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脊髓肌萎缩症 1 型患儿在接受onasemnogene abeparvovec 基因治疗后的脊髓表现 - SMA REACH UK 网络经验。

Spinal presentations in children with spinal muscular atrophy type 1 following gene therapy treatment with onasemnogene abeparvovec - The SMA REACH UK network experience.

机构信息

Department of Paediatric Neurology - Neuromuscular Service, Evelina London Children's Hospital, Guy's & St Thomas' NHS Foundation Trust, London, UK; Dubowitz Neuromuscular Centre, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK; Institute of Child Health, University College London, Gower St, London WC1E 6BT, UK.

Department of Paediatric Neurology - Neuromuscular Service, Evelina London Children's Hospital, Guy's & St Thomas' NHS Foundation Trust, London, UK.

出版信息

Neuromuscul Disord. 2024 Nov;44:104451. doi: 10.1016/j.nmd.2024.104451. Epub 2024 Sep 15.

Abstract

Spinal muscular atrophy (SMA) is a neuromuscular disorder of mainly early onset and variable severity. Prior to the introduction of disease modifying therapies (DMTs), children with SMA type 1 typically died before 2 years of age and management was primarily palliative. Onasemnogene abeparvovec (OA), nusinersen, and risdiplam are novel DMTs which ameliorate the effects of the underlying genetic defect at least partially making SMA a treatable condition. Survival and achievement of previously unmet developmental milestones result in treated SMA type 1 children spending more time upright than expected based on the natural history of the treatment-naïve condition. Consequently, spinal asymmetry and kyphosis, features not typically seen in untreated SMA type 1 children due to early mortality, are increasingly common complications. Precise data regarding their prevalence, severity, and management are currently limited. This study describes the spinal features and management in 75 children with SMA type 1 who received OA between March 2021 and December 2022. Retrospective analysis from SMA REACH UK data showed that 44/75 (59 %) clinically had spinal asymmetry and 37 (49 %) had kyphosis. This study aims to raise awareness of this important feature as part of the changed natural history of SMA type 1 post OA treatment.

摘要

脊髓性肌萎缩症(SMA)是一种主要为早发型且具有不同严重程度的神经肌肉疾病。在引入疾病修正疗法(DMT)之前,SMA 1 型患儿通常在 2 岁之前死亡,治疗主要是姑息性的。onasemnogene abeparvovec(OA)、nusinersen 和 risdiplam 是新型 DMT,它们至少部分改善了潜在遗传缺陷的影响,使 SMA 成为一种可治疗的疾病。生存和实现以前未满足的发育里程碑,使接受治疗的 SMA 1 型儿童比基于未经治疗的疾病自然史预期的时间更长时间保持直立。因此,脊柱不对称和脊柱后凸,由于早期死亡率,在未经治疗的 SMA 1 型儿童中通常不会出现这些特征,越来越成为常见的并发症。目前关于其患病率、严重程度和管理的精确数据有限。本研究描述了 75 名接受 OA 治疗的 SMA 1 型患儿的脊柱特征和管理情况,这些患儿均来自 SMA REACH UK 数据。回顾性分析显示,44/75(59%)患儿临床存在脊柱不对称,37(49%)患儿存在脊柱后凸。本研究旨在提高对这一重要特征的认识,因为这是 SMA 1 型患儿接受 OA 治疗后疾病自然史改变的一部分。

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