Department of Neurology, Taipei Medical University Shuang Ho Hospital, New Taipei City.
Department of Neurology, School of Medicine, College of Medicine, Taipei Medical University.
Medicine (Baltimore). 2021 Jan 29;100(4):e24191. doi: 10.1097/MD.0000000000024191.
Parkinson disease (PD), the second most common neurodegenerative disease, has no cure or applicable disease-modifying approach, only symptomatic therapy. Oxidative stress and mitochondrial dysfunction play key roles in PD pathophysiology. Animal studies have demonstrated that photobiomodulation (PBM) may enhance mitochondrial function and boost adenosine triphosphate production, thus alleviating PD symptoms; however, this process can cause increased reactive oxygen species (ROS) production. Molecular hydrogen (H2) is a potent and possibly therapeutic antioxidant that can mitigate the effect of ROS. PBM targeting the brainstem may facilitate neuronal activity, and the concomitant H2 may clear additional ROS produced by PBM. Therefore, this study aimed to determine the safety and effectiveness of PBM + H2 in patients with PD.
We included 18 patients with PD (age 30-80 years) who were at Hoehn and Yahr stages II-III. All the participants received daily PBM + H2 therapy for 2 weeks. The adverse event and the Unified Parkinson Disease Rating Scale (UPDRS) scores were recorded.
We noted that the UPDRS scores began significantly decreasing from the first week, and this improvement persisted until the end of therapy. Moreover, no adverse event was recorded. After 1 week of therapy cessation, UPDRS scores slightly increased but the improvement remained significant compared with the baseline.
This novel, proof-of-concept study demonstrated that PBM+H2 therapy is safe and reduces disease severity. A larger-scaled clinical trial is warranted to completely investigate the effects of PBM + H2 therapy on PD.
帕金森病(PD)是第二常见的神经退行性疾病,目前尚无治愈方法或适用的疾病修正方法,只有对症治疗。氧化应激和线粒体功能障碍在 PD 病理生理学中起关键作用。动物研究表明,光生物调节(PBM)可能增强线粒体功能并增加三磷酸腺苷的产生,从而缓解 PD 症状;然而,这一过程会导致活性氧(ROS)产生增加。分子氢(H2)是一种有效的抗氧化剂,可以减轻 ROS 的影响。针对脑干的 PBM 可能促进神经元活动,同时伴随的 H2 可能清除 PBM 产生的额外 ROS。因此,本研究旨在确定 PBM+H2 治疗 PD 患者的安全性和有效性。
我们纳入了 18 名 PD 患者(年龄 30-80 岁),他们处于 Hoehn 和 Yahr 分期 II-III 期。所有参与者每天接受 PBM+H2 治疗 2 周。记录不良事件和统一帕金森病评定量表(UPDRS)评分。
我们注意到,UPDRS 评分从第一周开始显著下降,这种改善持续到治疗结束。此外,未记录到不良反应。治疗停止 1 周后,UPDRS 评分略有升高,但与基线相比仍有显著改善。
这项新颖的概念验证研究表明,PBM+H2 治疗是安全的,可以降低疾病严重程度。需要更大规模的临床试验来全面研究 PBM+H2 治疗对 PD 的影响。