From the Division of Neurology (R.G.-M.), Children's Mercy Kansas City; School of Medicine (R.G.-M., J.S.L.), University of Missouri-Kansas City; Department of Pediatrics (R.G.-M., J.S.L.), University of Kansas Medical Center, Kansas City; Department of Pediatrics (C.S.), Department of Neurology (C.S.), and Mallinckrodt Institute of Radiology (C.S.), Washington University in St. Louis; and Division of Clinical Pharmacology, Toxicology & Therapeutic Innovation (J.S.L.), Children's Mercy Kansas City, MO.
Neurology. 2023 Oct 24;101(17):752-759. doi: 10.1212/WNL.0000000000207593. Epub 2023 Jul 18.
Recent focus on improving the recognition of dystonia in cerebral palsy (DCP) has highlighted the need for more effective treatments. Evidence supports improved functional outcomes with early interventions for patients with cerebral palsy, but it is not known which interventions are most effective for DCP. Current pharmacologic recommendations for DCP are based largely on anecdotal evidence, with medications demonstrating minimal to moderate improvements in dystonia and variable efficacy between patients. Patients, families, and clinicians have identified the need for new and improved treatments in DCP, naming this as the top research theme in a recent ® publication. Precision therapeutics focuses on providing early effective interventions that are individualized to every patient and can guide research priorities to improve treatments for DCP. This commentary outlines current obstacles to improving treatment of DCP and addresses how precision therapeutics can address each of these obstacles through 4 key components: (1) identification of to select patients likely to develop DCP in the future and for whom early intervention may be appropriate to delay or prevent full manifestation of dystonia, (2) stratification of patients with DCP into subgroups according to shared features (clinical, functional, biochemical, etc) to provide a based on those shared features, (3) administration of an of an effective intervention to ensure adequate concentrations of the therapeutic entity at the site of action, and (4) monitoring of objective to intervention. With implementation of each of these components of precision therapeutics, new and more effective treatments for every person with DCP can be realized.
最近,人们关注如何提高对脑瘫性肌张力障碍(DCP)的认识,这凸显了对更有效治疗方法的需求。有证据表明,对于脑瘫患者来说,早期干预可以改善其功能结局,但尚不清楚哪些干预措施对 DCP 最有效。目前针对 DCP 的药物治疗建议主要基于传闻证据,这些药物在改善肌张力障碍方面的效果甚微或中等,而且对不同患者的疗效也各不相同。患者、家属和临床医生都指出,需要对 DCP 进行新的和改进的治疗,这是最近 ®出版物中确定的首要研究主题。精准治疗侧重于提供对每个患者都有效的早期干预措施,并能够指导研究重点,以改善 DCP 的治疗效果。本述评概述了改善 DCP 治疗目前面临的障碍,并讨论了精准治疗如何通过以下 4 个关键组成部分来解决这些障碍:(1)确定标志物,以选择未来可能发生 DCP 的患者,以及对于哪些患者早期干预可能合适,以延缓或防止肌张力障碍完全表现;(2)根据共同特征(临床、功能、生化等)将 DCP 患者分层到亚组中,根据这些共同特征提供个体化治疗;(3)给予有效的干预措施,以确保治疗实体在作用部位达到足够的浓度;(4)监测客观指标,以评估干预效果。通过实施精准治疗的这些组成部分,可以为每一位 DCP 患者实现新的、更有效的治疗方法。