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青少年肌阵挛癫痫和额叶癫痫的辅助运动区连通性。

Connectivity of the supplementary motor area in juvenile myoclonic epilepsy and frontal lobe epilepsy.

机构信息

National Society for Epilepsy MRI Unit, Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology and National Hospital for Neurology and Neurosurgery, Queen Square, London, United Kingdom.

出版信息

Epilepsia. 2011 Mar;52(3):507-14. doi: 10.1111/j.1528-1167.2010.02770.x. Epub 2010 Nov 3.

Abstract

PURPOSE

Subtle structural abnormalities of frontal lobe gray and white matter have been described in cryptogenic frontal lobe and idiopathic generalized epilepsies. The supplementary motor area (SMA) has a role in motor control, and its involvement during frontal lobe epileptic seizures is characterized by a typical asymmetric tonic posturing. Moreover, motor networks are dysfunctional in juvenile myoclonic epilepsy (JME). We tested the hypothesis that SMA structural connectivity is altered in focal frontal lobe epilepsy (FLE) and JME compared to healthy controls.

METHODS

Diffusion tensor imaging (DTI) and probabilistic tractography were used to map the structural connectivity of the SMA, defined by motor functional magnetic resonance imaging (MRI), in 15 patients with JME, 36 patients with FLE, and 18 healthy controls.

KEY FINDINGS

Structural connectivity of the SMA was significantly reduced in JME compared to controls (reduced fractional anisotropy and increased mean diffusivity). In FLE there was no significant difference compared to controls, and in all groups there was stronger connectivity in the left hemisphere (higher fractional anisotropy) compared to the right. There was no difference in SMA connectivity between patients with medial or lateral frontal lobe epileptic foci.

SIGNIFICANCE

Reduced white matter connectivity is the structural correlate of functional frontal lobe abnormalities in JME. In FLE, the structural connectivity of the SMA was preserved, suggesting a robust motor network that is not compromised by longstanding epilepsy involving the medial frontal lobes.

摘要

目的

在隐源性额叶癫痫和特发性全面性癫痫中,已经描述了额叶灰白质的细微结构异常。补充运动区(SMA)在运动控制中起作用,其在额叶癫痫发作期间的参与表现为典型的非对称强直姿势。此外,运动网络在青少年肌阵挛性癫痫(JME)中功能失调。我们检验了这样一个假设,即与健康对照组相比,SMA 的结构连接在局灶性额叶癫痫(FLE)和 JME 中发生了改变。

方法

使用弥散张量成像(DTI)和概率追踪技术,对 15 例 JME 患者、36 例 FLE 患者和 18 名健康对照者的 SMA 结构连接进行了磁共振成像(MRI)运动功能定位。

主要发现

与对照组相比,JME 患者的 SMA 结构连接明显减少(各向异性分数降低,平均弥散度增加)。与对照组相比,FLE 患者无显著差异,且在所有组中,左侧半球的连接均较强(各向异性分数较高)。内侧或外侧额叶癫痫灶患者的 SMA 连接无差异。

意义

白质连接减少是 JME 中功能性额叶异常的结构相关因素。在 FLE 中,SMA 的结构连接保持不变,这表明存在一个稳健的运动网络,不会因涉及内侧额叶的长期癫痫而受到影响。

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