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接受脊髓性肌萎缩治疗的新生儿和幼儿的纵向发育概况。

Longitudinal developmental profile of newborns and toddlers treated for spinal muscular atrophy.

作者信息

Ngawa Magali, Dal Farra Fabian, Marinescu Andrei-Dan, Servais Laurent

机构信息

Neuromuscular Reference Center, Department of Paediatrics, University Hospital Liège & University of Liège, Belgium.

Division of Child Neurology, Centre de Références des Maladies Neuromusculaires, Department of Pediatrics, University Hospital Liège & University of Liège, Liège, Belgium.

出版信息

Ther Adv Neurol Disord. 2023 Feb 20;16:17562864231154335. doi: 10.1177/17562864231154335. eCollection 2023.

Abstract

BACKGROUND

Spinal muscular atrophy (SMA) results from a loss-of-function mutation in the gene. SMA patients suffer progressive motor disability, although no intellectual impairments have been described. Three drugs have been recently approved by the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA). These drugs result in longer life expectancy for SMA type 1 (SMA1) patients.

OBJECTIVE

The objective of the study was to assess longitudinally the psychomotor development of patients with SMA1 treated after the symptom onset and of patients treated presymptomatically.

DESIGN

Longitudinal, monocentric, noninterventional, prospective study.

METHODS

Our study included 11 SMA1 patients and seven presymptomatic SMA patients. The SMA1 patients were treated with an approved drug beginning after onset of symptoms; treatment for the presymptomatic patients was begun before symptom onset. They were longitudinally evaluated between September 2018 and January 2022 using the Bayley Scales of Infant and Toddler Development™ - Third Edition.

RESULTS

At each time point, all patients treated presymptomatically scored above those treated postsymptomatically on the motor scale. The cognitive scores of six of the seven patients treated presymptomatically were average; one patient was in the low average range. In the 11 postsymptomatically treated patients, four scored either in the low average or the abnormal range on the cognitive scale, but a positive trend was observed during the follow-up.

CONCLUSION

A significant proportion of patients treated postsymptomatically scored below average on cognitive and communicative scales, with most significant concerns raised about the age of 1 year. Our study indicates that intellectual development should be considered as an important outcome in treated SMA1 patients. Cognitive and communicative evaluations should be performed as part of standard of care, and guidance should be provided to parents for optimal stimulation.

摘要

背景

脊髓性肌萎缩症(SMA)由该基因的功能丧失突变引起。SMA患者会出现进行性运动功能障碍,不过尚未有智力受损的相关描述。最近,三种药物已获得美国食品药品监督管理局(FDA)和欧洲药品管理局(EMA)的批准。这些药物可延长1型脊髓性肌萎缩症(SMA1)患者的预期寿命。

目的

本研究的目的是纵向评估症状出现后接受治疗的SMA1患者以及症状前接受治疗的患者的心理运动发育情况。

设计

纵向、单中心、非干预性、前瞻性研究。

方法

我们的研究纳入了11名SMA1患者和7名症状前SMA患者。SMA1患者在症状出现后开始使用一种获批药物进行治疗;症状前患者在症状出现前开始治疗。在2018年9月至2022年1月期间,使用贝利婴幼儿发展量表第三版对他们进行纵向评估。

结果

在每个时间点,所有症状前接受治疗的患者在运动量表上的得分均高于症状后接受治疗的患者。7名症状前接受治疗的患者中有6名的认知得分处于平均水平;1名患者处于低平均水平范围。在11名症状后接受治疗的患者中,4名在认知量表上的得分处于低平均或异常范围,但在随访期间观察到了积极趋势。

结论

相当一部分症状后接受治疗的患者在认知和交流量表上的得分低于平均水平,其中在1岁左右时问题最为突出。我们的研究表明,智力发育应被视为接受治疗的SMA1患者的一项重要结局。应将认知和交流评估作为标准护理的一部分进行,并应为家长提供最佳刺激的指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec4/9944336/66430dd4ffdc/10.1177_17562864231154335-fig1.jpg

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