Schierbaum Luca, Quiroz Vicente, Yang Kathryn, Rong Joshua, Battaglia Nicole, Zubair Umar, Christie Michelle, Davis Marie, Calame Daniel, Danzi Matt C, Finkel Richard S, Burns Joshua, Gilbert Donald L, Mingbunjerdsuk Dararat, Pruitt Greg, Pruitt Norma, Cobb John, Sadjadi Reza, Cashman Christopher R, Blackstone Craig, Fink John K, Shy Michael E, Zuchner Stephan, Ebrahimi-Fakhari Darius
Movement Disorders Program, Department of Neurology, Boston Children's Hospital.
Division of Neurology and Rehabilitation Medicine, Scottish Rite Hospital for Children.
Neurol Genet. 2025 Feb 21;11(2):e200249. doi: 10.1212/NXG.0000000000200249. eCollection 2025 Apr.
The primary objective of this paper was to present the establishment of the Spastic Paraplegia-Centers of Excellence Research Network (SP-CERN) aimed at promoting clinical trial readiness for hereditary spastic paraplegia (HSP). SP-CERN is unique in its approach to addressing the diagnostic and therapeutic challenges associated with HSP through a large-scale, collaborative effort.
Participants with HSP are identified through multicenter collaborations across 11 institutions in the United States. SP-CERN systematically collects longitudinal clinical data, biospecimens, and wearable device data from patients. Data are stored in a centralized REDCap database, facilitating shared access for analysis. Patients are evaluated using standardized assessment tools for motor function, biomarkers, and digital outcome measures.
SP-CERN has established a biorepository, centralized data collection methods, and standardized clinical assessments. It is conducting natural history studies for all HSP subtypes, enabling the validation of biomarkers and development of gene-based therapies.
SP-CERN's collaborative approach bridges gaps in clinical care and research for HSP by improving diagnostic capabilities and promoting clinical trial readiness. This initiative represents a framework for rare disease research, accelerating the development of novel therapies and improving patient outcomes through standardized, multi-institutional collaboration.
本文的主要目标是介绍痉挛性截瘫卓越研究网络(SP - CERN)的建立,该网络旨在推动遗传性痉挛性截瘫(HSP)的临床试验准备工作。SP - CERN在应对与HSP相关的诊断和治疗挑战方面具有独特的方法,通过大规模的协作努力来实现这一目标。
通过美国11家机构的多中心合作确定HSP患者。SP - CERN系统地收集患者的纵向临床数据、生物样本和可穿戴设备数据。数据存储在集中式的REDCap数据库中,便于共享分析。使用标准化评估工具对患者进行运动功能、生物标志物和数字结局指标的评估。
SP - CERN已经建立了生物样本库、集中数据收集方法和标准化临床评估。它正在对所有HSP亚型进行自然史研究,以验证生物标志物并开发基于基因的疗法。
SP - CERN的协作方法通过提高诊断能力和推动临床试验准备工作,弥合了HSP临床护理和研究之间的差距。这一举措代表了罕见病研究的一个框架,通过标准化的多机构合作加速新型疗法的开发并改善患者预后。