Chahboune H, Mishra A M, DeSalvo M N, Staib L H, Purcaro M, Scheinost D, Papademetris X, Fyson S J, Lorincz M L, Crunelli V, Hyder F, Blumenfeld H
Magnetic Resonance Research Center, Yale University School of Medicine, 333 Cedar Street, New Haven, CT 06520, USA.
Neuroimage. 2009 Aug 15;47(2):459-66. doi: 10.1016/j.neuroimage.2009.04.060. Epub 2009 May 3.
Absence epilepsy is a common seizure disorder in children which can produce chronic psychosocial sequelae. Human patients and rat absence models show bilateral spike-wave discharges (SWD) in cortical regions. We employed diffusion tensor imaging (DTI) in rat absence models to detect abnormalities in white matter pathways connecting regions of seizure activity.
We studied Wistar albino Glaxo rats of Rijswijk (WAG/Rij), genetic absence epilepsy rats of Strasbourg (GAERS), and corresponding nonepileptic control strains. Ex vivo DTI was performed at 9.4 T with diffusion gradients applied in 16 orientations. We compared fractional anisotropy (FA), perpendicular (lambda(perpendicular)) and parallel (lambda(||)) diffusivity between groups using t-maps and region of interest (ROI) measurements.
Adult epileptic WAG/Rij rats exhibited a localized decrease in FA in the anterior corpus callosum. This area was confirmed by tractography to interconnect somatosensory cortex regions most intensely involved in seizures. This FA decrease was not present in young WAG/Rij rats before onset of SWD. GAERS, which have more severe SWD than WAG/Rij, exhibited even more pronounced callosal FA decreases. Reduced FA in the epileptic animals originated from an increased lambda(perpendicular) with no significant changes in lambda(||).
Reduced FA with increased lambda(perpendicular) suggests that chronic seizures cause reduction in myelin or decreased axon fiber density in white matter pathways connecting regions of seizure activity. These DTI abnormalities may improve the understanding of chronic neurological difficulties in children suffering with absence epilepsy, and may also serve as a noninvasive biomarker for monitoring beneficial effects of treatment.
失神癫痫是儿童常见的癫痫发作疾病,可产生慢性心理社会后遗症。人类患者和大鼠失神模型在皮质区域均显示双侧棘慢波放电(SWD)。我们在大鼠失神模型中采用扩散张量成像(DTI)来检测连接癫痫活动区域的白质通路异常。
我们研究了里杰斯维克的Wistar白化Glaxo大鼠(WAG/Rij)、斯特拉斯堡遗传性失神癫痫大鼠(GAERS)以及相应的非癫痫对照品系。在9.4 T条件下进行离体DTI,施加16个方向的扩散梯度。我们使用t检验图和感兴趣区域(ROI)测量比较了各组之间的分数各向异性(FA)、垂直扩散率(lambda(垂直))和平行扩散率(lambda(||))。
成年癫痫WAG/Rij大鼠胼胝体前部的FA局部降低。通过纤维束成像证实该区域最强烈地连接了癫痫发作中涉及的体感皮质区域。在SWD发作前的幼年WAG/Rij大鼠中未出现这种FA降低。GAERS的SWD比WAG/Rij更严重,其胼胝体FA降低更为明显。癫痫动物中FA降低源于lambda(垂直)增加,而lambda(||)无显著变化。
FA降低且lambda(垂直)增加表明慢性癫痫发作会导致连接癫痫活动区域的白质通路中髓鞘减少或轴突纤维密度降低。这些DTI异常可能有助于更好地理解失神癫痫患儿的慢性神经功能障碍,也可作为监测治疗有益效果的非侵入性生物标志物。