Division of Neurology, St. Michael's Hospital, University of Toronto, 30 Bond Street, Toronto, ON, M5B 1W8, Canada.
Department of Neurosciences, Université de Montréal and Centre hospitalier de l'Université de Montréal, 900 rue St. Denis, Montreal, QC, H2X 0A9, Canada.
BMC Neurol. 2021 Oct 27;21(1):418. doi: 10.1186/s12883-021-02447-7.
Neurological disability progression occurs across the spectrum of people living with multiple sclerosis (MS). Although there are a handful of disease-modifying treatments approved for use in progressive phenotypes of MS, there are no treatments that substantially modify the course of clinical progression in MS. Characterizing the determinants of clinical progression can inform the development of novel therapeutic agents and treatment approaches that target progression in MS, which is one of the greatest unmet needs in clinical practice. Canada, having one of the world's highest rates of MS and a publicly-funded health care system, represents an optimal country to achieve in-depth analysis of progression. Accordingly, the overarching aim of the Canadian Prospective Cohort Study to Understand Progression in MS (CanProCo) is to evaluate a wide spectrum of factors associated with the clinical onset and rate of disease progression in MS, and to describe how these factors relate to one another to influence progression.
CanProCo is a prospective, observational cohort study with investigators specializing in epidemiology, neuroimaging, neuroimmunology, health services research and health economics. CanProCo's study design was approved by an international review panel, comprised of content experts and key stakeholders. One thousand individuals with radiologically-isolated syndrome, relapsing-remitting MS, and primary-progressive MS within 10-15 years of disease onset will be recruited from 5 academic MS centres in Canada. Participants will undergo detailed clinical evaluation annually over 5 years (including advanced, app-based clinical data collection). In a subset of participants within 5-10 years of disease onset (n = 500), blood, cerebrospinal fluid, and research MRIs will be collected allowing an integrated, in-depth evaluation of factors contributing to progression in MS from multiple perspectives. Factors of interest range from biological measures (e.g. single-cell RNA-sequencing), MRI-based microstructural assessment, participant characteristics (self-reported, performance-based, clinician-assessed, health-system based), and micro and macro-environmental factors.
Halting the progression of MS remains a fundamental need to improve the lives of people living with MS. Achieving this requires leveraging transdisciplinary approaches to better characterize why clinical progression occurs. CanProCo is a pioneering multi-dimensional cohort study aiming to characterize these determinants to inform the development and implementation of efficacious and effective interventions.
神经功能障碍在多发性硬化症(MS)患者中广泛存在。尽管有一些疾病修正治疗药物被批准用于 MS 的进行性表型,但没有治疗方法能显著改变 MS 的临床进展进程。明确临床进展的决定因素可以为开发针对 MS 进展的新型治疗药物和治疗方法提供信息,这是临床实践中最大的未满足需求之一。加拿大是世界上多发性硬化症发病率最高的国家之一,拥有公共资助的医疗保健系统,是深入分析进展情况的理想国家。因此,了解多发性硬化症进展的加拿大前瞻性队列研究(CanProCo)的总体目标是评估与 MS 临床发病和疾病进展率相关的广泛因素,并描述这些因素如何相互关联以影响进展。
CanProCo 是一项前瞻性、观察性队列研究,研究人员专门从事流行病学、神经影像学、神经免疫学、卫生服务研究和卫生经济学。CanProCo 的研究设计得到了一个由内容专家和主要利益相关者组成的国际审查小组的批准。该研究将从加拿大 5 个学术性多发性硬化症中心招募 1000 名处于疾病发病后 10-15 年内的放射孤立综合征、复发缓解型 MS 和原发性进展型 MS 患者。参与者将在 5 年内每年接受详细的临床评估(包括先进的、基于应用程序的临床数据收集)。在疾病发病后 5-10 年内的一部分参与者(n=500)中,将采集血液、脑脊液和研究性 MRI,从而从多个角度对导致 MS 进展的因素进行综合深入评估。感兴趣的因素包括生物学指标(如单细胞 RNA 测序)、基于 MRI 的微观结构评估、参与者特征(自我报告、表现为基础、临床医生评估、基于健康系统)和微观和宏观环境因素。
阻止 MS 的进展仍然是改善 MS 患者生活的基本需求。要实现这一目标,需要利用跨学科方法更好地描述为什么会出现临床进展。CanProCo 是一项开创性的多维队列研究,旨在对这些决定因素进行特征描述,为开发和实施有效和有效的干预措施提供信息。