Laakso E-Liisa, Ewais Tatjana, McMahon Katie, Forbes Josephine, Phillips Liza
Mater Research Institute, The University of Queensland, Aubigny Place, Raymond Terrace, South Brisbane, QLD 4101, Australia.
School of Health Sciences and Social Work, Griffith University, Brisbane, QLD 4111, Australia.
J Clin Med. 2025 Mar 17;14(6):2047. doi: 10.3390/jcm14062047.
: There is no cure for mitochondrial diseases which manifest in numerous ways including fatigue, muscle weakness, and exercise intolerance. Medical treatment varies and focuses on managing symptoms. Photobiomodulation (PBM) can decrease mitochondrial damage thereby increasing energy production and decreasing cell death. This pilot study will apply PBM to people with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) to examine the safety of application, and if changes occur in symptoms and signs after cross-over application/withdrawal of a sham or active PBM treatment including a two-week period of washout. : This study is an exploratory, prospective series N-of-1 (single patient) studies. The protocol is guided by the CONSORT extension for reporting N-of-1 trials (CENT 2015), chosen due to the rarity of mitochondrial diseases, the fluctuating symptomology, and heterogeneity of the clinical presentation. The primary outcome is patient-reported fatigue assessed using the Checklist of Individual Strength and with concomitant evaluation of safety. Secondary measures are of depression, anxiety and stress, sleepiness, physical activity, blood lactate and creatine kinase, physical measures of sit-to-stand, and heel raise capability. Mitochondrial function will be evaluated using hydrogen magnetic resonance spectroscopy for lactate. PBM will be a participant-administered, home-based therapy using a multiple diode flexible array (BeniLight iLED-Pro Multi-Wave Multi-Pulse belt; 465 nm, 660 nm, 850 nm; average irradiance 5.23 mW/cm; total joules: 770.1 J/treatment, all sites; 5 KHz; 20% duty ratio) over the anterior thigh muscles, posterior calf muscles and abdomen for 10 min to each site, three times/week. The safety of the intervention will be assessed. Descriptive statistics, causal analyses of time series data and dynamic modelling will be applied as relevant to the variables collected. Hydrogen magnetic resonance spectra will be acquired and averaged to obtain the content of the targeted hydrogen levels. : The study will provide guidance on whether and how to progress to a larger, randomised cohort study with sham control.
线粒体疾病无法治愈,其表现形式多种多样,包括疲劳、肌肉无力和运动不耐受。医学治疗方法各异,主要侧重于控制症状。光生物调节(PBM)可减少线粒体损伤,从而增加能量生成并减少细胞死亡。这项初步研究将对患有线粒体脑肌病、乳酸酸中毒和卒中样发作(MELAS)的患者应用PBM,以检查应用的安全性,以及在交叉应用/停用假PBM或活性PBM治疗(包括两周的洗脱期)后症状和体征是否发生变化。:本研究是一项探索性的前瞻性系列N-of-1(单病例)研究。该方案以CONSORT扩展版报告N-of-1试验(CENT 2015)为指导,选择该方案是由于线粒体疾病的罕见性、症状的波动性以及临床表现的异质性。主要结局是使用个人力量检查表评估患者报告的疲劳情况,并同时评估安全性。次要指标包括抑郁、焦虑和压力、嗜睡、身体活动、血乳酸和肌酸激酶、从坐到站的身体测量以及踮脚跟能力。将使用氢磁共振波谱法评估乳酸的线粒体功能。PBM将是一种由参与者自行在家进行的治疗方法,使用多二极管柔性阵列(BeniLight iLED-Pro多波多脉冲腰带;465纳米、660纳米、850纳米;平均辐照度5.23毫瓦/平方厘米;总焦耳数:每个部位每次治疗770.1焦耳;所有部位;5千赫兹;20%占空比)照射大腿前侧肌肉、小腿后侧肌肉和腹部,每个部位照射10分钟,每周三次。将评估干预措施的安全性。将根据收集到的变量应用描述性统计、时间序列数据的因果分析和动态建模。将采集氢磁共振波谱并进行平均,以获得目标氢水平的含量。:该研究将为是否以及如何推进到更大规模的、有假对照的随机队列研究提供指导。