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Updated: Jun 24, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Increased basal myocardial perfusion in patients with chronic kidney disease without symptomatic coronary artery
Niina Koivuviita1, Risto Tertti, Mikko Järvisalo
1Department of Medicine, Turku University Hospital, Finland. niina.koivuviita@tyks.fi
Insights
Chronic kidney disease (CKD) patients show increased baseline myocardial blood flow and peripheral endothelial dysfunction. Coronary flow reserve remains normal, suggesting distinct vascular mechanisms in CKD.
Area of Science:
- Cardiovascular research
- Nephrology
- Vascular biology
Background:
- Minor renal dysfunction is a significant cardiovascular risk factor.
- Vascular abnormalities in chronic kidney disease (CKD) are not fully understood.
- Investigating early microvascular dysfunction in CKD is crucial.
Purpose of the Study:
- To determine if microvascular dysfunction, an early indicator of coronary dysfunction, is present in early stages of CKD.
- To assess coronary and peripheral artery function in CKD patients using positron emission tomography (PET).
Main Methods:
- Myocardial blood flow measured by PET at rest and during dipyridamole-induced hyperemia.
- Peripheral artery endothelial function assessed via flow-mediated dilatation (FMD) of the brachial artery.
- Study included 22 CKD patients and 10 healthy controls, excluding diabetics.
Main Results:
- CKD patients exhibited significantly higher basal myocardial perfusion compared to controls.
- A negative correlation was found between baseline myocardial perfusion and estimated glomerular filtration rate.
- Peripheral endothelial dysfunction (reduced FMD) was observed in all CKD patients, irrespective of disease stage.
Conclusions:
- Coronary flow reserve was normal in CKD patients, despite increased baseline myocardial blood flow.
- Peripheral endothelial dysfunction is a consistent finding in CKD patients.
- Coronary perfusion and peripheral vascular function appear to be affected by different mechanisms in CKD.
Background:
Even minor renal dysfunction is a powerful cardiovascular risk factor. The abnormalities in coronary and peripheral artery function in different stages of chronic kidney disease (CKD) remain poorly understood. Our aim was to test by a positron emission tomography (PET)-based method whether microvascular dysfunction, an early marker of coronary dysfunction, exists already in early stages of CKD.
Methods:
Myocardial blood flow was measured at baseline and during dipyridamole-induced hyperaemia by PET. Peripheral artery endothelial function was examined by measuring flow-mediated dilatation (FMD) of the brachial artery at rest and during reactive hyperaemia. Twenty-two patients with moderate to severe kidney failure and 10 healthy controls were investigated. Diabetic patients were excluded. Baseline characteristics were similar between the groups with the exception of antihypertensive medication in all CKD patients.
Results:
The basal myocardial perfusion was statistically significantly higher in CKD patients than observed values in similarly aged controls. There was a statistically significant negative correlation between the baseline myocardial perfusion and the estimated glomerular filtration rate. Coronary flow reserve was comparable to healthy controls in all patients. FMD was significantly reduced in all patients with CKD regardless of the stage of kidney failure.
Conclusions:
Coronary flow reserve was normal although baseline myocardial blood flow was increased in all CKD patients as compared to healthy controls. Peripheral endothelial dysfunction was detected in all patients. Our findings suggest that coronary perfusion and peripheral vascular function are disturbed by different mechanisms in patients with CKD.
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