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Reliability of rubidium-82 PET/CT for renal perfusion determination in healthy subjects
BACKGROUND: Changes in renal perfusion may play a pathophysiological role in hypertension and kidney disease, however to date, no method for renal blood flow (RBF) determination in humans has been implemented in clinical practice. In a previous study, we demonstrated that estimation of renal perfusi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9706837/ https://www.ncbi.nlm.nih.gov/pubmed/36443713 http://dx.doi.org/10.1186/s12882-022-02962-w |
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author | Langaa, Stine Sundgaard Mose, Frank Holden Fynbo, Claire Anne Theil, Jørn Bech, Jesper Nørgaard |
author_facet | Langaa, Stine Sundgaard Mose, Frank Holden Fynbo, Claire Anne Theil, Jørn Bech, Jesper Nørgaard |
author_sort | Langaa, Stine Sundgaard |
collection | PubMed |
description | BACKGROUND: Changes in renal perfusion may play a pathophysiological role in hypertension and kidney disease, however to date, no method for renal blood flow (RBF) determination in humans has been implemented in clinical practice. In a previous study, we demonstrated that estimation of renal perfusion based on a single positron emission tomography/computed tomography (PET/CT) scan with Rubidium-82 ((82)Rb) is feasible and found an approximate 5% intra-assay coefficient of variation for both kidneys, indicative of a precise method.This study’s aim was to determine the day-to day variation of (82)Rb PET/CT and to test the method’s ability to detect increased RBF induced by infusion of amino acids. METHODS: Seventeen healthy subjects underwent three dynamic (82)Rb PET/CT scans over two examination days comprising: Day A, a single 8-minute dynamic scan and Day B, two scans performed before (baseline) and after RBF stimulation by a 2-hour amino acid-infusion. The order of examination days was determined by randomization. Time activity curves for arterial and renal activity with a 1-tissue compartment model were used for flow estimation; the K(1) kinetic parameter representing renal (82)Rb clearance. Day-to-day variation was calculated based on the difference between the unstimulated K(1) values on Day A and Day B and paired t-testing was performed to compare K(1) values at baseline and after RBF stimulation on Day B. RESULTS: Day-to-day variation was observed to be 5.5% for the right kidney and 6.0% for the left kidney (n = 15 quality accepted scans). K(1) values determined after amino acid-infusion were significantly higher than pre-infusion values (n = 17, p = 0.001). The mean percentage change in K(1) from baseline was 13.2 ± 12.9% (range − 10.4 to 35.5) for the right kidney; 12.9 ± 13.2% (range − 15.7 to 35.3) for the left kidney. CONCLUSION: Day-to-day variation is acceptably low. A significant K(1) increase from baseline is detected after application of a known RBF stimulus, indicating that (82)Rb PET/CT scanning can provide a precise method for evaluation of RBF and it is able to determine changes herein. CLINICAL TRIAL REGISTRATION: EU Clinical Trials Register, 2017-005008-88. Registered 18/01/2018. |
format | Online Article Text |
id | pubmed-9706837 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97068372022-11-30 Reliability of rubidium-82 PET/CT for renal perfusion determination in healthy subjects Langaa, Stine Sundgaard Mose, Frank Holden Fynbo, Claire Anne Theil, Jørn Bech, Jesper Nørgaard BMC Nephrol Research BACKGROUND: Changes in renal perfusion may play a pathophysiological role in hypertension and kidney disease, however to date, no method for renal blood flow (RBF) determination in humans has been implemented in clinical practice. In a previous study, we demonstrated that estimation of renal perfusion based on a single positron emission tomography/computed tomography (PET/CT) scan with Rubidium-82 ((82)Rb) is feasible and found an approximate 5% intra-assay coefficient of variation for both kidneys, indicative of a precise method.This study’s aim was to determine the day-to day variation of (82)Rb PET/CT and to test the method’s ability to detect increased RBF induced by infusion of amino acids. METHODS: Seventeen healthy subjects underwent three dynamic (82)Rb PET/CT scans over two examination days comprising: Day A, a single 8-minute dynamic scan and Day B, two scans performed before (baseline) and after RBF stimulation by a 2-hour amino acid-infusion. The order of examination days was determined by randomization. Time activity curves for arterial and renal activity with a 1-tissue compartment model were used for flow estimation; the K(1) kinetic parameter representing renal (82)Rb clearance. Day-to-day variation was calculated based on the difference between the unstimulated K(1) values on Day A and Day B and paired t-testing was performed to compare K(1) values at baseline and after RBF stimulation on Day B. RESULTS: Day-to-day variation was observed to be 5.5% for the right kidney and 6.0% for the left kidney (n = 15 quality accepted scans). K(1) values determined after amino acid-infusion were significantly higher than pre-infusion values (n = 17, p = 0.001). The mean percentage change in K(1) from baseline was 13.2 ± 12.9% (range − 10.4 to 35.5) for the right kidney; 12.9 ± 13.2% (range − 15.7 to 35.3) for the left kidney. CONCLUSION: Day-to-day variation is acceptably low. A significant K(1) increase from baseline is detected after application of a known RBF stimulus, indicating that (82)Rb PET/CT scanning can provide a precise method for evaluation of RBF and it is able to determine changes herein. CLINICAL TRIAL REGISTRATION: EU Clinical Trials Register, 2017-005008-88. Registered 18/01/2018. BioMed Central 2022-11-28 /pmc/articles/PMC9706837/ /pubmed/36443713 http://dx.doi.org/10.1186/s12882-022-02962-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Langaa, Stine Sundgaard Mose, Frank Holden Fynbo, Claire Anne Theil, Jørn Bech, Jesper Nørgaard Reliability of rubidium-82 PET/CT for renal perfusion determination in healthy subjects |
title | Reliability of rubidium-82 PET/CT for renal perfusion determination in healthy subjects |
title_full | Reliability of rubidium-82 PET/CT for renal perfusion determination in healthy subjects |
title_fullStr | Reliability of rubidium-82 PET/CT for renal perfusion determination in healthy subjects |
title_full_unstemmed | Reliability of rubidium-82 PET/CT for renal perfusion determination in healthy subjects |
title_short | Reliability of rubidium-82 PET/CT for renal perfusion determination in healthy subjects |
title_sort | reliability of rubidium-82 pet/ct for renal perfusion determination in healthy subjects |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9706837/ https://www.ncbi.nlm.nih.gov/pubmed/36443713 http://dx.doi.org/10.1186/s12882-022-02962-w |
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