Cox regression is robust to inaccurate EHR-extracted event time: an application to EHR-based GWAS

Author:

Irlmeier Rebecca1ORCID,Hughey Jacob J23,Bastarache Lisa2,Denny Joshua C4,Chen Qingxia12

Affiliation:

1. Department of Biostatistics, Vanderbilt University Medical Center , Nashville, TN 37203, USA

2. Department of Biomedical Informatics, Vanderbilt University Medical Center , Nashville, TN 37203, USA

3. Department of Biomedical Sciences, Vanderbilt University , Nashville, TN 37203, USA

4. All of Us Research Program, National Institutes of Health , Bethesda, MD 20892, USA

Abstract

Abstract Motivation Logistic regression models are used in genomic studies to analyze the genetic data linked to electronic health records (EHRs), and do not take full usage of the time-to-event information available in EHRs. Previous work has shown that Cox regression, which can account for left truncation and right censoring in EHRs, increased the power to detect genotype–phenotype associations compared to logistic regression. We extend this to evaluate the relative performance of Cox regression and various logistic regression models in the presence of positive errors in event time (delayed event time), relating to recorded event time accuracy. Results One Cox model and three logistic regression models were considered under different scenarios of delayed event time. Extensive simulations and a genomic study application were used to evaluate the impact of delayed event time. While logistic regression does not model the time-to-event directly, various logistic regression models used in the literature were more sensitive to delayed event time than Cox regression. Results highlighted the importance to identify and exclude the patients diagnosed before entry time. Cox regression had similar or modest improvement in statistical power over various logistic regression models at controlled type I error. This was supported by the empirical data, where the Cox models steadily had the highest sensitivity to detect known genotype–phenotype associations under all scenarios of delayed event time. Availability and implementation Access to individual-level EHR and genotype data is restricted by the IRB. Simulation code and R script for data process are at: https://github.com/QingxiaCindyChen/CoxRobustEHR.git Supplementary information Supplementary data are available at Bioinformatics online.

Funder

National Institutes of Health

NLM

NIGMS

NCI

Vanderbilt University Medical Center

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

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3. The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019;Buniello;Nucleic Acids Res,2019

4. Chapter 11: Genome-wide association studies;Bush W.S;PLoS Comput Biol,2012

5. Simulation-extrapolation estimation in parametric measurement error models;Cook;J. Am. Stat. Assoc,1994

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