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Mining clinical and laboratory data of neurodegenerative diseases by Machine Learning: transcriptomic biomarkers

机译:通过机器学习挖掘神经退行性疾病的临床和实验室数据:转录组生物标记

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Low sensitivity and specificity of current diagnostic methodologies lead to frequent misdiagnosis of Alzheimer's and other dementia, causing an extra economic and social burden. We aim to compare real word data with the largest public databases, to extract new diagnostic models for an earlier and more accurate diagnosis of cognitive impairment. We analyzed both neuropsychological, neurological, physical assessments and transcriptomic data from biosamples. We used Machine Learning approaches and biostatistical methods to analyze the transcriptome from the large-scale ADNI and AddNeuroMed international projects: we selected some genes as potential transcriptomic biomarkers and highlighted affected cellular processes. Furthermore the analysis, by machine learning, of real-world data provided by European clinical dementia centres, resulted in a small subset of comorbidities able to discriminate diagnostic classes with a good classifier performance.
机译:当前诊断方法的低敏感性和特异性导致对阿尔茨海默氏病和其他痴呆症的频繁误诊,从而造成额外的经济和社会负担。我们旨在将真实单词数据与最大的公共数据库进行比较,以提取新的诊断模型,以更早,更准确地诊断认知障碍。我们分析了来自生物样本的神经心理学,神经生物学,身体评估和转录组数据。我们使用机器学习方法和生物统计学方法来分析来自大规模ADNI和AddNeuroMed国际项目的转录组:我们选择了一些基因作为潜在的转录组生物标记,并突出显示了受影响的细胞过程。此外,通过机器学习对欧洲临床痴呆中心提供的真实数据进行分析,结果发现一小部分合并症能够区分具有良好分类器性能的诊断类别。

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