Multi-Omics and Artificial Intelligence in Cardiovascular Medicine: From Mechanistic Insights to Clinical Translation
Ewelina Młynarska1, Kinga Bojdo1, Oliwia Mazur1
1Department of Nephrocardiology, Medical University of Lodz, 90-419 Lodz, Poland.
Insights
Integrating multi-omics data with artificial intelligence (AI) can bridge the gap in cardiovascular disease (CVD) prediction. This approach moves beyond descriptive markers to enable precision cardiology and personalized patient risk models.
Area of Science:
- Cardiovascular research
- Bioinformatics
- Artificial Intelligence in Medicine
Background:
- Cardiovascular diseases (CVDs) are the leading cause of death globally.
- A significant translational gap exists, with conventional biomarkers failing to predict individual disease trajectories.
- Current single-omics studies lack a unified framework for integrating molecular data with computational intelligence.
Purpose of the Study:
- To evaluate the integration of multi-omics and AI for predictive precision cardiology.
- To transition from descriptive biomarkers to actionable risk prediction models.
- To address the translational gap in cardiovascular disease research.
Main Methods:
- Synthesizing evidence from non-coding RNA networks (miRNAs, lncRNAs) and exosomal trafficking.
- Assessing Machine Learning (ML) architectures, including supervised, unsupervised, and deep learning (DL) models.
- Delineating pipelines to deconvolute high-dimensional signatures into risk models.
Main Results:
- Identified lack of standardized bioinformatic workflows and model interpretability as key barriers to clinical translation.
- Demonstrated pathways to translate multi-omic signatures (e.g., TMAO, miRNAs) into risk models for heart failure and post-infarction outcomes.
- Highlighted the potential of multi-omics and AI to overcome limitations of single-omics approaches.
Conclusions:
- Proposes an integrated molecular-computational framework for precision cardiology.
- Emphasizes the need for Explainable AI (XAI) and standardized multi-omic protocols.
- Advocates for bridging the gap between high-dimensional biological data and clinical decision-making.
Abstract:
Background: Cardiovascular diseases (CVDs) remain the leading global cause of mortality, yet a critical "translational gap" persists: Conventional biomarkers often fail to detect subclinical stages or predict individual disease trajectories. While single-omics studies have proliferated, the field lacks a unified framework synthesizing these molecular layers with advanced computational intelligence. Aim: This review addresses this gap by evaluating the synergistic integration of multi-omics and Artificial Intelligence (AI) to transition from descriptive markers toward predictive precision cardiology. Scope: Evidence from non-coding RNA networks (miRNAs, lncRNAs) and exosomal trafficking is synthesized alongside a critical assessment of Machine Learning (ML) architectures, including supervised, unsupervised, and deep learning (DL) models. Findings: Unlike traditional reviews, this work delineates the specific pipelines required to deconvolute high-dimensional signatures-such as TMAO, acylcarnitines, and cardiac-enriched miRNAs-into actionable risk models for heart failure (HF) and post-infarction outcomes. The primary barrier to clinical translation is identified not as data scarcity but as the lack of standardized bioinformatic workflows and model interpretability. Conclusions: This review distinguishes itself by proposing an integrated molecular-computational framework that prioritizes Explainable AI (XAI) and standardized multi-omic protocols. Such a shift is essential to bridge the gap between high-dimensional biological insights and routine clinical decision-making.
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