Willis Gregory L, Boda Jamilee, Freelance Christopher B
The Bronowski Institute of Behavioural Neuroscience, The Bronowski Clinic, Coliban Medical Centre, Kyneton, VIC, Australia.
Front Neurol. 2018 Sep 19;9:741. doi: 10.3389/fneur.2018.00741. eCollection 2018.
Parkinson's disease (PD) is a disorder characterized by loss of dopamine (DA) in the nigro-striatal dopamine (NSD) system with the primary symptoms of bradykinaesia, rigidity, tremor, and altered gate. Secondary symptoms including depression, insomnia, involuntary movement, and psychiatric side effects are also commonly observed. While the treatment focus for the past 50 years has been aimed at replacing deficient DA, to relieve the primary symptoms, more recent studies have suggested that the circadian system plays a critical role in the etiology and treatment of this disorder. Several case studies and open label trials have implemented bright light therapy (BT) in an attempt to repair sleep, depression and even the primary motor symptoms of this disorder, however controlled studies are yet to be fully implemented. In this controlled trial, patients that had been maintained on BT daily for 4 months to 5 years previously were assigned to one of three groups: continued polychromatic light, continued with red light or discontinued polychromatic light for a 2 week period. The Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDSUPDRS), The Parkinson's Disease Questionnaire (PDQ-39), The Beck Depression Inventory II, The Beck Anxiety Inventory, The Epworth Sleep Scale (ESS) and a global rating scale were used to assess patients prior to and at 1 and 2 weeks after commencing the trial. Patients continuing polychromatic BT showed significant improvement on the MDSUPDRS Rating Scale (12 points; = 0.028), the PDQ-39 (10 points; = 0.011), ESS (4 points; = 0.013), and numerous motor and secondary symptoms on a global rating scale. Performance on standardized motor tests also incrementally improved in this group while those exposed to red light and those that discontinued BT treatment deteriorated. These results demonstrate that strategically applied polychromatic light was beneficial in reducing many primary motor and secondary symptoms of PD. Further work investigating the role of light in mitigating PD symptoms and involvement of the circadian system will provide further advances in the treatment of PD. : http://www.anzctr.org.au, identifier ACTRN12617001309370.
帕金森病(PD)是一种以黑质 - 纹状体多巴胺(NSD)系统中多巴胺(DA)缺失为特征的疾病,主要症状包括运动迟缓、僵硬、震颤和步态改变。还普遍观察到包括抑郁、失眠、不自主运动和精神副作用在内的继发症状。虽然过去50年的治疗重点一直是补充缺失的多巴胺以缓解主要症状,但最近的研究表明,昼夜节律系统在这种疾病的病因和治疗中起着关键作用。一些病例研究和开放标签试验已采用强光疗法(BT),试图改善睡眠、缓解抑郁,甚至改善这种疾病的主要运动症状,然而对照研究尚未全面开展。在这项对照试验中,此前每天接受BT治疗4个月至5年的患者被分为三组之一:继续接受多色光治疗、继续接受红光治疗或在2周内停止多色光治疗。在试验开始前以及开始后1周和2周,使用运动障碍协会统一帕金森病评定量表(MDSUPDRS)、帕金森病问卷(PDQ - 39)、贝克抑郁量表第二版、贝克焦虑量表、爱泼华嗜睡量表(ESS)和一个整体评定量表对患者进行评估。继续接受多色光BT治疗的患者在MDSUPDRS评定量表(12分;P = 0.028)、PDQ - 39(10分;P = 0.011)、ESS(4分;P = 0.013)以及整体评定量表上的多项运动和继发症状方面均有显著改善。该组在标准化运动测试中的表现也逐步提高,而接受红光治疗的患者和停止BT治疗的患者则病情恶化。这些结果表明,策略性应用多色光有助于减轻帕金森病的许多主要运动和继发症状。进一步研究光在减轻帕金森病症状中的作用以及昼夜节律系统的参与情况,将为帕金森病的治疗带来进一步进展。:http://www.anzctr.org.au,标识符ACTRN12617001309370