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# Coronary Artery Disease

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  1. medRxiv

    Coronary risk scores stop giving one number: eight biological axes separate people with the same genetic liability

    Polygenic risk for coronary artery disease no longer collapses into a single number. Conventional scores identify who is at high risk but not which biological processes drive that risk. Decomposing 526 genome-wide significant variants by their associations with 78 CAD-related traits yielded eight latent components: cholesterol-enriched lipoproteins, triglyceride-rich lipoproteins, lipoprotein(a), metabolically unhealthy normal weight, obesity, endothelial dysfunction, coagulation and cardiac remodeling. Process-specific scores built in UK Biobank, SCAPIS and Mass General Brigham Biobank tracked clinical coronary events, subclinical atherosclerosis and distinct biomarker and comorbidity profiles.

  2. Integrating AI quantitative CT, photon-counting CT, and FFR-CT brings coronary plaque burden and ischemia assessment into one CCTA workflow

    This review surveys recent advances in coronary CT angiography (CCTA) for coronary artery disease: AI-driven plaque and stenosis quantification can cut analysis time from over 25 minutes to typically under 60 seconds per case with correlation coefficients of 0.92-0.95 against intravascular ultrasound, photon-counting detector CT (PCD-CT) reduces calcium blooming at ultra-high resolution and reclassifies some cases to lower CAD-RADS categories, and FFR-CT adds noninvasive lesion-specific physiologic assessment, so that combining the three can support more refined risk stratification for major adverse cardiovascular events and preventive therapy decisions.

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