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Risk factors affecting polygenic score performance across diverse cohorts.
Hui, Daniel; Dudek, Scott; Kiryluk, Krzysztof; Walunas, Theresa L; Kullo, Iftikhar J; Wei, Wei-Qi; Tiwari, Hemant K; Peterson, Josh F; Chung, Wendy K; Davis, Brittney; Khan, Atlas; Kottyan, Leah; Limdi, Nita A; Feng, Qiping; Puckelwartz, Megan J; Weng, Chunhua; Smith, Johanna L; Karlson, Elizabeth W; Jarvik, Gail P; Ritchie, Marylyn D.
Affiliation
  • Hui D; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Dudek S; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Kiryluk K; Division of Nephrology, Department of Medicine, Columbia University, NY, New York.
  • Walunas TL; Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
  • Kullo IJ; Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN.
  • Wei WQ; Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN.
  • Tiwari HK; Department of Pediatrics, University of Alabama at Birmingham, Birmingham, AL.
  • Peterson JF; Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN.
  • Chung WK; Departments of Pediatrics and Medicine, Columbia University Irving Medical Center, Columbia University, New York, NY.
  • Davis B; Department of Neurology, School of Medicine, University of Alabama at Birmingham, Birmingham, AL.
  • Khan A; Division of Nephrology, Department of Medicine, Columbia University, NY, New York.
  • Kottyan L; The Center for Autoimmune Genomics and Etiology, Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
  • Limdi NA; Department of Neurology, School of Medicine, University of Alabama at Birmingham, Birmingham, AL.
  • Feng Q; Division of Clinical Pharmacology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Puckelwartz MJ; Center for Genetic Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL.
  • Weng C; Department of Biomedical Informatics, Vagelos College of Physicians & Surgeons, Columbia University, New York, NY.
  • Smith JL; Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN.
  • Karlson EW; Division of Rheumatology, Inflammation, and Immunity, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA.
  • Jarvik GP; Departments of Medicine (Medical Genetics) and Genome Sciences, University of Washington Medical Center, Seattle, WA.
  • Ritchie MD; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
medRxiv ; 2024 Apr 10.
Article in En | MEDLINE | ID: mdl-38645167
ABSTRACT
Apart from ancestry, personal or environmental covariates may contribute to differences in polygenic score (PGS) performance. We analyzed effects of covariate stratification and interaction on body mass index (BMI) PGS (PGSBMI) across four cohorts of European (N=491,111) and African (N=21,612) ancestry. Stratifying on binary covariates and quintiles for continuous covariates, 18/62 covariates had significant and replicable R2 differences among strata. Covariates with the largest differences included age, sex, blood lipids, physical activity, and alcohol consumption, with R2 being nearly double between best and worst performing quintiles for certain covariates. 28 covariates had significant PGSBMI-covariate interaction effects, modifying PGSBMI effects by nearly 20% per standard deviation change. We observed overlap between covariates that had significant R2 differences among strata and interaction effects - across all covariates, their main effects on BMI were correlated with their maximum R2 differences and interaction effects (0.56 and 0.58, respectively), suggesting high-PGSBMI individuals have highest R2 and increase in PGS effect. Using quantile regression, we show the effect of PGSBMI increases as BMI itself increases, and that these differences in effects are directly related to differences in R2 when stratifying by different covariates. Given significant and replicable evidence for context-specific PGSBMI performance and effects, we investigated ways to increase model performance taking into account non-linear effects. Machine learning models (neural networks) increased relative model R2 (mean 23%) across datasets. Finally, creating PGSBMI directly from GxAge GWAS effects increased relative R2 by 7.8%. These results demonstrate that certain covariates, especially those most associated with BMI, significantly affect both PGSBMI performance and effects across diverse cohorts and ancestries, and we provide avenues to improve model performance that consider these effects.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: MedRxiv Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: MedRxiv Year: 2024 Document type: Article