Fine-mapping of retinal vascular complexity loci identifies Notch regulation as a shared mechanism with myocardial infarction outcomes
Fine-mapping of retinal vascular complexity loci identifies Notch regulation as a shared mechanism with myocardial infarction outcomes
A. Villaplana-Velasco,M. Pigeyre,13 Authors,M. Bernabeu
TLDR
A genome-wide association study of 38,000 individuals with white British ancestry from the UK Biobank finds an inverse relationship between progression of coronary artery disease and retinal vasculature’s complexity measured as fractal dimension, and validates a predictive model for myocardial infarction.
Abstract
There is increasing evidence that the complexity of the retinal vasculature measured as fractal dimension, D_f, might offer earlier insights into the progression of coronary artery disease (CAD) before traditional biomarkers can be detected. This association could be partly explained by a common genetic basis; however, the genetic component of D_f is poorly understood. We present a genome-wide association study (GWAS) of 38,000 individuals with white British ancestry from the UK Biobank aimed to comprehensively study the genetic component of D_f and analyse its relationship with CAD. We replicated 5 D_f loci and found 4 additional loci with suggestive significance ( P < 1e−05) to contribute to D_f variation, which previously were reported in retinal tortuosity and complexity, hypertension, and CAD studies. Significant negative genetic correlation estimates support the inverse relationship between D_f and CAD, and between D_f and myocardial infarction (MI), one of CAD’s fatal outcomes. Fine-mapping of D_f loci revealed Notch signalling regulatory variants supporting a shared mechanism with MI outcomes. We developed a predictive model for MI incident cases, recorded over a 10-year period following clinical and ophthalmic evaluation, combining clinical information, D_f, and a CAD polygenic risk score. Internal cross-validation demonstrated a considerable improvement in the area under the curve (AUC) of our predictive model (AUC = 0.770 ± 0.001) when comparing with an established risk model, SCORE, (AUC = 0.741 ± 0.002) and extensions thereof leveraging the PRS (AUC = 0.728 ± 0.001). This evidences that D_f provides risk information beyond demographic, lifestyle, and genetic risk factors. Our findings shed new light on the genetic basis of D_f, unveiling a common control with MI, and highlighting the benefits of its application in individualised MI risk prediction. A genome-wide association study finds an inverse relationship between progression of coronary artery disease and retinal vasculature’s complexity measured as fractal dimension, and validates a predictive model for myocardial infarction.
