Impact of myocardial phenotype on optimal atrioventricular delay settings during biventricular and left bundle branch pacing at rest and during exercise: insights from a virtual patient study

Europace. 2025 Mar 28;27(4):euaf082. doi: 10.1093/europace/euaf082.

Abstract

Aims: Previous studies have not examined the role of non-electrical myocardial disease substrates in determining the optimal atrio-ventricular delay (AVD) settings. We conducted virtual patient simulations to evaluate whether myocardial disease substrates influence the acute response to AVD optimization at rest and during exercise.

Methods and results: The CircAdapt cardiovascular model was used to simulate various left ventricular (LV) remodelling found in cardiac resynchronization therapy candidates. We simulated electrical dyssynchrony, LV dilatation with preserved and reduced contractility, and increased LV passive stiffness. We simulated cardiac resynchronization following biventricular (BiVP) and non-selective LBB pacing (nsLBBP). The paced-AVD ranged from 220 to 40 ms. Cardiac output and heart rate were increased to simulate different levels of exercise. The optimal AVD was the one leading to the highest stroke volume (SV) and the lowest mean left atrial pressure (mLAP). At rest, in simulations with healthy myocardium the gain in SV by AVD optimization was larger compared to those with reduced contractility and stiff myocardium. However, mLAP was comparably decreased by AVD optimization in both healthy and diseased myocardium. During exercise, the optimal AVD shifted to shorter values, and mLAP was more sensitive to AVD, particularly in the presence of hypo-contractile and stiff myocardium.

Conclusion: Simulations show that hypocontractility and stiffness reduce the effect of AVD optimization on SV but enhance its benefit in lowering mLAP. Notably, virtual patients with stiff ventricles experience greater benefits from AVD optimization during exercise compared to resting conditions. Furthermore, nsLBBP provides more favourable improvements in mLAP than BiVP.

Keywords: In silico trial; Atrio-ventricular delay optimization; CircAdapt; Computational modelling and simulation; Stiffness.

MeSH terms

  • Bundle-Branch Block* / diagnosis
  • Bundle-Branch Block* / physiopathology
  • Bundle-Branch Block* / therapy
  • Cardiac Resynchronization Therapy* / methods
  • Computer Simulation
  • Exercise*
  • Heart Rate
  • Humans
  • Models, Cardiovascular*
  • Myocardial Contraction
  • Patient-Specific Modeling*
  • Phenotype
  • Rest
  • Stroke Volume
  • Time Factors
  • Ventricular Function, Left*
  • Ventricular Remodeling*