Highly elevated polygenic risk scores are better predictors of myocardial infarction risk early in life than later

Figures

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  Fig. 1. Cross-validation scheme for logistic regression training and testing. a Schema indicating how each risk score was generated using a logistic regression algorithm trained with a selection of variable features and a dependent outcome label (IHD, MI, early MI). Ten folds of cross-validation were performed after dividing the full UKB dataset into ten equal subsets, each of which was iteratively used as a test set (1/10 of the data) after training on the others (9/10 of the data). In each iteration of the training, all cases were matched with an equal number of randomly sampled controls. b List of features included in each of five different LR models

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  Fig. 2. Modeling cardiovascular risk in the UKB with genetics and non-fixed factors. Panels on the left-hand side show the prevalence in the White British and Irish European UKB sample versus modeled risk percentile, for the 9% with ischemic heart disease (IHD, dark blue), approaching 5% who have had a myocardial infarction (MI, cyan), and 0.15% who had MI before the age of 50 (early MI, red). Panels on the right show receiver-operating curves of sensitivity against specificity. Each curve represents one of 10 cross-validated estimates, with point estimates plus standard deviation on the left. a 9-feature established-at-birth model. b 18-feature full-model. c Effect of adding features for MI prediction alone, yielding 4-feature, 9-feature, 14-feature, and 18-feature models as outlined in Fig. 1a

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  Fig. 3. Prevalence vs. risk percentile and ROC plots for four risk models for early MI. Plots show the predictive> performance and accuracy for the polygenic risk scores (PRS) only model (yellow), the 9-feature established-at-birth plus PRS model (red), 14-feature established-at-birth plus non-fixed model without PRS (light blue), and the 18-feature full model (dark blue). Each curve represents one of 10 cross-validated estimates, with point estimates plus standard deviation on the left

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  Fig. 4. Adjustment for ancestry by logistic regression. a-c Prevalence vs. Risk percentile plots for MI for the White British and Irish Europeans (a), full UK Biobank (b) and a model including genotypic PC1 and PC2 to control for ancestry (c). d shows frequency distributions of European-derived PRS in each of the indicated ancestry groups, standardized to equivalent size (European n = 441,173; African 7190; East Asian 1471; South Asian 7413). e Prevalence of MI in each ancestry group

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  Fig. 5. Comparison of MI Risk Scores with and without non-fixed risk factors. a Scatterplots of the full model (18-feature established-at-birth + non-fixed + PRS score) against the non-modifiable risk model (9-feature established-at-birth + PRS score). Individuals below the regression line (red, Group A in the middle panel) have comparatively lower predicted risk later in life compared to their predicted risk at birth, whereas those above the regression line (blue, Group B) have higher predicted risk of MI later in life; both groups represent the 2% extremes. The right -hand panel highlights individuals with relatively low risk according to both models (Group C, orange) or relatively high risk according to both models (cyan, Group D). b, c Standardized distributions of indicated non-fixed risk factors for the selected subsets of individuals, implying that high risk individuals are older and more overweight

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  Fig. 6. Effect of genetics on prevalence as a function of medication. a Prevalence vs. risk decile plots showing overall greater apparent influence of genetics for patients on blood pressure medication. This analysis is based on the 18-feature logistic regression model run for White British and Irish-only patients with MI as the label. b Frequency distributions of propensity scores showing close similarity for the three groups