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Updated: Jan 3, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
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.).
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.
Background:
Cardiac dysfunction and cardiovascular events are prevalent among patients with chronic kidney disease without overt obstructive coronary artery disease, but the mechanisms remain poorly understood. Coronary microvascular dysfunction has been proposed as a link between abnormal renal function and impairment of cardiac function and cardiovascular events. We aimed to investigate the relations between chronic kidney disease, coronary microvascular dysfunction, cardiac dysfunction, and adverse cardiovascular outcomes.
Methods:
Patients undergoing cardiac stress positron emission tomography, echocardiogram, and renal function ascertainment at Brigham and Women's Hospital were studied longitudinally. Patients free of overt coronary (summed stress score <3 and without a history of ischemic heart disease), valvular, and end-organ disease were followed up for the adverse composite outcome of death or hospitalization for myocardial infarction or heart failure. Coronary flow reserve (CFR) was determined from positron emission tomography. Echocardiograms were used to measure cardiac mechanics: diastolic (lateral and septal E/e') and systolic (global longitudinal, radial, and circumferential strain). Image analyses and event adjudication were blinded. The associations between estimated glomerular filtration rate (eGFR), CFR, diastolic and systolic indices, and adverse cardiovascular outcomes were assessed in adjusted models and mediation analyses.
Results:
Of the 352 patients (median age, 65 years; 63% female; 22% black) studied, 35% had an eGFR <60 mL·min-1·1.73 m-2, a median left ventricular ejection fraction of 62%, and a median CFR of 1.8. eGFR and CFR were associated with diastolic and systolic indices, as well as future cardiovascular events (all P<0.05). In multivariable models, CFR, but not eGFR, was independently associated with cardiac mechanics and cardiovascular events. The associations between eGFR, cardiac mechanics, and cardiovascular events were partly mediated via CFR.
Conclusions:
Coronary microvascular dysfunction, but not eGFR, was independently associated with abnormal cardiac mechanics and an increased risk of cardiovascular events. Coronary microvascular dysfunction may mediate the effect of chronic kidney disease on abnormal cardiac function and cardiovascular events in those without overt coronary artery disease.
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