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首页> 外文期刊>Human brain mapping >Default mode network modifications in F F abry disease: A resting‐state fMRI study with structural correlations
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Default mode network modifications in F F abry disease: A resting‐state fMRI study with structural correlations

机译:F F Abry病中默认模式网络修改:具有结构相关性的休息状态FMRI研究

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摘要

Abstract Aim of the study was to evaluate the presence of Default Mode Network (DMN) modifications in Fabry Disease (FD), and their possible correlations with structural alterations and neuropsychological scores. Thirty‐two FD patients with a genetically confirmed diagnosis of classical FD (12 males, mean age 43.3?±?12.2) were enrolled, along with 35 healthy controls (HC) of comparable age and sex (14 males, mean age 42.1?±?14.5). Resting‐State fMRI data were analyzed using a seed‐based approach, with six different seeds sampling the main hubs of the DMN. Structural modifications were assessed by means of Voxel‐Based Morphometry (VBM) and Tract‐Based Spatial Statistics analyses. Between‐group differences and correlations with neuropsychological variables were probed voxelwise over the whole brain. Possible correlations between FC modifications and global measures of microstructural alteration were also tested in FD patients with a partial correlation analysis. In the FD group, clusters of increased functional connectivity involving both supratentorial and infratentorial regions emerged, partially correlated to the widespread white matter (WM) damage found in these patients. No gray matter volume differences were found at VBM between the two groups. The connectivity between right inferior frontal gyrus and precuneus was significantly correlated with the Corsi block‐tapping test results ( p ?=?.0001). Widespread DMN changes are present in FD patients that correlate with WM alterations and cognitive performance. Our results confirm the current view of a cerebral involvement in FD patients not simply associated to major cerebrovascular events, but also related to significant and diffuse microstructural and functional changes.
机译:摘要该研究的目的是评估法布里疾病(FD)中默认模式网络(DMN)修饰的存在,以及它们与结构改变和神经心理学评分的可能相关性。三十二次FD患者患有遗传证实的古典FD(12名男性,平均43.3〜±12.2)的诊断,以及35例健康对照(HC)可比年龄和性别(14名男性,平均42.1岁(42.1) ?14.5)。使用基于种子的方法进行分析休息状态的FMRI数据,其中六种不同的种子采样DMN的主枢纽。通过基于体素的形态学(VBM)和基于传道的空间统计分析来评估结构修饰。在整个大脑上探测组差异和与神经心理变量的相关性。在FD患者中还测试了FC修饰与全球微观变化测量的可能相关性,其在FD患者中进行了部分相关分析。在FD组中,出现了涉及超级和Infactental区域的功能连通性增加,部分与这些患者中发现的广泛白质(WM)损伤相关。在两组之间没有在VBM之间发现灰质体积差异。右下额相回流和前象之间的连接与COSI块攻丝测试结果显着相关(P?= 0001)。在FD患者中存在普遍的DMN变化,其与WM改变和认知性能相关。我们的结果证实了目前对FD患者的脑卒中的目前看法不与主要脑血管事件相关的患者,也与显着和弥漫性微观结构和功能变化有关。

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