Amiodarone attenuates cardiac Rubidium-82 in consecutive PET/CT scans in a rodent model

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Amiodarone attenuates cardiac Rubidium-82 in consecutive PET/CT scans in a rodent model. / Bentsen, Simon; Bang, Lia E; Hasbak, Philip; Kjaer, Andreas; Ripa, Rasmus S.

In: Journal of Nuclear Cardiology, Vol. 29, 2022, p. 2853–2862.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Bentsen, S, Bang, LE, Hasbak, P, Kjaer, A & Ripa, RS 2022, 'Amiodarone attenuates cardiac Rubidium-82 in consecutive PET/CT scans in a rodent model', Journal of Nuclear Cardiology, vol. 29, pp. 2853–2862. https://doi.org/10.1007/s12350-021-02785-6

APA

Bentsen, S., Bang, L. E., Hasbak, P., Kjaer, A., & Ripa, R. S. (2022). Amiodarone attenuates cardiac Rubidium-82 in consecutive PET/CT scans in a rodent model. Journal of Nuclear Cardiology, 29, 2853–2862. https://doi.org/10.1007/s12350-021-02785-6

Vancouver

Bentsen S, Bang LE, Hasbak P, Kjaer A, Ripa RS. Amiodarone attenuates cardiac Rubidium-82 in consecutive PET/CT scans in a rodent model. Journal of Nuclear Cardiology. 2022;29:2853–2862. https://doi.org/10.1007/s12350-021-02785-6

Author

Bentsen, Simon ; Bang, Lia E ; Hasbak, Philip ; Kjaer, Andreas ; Ripa, Rasmus S. / Amiodarone attenuates cardiac Rubidium-82 in consecutive PET/CT scans in a rodent model. In: Journal of Nuclear Cardiology. 2022 ; Vol. 29. pp. 2853–2862.

Bibtex

@article{8dbf7a5632534040958502f49be2e158,
title = "Amiodarone attenuates cardiac Rubidium-82 in consecutive PET/CT scans in a rodent model",
abstract = "BACKGROUND: Risk stratification and diagnosis using Rubidium-82 (82Rb) positron emission tomography (PET) is a routine clinical approach in coronary artery disease (CAD). Various drugs are used to treat CAD; however, whether any of them change the uptake of 82Rb in the heart has not been investigated. The aim of this study is to determine whether drugs used in treatment of CAD affect the uptake of 82Rb in the heart in healthy rats.METHODS: Seventy-seven Sprague-Dawley rats were included in the cross-sectional study. All rats underwent baseline 82Rb PET/CT and divided into eleven groups treated with different drugs. One group was control group (no treatment), eight groups were treated with monotherapy (amiodarone, acetylsalicylic acid (ASA), clopidogrel, ticagrelor, atorvastatin, enalapril, amlodipine, metoprolol succinate), and two groups were treated with polypharmacy (ASA, ticagrelor, atorvastatin, amlodipine or ASA, clopidogrel, atorvastatin, amlodipine). Once a day, they were administered pharmacological therapy through oral gavage, and on day seven, follow-up scanned with 82Rb PET/CT.RESULTS: In the control group without pharmacological treatment, no difference in the standard uptake value (SUV) ratio between heart and muscle from baseline to follow-up (5.8 vs 7.0, P = .3) was found. The group treated with amiodarone had a significantly reduced SUV ratio from baseline to follow-up (5.8 vs 5.1, P = .008). All other drugs investigated had no difference in SUV ratio from baseline to follow-up.CONCLUSION: In this study, we showed that drugs normally used to treat CAD do not affect the uptake of 82Rb. However, amiodarone result in a significantly lowered 82Rb uptake, compared to control. This information about amiodarone would probably not change the size assessment of a myocardial perfusion defect in a clinical setting. However, it could change the kinetic parameters when assessing absolute myocardial blood flow in patients treated with amiodarone.",
author = "Simon Bentsen and Bang, {Lia E} and Philip Hasbak and Andreas Kjaer and Ripa, {Rasmus S}",
note = "{\textcopyright} 2021. American Society of Nuclear Cardiology.",
year = "2022",
doi = "10.1007/s12350-021-02785-6",
language = "English",
volume = "29",
pages = "2853–2862",
journal = "Journal of Nuclear Cardiology",
issn = "1071-3581",
publisher = "Springer",

}

RIS

TY - JOUR

T1 - Amiodarone attenuates cardiac Rubidium-82 in consecutive PET/CT scans in a rodent model

AU - Bentsen, Simon

AU - Bang, Lia E

AU - Hasbak, Philip

AU - Kjaer, Andreas

AU - Ripa, Rasmus S

N1 - © 2021. American Society of Nuclear Cardiology.

PY - 2022

Y1 - 2022

N2 - BACKGROUND: Risk stratification and diagnosis using Rubidium-82 (82Rb) positron emission tomography (PET) is a routine clinical approach in coronary artery disease (CAD). Various drugs are used to treat CAD; however, whether any of them change the uptake of 82Rb in the heart has not been investigated. The aim of this study is to determine whether drugs used in treatment of CAD affect the uptake of 82Rb in the heart in healthy rats.METHODS: Seventy-seven Sprague-Dawley rats were included in the cross-sectional study. All rats underwent baseline 82Rb PET/CT and divided into eleven groups treated with different drugs. One group was control group (no treatment), eight groups were treated with monotherapy (amiodarone, acetylsalicylic acid (ASA), clopidogrel, ticagrelor, atorvastatin, enalapril, amlodipine, metoprolol succinate), and two groups were treated with polypharmacy (ASA, ticagrelor, atorvastatin, amlodipine or ASA, clopidogrel, atorvastatin, amlodipine). Once a day, they were administered pharmacological therapy through oral gavage, and on day seven, follow-up scanned with 82Rb PET/CT.RESULTS: In the control group without pharmacological treatment, no difference in the standard uptake value (SUV) ratio between heart and muscle from baseline to follow-up (5.8 vs 7.0, P = .3) was found. The group treated with amiodarone had a significantly reduced SUV ratio from baseline to follow-up (5.8 vs 5.1, P = .008). All other drugs investigated had no difference in SUV ratio from baseline to follow-up.CONCLUSION: In this study, we showed that drugs normally used to treat CAD do not affect the uptake of 82Rb. However, amiodarone result in a significantly lowered 82Rb uptake, compared to control. This information about amiodarone would probably not change the size assessment of a myocardial perfusion defect in a clinical setting. However, it could change the kinetic parameters when assessing absolute myocardial blood flow in patients treated with amiodarone.

AB - BACKGROUND: Risk stratification and diagnosis using Rubidium-82 (82Rb) positron emission tomography (PET) is a routine clinical approach in coronary artery disease (CAD). Various drugs are used to treat CAD; however, whether any of them change the uptake of 82Rb in the heart has not been investigated. The aim of this study is to determine whether drugs used in treatment of CAD affect the uptake of 82Rb in the heart in healthy rats.METHODS: Seventy-seven Sprague-Dawley rats were included in the cross-sectional study. All rats underwent baseline 82Rb PET/CT and divided into eleven groups treated with different drugs. One group was control group (no treatment), eight groups were treated with monotherapy (amiodarone, acetylsalicylic acid (ASA), clopidogrel, ticagrelor, atorvastatin, enalapril, amlodipine, metoprolol succinate), and two groups were treated with polypharmacy (ASA, ticagrelor, atorvastatin, amlodipine or ASA, clopidogrel, atorvastatin, amlodipine). Once a day, they were administered pharmacological therapy through oral gavage, and on day seven, follow-up scanned with 82Rb PET/CT.RESULTS: In the control group without pharmacological treatment, no difference in the standard uptake value (SUV) ratio between heart and muscle from baseline to follow-up (5.8 vs 7.0, P = .3) was found. The group treated with amiodarone had a significantly reduced SUV ratio from baseline to follow-up (5.8 vs 5.1, P = .008). All other drugs investigated had no difference in SUV ratio from baseline to follow-up.CONCLUSION: In this study, we showed that drugs normally used to treat CAD do not affect the uptake of 82Rb. However, amiodarone result in a significantly lowered 82Rb uptake, compared to control. This information about amiodarone would probably not change the size assessment of a myocardial perfusion defect in a clinical setting. However, it could change the kinetic parameters when assessing absolute myocardial blood flow in patients treated with amiodarone.

U2 - 10.1007/s12350-021-02785-6

DO - 10.1007/s12350-021-02785-6

M3 - Journal article

C2 - 34611850

VL - 29

SP - 2853

EP - 2862

JO - Journal of Nuclear Cardiology

JF - Journal of Nuclear Cardiology

SN - 1071-3581

ER -

ID: 283513347