Coronary Microvascular Dysfunction, Left Ventricular Remodeling, and Clinical Outcomes in Patients With Chronic

Navkaranbir S Bajaj1,2, Amitoj Singh1, Wunan Zhou1

  • 1Cardiovascular Imaging Program, Departments of Radiology and Medicine; Division of Nuclear Medicine and Molecular Imaging, Department of Radiology; and Divisions of Cardiovascular Medicine and Nephrology, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA (N.S.B., A.S., W.Z., A.G., K.F., C.B., H.J.H., P.B., E.A., S.D., C.F.B., J.H., H.S., V.T., M.S., S.D., R.B., R.C.D., S.D.S., M.F.D.C.).

Circulation
|November 30, 2019
PubMed

Insights

Coronary microvascular dysfunction, not kidney function, independently predicts heart problems in patients without obvious coronary artery disease. This dysfunction may link kidney disease to heart issues and adverse cardiovascular events.

Area of Science:

  • Cardiology
  • Nephrology
  • Cardiovascular Imaging

Background:

  • Patients with chronic kidney disease (CKD) often experience cardiac dysfunction and cardiovascular events, even without obstructive coronary artery disease.
  • The underlying mechanisms linking CKD to cardiac impairment and adverse outcomes remain unclear.
  • Coronary microvascular dysfunction (CMD) is hypothesized to bridge the relationship between renal dysfunction and cardiac issues.

Purpose of the Study:

  • To investigate the associations between CKD, CMD, cardiac dysfunction, and cardiovascular outcomes.
  • To determine if CMD mediates the link between CKD and adverse cardiovascular events in patients without overt coronary artery disease.

Main Methods:

  • Longitudinal study of 352 patients undergoing cardiac stress positron emission tomography (PET) and echocardiography.
  • Renal function assessed via estimated glomerular filtration rate (eGFR).
  • Coronary flow reserve (CFR) measured by PET; cardiac mechanics assessed by echocardiography (diastolic and systolic indices).
  • Patients followed for composite outcomes of death, myocardial infarction, or heart failure hospitalization.
  • Statistical analyses included multivariable models and mediation analyses.

Main Results:

  • 35% of patients had eGFR <60 mL·min-1·1.73 m-2; median CFR was 1.8.
  • Both eGFR and CFR were associated with cardiac mechanics and cardiovascular events (P<0.05).
  • In multivariable models, CFR, but not eGFR, was independently associated with cardiac mechanics and cardiovascular events.
  • The relationship between eGFR, cardiac mechanics, and cardiovascular events was partly mediated by CFR.

Conclusions:

  • Coronary microvascular dysfunction, rather than eGFR alone, is independently linked to abnormal cardiac mechanics and increased cardiovascular event risk.
  • CMD may serve as a key mediator connecting CKD to cardiac dysfunction and adverse cardiovascular outcomes in patients without overt coronary artery disease.
Abstract

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