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Could Artificial Intelligence/Machine Learning and Inclusion of Diet-Gut Microbiome Interactions Improve Disease Risk
Baiba Vilne1,2, Juris Ķibilds3, Inese Siksna3
1Bioinformatics Lab, Riga Stradins University, Riga, Latvia.
Insights
Integrating diet and gut microbiome data with AI can improve coronary artery disease (CAD) risk prediction. This approach addresses limitations of traditional factors and personalized responses for better cardiovascular health outcomes.
Area of Science:
- Cardiovascular Disease Research
- Nutritional Science
- Microbiome Research
Background:
- Coronary artery disease (CAD) is a leading cause of global mortality, necessitating improved risk prediction.
- Current models using traditional risk factors are insufficient due to CAD's complex, multifactorial nature.
- Individual responses to diet vary, highlighting the need for personalized approaches beyond "one-size-fits-all".
Purpose of the Study:
- To review Artificial Intelligence (AI) and Machine Learning (ML) applications in CAD risk prediction.
- To explore the role of diet and gut microbiome in CAD.
- To discuss the integration of diet-gut microbiome interactions for personalized CAD risk assessment.
Main Methods:
- Review of AI/ML approaches for CAD risk prediction.
- Analysis of dietary factors' impact on CAD.
- Classification of individuals based on gut microbiome composition.
- Modeling of diet-gut microbiome interactions.
Main Results:
- AI/ML can capture complex data and interactions for improved prediction.
- Diet and gut microbiome are significant, yet complex, contributors to CAD risk.
- Integrating these factors presents Big Data challenges but holds promise.
Conclusions:
- Personalized CAD risk prediction requires integrating diet, gut microbiome, and clinical data.
- AI/ML offers powerful tools to model these complex interactions.
- Future research should focus on developing integrated, personalized decision support systems for CAD prevention.
Abstract:
Coronary artery disease (CAD) is the most common cardiovascular disease (CVD) and the main leading cause of morbidity and mortality worldwide, posing a huge socio-economic burden to the society and health systems. Therefore, timely and precise identification of people at high risk of CAD is urgently required. Most current CAD risk prediction approaches are based on a small number of traditional risk factors (age, sex, diabetes, LDL and HDL cholesterol, smoking, systolic blood pressure) and are incompletely predictive across all patient groups, as CAD is a multi-factorial disease with complex etiology, considered to be driven by both genetic, as well as numerous environmental/lifestyle factors. Diet is one of the modifiable factors for improving lifestyle and disease prevention. However, the current rise in obesity, type 2 diabetes (T2D) and CVD/CAD indicates that the "one-size-fits-all" approach may not be efficient, due to significant variation in inter-individual responses. Recently, the gut microbiome has emerged as a potential and previously under-explored contributor to these variations. Hence, efficient integration of dietary and gut microbiome information alongside with genetic variations and clinical data holds a great promise to improve CAD risk prediction. Nevertheless, the highly complex nature of meals combined with the huge inter-individual variability of the gut microbiome poses several Big Data analytics challenges in modeling diet-gut microbiota interactions and integrating these within CAD risk prediction approaches for the development of personalized decision support systems (DSS). In this regard, the recent re-emergence of Artificial Intelligence (AI) / Machine Learning (ML) is opening intriguing perspectives, as these approaches are able to capture large and complex matrices of data, incorporating their interactions and identifying both linear and non-linear relationships. In this Mini-Review, we consider (1) the most used AI/ML approaches and their different use cases for CAD risk prediction (2) modeling of the content, choice and impact of dietary factors on CAD risk; (3) classification of individuals by their gut microbiome composition into CAD cases vs. controls and (4) modeling of the diet-gut microbiome interactions and their impact on CAD risk. Finally, we provide an outlook for putting it all together for improved CAD risk predictions.
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