基于支持向量机的核磁共振成像和心理测试数据分类。

IF 0.2 Q4 MEDICINE, RESEARCH & EXPERIMENTAL International journal of clinical and experimental medicine Pub Date : 2017-12-01
Wenlu Yang, Xinyun Chen, David S Cohen, Eric R Rosin, Arthur W Toga, Paul M Thompson, Xudong Huang
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引用次数: 0

摘要

阿尔茨海默病(AD)是一种渐进性的脑部疾病,通常是致命性的,它会引起神经变性,导致记忆力减退以及其他认知和行为问题。在此,我们提出了一种新颖的多模态方法,该方法结合了核磁共振成像测量和临床评估的独立成分,可将阿尔茨海默病患者或轻度认知障碍(MCI)受试者与健康老年对照组区分开来。我们分析了 70 名 AD 受试者(平均年龄:77.15 ± 6.2 岁)、98 名 MCI 受试者(平均年龄:76.91 ± 5.7 岁)和 150 名 HC 受试者(平均年龄:75.69 ± 3.8 岁)。我们的方法包括以下步骤:预处理、从磁共振图像数据中估算独立成分的数量、提取用于分类的有效体素,以及使用基于支持向量机(SVM)的分类器进行分类。结果,在将 AD 与健康对照组进行分类方面,我们取得了 97.7% 的分类准确率、99.2% 的灵敏度和 96.7% 的特异性;在将 MCI 与健康对照组进行区分方面,我们取得了 87.8% 的分类准确率、86.0% 的灵敏度和 89.6% 的特异性;这些结果均优于仅通过临床测量获得的结果(准确率 79.5%、灵敏度 74.0% 和特异性 85.1%)。我们发现:(1) AD 患者和 MCI 受试者都有脑组织损失,但 MCI 受试者的灰质损失量要少得多,这支持了 MCI 是 AD 前驱阶段的观点;(2) 与仅使用独立成分或临床测量进行分类相比,将 MRI 的灰质特征与精神状态、认知功能的三种常用测量方法相结合可提高分类的准确性、灵敏度和特异性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Classification of MRI and psychological testing data based on support vector machine.

Alzheimer's disease (AD) is a progressive, and often fatal, brain disease that causes neurodegeneration, resulting in memory loss as well as other cognitive and behavioral problems. Here, we propose a novel multimodal method combining independent components from MRI measures and clinical assessments to distinguish Alzheimer's patients or mild cognitive impairment (MCI) subjects from healthy elderly controls. 70 AD subjects (mean age: 77.15 ± 6.2 years), 98 MCI subjects (mean age: 76.91 ± 5.7 years), and 150 HC subjects (mean age: 75.69 ± 3.8 years) were analyzed. Our method includes the following steps: pre-processing, estimating the number of independent components from the MR image data, extracting effective voxels for classification, and classification using a support vector machine (SVM)-based classifier. As a result, with regards to classifying AD from healthy controls, we achieved a classification accuracy of 97.7%, sensitivity of 99.2%, and specificity of 96.7%; for differentiating MCI from healthy controls, we achieved a classification accuracy of 87.8%, a sensitivity of 86.0%, and a specificity of 89.6; these results are better than those obtained with clinical measurements alone (accuracy of 79.5%, sensitivity of 74.0%, and specificity of 85.1%). We found that (1) both AD patients and MCI subjects showed brain tissue loss, but the volumes of gray matter loss in MCI subjects was far less, supporting the notion that MCI is a prodromal stage of AD; and (2) combining gray matter features from MRI and three commonly used measures of mental status, cognitive function improved classification accuracy, sensitivity, and specificity compared with classification using only independent components or clinical measurements.

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