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dc.contributor.authorZhou, Shang-Ming
dc.contributor.authorFernandez-Gutierrez, Fabiola
dc.contributor.authorKennedy, Jonathan
dc.contributor.authorCooksey, Roxanne
dc.contributor.authorAtkinson, Mark
dc.contributor.authorDenaxas, Spiros
dc.contributor.authorSiebert, Stefan
dc.contributor.authorDixon, William G.
dc.contributor.authorO'Neill, Terence W.
dc.contributor.authorChoy, Ernest
dc.contributor.authorSudlow, Cathie
dc.contributor.authorUK Biobank Follow-up and Outcomes Group
dc.contributor.authorBrophy, Sinead
dc.contributor.authorSullivan, Frank
dc.date.accessioned2017-06-20T09:30:12Z
dc.date.available2017-06-20T09:30:12Z
dc.date.issued2016-05-02
dc.identifier.citationZhou , S-M , Fernandez-Gutierrez , F , Kennedy , J , Cooksey , R , Atkinson , M , Denaxas , S , Siebert , S , Dixon , W G , O'Neill , T W , Choy , E , Sudlow , C , UK Biobank Follow-up and Outcomes Group , Brophy , S & Sullivan , F 2016 , ' Defining disease phenotypes in primary care electronic health records by a machine learning approach : a case study in identifying rheumatoid arthritis ' , PLoS One , vol. 11 , no. 5 , e0154515 . https://doi.org/10.1371/journal.pone.0154515en
dc.identifier.issn1932-6203
dc.identifier.otherPURE: 250248295
dc.identifier.otherPURE UUID: 496386f3-7c68-4ea4-8e02-cc80475101fc
dc.identifier.otherPubMed: 27135409
dc.identifier.otherPubMedCentral: PMC4852928
dc.identifier.otherScopus: 84968543936
dc.identifier.otherORCID: /0000-0002-6623-4964/work/34245815
dc.identifier.urihttps://hdl.handle.net/10023/11028
dc.descriptionThe work was supported by the UK Biobank, and undertaken with the support of the National Centre for Population Health and Wellbeing Research (NCPHWR) and the Farr Institute of Health Informatics Research. The NCPHWR is funded by Health and Care Research Wales (grant ref. : CA02). The Farr Institute is funded by a consortium of ten UK research organisations (grant ref. : MR/K006525/1): Arthritis Research UK, the British Heart Foundation, Cancer Research UK, the Economic and Social Research Council, the Engineering and Physical Sciences Research Council, the Medical Research Council, the National Institute of Health Research, the National Institute for Social Care and Health Research (Welsh Government) and the Chief Scientist Office (Scottish Government Health Directorates). WGD was supported by an MRC Clinician Scientist Fellowship (G0902272).en
dc.description.abstractObjectives : 1) To use data-driven method to examine clinical codes (risk factors) of a medical condition in primary care electronic health records (EHRs) that can accurately predict a diagnosis of the condition in secondary care EHRs. 2) To develop and validate a disease phenotyping algorithm for rheumatoid arthritis using primary care EHRs. Methods : This study linked routine primary and secondary care EHRs in Wales, UK. A machine learning based scheme was used to identify patients with rheumatoid arthritis from primary care EHRs via the following steps: i) selection of variables by comparing relative frequencies of Read codes in the primary care dataset associated with disease case compared to non-disease control (disease/non-disease based on the secondary care diagnosis); ii) reduction of predictors/associated variables using a Random Forest method, iii) induction of decision rules from decision tree model. The proposed method was then extensively validated on an independent dataset, and compared for performance with two existing deterministic algorithms for RA which had been developed using expert clinical knowledge. Results : Primary care EHRs were available for 2,238,360 patients over the age of 16 and of these 20,667 were also linked in the secondary care rheumatology clinical system. In the linked dataset, 900 predictors (out of a total of 43,100 variables) in the primary care record were discovered more frequently in those with versus those without RA. These variables were reduced to 37 groups of related clinical codes, which were used to develop a decision tree model. The final algorithm identified 8 predictors related to diagnostic codes for RA, medication codes, such as those for disease modifying anti-rheumatic drugs, and absence of alternative diagnoses such as psoriatic arthritis. The proposed data-driven method performed as well as the expert clinical knowledge based methods. Conclusion : Data-driven scheme, such as ensemble machine learning methods, has the potential of identifying the most informative predictors in a cost-effective and rapid way to accurately and reliably classify rheumatoid arthritis or other complex medical conditions in primary care EHRs.
dc.format.extent14
dc.language.isoeng
dc.relation.ispartofPLoS Oneen
dc.rights© 2016 Zhou et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en
dc.subjectRA0421 Public health. Hygiene. Preventive Medicineen
dc.subjectZA4050 Electronic information resourcesen
dc.subjectT-DASen
dc.subjectBDCen
dc.subjectSDG 3 - Good Health and Well-beingen
dc.subject.lccRA0421en
dc.subject.lccZA4050en
dc.titleDefining disease phenotypes in primary care electronic health records by a machine learning approach : a case study in identifying rheumatoid arthritisen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. School of Medicineen
dc.identifier.doihttps://doi.org/10.1371/journal.pone.0154515
dc.description.statusPeer revieweden
dc.identifier.urlhttp://journals.plos.org/plosone/article?id=10.1371/journal.pone.0154515#sec018en


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