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Data-driven identification of complex disease phenotypes
Disease interaction in multimorbid patients is relevant to treatment and prognosis, yet poorly understood. In the present work, we combine approaches from network science, machine learning and computational phenotyping to assess interactions between two or more diseases in a transparent way across t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8315834/ https://www.ncbi.nlm.nih.gov/pubmed/34314651 http://dx.doi.org/10.1098/rsif.2020.1040 |
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author | Strauss, Markus J. Niederkrotenthaler, Thomas Thurner, Stefan Kautzky-Willer, Alexandra Klimek, Peter |
author_facet | Strauss, Markus J. Niederkrotenthaler, Thomas Thurner, Stefan Kautzky-Willer, Alexandra Klimek, Peter |
author_sort | Strauss, Markus J. |
collection | PubMed |
description | Disease interaction in multimorbid patients is relevant to treatment and prognosis, yet poorly understood. In the present work, we combine approaches from network science, machine learning and computational phenotyping to assess interactions between two or more diseases in a transparent way across the full diagnostic spectrum. We demonstrate that health states of hospitalized patients can be better characterized by including higher-order features capturing interactions between more than two diseases. We identify a meaningful set of higher-order diagnosis features that account for synergistic disease interactions in a population-wide (N = 9 M) medical claims dataset. We construct a generalized disease network where (higher-order) diagnosis features are linked if they predict similar diagnoses across the whole diagnostic spectrum. The fact that specific diagnoses are generally represented multiple times in the network allows for the identification of putatively different disease phenotypes that may reflect different disease aetiologies. At the example of obesity, we demonstrate the purely data-driven detection of two complex phenotypes of obesity. As indicated by a matched comparison between patients having these phenotypes, we show that these phenotypes show specific characteristics of what has been controversially discussed in the medical literature as metabolically healthy and unhealthy obesity, respectively. The findings also suggest that metabolically healthy patients show some progression towards more unhealthy obesity over time, a finding that is consistent with longitudinal studies indicating a transient nature of metabolically healthy obesity. The disease network is available for exploration at https://disease.network/. |
format | Online Article Text |
id | pubmed-8315834 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-83158342021-07-31 Data-driven identification of complex disease phenotypes Strauss, Markus J. Niederkrotenthaler, Thomas Thurner, Stefan Kautzky-Willer, Alexandra Klimek, Peter J R Soc Interface Life Sciences–Physics interface Disease interaction in multimorbid patients is relevant to treatment and prognosis, yet poorly understood. In the present work, we combine approaches from network science, machine learning and computational phenotyping to assess interactions between two or more diseases in a transparent way across the full diagnostic spectrum. We demonstrate that health states of hospitalized patients can be better characterized by including higher-order features capturing interactions between more than two diseases. We identify a meaningful set of higher-order diagnosis features that account for synergistic disease interactions in a population-wide (N = 9 M) medical claims dataset. We construct a generalized disease network where (higher-order) diagnosis features are linked if they predict similar diagnoses across the whole diagnostic spectrum. The fact that specific diagnoses are generally represented multiple times in the network allows for the identification of putatively different disease phenotypes that may reflect different disease aetiologies. At the example of obesity, we demonstrate the purely data-driven detection of two complex phenotypes of obesity. As indicated by a matched comparison between patients having these phenotypes, we show that these phenotypes show specific characteristics of what has been controversially discussed in the medical literature as metabolically healthy and unhealthy obesity, respectively. The findings also suggest that metabolically healthy patients show some progression towards more unhealthy obesity over time, a finding that is consistent with longitudinal studies indicating a transient nature of metabolically healthy obesity. The disease network is available for exploration at https://disease.network/. The Royal Society 2021-07-28 /pmc/articles/PMC8315834/ /pubmed/34314651 http://dx.doi.org/10.1098/rsif.2020.1040 Text en © 2021 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Life Sciences–Physics interface Strauss, Markus J. Niederkrotenthaler, Thomas Thurner, Stefan Kautzky-Willer, Alexandra Klimek, Peter Data-driven identification of complex disease phenotypes |
title | Data-driven identification of complex disease phenotypes |
title_full | Data-driven identification of complex disease phenotypes |
title_fullStr | Data-driven identification of complex disease phenotypes |
title_full_unstemmed | Data-driven identification of complex disease phenotypes |
title_short | Data-driven identification of complex disease phenotypes |
title_sort | data-driven identification of complex disease phenotypes |
topic | Life Sciences–Physics interface |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8315834/ https://www.ncbi.nlm.nih.gov/pubmed/34314651 http://dx.doi.org/10.1098/rsif.2020.1040 |
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