Abstract

Biomedical literature articles and narrative content from Electronic Health Records (EHRs) both constitute rich sources of disease-phenotype information. Phenotype concepts may be mentioned in text in multiple ways, using phrases with a variety of structures. This variability stems partly from the different backgrounds of the authors, but also from the different writing styles typically used in each text type. Since EHR narrative reports and literature articles contain different but complementary types of valuable information, combining details from each text type can help to uncover new disease-phenotype associations. However, the alternative ways in which the same concept may be mentioned in each source constitutes a barrier to the automatic integration of information. Accordingly, identification of the unique concepts represented by phrases in text can help to bridge the gap between text types. We describe our development of a novel method, PhenoNorm, which integrates a number of different similarity measures to allow automatic linking of phenotype concept mentions to known concepts in the UMLS Metathesaurus, a biomedical terminological resource. PhenoNorm was developed using the PhenoCHF corpus—a collection of literature articles and narratives in EHRs, annotated for phenotypic information relating to congestive heart failure (CHF). We evaluate the performance of PhenoNorm in linking CHF-related phenotype mentions to Metathesaurus concepts, using a newly enriched version of PhenoCHF, in which each phenotype mention has an expert-verified link to a concept in the UMLS Metathesaurus. We show that PhenoNorm outperforms a number of alternative methods applied to the same task. Furthermore, we demonstrate PhenoNorm’s wider utility, by evaluating its ability to link mentions of various other types of medically-related information, occurring in texts covering wider subject areas, to concepts in different terminological resources. We show that PhenoNorm can maintain performance levels, and that its accuracy compares favourably to other methods applied to these tasks.

Highlights

  • IntroductionHuman phenotypic information constitutes the observable traits of human beings (e.g., height, eye colour, etc.) resulting from genetic make-up and environmental influences

  • Human phenotypic information constitutes the observable traits of human beings resulting from genetic make-up and environmental influences

  • We have evaluated the performance of PhenoNorm in normalising phenotype mentions in PhenoCHF, and we show that it achieves higher accuracy than other, more general normalisation methods when they are applied to the same task

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Summary

Introduction

Human phenotypic information constitutes the observable traits of human beings (e.g., height, eye colour, etc.) resulting from genetic make-up and environmental influences. Narrative EHR information includes details about individual patient diagnoses, medication, family history, patient past history, signs, symptoms and findings, whilst scientific articles tend to summarise the latest research findings, results and advances in knowledge relevant to different diseases [2, 3]. Given that these different types of information can often be complementary to each other, important details may be overlooked if only a single source (or text type) is considered. As such, automated methods to combine relevant details from different text types can be extremely useful, to discover extended information about a given concept (e.g., to gather alternative perspectives regarding risk factors contributing to a given disease), and to uncover novel associations between diseases and phenotypes, which may be scattered amongst documents, both within a given text type and across different text types

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