Cicuttini , C.K. Kwoh , X. Li , F.W. Roemer , T. Turmezei , T.M. Link
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引用次数: 0

Abstract

INTRODUCTION

The OARSI Imaging Discussion Group was established to stimulate discussion of imaging related research and developments at OARSI with an inclusive group including clinicians, radiologists, imaging researchers and representatives from the pharmaceutical industry. The focus of the 2024 Discussion Group was ‘Pain and Structural Phenotypes’.

OBJECTIVE

To gain insights on the relationship between pain and structural damage in OA from attendees at the 2024 OARSI World Congress on Osteoarthritis.

METHODS

After short presentations on OA pain phenotypes, structure phenotypes, and the pain and structure challenge, attendees participated in an online poll. Questions were as follows: 1) Which pain questionnaire best captures structural damage? 2) What changes in imaging features are best associated with changes in pain in the same direction? 3) Does structure/composition explain pain? 4a) Should patients with pain sensitization/neuropathic pain be excluded from trials of DMOAD? 4b) If yes – How should we exclude them? 5) Does the relationship between pain and structure differ between joints? 6) Does the relationship between pain and structure differ according to disease stage? 7) What is the reason why we do not find a satisfactory relationship between structure and pain in clinical trials?

RESULTS

The number of respondents varied between 18 (Q3-6) and 23 (Q2); 45% of respondents stated that WOMAC pain scores best capture structural damage, followed by KOOS (25%), ICOAP (20%) and VAS (10%). 22% Responded that structure explains pain while 50% and 22% stated that it will once we find the right structural measures or pain measures, respectively. Two of three participants indicated that patients with sensitization/neuropathic pain should be excluded from DMOAD trials; most (78%) stated that this should be done with a questionnaire such as PainDETECT, and 17% with quantitative sensatory testing. 50% of respondents indicated that there is variation between pain and structure in weight-bearing versus non-weight-bearing joints or all joints (39%). All but one participant (94%) indicated that the relationship between pain and structure differs according to both clinical and structural disease stage; the remaining respondent answered that it varies according to structural disease stage only. BMLs and synovitis were identified as imaging features best associated with pain changes (Figure 1). The heterogeneity of patient populations (regarding pain and structure) was the most common reason for lack of a relationship between pain and structure in clinical trials.

CONCLUSION

The heterogeneity of pain and structure in OA populations remains a challenge for clinical trials. Considerations should be given to excluding patients with pain due to non-nociceptive pain.

疼痛和结构性 OA 表型:OARSI 2024 成像讨论组会议与会者民意调查
OARSI 影像学讨论组的成立旨在促进 OARSI 影像学相关研究和发展的讨论,讨论组成员包括临床医生、放射科医生、影像学研究人员和制药业代表。2024年讨论组的重点是 "疼痛与结构表型"。目的从2024年OARSI世界骨关节炎大会的与会者那里获得关于OA中疼痛与结构损伤之间关系的见解。方法在关于OA疼痛表型、结构表型以及疼痛与结构挑战的简短介绍之后,与会者参与了在线投票。问题如下1) 哪种疼痛问卷最能反映结构损伤?2)影像学特征的哪些变化与疼痛的同方向变化最相关?3) 结构/组成能否解释疼痛?4a) 是否应将痛觉过敏/神经病理性疼痛患者排除在 DMOAD 试验之外?4b) 如果是--我们应该如何将他们排除在外?5) 疼痛与关节结构之间的关系是否因关节而异?6) 疼痛与结构之间的关系是否因疾病阶段而异?7)在临床试验中,我们没有找到令人满意的结构与疼痛之间关系的原因是什么?结果受访者人数在 18 人(Q3-6)和 23 人(Q2)之间变化;45% 的受访者表示 WOMAC 疼痛评分最能反映结构性损伤,其次是 KOOS(25%)、ICOAP(20%)和 VAS(10%)。22%的受访者认为结构可以解释疼痛,而50%和22%的受访者则分别表示,一旦我们找到正确的结构测量方法或疼痛测量方法,结构就可以解释疼痛。三分之二的受访者表示,DMOAD 试验应排除敏感化/神经病理性疼痛患者;大多数受访者(78%)表示,应通过疼痛检测等问卷调查来排除敏感化/神经病理性疼痛患者,17%的受访者表示应通过定量感觉测试来排除敏感化/神经病理性疼痛患者。50%的受访者表示,负重关节与非负重关节或所有关节的疼痛和结构之间存在差异(39%)。除一名受访者(94%)外,其余受访者均表示疼痛与结构之间的关系因临床和结构性疾病分期而异;其余受访者回答仅因结构性疾病分期而异。BMLs和滑膜炎被认为是与疼痛变化最相关的影像学特征(图1)。患者人群(疼痛和结构)的异质性是临床试验中疼痛和结构之间缺乏关系的最常见原因。应考虑排除非感觉性疼痛引起的疼痛患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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Osteoarthritis imaging
Osteoarthritis imaging Radiology and Imaging
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