Abstract

BackgroundChanges in renal blood flow (RBF) may play a pathophysiological role in hypertension and kidney disease. However, RBF determination in humans has proven difficult. We aimed to confirm the feasibility of RBF estimation based on positron emission tomography/computed tomography (PET/CT) and rubidium-82 (82Rb) using the abdominal aorta as input function in a 1-tissue compartment model.MethodsEighteen healthy subjects underwent two dynamic 82Rb PET/CT scans in two different fields of view (FOV). FOV-A included the left ventricular blood pool (LVBP), the abdominal aorta (AA) and the majority of the kidneys. FOV-B included AA and the kidneys in their entirety. In FOV-A, an input function was derived from LVBP and from AA, in FOV-B from AA. One-tissue compartmental modelling was performed using tissue time activity curves generated from volumes of interest (VOI) contouring the kidneys, where the renal clearance of 82Rb is represented by the K1 kinetic parameter. Total clearance for both kidneys was calculated by multiplying the K1 values with the volume of VOIs used for analysis. Intra-assay coefficients of variation and inter-observer variation were calculated.ResultsFor both kidneys, K1 values derived from AA did not differ significantly from values obtained from LVBP, neither were significant differences seen between AA in FOV-A and AA in FOV-B, nor between the right and left kidneys. For both kidneys, the intra-assay coefficients of variation were low (~ 5%) for both input functions. The measured K1 of 2.80 ml/min/cm3 translates to a total clearance for both kidneys of 766 ml/min/1.73 m2.ConclusionMeasurement of renal perfusion based on PET/CT and 82Rb using AA as input function in a 1-tissue compartment model is feasible in a single FOV. Based on previous studies showing 82Rb to be primarily present in plasma, the measured K1 clearance values are most likely representative of effective renal plasma flow (ERPF) rather than estimated RBF values, but as the accurate calculation of total clearance/flow is very much dependent on the analysed volume, a standardised definition for the employed renal volumes is needed to allow for proper comparison with standard ERPF and RBF reference methods.

Highlights

  • Changes in renal blood flow (RBF) may play a pathophysiological role in hypertension and kidney disease

  • Using the β-corrected Time activity curve (TAC) data, we find for both AA and left ventricular blood pool (LVBP), the intra-assay coefficients of variation are acceptably low, indicating that 82Rb positron emission tomography (PET)/Computed tomography (CT) is a precise method for evaluation of K1, allowing for determination of changes in K1

  • As a global quality control, we found no significant difference between K1 values derived from AA activity curves in fields of view (FOV)-A and those in FOV-B, supporting the assumption that in the studied population with healthy, lesion-free kidneys, quantitation obtained from truncated images of the kidney tissue is representative of values which would be obtained from imaging the kidneys in their entirety

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Summary

Introduction

Changes in renal blood flow (RBF) may play a pathophysiological role in hypertension and kidney disease. FOV-A included the left ventricular blood pool (LVBP), the abdominal aorta (AA) and the majority of the kidneys. One-tissue compartmental modelling was performed using tissue time activity curves generated from volumes of interest (VOI) contouring the kidneys, where the renal clearance of 82Rb is represented by the K1 kinetic parameter. Total clearance for both kidneys was calculated by multiplying the K1 values with the volume of VOIs used for analysis. Renal vasoconstriction has been identified in pre-hypertensive adults, indicating that renal vascular abnormalities could be a cause of hypertension rather than caused by hypertension [11, 12]

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