Please use this identifier to cite or link to this item:http://hdl.handle.net/20.500.12105/7901
Winner's Curse Correction and Variable Thresholding Improve Performance of Polygenic Risk Modeling Based on Genome-Wide Association Study Summary-Level Data
Shi, Jianxin | Park, Ju-Hyun | Duan, Jubao | Berndt, Sonja T | Moy, Winton | Yu, Kai | Song, Lei | Wheeler, William | Hua, Xing | Silverman, Debra | Garcia-Closas, Montserrat | Hsiung, Chao Agnes | Figueroa, Jonine D | Cortessis, Victoria K | Malats, Nuria CNIO | Karagas, Margaret R | Vineis, Paolo | Chang, I-Shou | Lin, Dongxin | Zhou, Baosen | Seow, Adeline | Matsuo, Keitaro | Hong, Yun-Chul | Caporaso, Neil E | Wolpin, Brian | Jacobs, Eric | Petersen, Gloria M | Klein, Alison P | Li, Donghui | Risch, Harvey | Sanders, Alan R | Hsu, Li | Schoen, Robert E | Brenner, Hermann | Stolzenberg-Solomon, Rachael | Gejman, Pablo | Lan, Qing | Rothman, Nathaniel | Amundadottir, Laufey T | Landi, Maria Teresa | Levinson, Douglas F | Chanock, Stephen J | Chatterjee, Nilanjan
PLoS Genet. 2016;12(12):e1006493.
Recent heritability analyses have indicated that genome-wide association studies (GWAS) have the potential to improve genetic risk prediction for complex diseases based on polygenic risk score (PRS), a simple modelling technique that can be implemented using summary-level data from the discovery samples. We herein propose modifications to improve the performance of PRS. We introduce threshold-dependent winner's-curse adjustments for marginal association coefficients that are used to weight the single-nucleotide polymorphisms (SNPs) in PRS. Further, as a way to incorporate external functional/annotation knowledge that could identify subsets of SNPs highly enriched for associations, we propose variable thresholds for SNPs selection. We applied our methods to GWAS summary-level data of 14 complex diseases. Across all diseases, a simple winner's curse correction uniformly led to enhancement of performance of the models, whereas incorporation of functional SNPs was beneficial only for selected diseases. Compared to the standard PRS algorithm, the proposed methods in combination led to notable gain in efficiency (25-50% increase in the prediction R2) for 5 of 14 diseases. As an example, for GWAS of type 2 diabetes, winner's curse correction improved prediction R2 from 2.29% based on the standard PRS to 3.10% (P = 0.0017) and incorporating functional annotation data further improved R2 to 3.53% (P = 2×10-5). Our simulation studies illustrate why differential treatment of certain categories of functional SNPs, even when shown to be highly enriched for GWAS-heritability, does not lead to proportionate improvement in genetic risk-prediction because of non-uniform linkage disequilibrium structure.
Algorithms | Computer Simulation | Genome-Wide Association Study | Humans | Linkage Disequilibrium | Multifactorial Inheritance | Polymorphism, Single Nucleotide | Risk Factors | Genetic Predisposition to Disease | Models, Genetic
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