Cargando…

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

OBJECTIVE: This 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 deta...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Shuang, Ma, Yu, Wang, Tianqi, Jin, Huimin, Du, Xiaonan, Wang, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9096167/
https://www.ncbi.nlm.nih.gov/pubmed/35573374
http://dx.doi.org/10.3389/fpsyt.2022.886028
_version_ 1784705916278407168
author Li, Shuang
Ma, Yu
Wang, Tianqi
Jin, Huimin
Du, Xiaonan
Wang, Yi
author_facet Li, Shuang
Ma, Yu
Wang, Tianqi
Jin, Huimin
Du, Xiaonan
Wang, Yi
author_sort Li, Shuang
collection PubMed
description OBJECTIVE: This 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. METHODS: Participants 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. RESULTS: A 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. CONCLUSION: Children 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.
format Online
Article
Text
id pubmed-9096167
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-90961672022-05-13 Epilepsy and Molecular Phenotype Affect the Neurodevelopment of Pediatric Angelman Syndrome Patients in China Li, Shuang Ma, Yu Wang, Tianqi Jin, Huimin Du, Xiaonan Wang, Yi Front Psychiatry Psychiatry OBJECTIVE: This 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. METHODS: Participants 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. RESULTS: A 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. CONCLUSION: Children 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. Frontiers Media S.A. 2022-04-28 /pmc/articles/PMC9096167/ /pubmed/35573374 http://dx.doi.org/10.3389/fpsyt.2022.886028 Text en Copyright © 2022 Li, Ma, Wang, Jin, Du and Wang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Psychiatry
Li, Shuang
Ma, Yu
Wang, Tianqi
Jin, Huimin
Du, Xiaonan
Wang, Yi
Epilepsy and Molecular Phenotype Affect the Neurodevelopment of Pediatric Angelman Syndrome Patients in China
title Epilepsy and Molecular Phenotype Affect the Neurodevelopment of Pediatric Angelman Syndrome Patients in China
title_full Epilepsy and Molecular Phenotype Affect the Neurodevelopment of Pediatric Angelman Syndrome Patients in China
title_fullStr Epilepsy and Molecular Phenotype Affect the Neurodevelopment of Pediatric Angelman Syndrome Patients in China
title_full_unstemmed Epilepsy and Molecular Phenotype Affect the Neurodevelopment of Pediatric Angelman Syndrome Patients in China
title_short Epilepsy and Molecular Phenotype Affect the Neurodevelopment of Pediatric Angelman Syndrome Patients in China
title_sort epilepsy and molecular phenotype affect the neurodevelopment of pediatric angelman syndrome patients in china
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9096167/
https://www.ncbi.nlm.nih.gov/pubmed/35573374
http://dx.doi.org/10.3389/fpsyt.2022.886028
work_keys_str_mv AT lishuang epilepsyandmolecularphenotypeaffecttheneurodevelopmentofpediatricangelmansyndromepatientsinchina
AT mayu epilepsyandmolecularphenotypeaffecttheneurodevelopmentofpediatricangelmansyndromepatientsinchina
AT wangtianqi epilepsyandmolecularphenotypeaffecttheneurodevelopmentofpediatricangelmansyndromepatientsinchina
AT jinhuimin epilepsyandmolecularphenotypeaffecttheneurodevelopmentofpediatricangelmansyndromepatientsinchina
AT duxiaonan epilepsyandmolecularphenotypeaffecttheneurodevelopmentofpediatricangelmansyndromepatientsinchina
AT wangyi epilepsyandmolecularphenotypeaffecttheneurodevelopmentofpediatricangelmansyndromepatientsinchina