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Heterogeneous multimodal biomarkers analysis for Alzheimer’s disease via Bayesian network

机译:通过贝叶斯网络对阿尔茨海默氏病进行异质多峰生物标志物分析

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摘要

By 2050, it is estimated that the number of worldwide Alzheimer’s disease (AD) patients will quadruple from the current number of 36 million, while no proven disease-modifying treatments are available. At present, the underlying disease mechanisms remain under investigation, and recent studies suggest that the disease involves multiple etiological pathways. To better understand the disease and develop treatment strategies, a number of ongoing studies including the Alzheimer’s Disease Neuroimaging Initiative (ADNI) enroll many study participants and acquire a large number of biomarkers from various modalities including demographic, genotyping, fluid biomarkers, neuroimaging, neuropsychometric test, and clinical assessments. However, a systematic approach that can integrate all the collected data is lacking. The overarching goal of our study is to use machine learning techniques to understand the relationships among different biomarkers and to establish a system-level model that can better describe the interactions among biomarkers and provide superior diagnostic and prognostic information. In this pilot study, we use Bayesian network (BN) to analyze multimodal data from ADNI, including demographics, volumetric MRI, PET, genotypes, and neuropsychometric measurements and demonstrate our approach to have superior prediction accuracy.
机译:据估计,到2050年,全世界阿尔茨海默氏病(AD)患者的数量将从目前的3600万增加到现在的四倍,而尚无行之有效的疾病缓解疗法。目前,潜在的疾病机制仍在研究中,最近的研究表明该疾病涉及多种病因途径。为了更好地了解疾病并制定治疗策略,包括阿尔茨海默氏病神经影像学倡议(ADNI)在内的许多正在进行的研究招募了许多研究参与者,并从人口统计学,基因分型,流体生物标志物,神经影像学,神经心理测验等各种方式中获得了大量生物标志物。以及临床评估。但是,缺乏可以整合所有收集到的数据的系统方法。我们研究的总体目标是使用机器学习技术来了解不同生物标志物之间的关系,并建立一个系统级模型,以更好地描述生物标志物之间的相互作用并提供出色的诊断和预后信息。在这项初步研究中,我们使用贝叶斯网络(BN)分析来自ADNI的多峰数据,包括人口统计学,体积MRI,PET,基因型和神经心理测量,并证明我们的方法具有出色的预测准确性。

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