Thivard Lionel, Lehéricy Stéphane, Krainik Alexandre, Adam Claude, Dormont Didier, Chiras Jacques, Baulac Michel, Dupont Sophie
Epileptology Unit, Hôpital de la Salpêtrière, 75013 Paris, France.
Neuroimage. 2005 Nov 15;28(3):682-90. doi: 10.1016/j.neuroimage.2005.06.045. Epub 2005 Aug 9.
Interictal diffusion imaging studies in patients with medial temporal lobe epilepsy (MTLE) accompanied by hippocampal sclerosis (HS) have shown an increased diffusivity in the epileptogenic hippocampus. In this study, we wanted to explore the whole brain in order to determine if MTLE could have an impact on the organization and the architecture of a large cerebral network and to identify clinical factors that could mediate diffusion abnormalities. Diffusion tensor imaging (DTI) and statistical parametric mapping of the entire brain were performed in 35 well-defined MTLE patients and in 36 healthy volunteers. SPM analyses identified three abnormal areas: an increased diffusivity was detected in the epileptic hippocampus and the ipsilateral temporal structures associated with a decreased anisotropy along the temporal lobe, a decreased diffusivity was found in the contralateral non-sclerotic hippocampus, the amygdala, and the temporal pole, and finally, a decreased anisotropy was noted ipsilaterally in posterior extratemporal regions. Duration of epilepsy, age at onset, and the frequency of generalized tonic-clonic seizures or partial complex seizures did not correlate with the presence of diffusion abnormalities. Region of interest analysis in the hippocampus/parahippocampus demonstrated a correlation between lower ipsilateral diffusivity values and occurrence of epigastric aura and between higher anisotropy values in both hemispheres and history of febrile seizures. In conclusion, this study showed that diffusion abnormalities are not restricted to the pathologic hippocampus and involve a larger network. This pattern may indirectly reflect the epileptogenic network and may be interpreted as a cause or a consequence of epilepsy.
对伴有海马硬化(HS)的内侧颞叶癫痫(MTLE)患者进行的发作间期扩散成像研究显示,致痫海马区的扩散率增加。在本研究中,我们希望对全脑进行探索,以确定MTLE是否会对大型脑网络的组织和结构产生影响,并确定可能介导扩散异常的临床因素。对35例明确诊断的MTLE患者和36名健康志愿者进行了全脑扩散张量成像(DTI)和统计参数映射分析。统计参数映射分析确定了三个异常区域:在癫痫海马区及同侧颞叶结构中检测到扩散率增加,同时沿颞叶各向异性降低;在对侧非硬化海马区、杏仁核和颞极发现扩散率降低;最后,在颞叶外后部区域同侧观察到各向异性降低。癫痫持续时间、发病年龄以及全身强直阵挛发作或部分性复杂发作的频率与扩散异常的存在无关。海马/海马旁回的感兴趣区分析表明,同侧较低的扩散率值与上腹部先兆的发生之间存在相关性,而双侧较高的各向异性值与热性惊厥病史之间存在相关性。总之,本研究表明,扩散异常并不局限于病理性海马区,而是涉及更大的网络。这种模式可能间接反映致痫网络,并且可以被解释为癫痫的原因或结果。