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Impaired Language Pathways in Tuberous Sclerosis Complex Patients with Autism Spectrum Disorders

机译:结节性硬化症伴自闭症谱系障碍患者的语言通路受损

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摘要

The purpose of this study was to examine the relationship between language pathways and autism spectrum disorders (ASDs) in patients with tuberous sclerosis complex (TSC). An advanced diffusion-weighted magnetic resonance imaging (MRI) was performed on 42 patients with TSC and 42 age-matched controls. Using a validated automatic method, white matter language pathways were identified and microstructural characteristics were extracted, including fractional anisotropy (FA) and mean diffusivity (MD). Among 42 patients with TSC, 12 had ASD (29%). After controlling for age, TSC patients without ASD had a lower FA than controls in the arcuate fasciculus (AF); TSC patients with ASD had even a smaller FA, lower than the FA for those without ASD. Similarly, TSC patients without ASD had a greater MD than controls in the AF; TSC patients with ASD had even a higher MD, greater than the MD in those without ASD. It remains unclear why some patients with TSC develop ASD, while others have better language and socio-behavioral outcomes. Our results suggest that language pathway microstructure may serve as a marker of the risk of ASD in TSC patients. Impaired microstructure in language pathways of TSC patients may indicate the development of ASD, although prospective studies of language pathway development and ASD diagnosis in TSC remain essential.
机译:这项研究的目的是检查结节性硬化症(TSC)患者的语言通路与自闭症谱系障碍(ASD)之间的关系。对42例TSC患者和42例年龄匹配的对照者进行了先进的扩散加权磁共振成像(MRI)。使用经过验证的自动方法,确定了白质语言途径,并提取了微结构特征,包括分数各向异性(FA)和平均扩散率(MD)。在42例TSC患者中,有12例患有自闭症(29%)。在控制了年龄之后,没有ASD的TSC患者的FA比弓状筋膜(AF)的FA低。患有ASD的TSC患者的FA甚至更小,低于没有ASD的患者的FA。同样,没有ASD的TSC患者在AF方面的MD值要高于对照组。患有ASD的TSC患者的MD甚至更高,高于没有ASD的MD。尚不清楚为什么某些TSC患者会发展为ASD,而另一些则具有更好的语言和社会行为结果。我们的结果表明,语言通路的微观结构可能成为TSC患者ASD风险的标志。 TSC患者语言通路的微观结构受损可能表明ASD的发展,尽管对TSC语言通路发展和ASD诊断的前瞻性研究仍然很重要。

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