McGee Claire, Liebert Ann, Bicknell Brian, Pang Vincent, Isaac Vivian, McLachlan Craig S, Kiat Hosen, Herkes Geoffrey
Faculty of Health Sciences, Torrens University Australia, Sydney, NSW 2000, Australia.
School of Medical Sciences, University of Sydney, Camperdown, NSW 2050, Australia.
J Clin Med. 2023 Apr 13;12(8):2846. doi: 10.3390/jcm12082846.
Emerging evidence is increasingly supporting the use of transcranial photobiomodulation (tPBM) to improve symptoms of neurodegenerative diseases, including Parkinson's disease (PD). The objective of this study was to analyse the safety and efficacy of tPBM for PD motor symptoms. The study was a triple blind, randomized placebo-controlled trial with 40 idiopathic PD patients receiving either active tPBM (635 nm plus 810 nm LEDs) or sham tPBM for 24 min per day (56.88J), six days per week, for 12 weeks. The primary outcome measures were treatment safety and a 37-item MDS-UPDRS-III (motor domain) assessed at baseline and 12 weeks. Individual MDS-UPDRS-III items were clustered into sub-score domains (facial, upper-limb, lower-limb, gait, and tremor). The treatment produced no safety concerns or adverse events, apart from occasional temporary and minor dizziness. There was no significant difference in total MDS-UPDRS-III scores between groups, presumably due to the placebo effect. Additional analyses demonstrated that facial and lower-limb sub-scores significantly improved with active treatment, while gait and lower-limb sub-scores significantly improved with sham treatment. Approximately 70% of participants responded to active treatment (≥5 decrease in MDS-UPDRS-III score) and improved in all sub-scores, while sham responders improved in lower-limb sub-scores only. tPBM appears to be a safe treatment and improved several PD motor symptoms in patients that responded to treatment. tPBM is proving to be increasingly attractive as a possible non-pharmaceutical adjunct therapy.
越来越多的新证据支持使用经颅光生物调节疗法(tPBM)来改善神经退行性疾病的症状,包括帕金森病(PD)。本研究的目的是分析tPBM对帕金森病运动症状的安全性和有效性。该研究是一项三盲、随机、安慰剂对照试验,40名特发性帕金森病患者每天接受24分钟的活性tPBM(635纳米加810纳米发光二极管)或假tPBM治疗(56.88焦耳),每周6天,共12周。主要结局指标是治疗安全性以及在基线和12周时评估的37项MDS-UPDRS-III(运动领域)。MDS-UPDRS-III的各个项目被聚类为子评分领域(面部、上肢、下肢、步态和震颤)。除了偶尔出现的短暂轻微头晕外,该治疗未产生安全问题或不良事件。两组之间的MDS-UPDRS-III总分没有显著差异,可能是由于安慰剂效应。进一步分析表明,活性治疗使面部和下肢子评分显著改善,而假治疗使步态和下肢子评分显著改善。大约70%的参与者对活性治疗有反应(MDS-UPDRS-III评分降低≥5分)且所有子评分均有所改善,而假治疗有反应者仅下肢子评分有所改善。tPBM似乎是一种安全的治疗方法,并且在有反应的患者中改善了几种帕金森病运动症状。tPBM作为一种可能的非药物辅助治疗方法正变得越来越有吸引力。