阿尔茨海默病的诊断方法。

Wen-Chin Hsu, Christopher Denq, Su-Shing Chen
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引用次数: 8

摘要

背景:像所有其他神经退行性疾病一样,阿尔茨海默病(AD)的诊断和治疗仍然是一个非常具有挑战性和困难的问题。多年来,只有历史、行为和精神方面的措施可用于阿尔茨海默病。最近,一个明确的诊断框架,使用生物标志物和成像,已被提出。在本文中,我们提出了一个有前途的诊断方法的框架。方法:在之前的一篇论文中,我们开发了一种高效的基于支持向量机(SVM)的方法,我们现在已经应用于发现重要的生物标志物和靶标网络,为阿尔茨海默病的治疗提供策略。结果:该方法选择了一些基于血液的生物标志物(少于NCBI三个AD数据集初始数量的10%),并通过交叉验证对结果进行了统计验证。所得的支持向量机是AD与正常受试者的分类器。我们基于互信息构建了AD目标网络。此外,对初始数据进行分层聚类,聚类基因在热图中可视化。该方法还通过基于性别对受试者进行分类来进行性别分析。结论:与其他传统的统计分析不同,我们的方法使用了基于机器学习的算法。我们的方法选择了一小组重要的AD生物标志物,将嘈杂的(不相关的)生物标志物与相关的生物标志物区分开来,并提供了所选生物标志物的目标网络,这将有助于诊断和治疗设计。最后,在性别分析的基础上,我们观察到性别可能在AD的诊断中发挥作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A diagnostic methodology for Alzheimer's disease.

A diagnostic methodology for Alzheimer's disease.

A diagnostic methodology for Alzheimer's disease.

A diagnostic methodology for Alzheimer's disease.

Background: Like all other neurodegenerative diseases, Alzheimer's disease (AD) remains a very challenging and difficult problem for diagnosis and therapy. For many years, only historical, behavioral and psychiatric measures have been available to AD cases. Recently, a definitive diagnostic framework, using biomarkers and imaging, has been proposed. In this paper, we propose a promising diagnostic methodology for the framework.

Methods: In a previous paper, we developed an efficient SVM (Support Vector Machine) based method, which we have now applied to discover important biomarkers and target networks which provide strategies for AD therapy.

Results: The methodology selects a number of blood-based biomarkers (fewer than 10% of initial numbers on three AD datasets from NCBI), and the results are statistically verified by cross-validation. The resulting SVM is a classifier of AD vs. normal subjects. We construct target networks of AD based on MI (mutual information). In addition, a hierarchical clustering is applied on the initial data and clustered genes are visualized in a heatmap. The proposed method also performs gender analysis by classifying subjects based on gender.

Conclusions: Unlike other traditional statistical analyses, our method uses a machine learning-based algorithm. Our method selects a small set of important biomarkers for AD, differentiates noisy (irrelevant) from relevant biomarkers and also provides the target networks of the selected biomarkers, which will be useful for diagnosis and therapeutic design. Finally, based on the gender analysis, we observe that gender could play a role in AD diagnosis.

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