Brain structure in triple X syndrome: regional gray matter volume and cortical thickness in adult women with 47,XXX karyotype.

IF 4.1 2区 医学 Q1 CLINICAL NEUROLOGY
Gregor Domes, Marie-Anne Croyé, Petra Freilinger, Andreas Bohlscheid, Winfried A Willinek, Jobst Meyer
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引用次数: 0

Abstract

Background: Changes in the brain structure of women with Triple X syndrome (karyotype 47,XXX) have been described in a few studies to date, including reduced total brain volume and regional reductions in gray substance in cortical and subcortical areas. However, the empirical evidence from adults is very limited and group comparison on a voxel-wise basis for gray matter volume and cortical thickness is still missing.

Methods: Using voxel-based morphometry (VBM) and surface-based morphometry (SBM), we investigated regional gray matter changes in a sample of n = 20 adult women (aged 18-49 years) with 47,XXX karyotype using T1-weighted 3T MRI scans.

Results: Compared to an age- and education-matched control group (and controlled for differences in total intracranial volume), the VBM revealed decreased regional gray matter volumes in the hippocampus, amygdala, parts of the basal ganglia, insula, prefrontal areas and cerebellum. To a lesser extent, we also noted specific reductions in cortical thickness in a smaller part of those regions.

Conclusion: The observed network is significantly involved in the processing of cognitive, affective, and social stimuli and might be a potential neuronal correlate of the autism-like social-cognitive problems described in 47,XXX in the literature.

X染色体综合征的脑结构:核型为47,xxx的成年女性的区域灰质体积和皮质厚度
背景:迄今为止,一些研究已经描述了患有三重X综合征(核型47,XXX)的女性大脑结构的变化,包括脑总量减少和皮层和皮层下区域灰色物质的局部减少。然而,来自成年人的经验证据非常有限,在体素基础上的灰质体积和皮层厚度的组比较仍然缺失。方法:采用体素形态测定法(VBM)和表面形态测定法(SBM),采用t1加权3T MRI扫描,研究了n = 20例核型为47xxx的成年女性(18-49岁)的区域灰质变化。结果:与年龄和教育程度匹配的对照组(并控制总颅内容积差异)相比,VBM显示海马、杏仁核、部分基底节区、脑岛、前额叶区和小脑的区域灰质体积减少。在较小程度上,我们也注意到这些区域中较小部分的皮层厚度特异性减少。结论:观察到的神经网络显著参与认知、情感和社会刺激的处理,可能是文献47,XXX中描述的自闭症样社会认知问题的潜在神经元关联。
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来源期刊
CiteScore
7.60
自引率
4.10%
发文量
58
审稿时长
>12 weeks
期刊介绍: Journal of Neurodevelopmental Disorders is an open access journal that integrates current, cutting-edge research across a number of disciplines, including neurobiology, genetics, cognitive neuroscience, psychiatry and psychology. The journal’s primary focus is on the pathogenesis of neurodevelopmental disorders including autism, fragile X syndrome, tuberous sclerosis, Turner Syndrome, 22q Deletion Syndrome, Prader-Willi and Angelman Syndrome, Williams syndrome, lysosomal storage diseases, dyslexia, specific language impairment and fetal alcohol syndrome. With the discovery of specific genes underlying neurodevelopmental syndromes, the emergence of powerful tools for studying neural circuitry, and the development of new approaches for exploring molecular mechanisms, interdisciplinary research on the pathogenesis of neurodevelopmental disorders is now increasingly common. Journal of Neurodevelopmental Disorders provides a unique venue for researchers interested in comparing and contrasting mechanisms and characteristics related to the pathogenesis of the full range of neurodevelopmental disorders, sharpening our understanding of the etiology and relevant phenotypes of each condition.
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