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Discovering comorbid diseases using an inter-disease interactivity network based on biobank-scale PheWAS data

MOTIVATION: Understanding comorbidity is essential for disease prevention, treatment and prognosis. In particular, insight into which pairs of diseases are likely or unlikely to co-occur may help elucidate the potential relationships between complex diseases. Here, we introduce the use of an inter-d...

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Autores principales: Nam, Yonghyun, Jung, Sang-Hyuk, Yun, Jae-Seung, Sriram, Vivek, Singhal, Pankhuri, Byrska-Bishop, Marta, Verma, Anurag, Shin, Hyunjung, Park, Woong-Yang, Won, Hong-Hee, Kim, Dokyoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9825330/
https://www.ncbi.nlm.nih.gov/pubmed/36571484
http://dx.doi.org/10.1093/bioinformatics/btac822
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author Nam, Yonghyun
Jung, Sang-Hyuk
Yun, Jae-Seung
Sriram, Vivek
Singhal, Pankhuri
Byrska-Bishop, Marta
Verma, Anurag
Shin, Hyunjung
Park, Woong-Yang
Won, Hong-Hee
Kim, Dokyoon
author_facet Nam, Yonghyun
Jung, Sang-Hyuk
Yun, Jae-Seung
Sriram, Vivek
Singhal, Pankhuri
Byrska-Bishop, Marta
Verma, Anurag
Shin, Hyunjung
Park, Woong-Yang
Won, Hong-Hee
Kim, Dokyoon
author_sort Nam, Yonghyun
collection PubMed
description MOTIVATION: Understanding comorbidity is essential for disease prevention, treatment and prognosis. In particular, insight into which pairs of diseases are likely or unlikely to co-occur may help elucidate the potential relationships between complex diseases. Here, we introduce the use of an inter-disease interactivity network to discover/prioritize comorbidities. Specifically, we determine disease associations by accounting for the direction of effects of genetic components shared between diseases, and categorize those associations as synergistic or antagonistic. We further develop a comorbidity scoring algorithm to predict whether diseases are more or less likely to co-occur in the presence of a given index disease. This algorithm can handle networks that incorporate relationships with opposite signs. RESULTS: We finally investigate inter-disease associations among 427 phenotypes in UK Biobank PheWAS data and predict the priority of comorbid diseases. The predicted comorbidities were verified using the UK Biobank inpatient electronic health records. Our findings demonstrate that considering the interaction of phenotype associations might be helpful in better predicting comorbidity. AVAILABILITY AND IMPLEMENTATION: The source code and data of this study are available at https://github.com/dokyoonkimlab/DiseaseInteractiveNetwork. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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spelling pubmed-98253302023-01-10 Discovering comorbid diseases using an inter-disease interactivity network based on biobank-scale PheWAS data Nam, Yonghyun Jung, Sang-Hyuk Yun, Jae-Seung Sriram, Vivek Singhal, Pankhuri Byrska-Bishop, Marta Verma, Anurag Shin, Hyunjung Park, Woong-Yang Won, Hong-Hee Kim, Dokyoon Bioinformatics Original Paper MOTIVATION: Understanding comorbidity is essential for disease prevention, treatment and prognosis. In particular, insight into which pairs of diseases are likely or unlikely to co-occur may help elucidate the potential relationships between complex diseases. Here, we introduce the use of an inter-disease interactivity network to discover/prioritize comorbidities. Specifically, we determine disease associations by accounting for the direction of effects of genetic components shared between diseases, and categorize those associations as synergistic or antagonistic. We further develop a comorbidity scoring algorithm to predict whether diseases are more or less likely to co-occur in the presence of a given index disease. This algorithm can handle networks that incorporate relationships with opposite signs. RESULTS: We finally investigate inter-disease associations among 427 phenotypes in UK Biobank PheWAS data and predict the priority of comorbid diseases. The predicted comorbidities were verified using the UK Biobank inpatient electronic health records. Our findings demonstrate that considering the interaction of phenotype associations might be helpful in better predicting comorbidity. AVAILABILITY AND IMPLEMENTATION: The source code and data of this study are available at https://github.com/dokyoonkimlab/DiseaseInteractiveNetwork. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2022-12-26 /pmc/articles/PMC9825330/ /pubmed/36571484 http://dx.doi.org/10.1093/bioinformatics/btac822 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Paper
Nam, Yonghyun
Jung, Sang-Hyuk
Yun, Jae-Seung
Sriram, Vivek
Singhal, Pankhuri
Byrska-Bishop, Marta
Verma, Anurag
Shin, Hyunjung
Park, Woong-Yang
Won, Hong-Hee
Kim, Dokyoon
Discovering comorbid diseases using an inter-disease interactivity network based on biobank-scale PheWAS data
title Discovering comorbid diseases using an inter-disease interactivity network based on biobank-scale PheWAS data
title_full Discovering comorbid diseases using an inter-disease interactivity network based on biobank-scale PheWAS data
title_fullStr Discovering comorbid diseases using an inter-disease interactivity network based on biobank-scale PheWAS data
title_full_unstemmed Discovering comorbid diseases using an inter-disease interactivity network based on biobank-scale PheWAS data
title_short Discovering comorbid diseases using an inter-disease interactivity network based on biobank-scale PheWAS data
title_sort discovering comorbid diseases using an inter-disease interactivity network based on biobank-scale phewas data
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9825330/
https://www.ncbi.nlm.nih.gov/pubmed/36571484
http://dx.doi.org/10.1093/bioinformatics/btac822
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