Epilepsy and Molecular Phenotype Affect the Neurodevelopment of Pediatric Angelman Syndrome Patients in China

Frontiers in Psychiatry

卷:13

Xiaonan Du¹  Yi Wang¹  Shuang Li¹  Tianqi Wang¹  Yu Ma¹  Huimin Jin² 

[1] Department of Neurology, Children's Hospital of Fudan University, Shanghai, China;

[2] Shanghai YangZhi Rehabilitation Hospital, School of Medicine, Tongji University, Shanghia, China;

关键词: Angelman syndrome;    neurodevelopment;    GMDS-C;    children;    epilepsy;   

DOI  :  10.3389/fpsyt.2022.886028

来源: DOAJ

【 摘 要 】

ObjectiveThis study investigated the mental development of children with Angelman syndrome (AS) in China and evaluated the relationship between neurodevelopment and molecular subtype, age, epilepsy, and sex using the Chinese version of the Griffith Mental Development Scale (GMDS-C) to provide detailed baseline data regarding neurodevelopment with AS in China.MethodsParticipants were recruited from the AS Natural History Study. The GMDS-C was used to evaluate all participants' mental age and developmental quotients. The general quotient (GQ) and quotients of five subscales (sports, personal-social, auditory language, eye-hand coordination, and comprehensive performance) were calculated.ResultsA total of 119 children (average age: 42.12 months; range, 7.5–95.5 months) with a genetic diagnosis of AS were enrolled. The median GQ score of the GMDS was 29.6 points (95% confidence interval, 28.6–33.25). The children had relatively good locomotor and personal-social skills but poor language skills. Overall, 89% (106/119) had mental ages younger than 24 months for all five subscales. The non-deletion group (i.e., without deletion in chromosome 15q11–13) had higher GQs and locomotor, personal-social, and performance subscale quotients. The GQ was significantly different among the three age subgroups and significantly correlated with age. Compared with the non-epilepsy group, the epilepsy group had lower GQs and lower quotients for the locomotor, personal-social, speech, language, and eye-hand coordination subscales.ConclusionChildren with AS in China experience severe neurodevelopmental deterioration. In addition to age, molecular subtypes and the onset of seizures may also correlate with these patients' intellectual development. The GMDS-C is an accurate tool that can assess the clinical characteristics of AS. The data of this study can be used as baseline data for clinical trials performed to evaluate drug development or other AS treatment development.

【 授权许可】

Unknown