Brain perfusion estimation by Tikhonov model-free deconvolution in a long axial field of view PET/CT scanner exploring five different PET tracers

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Brain perfusion estimation by Tikhonov model-free deconvolution in a long axial field of view PET/CT scanner exploring five different PET tracers. / Larsson, Henrik Bo Wiberg; Law, Ian; Andersen, Thomas L.; Andersen, Flemming L.; Fischer, Barbara M.; Vestergaard, Mark B.; Larsson, Tanne S.W.; Lindberg, Ulrich.

In: European Journal of Nuclear Medicine and Molecular Imaging, Vol. 51, No. 3, 2024, p. 707-720.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Larsson, HBW, Law, I, Andersen, TL, Andersen, FL, Fischer, BM, Vestergaard, MB, Larsson, TSW & Lindberg, U 2024, 'Brain perfusion estimation by Tikhonov model-free deconvolution in a long axial field of view PET/CT scanner exploring five different PET tracers', European Journal of Nuclear Medicine and Molecular Imaging, vol. 51, no. 3, pp. 707-720. https://doi.org/10.1007/s00259-023-06469-w

APA

Larsson, H. B. W., Law, I., Andersen, T. L., Andersen, F. L., Fischer, B. M., Vestergaard, M. B., Larsson, T. S. W., & Lindberg, U. (2024). Brain perfusion estimation by Tikhonov model-free deconvolution in a long axial field of view PET/CT scanner exploring five different PET tracers. European Journal of Nuclear Medicine and Molecular Imaging, 51(3), 707-720. https://doi.org/10.1007/s00259-023-06469-w

Vancouver

Larsson HBW, Law I, Andersen TL, Andersen FL, Fischer BM, Vestergaard MB et al. Brain perfusion estimation by Tikhonov model-free deconvolution in a long axial field of view PET/CT scanner exploring five different PET tracers. European Journal of Nuclear Medicine and Molecular Imaging. 2024;51(3):707-720. https://doi.org/10.1007/s00259-023-06469-w

Author

Larsson, Henrik Bo Wiberg ; Law, Ian ; Andersen, Thomas L. ; Andersen, Flemming L. ; Fischer, Barbara M. ; Vestergaard, Mark B. ; Larsson, Tanne S.W. ; Lindberg, Ulrich. / Brain perfusion estimation by Tikhonov model-free deconvolution in a long axial field of view PET/CT scanner exploring five different PET tracers. In: European Journal of Nuclear Medicine and Molecular Imaging. 2024 ; Vol. 51, No. 3. pp. 707-720.

Bibtex

@article{4b49c55607304ffd9d01fdd87878d958,
title = "Brain perfusion estimation by Tikhonov model-free deconvolution in a long axial field of view PET/CT scanner exploring five different PET tracers",
abstract = "Purpose: New total-body PET scanners with a long axial field of view (LAFOV) allow for higher temporal resolution due to higher sensitivity, which facilitates perfusion estimation by model-free deconvolution. Fundamental tracer kinetic theory predicts that perfusion can be estimated for all tracers despite their different fates given sufficiently high temporal resolution of 1 s or better, bypassing the need for compartment modelling. The aim of this study was to investigate whether brain perfusion could be estimated using model-free Tikhonov generalized deconvolution for five different PET tracers, [15O]H2O, [11C]PIB, [18F]FE-PE2I, [18F]FDG and [18F]FET. To our knowledge, this is the first example of a general model-free approach to estimate cerebral blood flow (CBF) from PET data. Methods: Twenty-five patients underwent dynamic LAFOV PET scanning (Siemens, Quadra). PET images were reconstructed with an isotropic voxel resolution of 1.65 mm3. Time framing was 40 × 1 s during bolus passage followed by increasing framing up to 60 min. AIF was obtained from the descending aorta. Both voxel- and region-based calculations of perfusion in the thalamus were performed using the Tikhonov method. The residue impulse response function was used to estimate the extraction fraction of tracer leakage across the blood–brain barrier. Results: CBF ranged from 37 to 69 mL blood min−1 100 mL of tissue−1 in the thalamus. Voxelwise calculation of CBF resulted in CBF maps in the physiologically normal range. The extraction fractions of [15O]H2O, [18F]FE-PE2I, [11C]PIB, [18F]FDG and [18F]FET in the thalamus were 0.95, 0.78, 0.62, 0.19 and 0.03, respectively. Conclusion: The high temporal resolution and sensitivity associated with LAFOV PET scanners allow for noninvasive perfusion estimation of multiple tracers. The method provides an estimation of the residue impulse response function, from which the fate of the tracer can be studied, including the extraction fraction, influx constant, volume of distribution and transit time distribution, providing detailed physiological insight into normal and pathologic tissue.",
keywords = "Cerebral blood flow, Extraction fraction, Long-axial field of view PET, Model-free deconvolution",
author = "Larsson, {Henrik Bo Wiberg} and Ian Law and Andersen, {Thomas L.} and Andersen, {Flemming L.} and Fischer, {Barbara M.} and Vestergaard, {Mark B.} and Larsson, {Tanne S.W.} and Ulrich Lindberg",
note = "Publisher Copyright: {\textcopyright} 2023, The Author(s).",
year = "2024",
doi = "10.1007/s00259-023-06469-w",
language = "English",
volume = "51",
pages = "707--720",
journal = "European Journal of Nuclear Medicine and Molecular Imaging",
issn = "1619-7070",
publisher = "Springer",
number = "3",

}

RIS

TY - JOUR

T1 - Brain perfusion estimation by Tikhonov model-free deconvolution in a long axial field of view PET/CT scanner exploring five different PET tracers

AU - Larsson, Henrik Bo Wiberg

AU - Law, Ian

AU - Andersen, Thomas L.

AU - Andersen, Flemming L.

AU - Fischer, Barbara M.

AU - Vestergaard, Mark B.

AU - Larsson, Tanne S.W.

AU - Lindberg, Ulrich

N1 - Publisher Copyright: © 2023, The Author(s).

PY - 2024

Y1 - 2024

N2 - Purpose: New total-body PET scanners with a long axial field of view (LAFOV) allow for higher temporal resolution due to higher sensitivity, which facilitates perfusion estimation by model-free deconvolution. Fundamental tracer kinetic theory predicts that perfusion can be estimated for all tracers despite their different fates given sufficiently high temporal resolution of 1 s or better, bypassing the need for compartment modelling. The aim of this study was to investigate whether brain perfusion could be estimated using model-free Tikhonov generalized deconvolution for five different PET tracers, [15O]H2O, [11C]PIB, [18F]FE-PE2I, [18F]FDG and [18F]FET. To our knowledge, this is the first example of a general model-free approach to estimate cerebral blood flow (CBF) from PET data. Methods: Twenty-five patients underwent dynamic LAFOV PET scanning (Siemens, Quadra). PET images were reconstructed with an isotropic voxel resolution of 1.65 mm3. Time framing was 40 × 1 s during bolus passage followed by increasing framing up to 60 min. AIF was obtained from the descending aorta. Both voxel- and region-based calculations of perfusion in the thalamus were performed using the Tikhonov method. The residue impulse response function was used to estimate the extraction fraction of tracer leakage across the blood–brain barrier. Results: CBF ranged from 37 to 69 mL blood min−1 100 mL of tissue−1 in the thalamus. Voxelwise calculation of CBF resulted in CBF maps in the physiologically normal range. The extraction fractions of [15O]H2O, [18F]FE-PE2I, [11C]PIB, [18F]FDG and [18F]FET in the thalamus were 0.95, 0.78, 0.62, 0.19 and 0.03, respectively. Conclusion: The high temporal resolution and sensitivity associated with LAFOV PET scanners allow for noninvasive perfusion estimation of multiple tracers. The method provides an estimation of the residue impulse response function, from which the fate of the tracer can be studied, including the extraction fraction, influx constant, volume of distribution and transit time distribution, providing detailed physiological insight into normal and pathologic tissue.

AB - Purpose: New total-body PET scanners with a long axial field of view (LAFOV) allow for higher temporal resolution due to higher sensitivity, which facilitates perfusion estimation by model-free deconvolution. Fundamental tracer kinetic theory predicts that perfusion can be estimated for all tracers despite their different fates given sufficiently high temporal resolution of 1 s or better, bypassing the need for compartment modelling. The aim of this study was to investigate whether brain perfusion could be estimated using model-free Tikhonov generalized deconvolution for five different PET tracers, [15O]H2O, [11C]PIB, [18F]FE-PE2I, [18F]FDG and [18F]FET. To our knowledge, this is the first example of a general model-free approach to estimate cerebral blood flow (CBF) from PET data. Methods: Twenty-five patients underwent dynamic LAFOV PET scanning (Siemens, Quadra). PET images were reconstructed with an isotropic voxel resolution of 1.65 mm3. Time framing was 40 × 1 s during bolus passage followed by increasing framing up to 60 min. AIF was obtained from the descending aorta. Both voxel- and region-based calculations of perfusion in the thalamus were performed using the Tikhonov method. The residue impulse response function was used to estimate the extraction fraction of tracer leakage across the blood–brain barrier. Results: CBF ranged from 37 to 69 mL blood min−1 100 mL of tissue−1 in the thalamus. Voxelwise calculation of CBF resulted in CBF maps in the physiologically normal range. The extraction fractions of [15O]H2O, [18F]FE-PE2I, [11C]PIB, [18F]FDG and [18F]FET in the thalamus were 0.95, 0.78, 0.62, 0.19 and 0.03, respectively. Conclusion: The high temporal resolution and sensitivity associated with LAFOV PET scanners allow for noninvasive perfusion estimation of multiple tracers. The method provides an estimation of the residue impulse response function, from which the fate of the tracer can be studied, including the extraction fraction, influx constant, volume of distribution and transit time distribution, providing detailed physiological insight into normal and pathologic tissue.

KW - Cerebral blood flow

KW - Extraction fraction

KW - Long-axial field of view PET

KW - Model-free deconvolution

U2 - 10.1007/s00259-023-06469-w

DO - 10.1007/s00259-023-06469-w

M3 - Journal article

C2 - 37843600

AN - SCOPUS:85174290314

VL - 51

SP - 707

EP - 720

JO - European Journal of Nuclear Medicine and Molecular Imaging

JF - European Journal of Nuclear Medicine and Molecular Imaging

SN - 1619-7070

IS - 3

ER -

ID: 381067094