June Christoph Kang, SuHyuk Chi, Young Eun Mok, Jeong-Ahn Kim, So Hyun Kim, Moon Soo Lee
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We examined fractional anisotropy (FA), radial diffusivity (RD), axial diffusivity, and mean diffusivity in 42 specific significant white matter tracts.</p><p><strong>Results: </strong>Our findings revealed notable differences in the children with tic disorders compared to the control group. Specifically, there was a significant reduction in FA in the parietal part and splenium of the corpus callosum and the left corticospinal tract. Increased RD was observed in the temporal and splenium areas of the corpus callosum, the left corticospinal tract, and the left acoustic radiation. A higher mean diffusivity was also noted in the left middle longitudinal fasciculus. A significant correlation emerged between the severity of motor symptoms, measured by the Yale Global Tic Severity Scale, and FA in the parietal part of the corpus callosum, as well as RD in the left acoustic radiation.</p><p><strong>Conclusion: </strong>These results indicate a pattern of reduced interhemispheric connectivity in the corpus callosum, aligning with previous studies and novel findings in the diffusion indices changes in the left corticospinal tract, left acoustic radiation, and left middle longitudinal fasciculus. 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引用次数: 0
摘要
背景介绍抽搐症是一种以不自主运动或发声为特征的神经精神疾病。以往利用弥散加权成像技术探讨抽搐症的白质改变的研究报告中,有关受影响束的结果并不一致。我们旨在通过采用一种新的束成像技术进行更详细的分析来填补这一空白:我们使用一种先进的自动概率束成像方法--TRActs Constrained by UnderLying Anatomy (TRACULA),分析了 23 名抽动障碍患儿和 23 名健康对照者的 MRI 数据。我们检测了 42 个特定重要白质束的分数各向异性(FA)、径向扩散率(RD)、轴向扩散率和平均扩散率:我们的研究结果表明,与对照组相比,患有抽搐症的儿童存在明显差异。具体来说,胼胝体顶叶部分和脾脏以及左侧皮质脊髓束的 FA 明显减少。在胼胝体的颞区和脾区、左侧皮质脊髓束和左侧声辐射中观察到 RD 增加。左侧中纵筋束的平均扩散率也较高。用耶鲁全球抽搐严重程度量表(Yale Global Tic Severity Scale)测量的运动症状严重程度与胼胝体顶叶部分的FA和左声辐射的RD之间存在明显的相关性:这些结果表明,胼胝体的半球间连通性降低,这与之前的研究以及左侧皮质脊髓束、左侧声辐射和左侧中纵筋束的弥散指数变化的新发现一致。抽搐症可能涉及关键白质束的结构异常,这为研究抽搐症的发病机制提供了新的视角。
Diffusion indices alteration in major white matter tracts of children with tic disorder using TRACULA.
Background: Tic disorder is a neuropsychiatric disorder characterized by involuntary movements or vocalizations. Previous studies utilizing diffusion-weighted imaging to explore white-matter alterations in tic disorders have reported inconsistent results regarding the affected tracts. We aimed to address this gap by employing a novel tractography technique for more detailed analysis.
Methods: We analyzed MRI data from 23 children with tic disorders and 23 healthy controls using TRActs Constrained by UnderLying Anatomy (TRACULA), an advanced automated probabilistic tractography method. We examined fractional anisotropy (FA), radial diffusivity (RD), axial diffusivity, and mean diffusivity in 42 specific significant white matter tracts.
Results: Our findings revealed notable differences in the children with tic disorders compared to the control group. Specifically, there was a significant reduction in FA in the parietal part and splenium of the corpus callosum and the left corticospinal tract. Increased RD was observed in the temporal and splenium areas of the corpus callosum, the left corticospinal tract, and the left acoustic radiation. A higher mean diffusivity was also noted in the left middle longitudinal fasciculus. A significant correlation emerged between the severity of motor symptoms, measured by the Yale Global Tic Severity Scale, and FA in the parietal part of the corpus callosum, as well as RD in the left acoustic radiation.
Conclusion: These results indicate a pattern of reduced interhemispheric connectivity in the corpus callosum, aligning with previous studies and novel findings in the diffusion indices changes in the left corticospinal tract, left acoustic radiation, and left middle longitudinal fasciculus. Tic disorders might involve structural abnormalities in key white matter tracts, offering new insights into their pathogenesis.
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.