脑结构的多变量模式分析:1型神经纤维瘤病的诊断工具

J. Duarte, M. Ribeiro, I. Violante, Gil Cunha, Mohammed Al-Rawi, João Paulo Silva Cunha, M. Castelo‐Branco
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引用次数: 1

摘要

1型神经纤维瘤病(NF1)是一种以肿瘤发展和认知缺陷易感性增加为特征的遗传性疾病。在这项工作中,我们使用磁共振(MR)脑结构扫描获得的灰质密度图,通过多变量模式分析技术(支持向量机)来区分NF1患者和健康对照组。多达83%的参与者被正确分类(平均敏感度为82%;平均特异性为84%;显著性水平p < 0.01)。NF1患者的高水平分类准确性表明该技术是一种潜在的诊断工具。此外,我们确定了该算法用于区分NF1患者和健康对照的大脑区域。使用单变量逐体素比较,这些区域未被识别为异常,这表明多变量技术是识别NF1大脑潜在结构缺陷的有用有力工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multivariate pattern analysis of brain structure: A diagnostic tool for Neurofibromatosis type 1
Neurofibromatosis type 1 (NF1) is a genetic disorder characterized by increased predisposition for tumor development and cognitive deficits. In this work, we used maps of grey matter density obtained from Magnetic Resonance (MR) brain structural scans to distinguish between NF1 patients and healthy controls with a multivariate pattern analysis technique, Support Vector Machines. Up to 83% of all participants were correctly classified (mean sensitivity of 82%; mean specificity of 84%; significance level p < 0.01). This high level of classification accuracy of NF1 patients suggests this technique as a potential diagnostic tool. In addition, we determined the brain regions that the algorithm used to distinguish between NF1 patients and healthy controls. These regions were not identified as abnormal using univariate voxel-by-voxel comparison indicating that multivariate techniques are a useful powerful tool with which to identify potential structural defects in the NF1 brain.
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