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Conditional Generative Adversarial Networks Aided Motion Correction of Dynamic (18)F-FDG PET Brain Studies

This work set out to develop a motion-correction approach aided by conditional generative adversarial network (cGAN) methodology that allows reliable, data-driven determination of involuntary subject motion during dynamic (18)F-FDG brain studies. Methods: Ten healthy volunteers (5 men/5 women; mean...

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Autores principales: Shiyam Sundar, Lalith Kumar, Iommi, David, Muzik, Otto, Chalampalakis, Zacharias, Klebermass, Eva-Maria, Hienert, Marius, Rischka, Lucas, Lanzenberger, Rupert, Hahn, Andreas, Pataraia, Ekaterina, Traub-Weidinger, Tatjana, Hummel, Johann, Beyer, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society of Nuclear Medicine 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8729870/
https://www.ncbi.nlm.nih.gov/pubmed/33246982
http://dx.doi.org/10.2967/jnumed.120.248856
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author Shiyam Sundar, Lalith Kumar
Iommi, David
Muzik, Otto
Chalampalakis, Zacharias
Klebermass, Eva-Maria
Hienert, Marius
Rischka, Lucas
Lanzenberger, Rupert
Hahn, Andreas
Pataraia, Ekaterina
Traub-Weidinger, Tatjana
Hummel, Johann
Beyer, Thomas
author_facet Shiyam Sundar, Lalith Kumar
Iommi, David
Muzik, Otto
Chalampalakis, Zacharias
Klebermass, Eva-Maria
Hienert, Marius
Rischka, Lucas
Lanzenberger, Rupert
Hahn, Andreas
Pataraia, Ekaterina
Traub-Weidinger, Tatjana
Hummel, Johann
Beyer, Thomas
author_sort Shiyam Sundar, Lalith Kumar
collection PubMed
description This work set out to develop a motion-correction approach aided by conditional generative adversarial network (cGAN) methodology that allows reliable, data-driven determination of involuntary subject motion during dynamic (18)F-FDG brain studies. Methods: Ten healthy volunteers (5 men/5 women; mean age ± SD, 27 ± 7 y; weight, 70 ± 10 kg) underwent a test–retest (18)F-FDG PET/MRI examination of the brain (n = 20). The imaging protocol consisted of a 60-min PET list-mode acquisition contemporaneously acquired with MRI, including MR navigators and a 3-dimensional time-of-flight MR angiography sequence. Arterial blood samples were collected as a reference standard representing the arterial input function (AIF). Training of the cGAN was performed using 70% of the total datasets (n = 16, randomly chosen), which was corrected for motion using MR navigators. The resulting cGAN mappings (between individual frames and the reference frame [55–60 min after injection]) were then applied to the test dataset (remaining 30%, n = 6), producing artificially generated low-noise images from early high-noise PET frames. These low-noise images were then coregistered to the reference frame, yielding 3-dimensional motion vectors. Performance of cGAN-aided motion correction was assessed by comparing the image-derived input function (IDIF) extracted from a cGAN-aided motion-corrected dynamic sequence with the AIF based on the areas under the curves (AUCs). Moreover, clinical relevance was assessed through direct comparison of the average cerebral metabolic rates of glucose (CMRGlc) values in gray matter calculated using the AIF and the IDIF. Results: The absolute percentage difference between AUCs derived using the motion-corrected IDIF and the AIF was (1.2% + 0.9%). The gray matter CMRGlc values determined using these 2 input functions differed by less than 5% (2.4% + 1.7%). Conclusion: A fully automated data-driven motion-compensation approach was established and tested for (18)F-FDG PET brain imaging. cGAN-aided motion correction enables the translation of noninvasive clinical absolute quantification from PET/MR to PET/CT by allowing the accurate determination of motion vectors from the PET data itself.
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spelling pubmed-87298702022-01-21 Conditional Generative Adversarial Networks Aided Motion Correction of Dynamic (18)F-FDG PET Brain Studies Shiyam Sundar, Lalith Kumar Iommi, David Muzik, Otto Chalampalakis, Zacharias Klebermass, Eva-Maria Hienert, Marius Rischka, Lucas Lanzenberger, Rupert Hahn, Andreas Pataraia, Ekaterina Traub-Weidinger, Tatjana Hummel, Johann Beyer, Thomas J Nucl Med Basic Science Investigation This work set out to develop a motion-correction approach aided by conditional generative adversarial network (cGAN) methodology that allows reliable, data-driven determination of involuntary subject motion during dynamic (18)F-FDG brain studies. Methods: Ten healthy volunteers (5 men/5 women; mean age ± SD, 27 ± 7 y; weight, 70 ± 10 kg) underwent a test–retest (18)F-FDG PET/MRI examination of the brain (n = 20). The imaging protocol consisted of a 60-min PET list-mode acquisition contemporaneously acquired with MRI, including MR navigators and a 3-dimensional time-of-flight MR angiography sequence. Arterial blood samples were collected as a reference standard representing the arterial input function (AIF). Training of the cGAN was performed using 70% of the total datasets (n = 16, randomly chosen), which was corrected for motion using MR navigators. The resulting cGAN mappings (between individual frames and the reference frame [55–60 min after injection]) were then applied to the test dataset (remaining 30%, n = 6), producing artificially generated low-noise images from early high-noise PET frames. These low-noise images were then coregistered to the reference frame, yielding 3-dimensional motion vectors. Performance of cGAN-aided motion correction was assessed by comparing the image-derived input function (IDIF) extracted from a cGAN-aided motion-corrected dynamic sequence with the AIF based on the areas under the curves (AUCs). Moreover, clinical relevance was assessed through direct comparison of the average cerebral metabolic rates of glucose (CMRGlc) values in gray matter calculated using the AIF and the IDIF. Results: The absolute percentage difference between AUCs derived using the motion-corrected IDIF and the AIF was (1.2% + 0.9%). The gray matter CMRGlc values determined using these 2 input functions differed by less than 5% (2.4% + 1.7%). Conclusion: A fully automated data-driven motion-compensation approach was established and tested for (18)F-FDG PET brain imaging. cGAN-aided motion correction enables the translation of noninvasive clinical absolute quantification from PET/MR to PET/CT by allowing the accurate determination of motion vectors from the PET data itself. Society of Nuclear Medicine 2021-06-01 2021-06-01 /pmc/articles/PMC8729870/ /pubmed/33246982 http://dx.doi.org/10.2967/jnumed.120.248856 Text en © 2021 by the Society of Nuclear Medicine and Molecular Imaging. https://creativecommons.org/licenses/by/4.0/Immediate Open Access: Creative Commons Attribution 4.0 International License (CC BY) allows users to share and adapt with attribution, excluding materials credited to previous publications. License: https://creativecommons.org/licenses/by/4.0/. Details: http://jnm.snmjournals.org/site/misc/permission.xhtml.
spellingShingle Basic Science Investigation
Shiyam Sundar, Lalith Kumar
Iommi, David
Muzik, Otto
Chalampalakis, Zacharias
Klebermass, Eva-Maria
Hienert, Marius
Rischka, Lucas
Lanzenberger, Rupert
Hahn, Andreas
Pataraia, Ekaterina
Traub-Weidinger, Tatjana
Hummel, Johann
Beyer, Thomas
Conditional Generative Adversarial Networks Aided Motion Correction of Dynamic (18)F-FDG PET Brain Studies
title Conditional Generative Adversarial Networks Aided Motion Correction of Dynamic (18)F-FDG PET Brain Studies
title_full Conditional Generative Adversarial Networks Aided Motion Correction of Dynamic (18)F-FDG PET Brain Studies
title_fullStr Conditional Generative Adversarial Networks Aided Motion Correction of Dynamic (18)F-FDG PET Brain Studies
title_full_unstemmed Conditional Generative Adversarial Networks Aided Motion Correction of Dynamic (18)F-FDG PET Brain Studies
title_short Conditional Generative Adversarial Networks Aided Motion Correction of Dynamic (18)F-FDG PET Brain Studies
title_sort conditional generative adversarial networks aided motion correction of dynamic (18)f-fdg pet brain studies
topic Basic Science Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8729870/
https://www.ncbi.nlm.nih.gov/pubmed/33246982
http://dx.doi.org/10.2967/jnumed.120.248856
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