Myotonic Dystrophy Foundation, 1004A O'Reilly Avenue, San Francisco, CA, USA, 94129.
Ther Innov Regul Sci. 2020 Sep;54(5):1010-1017. doi: 10.1007/s43441-020-00117-3. Epub 2020 Jan 22.
Myotonic dystrophy type 1 (DM1) and myotonic dystrophy type 2 (DM2) are multisystem, genetic disorders caused by repeat expansions on chromosome 19 (DM1) and chromosome 3 (DM2). Although the effects of DM on the skeletal, cardiac, and smooth muscles, as well as the endocrine and central nervous systems, can be disabling, there are no disease-modifying therapies for the disorder. Following a process established by the US Food and Drug Administration (FDA) in 2012 known as the Patient-Focused Drug Development (PFDD) Initiative, Myotonic (formerly the Myotonic Dystrophy Foundation) has been conducting patient- and caregiver-inclusive sessions to explore disease burden as defined by patients and caregivers, and what affected individuals want most from potential new therapies. In September 2017, at Myotonic's annual conference, a session titled "Bringing the Patient Voice to CNS-Targeting Drug Development in Myotonic Dystrophy" attracted some 350 members of the DM community. During the session, patients and caregivers described CNS disease symptoms, their impact on quality of life, and potential CNS-related targets that they considered important for drug development consideration. These included fatigue and daytime sleepiness; dysregulated sleep; cognitive deficits such as "brain fog," memory and focus impairment, learning and attention difficulties, and time management challenges; emotional/psychological/behavioral difficulties, including impulsivity, apathy, antisocial behavior, personality changes, and depression; social difficulties, including disconnection, lack of awareness, and feelings of isolation; and general anxieties about the future and potential loss of independence. Improvements in memory and lessening of "brain fog" were considered particularly important.
1 型肌强直性营养不良(DM1)和 2 型肌强直性营养不良(DM2)是由 19 号染色体(DM1)和 3 号染色体(DM2)上的重复扩展引起的多系统遗传性疾病。尽管 DM 对骨骼、心脏和平滑肌以及内分泌和中枢神经系统的影响可能导致残疾,但目前尚无针对该疾病的治疗方法。在 2012 年美国食品和药物管理局(FDA)建立的一个被称为以患者为中心的药物开发(PFDD)倡议的过程之后,Myotonic(以前称为肌强直性营养不良基金会)一直在进行包含患者和护理人员的会议,以探索患者和护理人员定义的疾病负担,以及受影响个体对潜在新疗法的最大需求。2017 年 9 月,在 Myotonic 的年会上,一个题为“将患者声音带入肌强直性营养不良的中枢神经系统靶向药物开发”的会议吸引了大约 350 名 DM 社区成员。在会议期间,患者和护理人员描述了中枢神经系统疾病的症状、对生活质量的影响,以及他们认为对药物开发考虑重要的潜在中枢神经系统相关靶点。这些靶点包括疲劳和白天嗜睡;睡眠失调;认知缺陷,如“脑雾”、记忆和注意力障碍、学习和注意力困难以及时间管理挑战;情绪/心理/行为困难,包括冲动、冷漠、反社会行为、人格改变和抑郁;社交困难,包括脱节、缺乏意识和孤立感;以及对未来的普遍焦虑和潜在的独立性丧失。改善记忆力和减轻“脑雾”被认为尤为重要。