采用定量生物标志物和深度学习方法的结构磁共振成像集成方法诊断阿尔茨海默病

HiteshB Shah, ChintanR Varnagar
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引用次数: 0

摘要

简介:阿尔茨海默病(AD)是一种神经退行性疾病,损害日常生活活动并急剧下降总体认知能力。到2050年,全世界将有超过1.52亿人面临寿命延长的可怕后果,使其成为一个紧迫的公共卫生问题。磁共振成像(MRI)提供了出色的软组织对比,并有助于在体内无创地成像大脑。目的和目的:总结AD的解剖、生理和病理生理变化,并从MRI中获得可量化的生物标志物,开发基于人工智能(AI)的计算机辅助检测(CAD)系统,将AD、轻度认知障碍(MCI)和认知正常(CN)的受试者进行分类。材料和方法:本回顾性研究使用1069名受试者的临床和标准化、预处理、质量控制和质量检查的结构MRI成像(诊断/标记)数据,这些数据来自阿尔茨海默病神经影像学倡议,年龄、性别和类别匹配。通过评估(1)皮质厚度,(2)全脑体积分割,以及(3)AD中受影响最大的感兴趣区域(ROI),开发了一种方法来获得量化的生物标志物。使用梯度增强方法来预测类标签。第二种方法实现了包含三维ROI的卷积神经网络(CNN)模型。结果:采用集成梯度增强方法实现的CAD系统显示出良好的接收机工作特性特征,平衡精度(BA)分别为82.31%、78.52%和72.73%,而CNN方法在分类任务AD vs CN、AD vs MCI和MCI vs CN上分别取得了88.44%、82.96%和74.34%的更好结果。结论:本研究使用了1069名受试者的大量数据集。基于深度学习的高效和最优CNN模型使用了非常大的基于roi的三维体积,与同类方法相比,性能有了令人印象深刻的提高。CNN模型在梯度增强上给出了更高的准确率(AD vs. CN为6.13%,AD vs. MCI为4.44%,MCI vs. CN为1.61%),因为该模型使用了非常大的基于roi的3D脑容量,并且它具有自动学习大多数判别特征的固有能力。然而,来自大脑形态测量学的定量生物标志物,可以获得结构变化,对整个大脑的病理生理变化产生合理的估计,并增强临床医生的洞察力和整体观点,从而比CNN预测的类别标签具有更高的置信度,并且更接近可解释的人工智能。MCI与CN的准确性下降,因为这些类别具有相似的特征和特征,可以通过整合其他MRI模式的生物标志物来提高。
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Ensemble method employing quantitative biomarkers and deep learning approach from structural magnetic resonance imaging to diagnose Alzheimer’s disease
Introduction: Alzheimer’s disease (AD) is a neurodegenerative condition that impairs activities of daily living and sharply declines gross cognitive ability. Over 152 million individuals worldwide will live with the dreaded consequence of a longer lifespan by the year 2050, making it a pressing public health issue. Magnetic resonance imaging (MRI) provides excellent soft tissue contrast and helps image the brain in vivo, non-invasively. Aims and Objectives: To summarize AD’s anatomical, physiological, and pathophysiological changes and derivation of quantifiable biomarkers from MRI to develop artificial intelligence (AI) based computer-aided detection (CAD) system to classify subjects among AD, mild cognitive impairment (MCI), and cognitively normal (CN). Materials and Methods: This retrospective study uses clinical and standardized, pre-processed, quality-controlled, and quality-checked—structural MRI imaging (diagnosed/labeled) data of 1069 subjects, age, gender, and class matched, taken from Alzheimer’s disease neuroimaging initiative. A pipeline is developed to get quantified biomarkers from the assessment of (1) cortical thickness, (2) volumetric segmentation for whole brain volumes, and (3) region of interest (ROI) areas most affected in AD. A gradient boosting method is used to predict class labels. The second approach implements a convolution neural network (CNN) model comprising 3D ROI. Results: Implemented CAD system using an ensemble gradient boosting approach has demonstrated good receiver operating characteristics characteristic and yielded balanced accuracy (BA) of 82.31%, 78.52%, and 72.73%, and the CNN approach has given better results 88.44%, 82.96%, and 74.34% for classification task AD versus CN, AD versus MCI, and MCI versus CN, respectively. Conclusion: This study has used a substantially large dataset of 1069 subjects. The deep learning-based efficient and optimal CNN model has used significantly large ROI-based 3-Dimentional volume, resulting in impressive performance improvements over comparable methods. The CNN model had given higher accuracy (6.13% for AD vs. CN, 4.44% for AD vs. MCI and 1.61% for MCI vs. CN) over gradient boosting, as the model uses significantly large ROI-based 3D brain volume and an inherent capability of it in learning most discriminative features automatically. However, quantitative biomarkers derived from brain morphometry, which accesses structural changes, yield reasonable estimates over pathophysiological alterations across the brain and augment a clinician with insightful and a holistic view, resulting in higher confidence over predicated class label by CNN and is a step closer to explainable AI. Accuracy for MCI versus CN drops as these classes share similar features and characteristics and can be improved by integrating biomarkers from other MRI modalities.
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