Prognostic Implications of Microvascular Resistance Reserve in Symptomatic Patients With

Seung Hun Lee1, Ki Hong Choi2, David Hong2

  • 1Division of Cardiology, Department of Internal Medicine, Heart Center, Chonnam National University Hospital, Chonnam National University Medical School, Gwangju, South Korea.

Insights

Microvascular resistance reserve (MRR) predicts adverse cardiovascular events in stable ischemic heart disease (IHD) patients. This coronary microvascular function index is valuable regardless of epicardial stenosis severity.

Area of Science:

  • Cardiology
  • Cardiovascular Physiology
  • Diagnostic Tools

Background:

  • Microvascular resistance reserve (MRR) assesses coronary microcirculatory function independently of epicardial stenosis.
  • Limited data exists on MRR's prognostic value in stable ischemic heart disease (IHD).

Purpose of the Study:

  • To evaluate clinical outcomes based on MRR in stable IHD patients.
  • To assess MRR's role with or without significant epicardial coronary artery stenosis.

Main Methods:

  • 547 patients with suspected stable IHD underwent echocardiography and invasive physiological assessment.
  • Significant epicardial stenosis defined as FFR ≤0.80; coronary microvascular dysfunction (CMD) as MRR ≤3.0.
  • Primary outcome: major adverse cardiovascular events (MACE) including cardiovascular death, MI, repeat revascularization, and heart failure admission.

Main Results:

  • 200 patients (36.6%) had CMD (MRR ≤3.0).
  • MRR correlated with microcirculatory resistance, natriuretic peptide levels, and diastolic dysfunction, but not FFR.
  • Decreased MRR was independently associated with increased MACE risk (HR: 1.23 per 1-U decrease).
  • CMD increased MACE risk in both FFR >0.80 and FFR ≤0.80 groups.

Conclusions:

  • Reduced MRR is linked to diastolic dysfunction and elevated filling pressures.
  • Coronary microvascular dysfunction (CMD) identified by MRR independently predicts MACE in stable IHD patients.
  • MRR's prognostic value is significant irrespective of epicardial coronary artery stenosis.
Abstract