Expressive language and social communication abilities in children with spinal muscular atrophy type 1.

IF 4.3 2区 医学 Q1 CLINICAL NEUROLOGY
Chiara Brusa, Bianca Buchignani, Chiara Cutri, Giorgia Coratti, Elaine Clark, Emily Johnson, Nikki Cornell, Mariacristina Scoto, Marika Pane, Eugenio Maria Mercuri, Francesco Muntoni, Giovanni Baranello
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Abstract

Aim: To investigate parent-reported expressive language and social communication abilities in children with spinal muscular atrophy type 1 (SMA1) treated with disease-modifying therapies.

Method: This was a cross-sectional feasibility study performed at the Dubowitz Neuromuscular Centre, London (UK), and the Centro Clinico Nemo Pediatrico, Rome (Italy), testing the use of the MacArthur-Bates Communicative Development Inventories (MB-CDIs, 8 months+) to explore vocabulary production, and the Social Communication Questionnaire (SCQ, 4 years+) to investigate social communication.

Results: Fifteen participants completed the MB-CDIs (age range 2 years 2 months-6 years 9 months). Thirteen out of the 15 acquired verbal skills, although with scores below normal ranges. Thirty-seven completed the SCQ (age range 4 years 0 months-9 years 0 months). Four out of the 37 scored 11 or more, suggesting the need for further assessment for autism spectrum disorder. Three out of four had completed the MB-CDIs and were among the children able to say the lowest number of words. Other areas of concern included routines/ritualized patterns of behaviour (14 out of 37) and hyperreactivity to sensory input (5 out of 37).

Interpretation: Treated children with SMA1 can acquire verbal skills, although this can be delayed. A percentage of them also present with social communication difficulties, especially when expressive language is more severely affected. Further assessments for language and social communication are, therefore, recommended and large prospective studies warranted to better characterize the spectrum of these abilities in treated children with or at risk of SMA1.

1型脊髓性肌萎缩症患儿的表达性语言和社交能力。
目的:探讨经疾病改善疗法治疗的1型脊髓性肌萎缩症(SMA1)患儿家长报告的表达性语言和社交能力。方法:这是一项横截面可行性研究,在伦敦(英国)的Dubowitz神经肌肉中心和罗马(意大利)的尼莫儿科中心进行,测试使用麦克阿瑟-贝茨交际发展量表(mb - cdi, 8个月以上)来探索词汇产生,使用社会交际问卷(SCQ, 4岁以上)来调查社会交际。结果:15名参与者完成了mb - cdi(年龄范围2岁2个月-6岁9个月)。15人中有13人获得了语言技能,尽管得分低于正常范围。37例完成SCQ(年龄范围4岁0个月-9岁0个月)。37人中有4人得分在11分以上,这表明需要对自闭症谱系障碍进行进一步评估。四分之三的孩子完成了mb - cdi测试,是能说最少单词的孩子之一。其他关注的领域包括常规/仪式化的行为模式(37人中有14人)和对感官输入的过度反应(37人中有5人)。解释:接受治疗的SMA1患儿可以获得语言技能,尽管这可能会延迟。他们中的一部分人还存在社会沟通困难,特别是当表达性语言受到更严重的影响时。因此,建议对语言和社会沟通进行进一步的评估,并进行大规模的前瞻性研究,以更好地描述患有或有SMA1风险的治疗儿童的这些能力的频谱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.80
自引率
13.20%
发文量
338
审稿时长
3-6 weeks
期刊介绍: Wiley-Blackwell is pleased to publish Developmental Medicine & Child Neurology (DMCN), a Mac Keith Press publication and official journal of the American Academy for Cerebral Palsy and Developmental Medicine (AACPDM) and the British Paediatric Neurology Association (BPNA). For over 50 years, DMCN has defined the field of paediatric neurology and neurodisability and is one of the world’s leading journals in the whole field of paediatrics. DMCN disseminates a range of information worldwide to improve the lives of disabled children and their families. The high quality of published articles is maintained by expert review, including independent statistical assessment, before acceptance.
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