Discovering comorbid diseases using an inter-disease interactivity network based on biobank-scale PheWAS data
Abstract 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...
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Veröffentlicht in: | Bioinformatics (Oxford, England) England), 2023-01, Vol.39 (1) |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Abstract
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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ISSN: | 1367-4811 1367-4803 1367-4811 |
DOI: | 10.1093/bioinformatics/btac822 |