遗传网络表明,阿斯伯格综合症是自闭症谱系障碍的一个独特亚型。

IF 2.2 4区 医学 Q1 EDUCATION, SPECIAL Research in Autism Spectrum Disorders Pub Date : 2024-09-27 DOI:10.1016/j.rasd.2024.102484
Sadiq Naveed , Adam A. Dmytriw , Sherief Ghozy , Sara Morsy
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引用次数: 0

摘要

背景《精神疾病诊断与统计手册》(DSM-V)发布了新的自闭症谱系障碍(ASD)诊断标准,导致一些阿斯伯格综合症(AS)病例被漏诊。这对患者获得的支持产生了负面影响。在这项研究中,我们通过基因共表达网络保存分析,探讨了自闭症是否可以从生物学上从更广泛的谱系中分层。方法我们分析了 24 名阿斯伯格综合征患者和 72 名自闭症患者的 GEO 微阵列数据。然后,我们使用加权基因共表达网络(WGCNA)管道构建了基因共表达网络。结果表明,自闭症的所有共表达模块在阿斯伯格综合征中都得到了保留。基因富集分析表明,这些模块涉及染色质重塑、免疫和神经炎症反应、突触和神经元发育。脑富集分析表明,在阿斯伯格综合症患者中,与社会识别能力受损相关的不同脑区的神经发育基因出现了明显的下调。结论已确定的遗传和分子特征表明,尽管阿斯伯格综合症与自闭症有许多相似之处,但它具有独特的遗传特征,使其成为自闭症的一个独特亚型。这种区别可能会对针对阿斯伯格综合症患者的管理和治疗策略产生重大影响。
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Genetic networks suggest Asperger’s syndrome as a distinct subtype of autism spectrum disorders.

Background

The Diagnostic and Statistical Manual of Mental Disorders (DSM-V) issued new diagnostic criteria for autism spectrum disorders (ASD) which resulted in missing the diagnosis of some cases of Asperger’s syndrome (AS). This negatively affected the support received by those affected. In this study, we explored if AS could be biologically stratified from the broader spectrum through a gene co-expression network preservation analysis.

Methods

We analysed the GEO microarray data of 24 individuals with Asperger’s syndrome and 72 individuals with autism. Then, we used a weighted gene co-expression network (WGCNA) pipeline to construct gene co-expression networks. We explored whether these modules share the same co-expression patterns between autism and Asperger’s syndrome using network preservation analysis.

Results

Our results showed that all co-expression modules of autism are preserved into the Asperger’s syndrome. However, three modules of Asperger’s syndrome out of 30 modules were not preserved in autism.
Gene enrichment analysis revealed that these modules were involved in chromatin remodelling, immune and neuroinflammatory response, synaptic and neuronal development. Brain enrichment analysis showed significant downregulation of neurodevelopment genes in different brain regions associated with impaired social recognition in Asperger’s syndrome.

Conclusions

The identified genetic and molecular profiles suggest that Asperger’s syndrome, despite sharing numerous similarities with autism, possesses a distinct genetic profile that makes it a distinct subtype of autism. This distinction could have significant implications for the management and treatment strategies tailored to individuals with Asperger’s syndrome.
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来源期刊
CiteScore
4.20
自引率
8.00%
发文量
108
期刊介绍: Research in Autism Spectrum Disorders (RASD) publishes high quality empirical articles and reviews that contribute to a better understanding of Autism Spectrum Disorders (ASD) at all levels of description; genetic, neurobiological, cognitive, and behavioral. The primary focus of the journal is to bridge the gap between basic research at these levels, and the practical questions and difficulties that are faced by individuals with ASD and their families, as well as carers, educators and clinicians. In addition, the journal encourages submissions on topics that remain under-researched in the field. We know shamefully little about the causes and consequences of the significant language and general intellectual impairments that characterize half of all individuals with ASD. We know even less about the challenges that women with ASD face and less still about the needs of individuals with ASD as they grow older. Medical and psychological co-morbidities and the complications they bring with them for the diagnosis and treatment of ASD represents another area of relatively little research. At RASD we are committed to promoting high-quality and rigorous research on all of these issues, and we look forward to receiving many excellent submissions.
期刊最新文献
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