使用共识聚类和无监督学习技术无监督地发现阿尔茨海默病的轻度认知障碍亚型

F. Nezhadmoghadam, Jose Gerardo Tamez-Peña
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引用次数: 0

摘要

在生物信息学和卫生信息学等许多领域,发现和描述可重复的疾病亚型结果是最苛刻和最基本的任务之一。它可以促进诊断,是迈向更个性化治疗的重要一步。本文旨在分析无监督学习方法识别少量可靠且稳定的轻度认知障碍(MCI)受试者亚型的能力,并发现MCI向AD转换风险受试者的原发性前驱阿尔茨海默病(AD)阶段。我们提出了一种新的无监督学习方法来识别显著的稳定和可重复的亚型。该方法利用了无监督聚类方法中的一致聚类。对于这个平均值,我们从阿尔茨海默病神经成像倡议研究中获得数据。346个特征,包括人口统计信息和mri衍生特征,描述了839名早期轻度认知障碍患者。我们将数据随机分成发现(70%)和验证(30%)两组。使用五种无监督聚类方法对发现集进行分析,并采用鲁棒共识聚类方法确定最稳定可靠的亚型。结果表明,该方法可识别出四种不同的MCI患者亚型。发现后,在测试集中预测亚型并与MCI转换相关。其中一种亚型有转化为阿尔茨海默病的高风险(OR = 2.99, 95%CI = 1.65 ~ 5.41)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unsupervised discovery of Mild Cognitive Impairment subtypes of Alzheimer's disease using consensus clustering and unsupervised learning techniques
Discovering and characterizing reproducible disease subtypes results is one of the most demanding and fundamental tasks in many fields, such as bioinformatics and health informatics. It could facilitate diagnosis and is a vital step toward more individualized therapy. This paper aims to analyze the ability of unsupervised learning methods to identify a small collection of reliable and stable subtypes of subjects with mild cognitive impairment (MCI) and to discover the primary prodromal Alzheimer's disease (AD) stages in subjects with MCI to AD conversion risk. We present a novel unsupervised learning methodology to identify the notable stable and reproducible subtypes. The proposed method takes advantage of the consensus clustering of unsupervised clustering methods. For this mean, we obtained the data from the Alzheimer's disease Neuroimaging Initiative study. 346 features, including demographic information and MRI-derived features, described 839 subjects with early MCI. We randomly split the data into discovery (70%) and validation (30%) sets. The discovery set was analyzed using five unsupervised clustering methods, and robust consensus clustering was used to determine the most stable and reliable subtypes. The results show that the proposed method identified four different MCI patient subtypes. After discovery, subtypes were predicted in the testing set and associated with MCI conversion. One subtype had a high-risk (OR = 2.99, 95%CI = 1.65 to 5.41) of converting to Alzheimer's disease.
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