Thomas Natalie, Chau Tracey, Tantanis Darcy, Huang Katherine, Scheinberg Adam, Gooley Paul R, Josev Elisha K, Knight Sarah J, Armstrong Christopher W
Department of Biochemistry and Pharmacology, The University of Melbourne Bio21 Molecular Science and Biotechnology Institute, Parkville, Victoria, Australia.
Neurodisability & Rehabilitation, Murdoch Children's Research Institute, Parkville, Victoria, Australia.
BMJ Open. 2024 Dec 10;14(12):e089038. doi: 10.1136/bmjopen-2024-089038.
Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a disabling condition that can affect adolescents during a vulnerable period of development. The underlying biological mechanisms for ME/CFS remain unclear and have rarely been investigated in the adolescent population, despite this period representing an age peak in the overall incidence. The primary objective of this is to provide a foundational set of biological data on adolescent ME/CFS patients. Data generated will be compared with controls and over several time points within each patient to potentially develop a biomarker signature of the disease, identify subsets or clusters of patients, and to unveil the pathomechanisms of the disease.
This protocol paper outlines a comprehensive, multilevel, longitudinal, observational study in paediatric ME/CFS. ME/CFS patients aged 12-19 years and controls will donate biosamples of urine, blood, and peripheral blood mononuclear cells for an in-depth omics profiling analysis (whole-genome sequencing, metabolomics and quantitative proteomics) while being assessed by gold-standard clinical and neuropsychological measures. ME/CFS patients will then be provided with a take-home kit that enables them to collect urine and blood microsamples during an average day and during days when they are experiencing postexertional malaise. The longitudinal repeated-measures study design is optimal for studying heterogeneous chronic diseases like ME/CFS as it can detect subtle changes, control for individual differences, enhance precision and boost statistical power. The outcomes of this research have the potential to identify biomarker signatures, aid in understanding the underlying mechanisms, and ultimately, improve the lives of children with ME/CFS.
This project was approved by the Royal Children's Hospital's Human Research Ethics Committee (HREC 74175). Findings from this study will be disseminated through peer-reviewed journal publications and presentations at relevant conferences. All participants will be provided with a summary of the study's findings once the project is completed.
肌痛性脑脊髓炎/慢性疲劳综合征(ME/CFS)是一种致残性疾病,可在青少年发育的脆弱期影响他们。尽管青少年时期是ME/CFS总体发病率的一个年龄高峰,但ME/CFS的潜在生物学机制仍不清楚,且在青少年人群中很少被研究。本研究的主要目的是提供一组关于青少年ME/CFS患者的基础生物学数据。所产生的数据将与对照组进行比较,并在每个患者的多个时间点进行比较,以潜在地开发该疾病的生物标志物特征,识别患者亚组或聚类,并揭示疾病的发病机制。
本方案文件概述了一项针对儿童ME/CFS的全面、多层次、纵向观察性研究。12至19岁的ME/CFS患者和对照组将捐赠尿液、血液和外周血单核细胞的生物样本,用于深入的组学分析(全基因组测序、代谢组学和定量蛋白质组学),同时接受金标准临床和神经心理学测量评估。然后将为ME/CFS患者提供一个家庭试剂盒,使他们能够在平均一天以及出现运动后不适的日子里收集尿液和血液微量样本。纵向重复测量研究设计对于研究像ME/CFS这样的异质性慢性疾病是最佳的,因为它可以检测细微变化,控制个体差异,提高精度并增强统计效力。本研究的结果有可能识别生物标志物特征,有助于理解潜在机制,并最终改善ME/CFS儿童的生活。
本项目已获得皇家儿童医院人类研究伦理委员会批准(HREC 74175)。本研究的结果将通过同行评审的期刊出版物以及在相关会议上的报告进行传播。项目完成后,将向所有参与者提供研究结果的摘要。