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接受 nusinersen 治疗的 II 型脊髓性肌萎缩症儿科患者的年龄相关治疗效果。

Age related treatment effect in type II Spinal Muscular Atrophy pediatric patients treated with nusinersen.

机构信息

Pediatric Neurology, Università Cattolica del Sacro Cuore, Rome, Italy; Centro Clinico Nemo, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.

Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.

出版信息

Neuromuscul Disord. 2021 Jul;31(7):596-602. doi: 10.1016/j.nmd.2021.03.012. Epub 2021 Apr 2.

Abstract

Previous natural history studies suggest that type II SMA patients remain stable over one year but show some progression over two years. Since nusinersen approval, there has been increasing attention to identify more specific age-related changes. The aim of the study was to establish 12-month changes in a cohort of pediatric type II SMA treated with nusinersen and to establish possible patterns of treatment effect in relation to different variables such as age, baseline value and SMN2 copy number. The Hammersmith Functional Motor Scale Expanded and the Revised Upper Limb Module were performed at T0 and 12 months after treatment (T12). Data in treated patients were compared to available data in untreated patients collected by the same evaluators.Seventy-seven patients of age between 2.64 and 17.88 years (mean:7.47, SD:3.79) were included. On t-test there was an improvement, with increased mean scores between T0 and T12 on both scales (p < 0.001). Using multivariate linear regression analysis, age and baseline scores were predictive of changes on both scales (p < 0.05) while SMN2 copy number was not. Differences were also found between study cohort and untreated data on both scales (p < 0.001). At 12 months, an increase in scores was observed in all the age subgroups at variance with natural history data. Our real-world data confirm the treatment effect of nusinersen in pediatric type II SMA patients and that the data interpretation should take into account different variables. These data confirm and expand the ones already reported in the Cherish study.

摘要

先前的自然病史研究表明,II 型 SMA 患者在一年内保持稳定,但在两年内会出现一些进展。自从 nusinersen 获批以来,人们越来越关注识别更具体的与年龄相关的变化。本研究旨在确定接受 nusinersen 治疗的儿科 II 型 SMA 患者队列在 12 个月内的变化,并确定与不同变量(如年龄、基线值和 SMN2 拷贝数)相关的可能治疗效果模式。在治疗前(T0)和治疗后 12 个月(T12)进行了 Hammersmith 功能运动量表扩展版和修订后的上肢模块评估。将治疗患者的数据与同一评估者收集的未治疗患者的可用数据进行比较。共有 77 名年龄在 2.64 至 17.88 岁之间的患者(平均年龄:7.47,标准差:3.79)被纳入研究。在 T 检验中,两个量表的评分均有所提高,T0 与 T12 之间的平均评分均有显著差异(p<0.001)。使用多元线性回归分析,年龄和基线评分是两个量表变化的预测因素(p<0.05),而 SMN2 拷贝数则不是。两个量表的研究队列与未治疗数据之间也存在差异(p<0.001)。在 12 个月时,所有年龄亚组的评分都有所增加,与自然病史数据不同。我们的真实世界数据证实了 nusinersen 在儿科 II 型 SMA 患者中的治疗效果,并且数据解释应考虑到不同的变量。这些数据证实并扩展了 Cherish 研究中已经报道的数据。

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