Journal article 660 views 167 downloads
Ranking sets of morbidities using hypergraph centrality
,
Alan Watkins ,
Jane Lyons,
Ronan Lyons ,
Ashley Akbari ,
Niels Peek,
Farideh Jalali-najafabadi,
Thamer Ba Dhafari,
Alexander Pate,
Glen P. Martin,
Rowena Bailey
Journal of Biomedical Informatics, Volume: 122, Start page: 103916
Swansea University Authors:
Jim Rafferty , Alan Watkins , Jane Lyons, Ronan Lyons , Ashley Akbari , Rowena Bailey
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DOI (Published version): 10.1016/j.jbi.2021.103916
Abstract
Multi-morbidity, the health state of having two or more concurrent chronic conditions, is becoming more common as populations age, but is poorly understood. Identifying and understanding commonly occurring sets of diseases is important to inform clinical decisions to improve patient services and out...
| Published in: | Journal of Biomedical Informatics |
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| ISSN: | 1532-0464 |
| Published: |
Elsevier BV
2021
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| Online Access: |
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| URI: | https://cronfa.swan.ac.uk/Record/cronfa57958 |
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| Abstract: |
Multi-morbidity, the health state of having two or more concurrent chronic conditions, is becoming more common as populations age, but is poorly understood. Identifying and understanding commonly occurring sets of diseases is important to inform clinical decisions to improve patient services and outcomes. Network analysis has been previously used to investigate multi-morbidity, but a classic application only allows for information on binary sets of diseases to contribute to the graph. We propose the use of hypergraphs, which allows for the incorporation of data on people with any number of conditions, and also allows us to obtain a quantitative understanding of the centrality, a measure of how well connected items in the network are to each other, of both single diseases and sets of conditions. Using this framework we illustrate its application with the set of conditions described in the Charlson morbidity index using data extracted from routinely collected population-scale, patient level electronic health records (EHR) for a cohort of adults in Wales, UK. Stroke and diabetes were found to be the most central single conditions. Sets of diseases featuring diabetes; diabetes with Chronic Pulmonary Disease, Renal Disease, Congestive Heart Failure and Cancer were the most central pairs of diseases. We investigated the differences between results obtained from the hypergraph and a classic binary graph and found that the cen-trality of diseases such as paraplegia, which are connected strongly to a single other disease is exaggerated in binary graphs compared to hypergraphs. The measure of centrality is derived from the weighting metrics calculated for disease sets and further investigation is needed to better understand the effect of the metric used in identifying the clinical significance and ranked centrality of grouped diseases. These initial results indicate that hypergraphs can be used as a valuable tool for analysing previously poorly understood relationships and in-formation available in EHR data. |
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| Keywords: |
Multi-morbidity, Network analysis, Hypergraph |
| College: |
Faculty of Medicine, Health and Life Sciences |
| Funders: |
This work was funded by the Medical Research Council (MRC) (Grant No.: MR/S027750/1); and supported by Health Data Research UK (Grant No.: HDR-9006), which receives its funding from the UK Medical Research Council, Engineering and Physical Sciences Research Council, Economic and Social Research Council, Department of Health and Social Care (England), Chief Scientist Office of the Scottish Government Health and Social Care Directorates, Health and Social Care Research and Development Division (Welsh Government), Public Health Agency (Northern Ireland), British Heart Foundation (BHF) and the Wellcome Trust; and Administrative Data Research UK, which is funded by the Economic and Social Research Council (Grant No.: ES/S007393/1). FJ is supported by an MRC/University of Manchester Skills Development Fellowship (Grant No. MR/R016615). The funder was not involved in the study design, analysis of the data or preparation of the manuscript. |
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103916 |