A pilot study on coronary microvascular dysfunction in obstructive hypertrophic cardiomyopathy: impact of

Taikan Terauchi1, Daigo Hiraya2, Kyohei Usami1

  • 1Department of Cardiology, Institute of Medicine, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, 3058575, Japan.

Insights

Percutaneous transluminal septal myocardial ablation (PTSMA) improved coronary microvascular dysfunction (CMD) in obstructive hypertrophic cardiomyopathy (oHCM) patients. This septal reduction therapy reduced pressure gradients and enhanced microcirculation.

Area of Science:

  • Cardiology
  • Cardiovascular Research
  • Interventional Cardiology

Background:

  • Coronary microvascular dysfunction (CMD) is recognized in coronary artery disease but poorly understood in obstructive hypertrophic cardiomyopathy (oHCM).
  • The effect of percutaneous transluminal septal myocardial ablation (PTSMA) on CMD in oHCM remains unevaluated.

Purpose of the Study:

  • To investigate the impact of PTSMA on CMD in patients with oHCM.
  • To assess changes in microcirculatory function following PTSMA.

Main Methods:

  • PTSMA was performed on 10 oHCM patients between October 2023 and May 2024.
  • Invasive assessment of CMD using a pressure guidewire in the left anterior descending artery (LAD) before and after PTSMA.
  • Measurements included resting full-cycle ratio (RFR), fractional flow reserve (FFR), coronary flow reserve (CFR), and index of microcirculatory resistance (IMR).

Main Results:

  • Pre-PTSMA, patients showed reduced CFR (1.8) and elevated IMR (31), indicating CMD, despite normal RFR and FFR.
  • Post-PTSMA, the left ventricular pressure gradient significantly decreased (from 44 to 5 mmHg).
  • Microcirculatory function improved, with increased CFR (to 2.5) and decreased IMR (to 22).

Conclusions:

  • Myocardial hypertrophy in oHCM contributes to both left ventricular outflow tract obstruction and CMD.
  • PTSMA effectively reduces the left ventricular pressure gradient in oHCM.
  • This study demonstrates that PTSMA improves coronary microvascular dysfunction in patients with oHCM.