Coronary artery disease as a risk factor for metabolic dysfunction-associated steatotic liver disease and liver

Luis Vega1, Daniela Simian1, Abraham I Gajardo2

  • 1Gastroenterology Section, Medicine Department, Hospital Clínico Universidad de Chile, Santiago, Chile.

PubMed

Insights

Metabolic dysfunction-associated steatotic liver disease (MASLD) is common in patients with coronary heart disease (CHD). Significant CHD increases the likelihood of liver fibrosis, suggesting further investigation in these patients.

Area of Science:

  • Cardiology
  • Hepatology
  • Metabolic Diseases

Background:

  • Patients with metabolic dysfunction-associated steatotic liver disease (MASLD) face elevated cardiovascular risk.
  • Non-alcoholic fatty liver disease (NAFLD) is frequently observed in individuals with coronary heart disease (CHD).
  • The relationship between significant CHD and the prevalence of liver fibrosis remains unclear.

Purpose of the Study:

  • To determine the frequency of MASLD and liver fibrosis in patients with CHD.
  • To assess the association between coronary stenosis severity and MASLD and liver fibrosis.

Main Methods:

  • An observational study involving 113 adult patients undergoing coronary angiography for suspected coronary artery disease.
  • Significant CHD defined as >50% stenosis in at least one coronary artery.
  • Liver stiffness measured via elastography (FibroScan®) to assess liver fibrosis (>6.5 Kpa).

Main Results:

  • 72% of patients had significant CHD; 52% had MASLD.
  • Liver fibrosis was present in 12% of patients, notably higher in the significant CHD group (p=0.007).
  • Increased coronary artery stenosis correlated with a higher probability of liver fibrosis (OR 1.79, p=0.029).

Conclusions:

  • MASLD is highly prevalent in patients with significant CHD, even without prior liver disease diagnosis.
  • These findings indicate a need to screen for MASLD and liver fibrosis in CHD patients.
  • Future research should explore confounding factors like type 2 diabetes mellitus.
Abstract

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