Division of Respiratory Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.
Department of Pediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada.
Pediatr Pulmonol. 2023 Jan;58(1):161-170. doi: 10.1002/ppul.26173. Epub 2022 Oct 17.
Spinal muscular atrophy type 1 (SMA1) is a neuromuscular disorder with a natural history of chronic respiratory failure and death during infancy without ventilation. Recently, disease-modifying therapies such as nusinersen have improved disease trajectory. However, objective data on the trajectory of polysomnography outcomes, the relationship between motor scores and respiratory parameters, respiratory technology dependence and healthcare utilization in children with SMA1 remain to be elucidated.
This was a retrospective observational study of children with SMA1 receiving nusinersen between October 2016 and February 2021 at two tertiary care hospitals in Canada. Baseline polysomnography data, motor scores, respiratory technology, and unanticipated healthcare utilization were examined.
Eleven children (five females, two SMN2 copies each) were included. Median (interquartile range [IQR]) age at diagnosis was 3.6 (2.8-5.0) months and age at diagnostic polysomnogram following nusinersen initiation was 9.4 (5.3-14.0) months. Nusinersen was initiated at a median (IQR) age of 5.4 (3.4-7.6) months and 8/11 children had respiratory symptoms at that time. Diagnostic polysomnography data showed a median (IQR) central apnea-hypopnea index (AHI) of 4.1 (1.8-10.0) and obstructive AHI of 2.2 (0-8.0) events/h. We observed an inverse relationship between motor scores and central apnea-hypopnea indices. All children required ventilatory support at the end of the study period.
This study showed abnormal polysomnography parameters and need for ventilation despite nusinersen suggesting ongoing need for regular monitoring with polysomnography. Understanding the respiratory disease trajectory of children undergoing treatment with nusinersen will inform decision-making regarding optimal timing of ventilatory support initiation.
脊髓性肌萎缩症 1 型(SMA1)是一种神经肌肉疾病,其自然病史为慢性呼吸衰竭,并在婴儿期因无通气而死亡。最近,诸如 nusinersen 等疾病修正疗法改善了疾病进程。然而,关于 SMA1 患儿的睡眠多导图结果的轨迹、运动评分与呼吸参数之间的关系、呼吸技术依赖和医疗保健利用情况的客观数据仍有待阐明。
这是一项回顾性观察研究,纳入了 2016 年 10 月至 2021 年 2 月期间在加拿大两家三级保健医院接受 nusinersen 治疗的 SMA1 患儿。检查了基线睡眠多导图数据、运动评分、呼吸技术和意外的医疗保健利用情况。
纳入了 11 名患儿(5 名女性,各有 2 个 SMN2 拷贝)。诊断时的中位(四分位间距[IQR])年龄为 3.6(2.8-5.0)个月,开始使用 nusinersen 后行诊断性睡眠多导图的中位(IQR)年龄为 9.4(5.3-14.0)个月。nusinersen 的起始中位(IQR)年龄为 5.4(3.4-7.6)个月,8/11 名患儿当时已有呼吸症状。诊断性睡眠多导图数据显示,中位(IQR)中枢性呼吸暂停-低通气指数(AHI)为 4.1(1.8-10.0),阻塞性 AHI 为 2.2(0-8.0)事件/小时。我们观察到运动评分与中枢性呼吸暂停-低通气指数呈负相关。研究结束时,所有患儿均需要通气支持。
本研究显示,尽管使用了 nusinersen,但患儿仍存在睡眠多导图参数异常和通气需求,这表明需要持续进行睡眠多导图监测。了解接受 nusinersen 治疗的患儿的呼吸疾病进程,将有助于确定开始通气支持的最佳时机。