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探索自闭症谱系障碍中的性别差异。

Towards understanding sex differences in autism spectrum disorders.

机构信息

Department of Physiology, Biomedical Discovery Institute, Monash University, Victoria, Australia.

Tianjin Institute of Infectious Disease, Second Hospital of Tianjin Medical University, China.

出版信息

Brain Res. 2024 Jun 15;1833:148877. doi: 10.1016/j.brainres.2024.148877. Epub 2024 Mar 19.

Abstract

Autism Spectrum Disorder (ASD) is a neurodevelopmental condition characterized by social deficits, repetitive behaviours and lack of empathy. Its significant genetic heritability and potential comorbidities often lead to diagnostic and therapeutic challenges. This review addresses the biological basis of ASD, focusing on the sex differences in gene expression and hormonal influences. ASD is more commonly diagnosed in males at a ratio of 4:1, indicating a potential oversight in female-specific ASD research and a risk of underdiagnosis in females. We consider how ASD manifests differently across sexes by exploring differential gene expression in female and male brains and consider how variations in steroid hormones influence ASD characteristics. Synaptic function, including excitation/inhibition ratio imbalance, is influenced by gene mutations and this is explored as a key factor in the cognitive and behavioural manifestations of ASD. We also discuss the role of micro RNAs (miRNAs) and highlight a novel mutation in miRNA-873, which affects a suite of key synaptic genes, neurexin, neuroligin, SHANK and post-synaptic density proteins, implicated in the pathology of ASD. Our review suggests that genetic predisposition, sex differences in brain gene expression, and hormonal factors significantly contribute to the presentation, identification and severity of ASD, necessitating sex-specific considerations in diagnosis and treatments. These findings advocate for personalized interventions to improve the outcomes for individuals with ASD.

摘要

自闭症谱系障碍 (ASD) 是一种神经发育障碍,其特征是社交缺陷、重复行为和缺乏同理心。其显著的遗传遗传性和潜在的共病性常常导致诊断和治疗方面的挑战。这篇综述探讨了 ASD 的生物学基础,重点关注基因表达和激素影响方面的性别差异。ASD 更常见于男性,男女比例为 4:1,这表明女性特定的 ASD 研究存在潜在的忽视,女性的诊断不足风险也更高。我们通过探讨女性和男性大脑中的差异基因表达,考虑 ASD 在性别之间的不同表现方式,并考虑类固醇激素的变化如何影响 ASD 特征。突触功能,包括兴奋/抑制比失衡,受基因突变的影响,这被认为是 ASD 认知和行为表现的一个关键因素。我们还讨论了 microRNAs (miRNAs) 的作用,并强调了 miRNA-873 的一个新突变,该突变影响了一系列关键的突触基因,包括神经连接蛋白、神经连接蛋白聚糖、SHANK 和突触后密度蛋白,这些基因与 ASD 的病理学有关。我们的综述表明,遗传易感性、大脑基因表达的性别差异和激素因素对 ASD 的表现、识别和严重程度有重要影响,因此在诊断和治疗中需要考虑性别特异性。这些发现提倡采取个性化干预措施,以改善 ASD 患者的预后。

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