Lundbom N, Gaily E, Vuori K, Paetau R, Liukkonen E, Rajapakse J C, Valanne L, Häkkinen A M, Granström M L
Department of Radiology, Helsinki University Central Hospital (HUCH), Helsinki, Finland.
Epilepsia. 2001 Dec;42(12):1507-14. doi: 10.1046/j.1528-1157.2001.15301.x.
Proton magnetic resonance spectroscopic imaging (1H MRSI) can lateralize the epileptogenic frontal lobe by detecting metabolic ratio abnormalities in frontal lobe epilepsy (FLE). We used 1H MRS to lateralize and localize the epileptogenic focus, and we also sought to characterize further the metabolic abnormality in FLE.
We measured signals from N-acetyl aspartate (NAA), choline-containing compounds (Cho), and creatine + phosphocreatine (Cr) in the supraventricular brain of 14 patients with frontal or frontoparietal epilepsy and their matched controls. The supratentorial brain also was segmented into gray matter, white matter, and cerebrospinal fluid classes. Regional metabolite alterations were compared with localizing and lateralizing results from other examination modalities and with histology from three patients.
Spectroscopy lateralized the epileptogenic focus in 10 patients in agreement with video-EEG and functional imaging. In four patients, spectroscopy showed bilateral, focal metabolic abnormality, whereas video-EEG suggested unilateral or midline abnormality. In the epileptogenic focus, Cho and Cr were increased by 23% and 14%, respectively, and NAA was decreased by 11%, suggesting metabolic disturbances both in the glial and in the neuronal cell pools. Two Taylor dysplasia lesions confirmed by histology and one with radiologic diagnosis showed high Cho and low or normal NAA, whereas two dysembryoplastic neurogenic tumors had normal Cho and low NAA. Contralateral hemisphere NAA/(Cho + Cr) was decreased in FLE, indicating diffusely altered brain metabolism. Segmentation of brain tissue did not reveal atrophic changes in FLE.
Spectroscopy is useful in lateralizing frontoparietal epilepsy and shows promise as a "noninvasive biopsy" in epileptogenic lesions.
质子磁共振波谱成像(1H MRSI)可通过检测额叶癫痫(FLE)患者额叶的代谢率异常来确定致痫额叶的位置。我们使用1H MRS来确定致痫灶的位置并进行定位,同时还试图进一步描述FLE中的代谢异常情况。
我们测量了14例额叶或额顶叶癫痫患者及其匹配对照组的大脑脑室上区域中N-乙酰天门冬氨酸(NAA)、含胆碱化合物(Cho)以及肌酸+磷酸肌酸(Cr)的信号。幕上脑区也被分为灰质、白质和脑脊液类别。将区域代谢物改变与其他检查方式的定位和定侧结果以及3例患者的组织学结果进行比较。
波谱分析在10例患者中确定了致痫灶的位置,与视频脑电图和功能成像结果一致。在4例患者中,波谱分析显示双侧局灶性代谢异常,而视频脑电图提示单侧或中线异常。在致痫灶中,Cho和Cr分别增加了23%和14%,NAA减少了11%,提示神经胶质细胞池和神经元细胞池均存在代谢紊乱。经组织学证实的2例泰勒发育异常病变和1例经放射学诊断的病变显示Cho升高,NAA降低或正常,而2例胚胎发育不良性神经上皮肿瘤的Cho正常,NAA降低。FLE患者对侧半球的NAA/(Cho + Cr)降低,表明大脑代谢存在弥漫性改变。脑组织分割未发现FLE存在萎缩性变化。
波谱分析有助于确定额顶叶癫痫的位置,并有望成为致痫性病变的“无创活检”方法。