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Conditional Disease Development extracted from Longitudinal Health Care Cohort Data using Layered Network Construction
Health care data holds great promise to be used in clinical decision support systems. However, frequent near-synonymous diagnoses recorded separately, as well as the sheer magnitude and complexity of the disease data makes it challenging to extract non-trivial conclusions beyond confirmatory associa...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4876508/ https://www.ncbi.nlm.nih.gov/pubmed/27211115 http://dx.doi.org/10.1038/srep26170 |
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author | Kannan, Venkateshan Swartz, Fredrik Kiani, Narsis A. Silberberg, Gilad Tsipras, Giorgos Gomez-Cabrero, David Alexanderson, Kristina Tegnèr, Jesper |
author_facet | Kannan, Venkateshan Swartz, Fredrik Kiani, Narsis A. Silberberg, Gilad Tsipras, Giorgos Gomez-Cabrero, David Alexanderson, Kristina Tegnèr, Jesper |
author_sort | Kannan, Venkateshan |
collection | PubMed |
description | Health care data holds great promise to be used in clinical decision support systems. However, frequent near-synonymous diagnoses recorded separately, as well as the sheer magnitude and complexity of the disease data makes it challenging to extract non-trivial conclusions beyond confirmatory associations from such a web of interactions. Here we present a systematic methodology to derive statistically valid conditional development of diseases. To this end we utilize a cohort of 5,512,469 individuals followed over 13 years at inpatient care, including data on disability pension and cause of death. By introducing a causal information fraction measure and taking advantage of the composite structure in the ICD codes, we extract an effective directed lower dimensional network representation (100 nodes and 130 edges) of our cohort. Unpacking composite nodes into bipartite graphs retrieves, for example, that individuals with behavioral disorders are more likely to be followed by prescription drug poisoning episodes, whereas women with leiomyoma were more likely to subsequently experience endometriosis. The conditional disease development represent putative causal relations, indicating possible novel clinical relationships and pathophysiological associations that have not been explored yet. |
format | Online Article Text |
id | pubmed-4876508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48765082016-06-06 Conditional Disease Development extracted from Longitudinal Health Care Cohort Data using Layered Network Construction Kannan, Venkateshan Swartz, Fredrik Kiani, Narsis A. Silberberg, Gilad Tsipras, Giorgos Gomez-Cabrero, David Alexanderson, Kristina Tegnèr, Jesper Sci Rep Article Health care data holds great promise to be used in clinical decision support systems. However, frequent near-synonymous diagnoses recorded separately, as well as the sheer magnitude and complexity of the disease data makes it challenging to extract non-trivial conclusions beyond confirmatory associations from such a web of interactions. Here we present a systematic methodology to derive statistically valid conditional development of diseases. To this end we utilize a cohort of 5,512,469 individuals followed over 13 years at inpatient care, including data on disability pension and cause of death. By introducing a causal information fraction measure and taking advantage of the composite structure in the ICD codes, we extract an effective directed lower dimensional network representation (100 nodes and 130 edges) of our cohort. Unpacking composite nodes into bipartite graphs retrieves, for example, that individuals with behavioral disorders are more likely to be followed by prescription drug poisoning episodes, whereas women with leiomyoma were more likely to subsequently experience endometriosis. The conditional disease development represent putative causal relations, indicating possible novel clinical relationships and pathophysiological associations that have not been explored yet. Nature Publishing Group 2016-05-23 /pmc/articles/PMC4876508/ /pubmed/27211115 http://dx.doi.org/10.1038/srep26170 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Kannan, Venkateshan Swartz, Fredrik Kiani, Narsis A. Silberberg, Gilad Tsipras, Giorgos Gomez-Cabrero, David Alexanderson, Kristina Tegnèr, Jesper Conditional Disease Development extracted from Longitudinal Health Care Cohort Data using Layered Network Construction |
title | Conditional Disease Development extracted from Longitudinal Health Care Cohort Data using Layered Network Construction |
title_full | Conditional Disease Development extracted from Longitudinal Health Care Cohort Data using Layered Network Construction |
title_fullStr | Conditional Disease Development extracted from Longitudinal Health Care Cohort Data using Layered Network Construction |
title_full_unstemmed | Conditional Disease Development extracted from Longitudinal Health Care Cohort Data using Layered Network Construction |
title_short | Conditional Disease Development extracted from Longitudinal Health Care Cohort Data using Layered Network Construction |
title_sort | conditional disease development extracted from longitudinal health care cohort data using layered network construction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4876508/ https://www.ncbi.nlm.nih.gov/pubmed/27211115 http://dx.doi.org/10.1038/srep26170 |
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