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首页> 外文期刊>Neurobiology of Aging: Experimental and Clinical Research >Brain structure in asymptomatic FMR1 premutation carriers at risk for fragile X-associated tremor/ataxia syndrome
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Brain structure in asymptomatic FMR1 premutation carriers at risk for fragile X-associated tremor/ataxia syndrome

机译:无症状FMR1突变前携带者的脑部结构易患X相关震颤/共济失调综合征

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摘要

Fragile X-associated tremor/ataxia syndrome (FXTAS), a late-onset movement disorder affecting FMR1 premutation carriers, is associated with cerebral and cerebellar lesions. The aim of this study was to test whether computational anatomy can detect similar patterns in asymptomatic FMR1 premutation carriers (mean age 46.7 years) with qualitatively normal -appearing grey and white matter on brain MRI. We used a multimodal imaging protocol to characterize brain anatomy by automated assessment of gray matter volume and white matter properties. Structural changes in the hippocampus and in the cerebellar motor network with decreased gray matter volume in lobule VI and white matter alterations of the corresponding afferent projections through the middle cerebellar peduncles are demonstrated. Diffuse subcortical white matter changes in both hemispheres, without corresponding gray matter alterations, are only identified through age × group interactions. We interpret the hippocampal fimbria and cerebellar changes as early alterations with a possible neurodevelopmental origin. In contrast, progression of the diffuse cerebral hemispheric white matter changes suggests a neurodegenerative process, leading to late-onset lesions, which may mark the imminent onset of FXTAS.
机译:易碎的X相关震颤/共济失调综合征(FXTAS)是影响FMR1突变前携带者的迟发性运动障碍,与脑和小脑病变有关。这项研究的目的是检验在大脑MRI上定性为正常的灰白色物质时,计算解剖学是否可以检测到无症状FMR1突变前携带者(平均年龄46.7岁)中的相似模式。我们使用多模式成像协议通过自动评估灰质体积和白质特性来表征大脑解剖结构。证明了海马和小脑运动网络的结构变化,小叶VI的灰质体积减少,并且穿过小脑中轴的相应传入突起的白质改变。仅通过年龄×群体相互作用识别两个半球中皮层下的弥漫性白质变化,而没有相应的灰质变化。我们将海马菌毛和小脑改变解释为可能具有神经发育起源的早期改变。相反,弥漫性脑半球白质变化的进展提示神经退行性过程,导致迟发性病变,这可能标志着FXTAS即将发作。

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