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基于体素形态测量学和 MRI T1 脑图像的皮质、皮质下和海马区的联合特征对阿尔茨海默病的早期诊断。

Early diagnosis of Alzheimer's disease using combined features from voxel-based morphometry and cortical, subcortical, and hippocampus regions of MRI T1 brain images.

机构信息

School of Information Communication Engineering, Chosun University, Gwangju, Republic of Korea.

National Research Center for Dementia, Chosun University, Gwangju, Republic of Korea.

出版信息

PLoS One. 2019 Oct 4;14(10):e0222446. doi: 10.1371/journal.pone.0222446. eCollection 2019.

DOI:10.1371/journal.pone.0222446
PMID:31584953
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6777799/
Abstract

In recent years, several high-dimensional, accurate, and effective classification methods have been proposed for the automatic discrimination of the subject between Alzheimer's disease (AD) or its prodromal phase {i.e., mild cognitive impairment (MCI)} and healthy control (HC) persons based on T1-weighted structural magnetic resonance imaging (sMRI). These methods emphasis only on using the individual feature from sMRI images for the classification of AD, MCI, and HC subjects and their achieved classification accuracy is low. However, latest multimodal studies have shown that combining multiple features from different sMRI analysis techniques can improve the classification accuracy for these types of subjects. In this paper, we propose a novel classification technique that precisely distinguishes individuals with AD, aAD (stable MCI, who had not converted to AD within a 36-month time period), and mAD (MCI caused by AD, who had converted to AD within a 36-month time period) from HC individuals. The proposed method combines three different features extracted from structural MR (sMR) images using voxel-based morphometry (VBM), hippocampal volume (HV), and cortical and subcortical segmented region techniques. Three classification experiments were performed (AD vs. HC, aAD vs. mAD, and HC vs. mAD) with 326 subjects (171 elderly controls and 81 AD, 35 aAD, and 39 mAD patients). For the development and validation of the proposed classification method, we acquired the sMR images from the dataset of the National Research Center for Dementia (NRCD). A five-fold cross-validation technique was applied to find the optimal hyperparameters for the classifier, and the classification performance was compared by using three well-known classifiers: K-nearest neighbor, support vector machine, and random forest. Overall, the proposed model with the SVM classifier achieved the best performance on the NRCD dataset. For the individual feature, the VBM technique provided the best results followed by the HV technique. However, the use of combined features improved the classification accuracy and predictive power for the early classification of AD compared to the use of individual features. The most stable and reliable classification results were achieved when combining all extracted features. Additionally, to analyze the efficiency of the proposed model, we used the Alzheimer's Disease Neuroimaging Initiative (ADNI) dataset to compare the classification performance of the proposed model with those of several state-of-the-art methods.

摘要

近年来,已经提出了几种高维、准确且有效的分类方法,用于基于 T1 加权结构磁共振成像 (sMRI) 自动区分阿尔茨海默病 (AD) 或其前驱阶段(即轻度认知障碍 (MCI))患者与健康对照 (HC) 个体。这些方法仅强调使用来自 sMRI 图像的个体特征来对 AD、MCI 和 HC 受试者进行分类,并且它们达到的分类准确性较低。然而,最新的多模态研究表明,结合来自不同 sMRI 分析技术的多个特征可以提高对这些类型的受试者的分类准确性。在本文中,我们提出了一种新颖的分类技术,可准确区分 AD、aAD(稳定的 MCI,在 36 个月内未转化为 AD)和 mAD(由 AD 引起的 MCI,在 36 个月内转化为 AD)个体与 HC 个体。该方法结合了基于体素的形态测量学 (VBM)、海马体积 (HV) 以及皮质和皮质下分割区域技术从结构磁共振 (sMR) 图像中提取的三种不同特征。对 326 名受试者(171 名老年对照组和 81 名 AD、35 名 aAD 和 39 名 mAD 患者)进行了三项分类实验(AD 与 HC、aAD 与 mAD、HC 与 mAD)。为了开发和验证所提出的分类方法,我们从国家老年痴呆症研究中心 (NRCD) 的数据集获取了 sMR 图像。应用五折交叉验证技术来找到分类器的最佳超参数,并使用三种著名的分类器比较分类性能:K-最近邻、支持向量机和随机森林。总体而言,在 NRCD 数据集上,使用 SVM 分类器的提出模型获得了最佳性能。对于单个特征,VBM 技术提供了最佳结果,其次是 HV 技术。然而,与使用单个特征相比,使用组合特征可提高 AD 的早期分类的分类准确性和预测能力。当组合所有提取的特征时,获得了最稳定和可靠的分类结果。此外,为了分析所提出模型的效率,我们使用了阿尔茨海默病神经影像倡议 (ADNI) 数据集来比较所提出模型与几种最先进方法的分类性能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bcb/6777799/919a3ea69285/pone.0222446.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bcb/6777799/919a3ea69285/pone.0222446.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bcb/6777799/919a3ea69285/pone.0222446.g001.jpg

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