用机器学习方法识别意大利与阿尔茨海默病有关的载脂蛋白E基因突变病例对照研究

Giorgia Francesca Saraceno, Diana Marisol Abrego-Guandique, Roberto Cannataro, M. Caroleo, E. Cione
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引用次数: 0

摘要

背景:人工智能的一种应用是机器学习,它允许计算机程序学习和创建数据。方法在这项工作中,我们旨在评估 MySLR 机器学习平台的性能,该平台在识别和筛选文献中关于意大利阿尔茨海默病患者载脂蛋白 E(ApoE)基因突变的论文时,采用了 Latent Dirichlet Allocation(LDA)算法。结果:MySLR 可排除重复论文并创建主题。MySLR 被用于分析一组 164 篇科学出版物。在剔除重复论文后,我们确定了 92 篇论文,并将其分为两个相关主题,以反映所调查研究领域的特点。主题 1 包含 70 篇论文,主题 2 包含其余 22 篇论文。尽管存在目前的局限性,但现有证据表明,包含对意大利阿尔茨海默病(AD)患者研究的文章占 65.22%(n = 60)。此外,关于突变(包括单核苷酸多态性(SNPs)载脂蛋白E基因,AD的主要遗传风险因素)的论文在意大利人群中占 5.4%(n = 5)。结论结果表明,机器学习平台有助于识别有关载脂蛋白E基因突变(包括SNPs)的病例对照研究,但并非仅在意大利进行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Machine Learning Approach to Identify Case-Control Studies on ApoE Gene Mutations Linked to Alzheimer’s Disease in Italy
Background: An application of artificial intelligence is machine learning, which allows computer programs to learn and create data. Methods: In this work, we aimed to evaluate the performance of the MySLR machine learning platform, which implements the Latent Dirichlet Allocation (LDA) algorithm in the identification and screening of papers present in the literature that focus on mutations of the apolipoprotein E (ApoE) gene in Italian Alzheimer’s Disease patients. Results: MySLR excludes duplicates and creates topics. MySLR was applied to analyze a set of 164 scientific publications. After duplicate removal, the results allowed us to identify 92 papers divided into two relevant topics characterizing the investigated research area. Topic 1 contains 70 papers, and topic 2 contains the remaining 22. Despite the current limitations, the available evidence suggests that articles containing studies on Italian Alzheimer’s Disease (AD) patients were 65.22% (n = 60). Furthermore, the presence of papers about mutations, including single nucleotide polymorphisms (SNPs) ApoE gene, the primary genetic risk factor of AD, for the Italian population was 5.4% (n = 5). Conclusion: The results show that the machine learning platform helped to identify case-control studies on ApoE gene mutations, including SNPs, but not only conducted in Italy.
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