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特发性全身性癫痫患者基于体素的形态学测量

Voxel-based morphometry in patients with idiopathic generalized epilepsies.

作者信息

Betting Luiz Eduardo, Mory Susana Barreto, Li Li Min, Lopes-Cendes Iscia, Guerreiro Marilisa M, Guerreiro Carlos A M, Cendes Fernando

机构信息

Department of Neurology, Brazil.

出版信息

Neuroimage. 2006 Aug 15;32(2):498-502. doi: 10.1016/j.neuroimage.2006.04.174. Epub 2006 May 15.

Abstract

Idiopathic generalized epilepsies (IGE) are a group of frequent age-related epilepsy syndromes. IGE are clinically characterized by generalized tonic-clonic, myoclonic and absence seizures. According to predominant seizure type and age of onset, IGE are divided in subsyndromes: childhood absence and juvenile absence epilepsy (AE), juvenile myoclonic epilepsy (JME) and generalized tonic-clonic seizures on awakening (GTCS). The limits between these subsyndromes are not well defined, supporting the existence of only one major syndrome. Visual assessment of routine magnetic resonance imaging (MRI) in patients with IGE is normal. MRI voxel-based morphometry (VBM) uses automatically segmented gray and white matter for comparisons, eliminating the investigator bias. We used VBM to study 120 individuals (47 controls, 44 with JME, 24 with AE and 15 with GTCS) to investigate the presence of subtle structural abnormalities in IGE subsyndromes. VBM was performed searching for abnormalities on gray matter concentration (GMC) between patients groups and controls. Compared to controls, JME presented increased GMC in frontobasal region and AE showed increased GMC in the superior mesiofrontal region. The GTCS group did not differ from controls. There were no areas of reduced GMC with the statistical level selected. Region of interest analysis showed increased GMC in the anterior portion of the thalamus in patients with absence seizures. Our results support subtle GMC abnormalities in patients with JME and AE when compared to controls. These findings suggest the existence of different patterns of cortical abnormalities in IGE subsyndromes.

摘要

特发性全身性癫痫(IGE)是一组常见的与年龄相关的癫痫综合征。IGE的临床特征为全身性强直阵挛发作、肌阵挛发作和失神发作。根据主要发作类型和发病年龄,IGE可分为以下亚综合征:儿童失神癫痫和青少年失神癫痫(AE)、青少年肌阵挛癫痫(JME)以及觉醒时全身性强直阵挛发作(GTCS)。这些亚综合征之间的界限并不明确,这支持了仅存在一种主要综合征的观点。IGE患者的常规磁共振成像(MRI)视觉评估结果正常。MRI基于体素的形态计量学(VBM)使用自动分割的灰质和白质进行比较,消除了研究者偏差。我们使用VBM研究了120名个体(47名对照、44名JME患者、24名AE患者和15名GTCS患者),以调查IGE亚综合征中是否存在细微的结构异常。通过VBM检测患者组与对照组之间灰质浓度(GMC)的异常情况。与对照组相比,JME患者额基底区域的GMC增加,AE患者额中回上部区域的GMC增加。GTCS组与对照组无差异。在所选择的统计水平下,没有发现GMC降低的区域。感兴趣区分析显示,失神发作患者丘脑前部的GMC增加。与对照组相比,我们的结果支持JME和AE患者存在细微的GMC异常。这些发现提示IGE亚综合征中存在不同模式的皮质异常。

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