Dubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health & Great Ormond Street Hospital, London, UK.
Dubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health & Great Ormond Street Hospital, London, UK.
Neuromuscul Disord. 2024 Sep;42:22-26. doi: 10.1016/j.nmd.2024.07.004. Epub 2024 Jul 11.
Spinal muscular atrophy (SMA) is an autosomal recessive disorder with progressive muscle atrophy and weakness, caused by biallelic mutations in the survival motor neuron 1 (SNM1) gene. Onasemnogene abeparvovec (OA) is an approved gene replacement therapy for patients with SMA. We report on two patients with SMA type 1, weighing 20 kg, previously treated with Nusinersen, who received OA infusion at 7 years of age. To our knowledge, these two patients are the heaviest treated in the real-world and we describe their different courses after gene therapy, including liver impairment requiring long-term steroid treatment and additional immunosuppression, with only transitory improvement in functional outcomes. Our cases illustrate how careful risk-benefit consideration is required in treating older and heavier SMA patients with OA, especially in view of the multiple treatment choices available for older patients with SMA.
脊髓性肌萎缩症(SMA)是一种常染色体隐性遗传病,表现为进行性肌肉萎缩和无力,由生存运动神经元 1(SMN1)基因的双等位基因突变引起。Onasemnogene abeparvovec(OA)是一种已获批用于治疗 SMA 患者的基因替代疗法。我们报告了两例体重为 20 公斤的 1 型 SMA 患者,他们之前曾接受过 nusinersen 治疗,在 7 岁时接受了 OA 输注。据我们所知,这两例患者是在真实世界中接受治疗的最重的患者,我们描述了他们在基因治疗后的不同病程,包括需要长期类固醇治疗和额外免疫抑制的肝损伤,仅有短暂的功能改善。我们的病例说明了在使用 OA 治疗年龄较大和体重较重的 SMA 患者时,需要仔细考虑风险-获益,特别是考虑到 SMA 老年患者有多种治疗选择。