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Reduced subcortical glutamate/glutamine in adults with autism spectrum disorders: a 1HMRS study

机译:成人自闭症谱系障碍患者皮层下谷氨酸/谷氨酰胺减少:一项1H MRS研究

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摘要

Dysfunctional glutamatergic neurotransmission has been implicated in autism spectrum disorder (ASD). However, relatively few studies have directly measured brain glutamate in ASD adults, or related variation in glutamate to clinical phenotype. We therefore set out to investigate brain glutamate levels in adults with an ASD, comparing these to healthy controls and also comparing results between individuals at different points on the spectrum of symptom severity. We recruited 28 adults with ASD and 14 matched healthy controls. Of those with ASD, 15 fulfilled the ‘narrowly' defined criteria for typical autism, whereas 13 met the ‘broader phenotype'. We measured the concentration of the combined glutamate and glutamine signal (Glx), and other important metabolites, using proton magnetic resonance spectroscopy in two brain regions implicated in ASD—the basal ganglia (including the head of caudate and the anterior putamen) and the dorsolateral prefrontal cortex—as well as in a parietal cortex ‘control' region. Individuals with ASD had a significant decrease (P<0.001) in concentration of Glx in the basal ganglia, and this was true in both the ‘narrow' and ‘broader' phenotype. Also, within the ASD sample, reduced basal ganglia Glx was significantly correlated with increased impairment in social communication (P=0.013). In addition, there was a significant reduction in the concentration of other metabolites such as choline, creatine (Cr) and N-acetylaspartate (NAA) in the basal ganglia. In the dorsolateral prefrontal cortex, Cr and NAA were reduced (P<0.05), although Glx was not. There were no detectable differences in Glx, or any other metabolite, in the parietal lobe control region. There were no significant between-group differences in age, gender, IQ, voxel composition or data quality. In conclusion, individuals across the spectrum of ASD have regionally specific abnormalities in subcortical glutamatergic neurotransmission that are associated with variation in social development.
机译:功能障碍的谷氨酸能神经传递与自闭症谱系障碍(ASD)有关。但是,很少有研究直接测量ASD成人的大脑谷氨酸或谷氨酸与临床表型的相关变化。因此,我们着手调查患有ASD的成年人的脑谷氨酸水平,将其与健康对照组进行比较,还比较症状严重程度谱上不同点的个体之间的结果。我们招募了28名患有ASD的成年人和14名相匹配的健康对照组。在患有自闭症的人群中,有15个满足了典型自闭症的“狭义”定义标准,而13个满足了“更广泛的表型”。我们使用质子磁共振波谱在涉及ASD的两个大脑区域(基底神经节(包括尾状头和前壳核)和背外侧)中使用质子磁共振波谱测量了谷氨酸和谷氨酰胺信号(Glx)和其他重要代谢产物的浓度前额叶皮层以及顶叶皮层的“对照”区域。患有ASD的个体的基底神经节中Glx的浓度显着降低(P <0.001),“狭窄”和“广泛”表型均是如此。同样,在ASD样本中,基底节神经节Glx减少与社交沟通障碍增加显着相关(P = 0.013)。此外,基底神经节中其他代谢物(例如胆碱,肌酸(Cr)和N-乙酰天冬氨酸(NAA))的浓度显着降低。在背外侧前额叶皮层中,Cr和NAA降低(P <0.05),而Glx未降低。在顶叶控制区中,Glx或任何其他代谢物没有可检测到的差异。年龄,性别,智商,体素组成或数据质量在组间无显着差异。总之,整个ASD谱系中的个体在皮层下谷氨酸能神经传递中具有与社会发展变化相关的区域性特定异常。

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