Polygenic risk prediction: why and when out-of-sample prediction R2 can exceed SNP-based heritability: why and when out-of-sample prediction R2 can exceed SNP-based heritability
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Polygenic risk prediction: why and when out-of-sample prediction R2 can exceed SNP-based heritability: why and when out-of-sample prediction R2 can exceed SNP-based heritability
Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium 2023, 'Polygenic risk prediction : why and when out-of-sample prediction R2 can exceed SNP-based heritability', American journal of human genetics, vol. 110, no. 7, pp. 1207-1215. https://doi.org/10.1016/j.ajhg.2023.06.006 Wang, X, Walker, A, Revez, J A, Ni, G, Adams, M J, McIntosh, A M & Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium 2023, 'Polygenic risk prediction : why and when out-of-sample prediction R 2 can exceed SNP-based heritability', American Journal of Human Genetics, vol. 110, no. 7, pp. 1207-1215. https://doi.org/10.1016/j.ajhg.2023.06.006
In polygenic score (PGS) analysis, the coefficient of determination (R2) is a key statistic to evaluate efficacy. R2 is the proportion of phenotypic variance explained by the PGS, calculated in a cohort that is independent of the genome-wide association study (GWAS) that provided estimates of allelic effect sizes. The SNP-based heritability (hSNP2, the proportion of total phenotypic variances attributable to all common SNPs) is the theoretical upper limit of the out-of-sample prediction R2. However, in real data analyses R2 has been reported to exceed hSNP2, which occurs in parallel with the observation that hSNP2 estimates tend to decline as the number of cohorts being meta-analyzed increases. Here, we quantify why and when these observations are expected. Using theory and simulation, we show that if heterogeneities in cohort-specific hSNP2 exist, or if genetic correlations between cohorts are less than one, hSNP2 estimates can decrease as the number of cohorts being meta-analyzed increases. We derive conditions when the out-of-sample prediction R2 will be greater than hSNP2 and show the validity of our derivations with real data from a binary trait (major depression) and a continuous trait (educational attainment). Our research calls for a better approach to integrating information from multiple cohorts to address issues of between-cohort heterogeneity.
In polygenic score (PGS) analysis, the coefficient of determination (R2) is a key statistic to evaluate efficacy. R2 is the proportion of phenotypic variance explained by the PGS, calculated in a cohort that is independent of the genome-wide association study (GWAS) that provided estimates of allelic effect sizes. The SNP-based heritability (hSNP2, the proportion of total phenotypic variances attributable to all common SNPs) is the theoretical upper limit of the out-of-sample prediction R2. However, in real data analyses R2 has been reported to exceed hSNP2, which occurs in parallel with the observation that hSNP2 estimates tend to decline as the number of cohorts being meta-analyzed increases. Here, we quantify why and when these observations are expected. Using theory and simulation, we show that if heterogeneities in cohort-specific hSNP2 exist, or if genetic correlations between cohorts are less than one, hSNP2 estimates can decrease as the number of cohorts being meta-analyzed increases. We derive conditions when the out-of-sample prediction R2 will be greater than hSNP2 and show the validity of our derivations with real data from a binary trait (major depression) and a continuous trait (educational attainment). Our research calls for a better approach to integrating information from multiple cohorts to address issues of between-cohort heterogeneity.
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