Evaluation of DNA damage induced by ionizing radiation from myocardial perfusion imaging: a pilot study

Abstract Background As patient exposure to ionizing radiation raises concern about malignancy risks, this study evaluated the effect of ionizing radiation on patients undergoing myocardial perfusion imaging (MPI) using the comet assay, a method for detection of DNA damage. Methods Patients without c...

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Main Authors: Anna Paula Arpini, Andrea De Lorenzo, Aniele Moritz, Julia Passarelli Pereira, Glauber Monteiro Dias
Format: Article
Language:English
Published: BMC 2022-09-01
Series:BMC Cardiovascular Disorders
Subjects:
Online Access:https://doi.org/10.1186/s12872-022-02839-8
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author Anna Paula Arpini
Andrea De Lorenzo
Aniele Moritz
Julia Passarelli Pereira
Glauber Monteiro Dias
author_facet Anna Paula Arpini
Andrea De Lorenzo
Aniele Moritz
Julia Passarelli Pereira
Glauber Monteiro Dias
author_sort Anna Paula Arpini
collection DOAJ
description Abstract Background As patient exposure to ionizing radiation raises concern about malignancy risks, this study evaluated the effect of ionizing radiation on patients undergoing myocardial perfusion imaging (MPI) using the comet assay, a method for detection of DNA damage. Methods Patients without cancer, acute or autoimmune diseases, recent surgery or trauma, were studied. Gated single-photon myocardial perfusion imaging was performed with Tc-99m sestamibi. Peripheral blood was collected before radiotracer injection at rest and 60–90 min after injection. Single-cell gel electrophoresis (comet assay) was performed with blood lymphocytes to detect strand breaks, which determine a “comet tail” of variable size, visually scored by 3 observers in a fluorescence microscope after staining (0: no damage, no tail; 1: small damage; 2: large damage; 3: full damage). A damage index was calculated as a weighted average of the cell scores. Results Among the 29 individuals included in the analysis, age was 65.3 ± 9.9 years and 18 (62.1%) were male. The injected radiotracer dose was 880.6 ± 229.4 MBq. Most cells (approximately 70%) remained without DNA fragmentation (class 0) after tracer injection. There were nonsignificant increases of classes 1 and 2 of damage. Class 3 was the least frequent both before and after radiotracer injection, but displayed a significant, 44% increase after injection. Conclusion While lymphocytes mostly remained in class 0, an increase in class 3 DNA damage was detected. This may suggest that, despite a probable lack of biologically relevant DNA damage, there is still a need for tracer dose reductions in MPI.
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spelling doaj.art-33a4788c645048a5b17c25dc9e5d41ba2022-12-22T04:23:59ZengBMCBMC Cardiovascular Disorders1471-22612022-09-012211610.1186/s12872-022-02839-8Evaluation of DNA damage induced by ionizing radiation from myocardial perfusion imaging: a pilot studyAnna Paula Arpini0Andrea De Lorenzo1Aniele Moritz2Julia Passarelli Pereira3Glauber Monteiro Dias4Coordenação de Ensino E Pesquisa, Instituto Nacional de CardiologiaCoordenação de Ensino E Pesquisa, Instituto Nacional de CardiologiaCoordenação de Ensino E Pesquisa, Instituto Nacional de CardiologiaCoordenação de Ensino E Pesquisa, Instituto Nacional de CardiologiaCoordenação de Ensino E Pesquisa, Instituto Nacional de CardiologiaAbstract Background As patient exposure to ionizing radiation raises concern about malignancy risks, this study evaluated the effect of ionizing radiation on patients undergoing myocardial perfusion imaging (MPI) using the comet assay, a method for detection of DNA damage. Methods Patients without cancer, acute or autoimmune diseases, recent surgery or trauma, were studied. Gated single-photon myocardial perfusion imaging was performed with Tc-99m sestamibi. Peripheral blood was collected before radiotracer injection at rest and 60–90 min after injection. Single-cell gel electrophoresis (comet assay) was performed with blood lymphocytes to detect strand breaks, which determine a “comet tail” of variable size, visually scored by 3 observers in a fluorescence microscope after staining (0: no damage, no tail; 1: small damage; 2: large damage; 3: full damage). A damage index was calculated as a weighted average of the cell scores. Results Among the 29 individuals included in the analysis, age was 65.3 ± 9.9 years and 18 (62.1%) were male. The injected radiotracer dose was 880.6 ± 229.4 MBq. Most cells (approximately 70%) remained without DNA fragmentation (class 0) after tracer injection. There were nonsignificant increases of classes 1 and 2 of damage. Class 3 was the least frequent both before and after radiotracer injection, but displayed a significant, 44% increase after injection. Conclusion While lymphocytes mostly remained in class 0, an increase in class 3 DNA damage was detected. This may suggest that, despite a probable lack of biologically relevant DNA damage, there is still a need for tracer dose reductions in MPI.https://doi.org/10.1186/s12872-022-02839-8Myocardial perfusion imagingRadiationComet assayDNA
spellingShingle Anna Paula Arpini
Andrea De Lorenzo
Aniele Moritz
Julia Passarelli Pereira
Glauber Monteiro Dias
Evaluation of DNA damage induced by ionizing radiation from myocardial perfusion imaging: a pilot study
BMC Cardiovascular Disorders
Myocardial perfusion imaging
Radiation
Comet assay
DNA
title Evaluation of DNA damage induced by ionizing radiation from myocardial perfusion imaging: a pilot study
title_full Evaluation of DNA damage induced by ionizing radiation from myocardial perfusion imaging: a pilot study
title_fullStr Evaluation of DNA damage induced by ionizing radiation from myocardial perfusion imaging: a pilot study
title_full_unstemmed Evaluation of DNA damage induced by ionizing radiation from myocardial perfusion imaging: a pilot study
title_short Evaluation of DNA damage induced by ionizing radiation from myocardial perfusion imaging: a pilot study
title_sort evaluation of dna damage induced by ionizing radiation from myocardial perfusion imaging a pilot study
topic Myocardial perfusion imaging
Radiation
Comet assay
DNA
url https://doi.org/10.1186/s12872-022-02839-8
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