Aging-driven metabolic abnormalities remodel intercellular communication through the gut–liver–heart axis and may promote coronary artery disease: the key role of bile acid metabolism - Scorecard - MDSpire
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Metabolic Changes Associated with Aging Alter Intercellular Interactions via the Gut–Liver–Heart Axis and May Contribute to Coronary Artery Disease: The Critical Function of Bile Acid Metabolism

  • By

  • Wei Chen

  • Yue Sun

  • Chu-fan Meng

  • Si-tong Wu

  • Xin-yi Jiang

  • Xian-meng Meng

  • Qing-feng Wang

  • July 6, 2026

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Clinical Scorecard: Metabolic Changes Associated with Aging Alter Intercellular Interactions via the Gut–Liver–Heart Axis and May Contribute to Coronary Artery Disease: The Critical Function of Bile Acid Metabolism

At a Glance

CategoryDetail
ConditionCoronary Artery Disease (CAD)
Key MechanismsAging-related dysbiosis, bile acid metabolism disruption, systemic inflammation via SASP.
Target PopulationOlder adults, particularly those aged 65 years and older.
Care SettingClinical research and cardiovascular health management.

Key Highlights

  • CAD is the leading cause of cardiovascular mortality worldwide.
  • Aging is a strong and independent risk factor for CAD.
  • Cellular senescence contributes to chronic low-grade systemic inflammation.
  • Endothelial dysfunction and large-artery stiffness are key vascular phenotypes of aging.
  • Dysregulated bile acid metabolism is crucial in the gut–liver–heart axis.

Guideline-Based Recommendations

Diagnosis

  • Consider age as a significant risk factor in CAD assessment.

Management

  • Explore microbiota remodeling and FXR/TGR5 agonists as potential interventions.

Monitoring & Follow-up

  • Monitor for signs of endothelial dysfunction and systemic inflammation in older adults.

Risks

  • Increased risk of CAD despite controlled classical risk factors in older populations.

Patient & Prescribing Data

Older adults with CAD or at high risk for CAD.

Emerging therapies include senolytic therapies and metformin, though evidence is primarily preclinical.

Clinical Best Practices

  • Integrate multi-omics approaches to understand CAD as a systemic process.
  • Assess gut microbiota composition in older adults for potential cardiovascular implications.
  • Utilize integrated biomarker frameworks for early risk stratification in CAD.

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