Benatar Michael, Heiman-Patterson Terry D, Cooper-Knock Johnathan, Brickman Daniel, Casaletto Kaitlin B, Goutman Stephen A, Vinceti Marco, Dratch Laynie, Arias Jalayne J, Swidler Jean, Turner Martin R, Shefner Jeremy, Westeneng Henk-Jan, van den Berg Leonard H, Al-Chalabi Ammar
Neurology, University of Miami Miller School of Medicine, Miami, Florida, USA
Department of Neurology, Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania, USA.
J Neurol Neurosurg Psychiatry. 2025 Jan 31;96(3). doi: 10.1136/jnnp-2024-334339.
There is a growing understanding of the presymptomatic stages of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) and nascent efforts aiming to prevent these devastating neurodegenerative diseases have emerged. This progress is attributable, in no small part, to the altruism of people living with pathogenic variants at elevated genetic risk for ALS/FTD via their willingness to participate in natural history studies and disease prevention trials. Increasingly, this community has also highlighted the urgent need to develop paradigms for providing appropriate clinical care for those at elevated risk for ALS and FTD. This manuscript summarises recommendations emanating from a multi-stakeholder Workshop (Malvern, Pennsylvania, 2023) that aimed to develop guidance for at-risk carriers and their treating physicians. Clinical care recommendations span genetic testing (including counselling and sociolegal implications); monitoring for the emergence of early motor, cognitive and behavioural signs of disease; and the use of Food and Drug Administration-approved small molecule drugs and gene-targeting therapies. Lifestyle recommendations focus on exercise, smoking, statin use, supplement use, caffeine intake and head trauma, as well as occupational and environmental exposures. While the evidence base to inform clinical and lifestyle recommendations is limited, this guidance document aims to appraise carriers and clinicians of the issues and best available evidence, and also to define the research agenda that could yield more evidence-informed guidelines.
人们对肌萎缩侧索硬化症(ALS)和额颞叶痴呆(FTD)的症状前阶段有了越来越多的认识,旨在预防这些毁灭性神经退行性疾病的初步努力也已出现。这一进展在很大程度上归因于携带ALS/FTD高遗传风险致病变体的人们的利他主义,他们愿意参与自然史研究和疾病预防试验。这个群体也越来越强调迫切需要制定为ALS和FTD高风险人群提供适当临床护理的模式。本手稿总结了多利益相关方研讨会(宾夕法尼亚州马尔文,2023年)提出的建议,该研讨会旨在为高风险携带者及其治疗医生制定指导意见。临床护理建议涵盖基因检测(包括咨询和社会法律影响);监测疾病早期运动、认知和行为症状的出现;以及使用美国食品药品监督管理局批准的小分子药物和基因靶向疗法。生活方式建议侧重于运动、吸烟、他汀类药物的使用、补充剂的使用、咖啡因摄入和头部创伤,以及职业和环境暴露。虽然为临床和生活方式建议提供依据的证据基础有限,但本指导文件旨在让携带者和临床医生了解这些问题和现有最佳证据,并确定能够产生更多循证指南的研究议程。