Literature DB >> 31609419

Improving the phenotype risk score as a scalable approach to identifying patients with Mendelian disease.

Lisa Bastarache1, Jacob J Hughey1, Jeffrey A Goldstein2, Julie A Bastraache3,4,5, Satya Das3, Neil Charles Zaki6, Chenjie Zeng3, Leigh Anne Tang1, Dan M Roden1,3,7, Joshua C Denny1,3.   

Abstract

OBJECTIVE: The Phenotype Risk Score (PheRS) is a method to detect Mendelian disease patterns using phenotypes from the electronic health record (EHR). We compared the performance of different approaches mapping EHR phenotypes to Mendelian disease features.
MATERIALS AND METHODS: PheRS utilizes Mendelian diseases descriptions annotated with Human Phenotype Ontology (HPO) terms. In previous work, we presented a map linking phecodes (based on International Classification of Diseases [ICD]-Ninth Revision) to HPO terms. For this study, we integrated ICD-Tenth Revision codes and lab data. We also created a new map between HPO terms using customized groupings of ICD codes. We compared the performance with cases and controls for 16 Mendelian diseases using 2.5 million de-identified medical records.
RESULTS: PheRS effectively distinguished cases from controls for all 15 positive controls and all approaches tested (P < 4 × 1016). Adding lab data led to a statistically significant improvement for 4 of 14 diseases. The custom ICD groupings improved specificity, leading to an average 8% increase for precision at 100 (-2% to 22%). Eight of 10 adults with cystic fibrosis tested had PheRS in the 95th percentile prio to diagnosis. DISCUSSION: Both phecodes and custom ICD groupings were able to detect differences between affected cases and controls at the population level. The ICD map showed better precision for the highest scoring individuals. Adding lab data improved performance at detecting population-level differences.
CONCLUSIONS: PheRS is a scalable method to study Mendelian disease at the population level using electronic health record data and can potentially be used to find patients with undiagnosed Mendelian disease.
© The Author(s) 2019. Published by Oxford University Press on behalf of the American Medical Informatics Association. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  Data mining; Diagnosis; Electronic health record; Mendelian genetics

Year:  2019        PMID: 31609419      PMCID: PMC6857501          DOI: 10.1093/jamia/ocz179

Source DB:  PubMed          Journal:  J Am Med Inform Assoc        ISSN: 1067-5027            Impact factor:   4.497


  23 in total

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2.  Case 40-2018: A Woman with Recurrent Sinusitis, Cough, and Bronchiectasis.

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4.  Evaluating electronic health record data sources and algorithmic approaches to identify hypertensive individuals.

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Journal:  J Am Med Inform Assoc       Date:  2016-08-07       Impact factor: 4.497

5.  Secondary use of clinical data: the Vanderbilt approach.

Authors:  Ioana Danciu; James D Cowan; Melissa Basford; Xiaoming Wang; Alexander Saip; Susan Osgood; Jana Shirey-Rice; Jacqueline Kirby; Paul A Harris
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6.  Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease.

Authors:  Kimberly Splinter; David R Adams; Carlos A Bacino; Hugo J Bellen; Jonathan A Bernstein; Alys M Cheatle-Jarvela; Christine M Eng; Cecilia Esteves; William A Gahl; Rizwan Hamid; Howard J Jacob; Bijal Kikani; David M Koeller; Isaac S Kohane; Brendan H Lee; Joseph Loscalzo; Xi Luo; Alexa T McCray; Thomas O Metz; John J Mulvihill; Stanley F Nelson; Christina G S Palmer; John A Phillips; Leslie Pick; John H Postlethwait; Chloe Reuter; Vandana Shashi; David A Sweetser; Cynthia J Tifft; Nicole M Walley; Michael F Wangler; Monte Westerfield; Matthew T Wheeler; Anastasia L Wise; Elizabeth A Worthey; Shinya Yamamoto; Euan A Ashley
Journal:  N Engl J Med       Date:  2018-10-10       Impact factor: 91.245

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8.  Diagnostic Utility of Exome Sequencing for Kidney Disease.

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Journal:  Front Genet       Date:  2014-06-17       Impact factor: 4.599

10.  McKusick's Online Mendelian Inheritance in Man (OMIM).

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6.  Association of Pathogenic Variants in Hereditary Cancer Genes With Multiple Diseases.

Authors:  Chenjie Zeng; Lisa A Bastarache; Ran Tao; Eric Venner; Scott Hebbring; Justin D Andujar; Sarah T Bland; David R Crosslin; Siddharth Pratap; Ayorinde Cooley; Jennifer A Pacheco; Kurt D Christensen; Emma Perez; Carrie L Blout Zawatsky; Leora Witkowski; Hana Zouk; Chunhua Weng; Kathleen A Leppig; Patrick M A Sleiman; Hakon Hakonarson; Marc S Williams; Yuan Luo; Gail P Jarvik; Robert C Green; Wendy K Chung; Ali G Gharavi; Niall J Lennon; Heidi L Rehm; Richard A Gibbs; Josh F Peterson; Dan M Roden; Georgia L Wiesner; Joshua C Denny
Journal:  JAMA Oncol       Date:  2022-06-01       Impact factor: 33.006

7.  Annual decline in lung function in adults with sickle cell disease is similar to that observed in adults with cystic fibrosis.

Authors:  Brock Hodges; Zalaya Ivy; Robert M Cronin; Mark Rodeghier; Michael R DeBaun; Shaina M Willen
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Review 8.  Artificial intelligence and the hunt for immunological disorders.

Authors:  Nicholas L Rider; Renganathan Srinivasan; Paneez Khoury
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Review 9.  Using the electronic health record for genomics research.

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10.  Examining the Prevalence of Previously Recorded Phenotypically Related Diagnoses Among Fee-for-Service Medicare Enrollees Newly Diagnosed with Mendelian Conditions.

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