髓鞘少突胶质细胞糖蛋白抗体相关疾病患儿的认知能力和学习成绩。

IF 3.8 2区 医学 Q1 CLINICAL NEUROLOGY Developmental Medicine and Child Neurology Pub Date : 2024-10-16 DOI:10.1111/dmcn.16093
Audrey Mittelman, Julie Pique, Vincent Desportes, Kumaran Deiva, Anne-Lise Poulat, Romain Marignier
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引用次数: 0

摘要

目的:描述小儿髓鞘少突胶质细胞糖蛋白抗体相关疾病(MOGAD)对学习和认知结果的影响:方法:这是一项观察性、回顾性和描述性的单中心研究,研究对象是患有髓鞘少突胶质细胞糖蛋白抗体相关疾病的儿科病例系列:共纳入 51 名患者(22 名女性),中位年龄为 8 岁,中位随访时间为 31.1 个月(四分位数间距为 23.5)。最常见的临床表现是急性播散性脑脊髓炎(54.9%),其次是视神经炎(35.5%)。在最后一次随访中,无论发病时的临床表型如何,39.5% 的 MOGAD 患者接受了学术和教育干预(p 解释:MOGAD 患者需要接受学术和教育干预:MOGAD 与需要学术支持有关;WISC-V 的得分较低。多发性骨髓增生异常综合征患者应接受认知和学业评估,以便为教育规划提供依据,并为学业成功提供支持。
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Cognitive and academic outcomes in children with myelin oligodendrocyte glycoprotein antibody-associated disease.

Aim: To describe the impact of paediatric myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) on academic and cognitive outcomes.

Method: This was an observational, retrospective, and descriptive single-centre study, carried out on a paediatric case series of children with MOGAD.

Results: A total of 51 patients were included (22 females); their median age was 8 years and the median follow-up duration was 31.1 months (interquartile range 23.5). The most frequent clinical presentation was acute disseminated encephalomyelitis (54.9%), followed by optic neuritis (35.5%). At the last follow-up, regardless of the clinical phenotype at disease onset, 39.5% of patients with MOGAD received academic and educational interventions (p < 0.05 compared to before disease onset), including academic accommodations (p < 0.05) or the need for a learning support assistant (p < 0.05). Ten patients were evaluated with the Wechsler Intelligence Scale for Children, Fifth Edition (WISC-V). The overall IQ was calculated for six patients (mean = 92); two of these patients had an IQ lower than 85. No difference was found regarding prenatal and neonatal neurodevelopmental characteristics between this cohort and the general population.

Interpretation: MOGAD was associated with a need for academic support; lower scores were found on the WISC-V. Patients with MOGAD should receive cognitive and academic assessments to inform educational planning and support academic success.

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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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