Department of Psychiatry & Behavioral Sciences, Stanford University, Stanford, California, USA.
Autism Res. 2022 Jun;15(6):1068-1082. doi: 10.1002/aur.2703. Epub 2022 Mar 8.
The neurobiology of autism has been shown to involve alterations in cortical morphology and gamma-aminobutyric acid A (GABA ) receptor density. We hypothesized that GABA receptor binding potential (GABA R BP ) would correlate with cortical thickness, but their correlations would differ between autistic adults and typically developing (TD) controls. We studied 50 adults (23 autism, 27 TD, mean age of 27 years) using magnetic resonance imaging to measure cortical thickness, and [ F]flumazenil positron emission tomography imaging to measure GABA R BP . We determined the correlations between cortical thickness and GABA R BP by cortical lobe, region-of-interest, and diagnosis of autism spectrum disorder (ASD). We also explored potential sex differences in the relationship between cortical thickness and autism characteristics, as measured by autism spectrum quotient (AQ) scores. Comparing autism and TD groups, no significant differences were found in cortical thickness or GABA R BP . In both autism and TD groups, a negative relationship between cortical thickness and GABA R BP was observed in the frontal and occipital cortices, but no relationship was found in the temporal or limbic cortices. A positive correlation was seen in the parietal cortex that was only significant for the autism group. Interestingly, in an exploratory analysis, we found sex differences in the relationships between cortical thickness and GABA R BP , and cortical thickness and AQ scores in the left postcentral gyrus. LAY SUMMARY: The thickness of the brain cortex and the density of the receptors associated with inhibitory neurotransmitter GABA have been hypothesized to underlie the neurobiology of autism. In this study, we found that these biomarkers correlate positively in the parietal cortex, but negatively in the frontal and occipital cortical regions of the brain. Furthermore, we collected preliminary evidence that the correlations between cortical thickness and GABA receptor density are sexdependent in a brain region where sensory inputs are registered.
自闭症的神经生物学已被证明涉及皮质形态和γ-氨基丁酸 A(GABA)受体密度的改变。我们假设 GABA 受体结合潜能(GABA RBP)与皮质厚度相关,但它们在自闭症成人和典型发育(TD)对照组之间的相关性不同。我们使用磁共振成像(MRI)研究了 50 名成年人(23 名自闭症,27 名 TD,平均年龄 27 岁),以测量皮质厚度,并使用[F]氟马西尼正电子发射断层扫描(PET)成像来测量 GABA RBP。我们通过皮质叶、感兴趣区域和自闭症谱系障碍(ASD)的诊断,确定了皮质厚度与 GABA RBP 之间的相关性。我们还探索了自闭症特征与皮质厚度之间关系的潜在性别差异,这些自闭症特征通过自闭症谱系商数(AQ)评分来衡量。与 TD 组相比,自闭症组的皮质厚度或 GABA RBP 没有显著差异。在自闭症和 TD 组中,在额叶和枕叶皮质中观察到皮质厚度与 GABA RBP 之间呈负相关,但在颞叶和边缘皮质中未发现相关性。在顶叶皮质中观察到正相关,仅在自闭症组中具有统计学意义。有趣的是,在探索性分析中,我们发现左中央后回的皮质厚度与 GABA RBP 之间的关系以及皮质厚度与 AQ 评分存在性别差异。