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Discovering comorbid diseases using an inter-disease interactivity network based on biobank-scale PheWAS dataoa mark
  • 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
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Publication Year
2023-01-01
Publisher
Oxford University Press
Citation
Bioinformatics, Vol.39
Mesh Keyword
AlgorithmsBiological Specimen BanksComorbidityPhenotypeSoftware
All Science Classification Codes (ASJC)
Statistics and ProbabilityBiochemistryMolecular BiologyComputer Science ApplicationsComputational Theory and MathematicsComputational Mathematics
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.
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/33185
DOI
https://doi.org/10.1093/bioinformatics/btac822
Fulltext

Type
Article
Funding
This work was supported by a National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIT) [No. 2022R1A2C2009998]; the Korea Health Technology R&D Project through the Korea Health Industry Development Institute, funded by the Ministry of Health and Welfare, Republic of Korea [HU21C0111]; and by the National Institute of General Medical Sciences (NIGMS) [R01 GM138597].
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