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EndoPRS: Incorporating Endophenotype Information to Improve Polygenic Risk Scores for Clinical Endpoints.
Kharitonova, Elena V; Sun, Quan; Ockerman, Frank; Chen, Brian; Zhou, Laura Y; Cao, Hongyuan; Mathias, Rasika A; Auer, Paul L; Ober, Carole; Raffield, Laura M; Reiner, Alexander P; Cox, Nancy J; Kelada, Samir; Tao, Ran; Li, Yun.
Afiliação
  • Kharitonova EV; Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
  • Sun Q; Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
  • Ockerman F; Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
  • Chen B; Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
  • Zhou LY; Department of Biostatistics and Health Data Science, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
  • Cao H; Department of Statistics, Florida State University, Tallahassee, FL 32306, USA.
  • Mathias RA; Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
  • Auer PL; Department of Biostatistics, Medical College of Wisconsin, Milwaukee, WI 53226, USA.
  • Ober C; Department of Human Genetics, University of Chicago, Chicago, IL 60637, USA.
  • Raffield LM; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
  • Reiner AP; Department of Epidemiology, University of Washington, Seattle, WA 98105, USA.
  • Cox NJ; Division of Genetic Medicine, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
  • Kelada S; Vanderbilt Genetics Institute, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
  • Tao R; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
  • Li Y; Marsico Lung Institute, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
medRxiv ; 2024 May 24.
Article em En | MEDLINE | ID: mdl-38826253
ABSTRACT
Polygenic risk score (PRS) prediction of complex diseases can be improved by leveraging related phenotypes. This has motivated the development of several multi-trait PRS methods that jointly model information from genetically correlated traits. However, these methods do not account for vertical pleiotropy between traits, in which one trait acts as a mediator for another. Here, we introduce endoPRS, a weighted lasso model that incorporates information from relevant endophenotypes to improve disease risk prediction without making assumptions about the genetic architecture underlying the endophenotype-disease relationship. Through extensive simulation analysis, we demonstrate the robustness of endoPRS in a variety of complex genetic frameworks. We also apply endoPRS to predict the risk of childhood onset asthma in UK Biobank by leveraging a paired GWAS of eosinophil count, a relevant endophenotype. We find that endoPRS significantly improves prediction compared to many existing PRS methods, including multi-trait PRS methods, MTAG and wMT-BLUP, which suggests advantages of endoPRS in real-life clinical settings.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article