White matter microstructure and functional connectivity in the brains of infants with Turner syndrome.

IF 2.9 2区 医学 Q2 NEUROSCIENCES Cerebral cortex Pub Date : 2024-09-03 DOI:10.1093/cercor/bhae351
Reid Blanchett,Haitao Chen,Roza M Vlasova,Emil Cornea,Maria Maza,Marsha Davenport,Debra Reinhartsen,Margaret DeRamus,Rebecca Edmondson Pretzel,John H Gilmore,Stephen R Hooper,Martin A Styner,Wei Gao,Rebecca C Knickmeyer
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Abstract

Turner syndrome, caused by complete or partial loss of an X-chromosome, is often accompanied by specific cognitive challenges. Magnetic resonance imaging studies of adults and children with Turner syndrome suggest these deficits reflect differences in anatomical and functional connectivity. However, no imaging studies have explored connectivity in infants with Turner syndrome. Consequently, it is unclear when in development connectivity differences emerge. To address this gap, we compared functional connectivity and white matter microstructure of 1-year-old infants with Turner syndrome to typically developing 1-year-old boys and girls. We examined functional connectivity between the right precentral gyrus and five regions that show reduced volume in 1-year old infants with Turner syndrome compared to controls and found no differences. However, exploratory analyses suggested infants with Turner syndrome have altered connectivity between right supramarginal gyrus and left insula and right putamen. To assess anatomical connectivity, we examined diffusivity indices along the superior longitudinal fasciculus and found no differences. However, an exploratory analysis of 46 additional white matter tracts revealed significant group differences in nine tracts. Results suggest that the first year of life is a window in which interventions might prevent connectivity differences observed at later ages, and by extension, some of the cognitive challenges associated with Turner syndrome.
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特纳综合征婴儿大脑白质微结构和功能连接。
特纳综合征是由完全或部分缺失 X 染色体引起的,通常伴有特定的认知障碍。对特纳综合征成人和儿童进行的磁共振成像研究表明,这些缺陷反映了解剖学和功能连接的差异。然而,目前还没有成像研究探讨特纳综合征婴儿的连接性。因此,目前还不清楚在发育过程中何时会出现连接性差异。为了填补这一空白,我们比较了特纳综合征 1 岁婴儿与发育正常的 1 岁男孩和女孩的功能连接性和白质微结构。我们研究了特纳综合征 1 岁婴儿与对照组相比右侧前脑回和五个体积缩小的区域之间的功能连接,结果发现两者之间没有差异。然而,探索性分析表明,特纳综合征婴儿的右侧边际上回与左侧岛叶和右侧丘脑之间的连通性发生了改变。为了评估解剖连接性,我们检查了沿上纵筋束的扩散指数,结果没有发现差异。然而,对另外46个白质束的探索性分析显示,9个白质束存在显著的群体差异。研究结果表明,出生后的第一年是一个窗口期,在这个时期采取干预措施可能会避免在晚年观察到的连接性差异,进而避免与特纳综合征相关的一些认知挑战。
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来源期刊
Cerebral cortex
Cerebral cortex 医学-神经科学
CiteScore
6.30
自引率
8.10%
发文量
510
审稿时长
2 months
期刊介绍: Cerebral Cortex publishes papers on the development, organization, plasticity, and function of the cerebral cortex, including the hippocampus. Studies with clear relevance to the cerebral cortex, such as the thalamocortical relationship or cortico-subcortical interactions, are also included. The journal is multidisciplinary and covers the large variety of modern neurobiological and neuropsychological techniques, including anatomy, biochemistry, molecular neurobiology, electrophysiology, behavior, artificial intelligence, and theoretical modeling. In addition to research articles, special features such as brief reviews, book reviews, and commentaries are included.
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