Antel Samson B, Collins D Louis, Bernasconi Neda, Andermann Frederick, Shinghal Rajjan, Kearney Robert E, Arnold Douglas L, Bernasconi Andrea
Department of Biomedical Engineering, Montreal Neurological Institute, McGill University, 3801 University Street, Montreal, Quebec H3A 2B4, Canada.
Neuroimage. 2003 Aug;19(4):1748-59. doi: 10.1016/s1053-8119(03)00226-x.
Focal cortical dysplasia (FCD), a malformation of cortical development, is a frequent cause of pharmacologically intractable epilepsy. FCD is characterized on Tl-weighted MRI by cortical thickening, blurring of the gray-matter/white-matter interface, and gray-level hyperintensity. We have previously used computational models of these characteristics to enhance visual lesion detection. In the present study we seek to improve our methods by combining these models with features derived from texture analysis of MRI, which allows measurement of image properties not readily accessible by visual analysis. These computational models and texture features were used to develop a two-stage Bayesian classifier to perform automated FCD lesion detection. Eighteen patients with histologically confirmed FCD and 14 normal controls were studied. On the MRI volumes of the 18 patients, 20 FCD lesions were manually labeled by an expert observer. Three-dimensional maps of the computational models and texture features were constructed for all subjects. A Bayesian classifier was trained on the computational models to classify voxels as cerebrospinal fluid, gray-matter, white-matter, transitional, or lesional. Voxels classified as lesional were subsequently reclassified based on the texture features. This process produced a 3D lesion map, which was compared to the manual lesion labels. The automated classifier identified 17/20 manually labeled lesions. No lesions were identified in controls. Thus, combining models of the T1-weighted MRI characteristics of FCD with texture analysis enabled successful construction of a classifier. This computer-based, automated method may be useful in the presurgical evaluation of patients with severe epilepsy related to FCD.
局灶性皮质发育不良(FCD)是一种皮质发育畸形,是药物难治性癫痫的常见病因。FCD在T1加权磁共振成像(MRI)上的特征为皮质增厚、灰质/白质界面模糊以及灰度高信号。我们之前已使用这些特征的计算模型来增强视觉病灶检测。在本研究中,我们试图通过将这些模型与从MRI纹理分析得出的特征相结合来改进我们的方法,MRI纹理分析能够测量视觉分析不易获取的图像属性。这些计算模型和纹理特征被用于开发一个两阶段贝叶斯分类器,以执行FCD病灶的自动检测。对18名经组织学确诊为FCD的患者和14名正常对照者进行了研究。在18名患者的MRI容积上,由一名专家观察者手动标记了20个FCD病灶。为所有受试者构建了计算模型和纹理特征三维图。在计算模型上训练一个贝叶斯分类器,将体素分类为脑脊液、灰质、白质、过渡性或病灶性。随后根据纹理特征对分类为病灶性的体素进行重新分类。这个过程产生了一个三维病灶图,并将其与手动病灶标记进行比较。自动分类器识别出了17/20个手动标记的病灶。在对照者中未识别出病灶。因此,将FCD的T1加权MRI特征模型与纹理分析相结合能够成功构建一个分类器。这种基于计算机的自动方法可能有助于对与FCD相关的严重癫痫患者进行术前评估。