Clinical Medicine Division, Korea Institute of Oriental Medicine, Daejeon 34054, Republic of Korea.
Clinical Research Coordinating Team, Korea Institute of Oriental Medicine, Daejeon 34054, Republic of Korea.
Int J Environ Res Public Health. 2023 Jan 18;20(3):1776. doi: 10.3390/ijerph20031776.
Pain in Parkinson's disease (PD) represents a complex phenotype known to decrease quality of life. This pragmatic randomized, controlled clinical trial evaluated the efficacy of pharmacopuncture (PA) for improving pain symptoms and investigated the corresponding therapeutic mechanisms in patients with PD. Ninety patients with PD-related pain were randomly allocated to receive either PA, manual acupuncture, or usual care in a 1:1:1 ratio; sixty healthy controls were included for comparative analysis of brain imaging data. Over 12 weeks, study treatment provided 2 days per week for 8 weeks with a follow-up period of 4 weeks. The primary outcome measure was the King's Parkinson's Disease Pain Scale score for assessing improvement in PD-related pain, including a sub-analysis to investigate the pattern of changes in pain according to a PD-related pain mechanism-based classification. Secondary outcome measures included a numerical rating scale-based assessment of the intensity and location of pain and changes in pain-associated symptoms, such as depression, anxiety, and sleep disorders. Exploratory outcome measures included structural and functional brain patterns on magnetic resonance imaging, blood molecular signature changes, gait analysis, facial expression and movement assessment in response to emotional stimuli, and a traditional Korean medicine syndrome differentiation questionnaire. The trial findings provided important clinical evidence for the effectiveness of PA in the management of PD-related pain and its associated symptoms, and helped elucidate the mechanism of its therapeutic effect on PD-related pain.
帕金森病(PD)疼痛表现为一种已知降低生活质量的复杂表型。这项实用、随机、对照临床试验评估了药针疗法(PA)改善疼痛症状的疗效,并探讨了 PD 患者的相应治疗机制。90 名 PD 相关疼痛患者按 1:1:1 的比例随机分为 PA 组、手针组和常规护理组;纳入 60 名健康对照者进行脑影像学数据的比较分析。在 12 周内,研究治疗提供每周 2 天,持续 8 周,随访 4 周。主要结局指标是帕金森病疼痛量表(King's Parkinson's Disease Pain Scale)评分,用于评估 PD 相关疼痛的改善情况,包括根据 PD 相关疼痛机制分类进行疼痛变化模式的亚分析。次要结局指标包括疼痛强度和位置的数字评定量表评估,以及疼痛相关症状的变化,如抑郁、焦虑和睡眠障碍。探索性结局指标包括磁共振成像的结构和功能脑模式、血液分子特征变化、步态分析、面部表情和对情绪刺激的运动反应,以及传统的韩国医学综合征鉴别问卷。试验结果为 PA 治疗 PD 相关疼痛及其相关症状的有效性提供了重要的临床证据,并有助于阐明其对 PD 相关疼痛的治疗效果的机制。