通过多尺度图分析揭示COVID-19与神经退行性疾病的共发病:生物数据库和文本挖掘的系统调查

IF 5.4
Negin Sadat Babaiha , Stefan Geissler , Vincent Nibart , Heval Atas Güvenilir , Vinay Srinivas Bharadhwaj , Alpha Tom Kodamullil , Juergen Klein , Marc Jacobs , Martin Hofmann-Apitius
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引用次数: 0

摘要

2019冠状病毒病大流行引发了大量研究,但其中大部分集中在个体疾病上,忽视了复杂的共病关系。虽然关于阿尔茨海默病和帕金森病等神经退行性疾病(ndd)以及COVID-19的文献很多,但它们的交集仍未得到充分探讨。合并症建模是至关重要的,特别是对于经常出现多种情况的住院患者。本研究通过整合从生物医学数据集和文本挖掘工具构建的知识图(KGs),调查了COVID-19与ndd之间的相互作用。我们对多个kg(如PrimeKG、DrugBank、OpenTargets和通过自然语言处理(NLP)方法生成的kg)进行了全面的分析,包括通径分析、表型覆盖以及细胞和遗传因素的映射。我们的研究结果揭示了图密度和连通性的显着差异,每个KG都为COVID-19与ndd之间的分子和表型联系提供了独特的见解。关键的遗传和炎症标志物,特别是免疫反应基因,一致地出现在图中,表明一个共同的致病基础。通过将结构化生物学数据与非结构化文本证据统一起来,我们增强了共发病建模,并提高了识别COVID-19-NDD相互作用机制的召回率。这一综合框架支持共同发病假设数据库的发展,旨在促进治疗靶点的发现。所有的数据,方法和说明访问合并症假设数据库是公开的:https://github.com/SCAI-BIO/covid-NDD-comorbidity-NLP。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unraveling the co-morbidity between COVID-19 and neurodegenerative diseases through multi-scale graph analysis: A systematic investigation of biological databases and text mining
The COVID-19 pandemic has generated a vast volume of research, yet much of it focuses on individual diseases, overlooking complex comorbidity relationships. While extensive literature exists on both neurodegenerative diseases (NDDs), such as Alzheimer’s and Parkinson’s, and COVID-19, their intersection remains underexplored. Co-morbidity modeling is crucial, particularly for hospitalized patients often presenting with multiple conditions. This study investigates the interplay between COVID-19 and NDDs by integrating knowledge graphs (KGs) built from curated biomedical datasets and text mining tools. We performed comprehensive analyses—including path analysis, phenotype coverage, and mapping of cellular and genetic factors—across multiple KGs, such as PrimeKG, DrugBank, OpenTargets, and those generated via natural language processing (NLP) methods. Our findings reveal notable variability in graph density and connectivity, with each KG offering unique insights into molecular and phenotypic links between COVID-19 and NDDs. Key genetic and inflammatory markers, especially immune response genes, consistently appeared across graphs, suggesting a shared pathogenic basis. By unifying structured biological data with unstructured textual evidence, we enhance co-morbidity modeling and improve recall in identifying mechanisms underlying COVID-19–NDD interactions. This integrative framework supports the development of a co-morbidity hypothesis database aimed at facilitating therapeutic target discovery. All data, methods, and instructions for accessing the co-morbidity hypothesis database are publicly available at: https://github.com/SCAI-BIO/covid-NDD-comorbidity-NLP.
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来源期刊
Artificial intelligence in the life sciences
Artificial intelligence in the life sciences Pharmacology, Biochemistry, Genetics and Molecular Biology (General), Computer Science Applications, Health Informatics, Drug Discovery, Veterinary Science and Veterinary Medicine (General)
CiteScore
5.00
自引率
0.00%
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0
审稿时长
15 days
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