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Ross Arena

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Review Aug 2026

Artificial intelligence for risk prediction in atherosclerotic cardiovascular disease: A narrative review of advances, validation challenges, and clinical translation (2020-2026).

Since 2020, artificial intelligence (AI) has been increasingly applied to atherosclerotic cardiovascular disease (ASCVD) risk prediction. This structured narrative review with systematic evidence mapping summarizes literature (2020-2026) examining study design, data sources, model architectures, multimodal fusion, model development and validation, performance evaluation, subgroup applications, and implementation barriers. Overall, 126 studies informed the review; 93 provided sufficient information for structured extraction, including prevention setting, exact input variables, comparator scores, validation strategies, discrimination, calibration, dominant model architecture, endpoint category, foundation-model or pretrained-model status, regulatory status, and implementation features. AI-based models may offer modest but clinically meaningful gains over conventional risk equations, especially with multimodal or longitudinal data. Among the 93 studies, traditional machine learning accounted for 83 (89%), deep learning for 7 (8%), and multimodal fusion for 3 (3%). Endpoint definitions were heterogeneous (23% ASCVD-specific; 63% expanded MACE composites). Among these studies, no large language model or federated learning was used for risk prediction. Appropriate comparators should now include contemporary equations such as PREVENT, rather than only legacy tools. Major barriers remain, including limited external validation, performance attenuation, data and algorithmic bias, limited interpretability, inconsistent reporting of calibration, fairness, and clinical utility, unclear regulatory status, and limited prospective evidence. Future work should prioritize calibration, robustness, transportability, fairness, interpretability, regulatory clarity, workflow integration, and prospective evidence of decision impact or post-deployment benefit. The central question is not only whether AI can detect complex patterns, but whether such models can be trusted, implemented, and shown to advance preventive cardiology in real-world settings.

Ruifeng Liu, Ross Arena, V. Vasile et al. · 0 citations
Review Aug 2026

The long-term prognostic value of triglyceride-glucose index in type 2 diabetics without clinical coronary artery disease.

BACKGROUND The triglyceride-glucose (TyG) index, a simple laboratory marker of insulin resistance, has been associated with cardiometabolic risk. OBJECTIVES The purpose of this study was to evaluate whether baseline TyG predicts long-term major adverse cardiovascular events (MACE) in patients with type 2 diabetes (T2DM) without clinical coronary artery disease (CAD), independent of traditional risk factors and coronary artery calcium scoring (CACS). METHODS We conducted a retrospective analysis of a prospectively recruited cohort of 735 patients with T2DM, aged 55-74 years (48% women), enrolled between 2006 and 2008. All participants had at least one additional cardiovascular risk factor, no history or symptoms of CAD, and underwent computed tomography for CACS assessment. Multivariate Cox proportional hazards models were used to investigate the association of baseline TyG with the occurrence of myocardial infarction, stroke, or all-cause death, adjusting for demographic factors, diabetes severity, and CACS. RESULTS Over a median follow-up of 16.4 years, 327 patients experienced a first MACE. Compared with patients with TyG <50th percentile (<9.26), multivariable-adjusted hazard ratios (95% CI) were 1.62 (1.30-2.03), 1.84 (1.43-2.38), and 2.09 (1.48-2.94) for TyG ≥50th (≥9.26), >75th (>9.68), and ≥90th (>10.16) percentiles, respectively. The association remained significant after additional adjustment for diabetes severity and CACS. In a combined TyG-CACS model, MACE incidence progressively increased from 1.29 (TyG <9.26; CACS=0) to 5.33 (TyG >9.68; CACS ≥100) events per 100 patient-years. CONCLUSIONS In a cohort without known CAD, baseline TyG independently predicts long-term MACE in T2DM. This simple, widely available metabolic marker may enhance cardiovascular risk stratification and MACE primary prevention strategies.

Yuval Avidan, D. Halon, Amir Yahav et al. · 0 citations