Zentrum für Seltene Erkrankungen, University Hospital Leipzig, Leipzig, Germany
AbbVie Deutschland GmbH & Co KG, Wiesbaden, Germany.
Ann Rheum Dis. 2024 Sep 30;83(10):1381-1388. doi: 10.1136/ard-2023-225414.
To determine the proportion of patients with rheumatoid arthritis (RA) with severe persisting pain and to identify predictive factors despite treatment-controlled disease activity.
This prospective multicentre study included outpatients with RA scheduled for escalation of anti-inflammatory treatment due to active disease and severe pain (Disease Activity Score 28 (DAS28)>3.2 and Visual Analogue Scale (VAS)>50). At week 24, patients were stratified into reference group (DAS28 improvement>1.2 or DAS28≤3.2 and VAS pain score<50), non-responders (DAS28 improvement≤1.2 and DAS28>3.2, regardless of VAS pain score) and persisting pain group (DAS28 improvement>1.2 or DAS28≤3.2 and VAS pain score≥50). The former two subgroups ended the study at week 24. The latter continued until week 48. Demographic data, DAS28-C reactive protein, VAS for pain, painDETECT Questionnaire (PD-Q) to identify neuropathic pain (NeP) and the Pain Catastrophising Scale were assessed and tested for relation to persisting pain.
Of 567 patients, 337 (59.4%) were classified as reference group, 102 (18.0%) as non-responders and 128 (22.6%) as patients with persisting pain. 21 (8.8%) responders, 28 (35.0%) non-responders and 27 (26.5%) persisting pain patients tested positive for NeP at week 24. Pain catastrophising (p=0.002) and number of tender joints (p=0.004) were positively associated with persisting pain at week 24. Baseline PD-Q was not related to subsequent persisting pain.
Persisting and non-nociceptive pain occur frequently in RA. Besides the potential involvement of NeP, pain catastrophising and a higher number of tender joints coincide with persisting pain.
确定类风湿关节炎(RA)患者中存在严重持续疼痛的比例,并确定尽管疾病活动得到控制但仍存在的预测因素。
这项前瞻性多中心研究纳入了因疾病活动和严重疼痛(疾病活动评分 28(DAS28)>3.2 和视觉模拟量表(VAS)>50)而计划进行抗炎治疗升级的 RA 门诊患者。在第 24 周,将患者分为参考组(DAS28 改善>1.2 或 DAS28≤3.2 和 VAS 疼痛评分<50)、无应答者(DAS28 改善≤1.2 和 DAS28>3.2,无论 VAS 疼痛评分如何)和持续疼痛组(DAS28 改善>1.2 或 DAS28≤3.2 和 VAS 疼痛评分≥50)。前两个亚组在第 24 周结束研究。后者继续进行至第 48 周。评估人口统计学数据、DAS28-C 反应蛋白、疼痛 VAS、用于识别神经病理性疼痛(NeP)的疼痛检测问卷(PD-Q)和疼痛灾难化量表,并测试与持续疼痛的关系。
在 567 名患者中,337 名(59.4%)被分类为参考组,102 名(18.0%)为无应答者,128 名(22.6%)为持续疼痛患者。在第 24 周时,21 名(8.8%)应答者、28 名(35.0%)无应答者和 27 名(26.5%)持续疼痛患者的 PD-Q 检测为阳性。在第 24 周时,疼痛灾难化(p=0.002)和压痛关节数(p=0.004)与持续疼痛呈正相关。基线 PD-Q 与随后的持续疼痛无关。
RA 中经常出现持续和非伤害性疼痛。除了潜在的 NeP 参与外,疼痛灾难化和更多的压痛关节与持续疼痛一致。