Independence of coronary artery disease to subclinical left ventricular dysfunction

Prasanna Venkataraman1,2, Leah Wright1, Quan Huynh1

  • 1Baker Heart and Diabetes Research Institute, Melbourne, Vic., Australia.

Insights

Subclinical left ventricular dysfunction (S-LVD) was not associated with coronary artery calcium (CAC) in intermediate-risk individuals. Early atherosclerosis markers do not predict early heart dysfunction in this population.

Area of Science:

  • Cardiology
  • Cardiovascular Imaging
  • Preventive Cardiology

Background:

  • Epicardial atherosclerosis and heart failure share inflammatory and endothelial dysfunction pathways.
  • Early detection of subclinical disease may enable timely intervention.
  • Investigating the link between coronary calcium score (CCS) and subclinical left ventricular dysfunction (S-LVD) is crucial.

Purpose of the Study:

  • To assess the association between coronary calcium score (CCS), cardiovascular risk factors, and echocardiographic markers of subclinical left ventricular dysfunction (S-LVD).

Main Methods:

  • 159 participants aged 40-70 with intermediate coronary artery disease risk were enrolled.
  • Computed tomography (CT) for CCS and 2-D transthoracic echocardiography were performed.
  • Subclinical left ventricular dysfunction (S-LVD) was defined by reduced global longitudinal strain (GLS), enlarged left atrial volume, and elevated E/e'.

Main Results:

  • 15 participants (9.4%) exhibited S-LVD (8 systolic, 7 diastolic).
  • Coronary calcium score (CCS) > 0 was found in 10 participants with S-LVD versus 75 without (67% vs 53%, P=0.47).
  • No significant differences in mean GLS, E/e', indexed LV mass, or indexed left atrial volume were observed between those with and without coronary artery calcium.

Conclusions:

  • In asymptomatic, low-to-intermediate-risk individuals, the processes driving atherosclerosis are not directly linked to subclinical left ventricular dysfunction.
  • Coronary artery calcium does not appear to be a reliable early indicator of subclinical left ventricular dysfunction in this population.
Abstract

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