| Literature DB >> 26958218 |
Joseph B Leader1, Sarah A Pendergrass2, Anurag Verma3, David J Carey4, Dustin N Hartzel1, Marylyn D Ritchie3, H Lester Kirchner1.
Abstract
Phenome-Wide Association Studies (PheWAS) comprehensively investigate the association between genetic variation and a wide array of outcome traits. Electronic health record (EHR) based PheWAS uses various abstractions of International Classification of Diseases, Ninth Revision (ICD-9) codes to identify case/control status for diagnoses that are used as the phenotypic variables. However, there have not been comparisons within a PheWAS between results from high quality derived phenotypes and high-throughput but potentially inaccurate use of ICD-9 codes for case/control definition. For this study we first developed a group of high quality algorithms for five phenotypes. Next we evaluated the association of these "gold standard" phenotypes and 4,636,178 genetic variants with minor allele frequency > 0.01 and compared the results from high-throughput associations at the 3 digit, 5 digit, and PheWAS codes for defining case/control status. We found that certain diseases contained similar patient populations across phenotyping methods but had differences in PheWAS.Entities:
Mesh:
Year: 2015 PMID: 26958218 PMCID: PMC4765620
Source DB: PubMed Journal: AMIA Annu Symp Proc ISSN: 1559-4076