Negin Sadat Babaiha , Stefan Geissler , Vincent Nibart , Heval Atas Güvenilir , Vinay Srinivas Bharadhwaj , Alpha Tom Kodamullil , Juergen Klein , Marc Jacobs , Martin Hofmann-Apitius
{"title":"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","authors":"Negin Sadat Babaiha , Stefan Geissler , Vincent Nibart , Heval Atas Güvenilir , Vinay Srinivas Bharadhwaj , Alpha Tom Kodamullil , Juergen Klein , Marc Jacobs , Martin Hofmann-Apitius","doi":"10.1016/j.ailsci.2025.100138","DOIUrl":null,"url":null,"abstract":"<div><div>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: <span><span>https://github.com/SCAI-BIO/covid-NDD-comorbidity-NLP</span><svg><path></path></svg></span>.</div></div>","PeriodicalId":72304,"journal":{"name":"Artificial intelligence in the life sciences","volume":"8 ","pages":"Article 100138"},"PeriodicalIF":5.4000,"publicationDate":"2025-07-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Unraveling the co-morbidity between COVID-19 and neurodegenerative diseases through multi-scale graph analysis: A systematic investigation of biological databases and text mining\",\"authors\":\"Negin Sadat Babaiha , Stefan Geissler , Vincent Nibart , Heval Atas Güvenilir , Vinay Srinivas Bharadhwaj , Alpha Tom Kodamullil , Juergen Klein , Marc Jacobs , Martin Hofmann-Apitius\",\"doi\":\"10.1016/j.ailsci.2025.100138\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>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. 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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.
Artificial intelligence in the life sciencesPharmacology, Biochemistry, Genetics and Molecular Biology (General), Computer Science Applications, Health Informatics, Drug Discovery, Veterinary Science and Veterinary Medicine (General)