Hyperpolarized 13C-MRSI and PET (hyperPET) in an Osteomyelitis Pig Model: A Pilot Study

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Hyperpolarized 13C-MRSI and PET (hyperPET) in an Osteomyelitis Pig Model : A Pilot Study. / Rahbek, Sofie; Gutte, Henrik; Johannesen, Helle H; Koch, Janne; Jensen, Louise Kruse; Dich-Jørgensen, Kristine; Jensen, Henrik Elvang; Hansen, Adam E; Kjær, Andreas.

In: IEEE Transactions on Radiation and Plasma Medical Sciences, Vol. 1, No. 2, 164-167, 03.2017.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Rahbek, S, Gutte, H, Johannesen, HH, Koch, J, Jensen, LK, Dich-Jørgensen, K, Jensen, HE, Hansen, AE & Kjær, A 2017, 'Hyperpolarized 13C-MRSI and PET (hyperPET) in an Osteomyelitis Pig Model: A Pilot Study', IEEE Transactions on Radiation and Plasma Medical Sciences, vol. 1, no. 2, 164-167. https://doi.org/10.1109/TNS.2016.2642478

APA

Rahbek, S., Gutte, H., Johannesen, H. H., Koch, J., Jensen, L. K., Dich-Jørgensen, K., Jensen, H. E., Hansen, A. E., & Kjær, A. (2017). Hyperpolarized 13C-MRSI and PET (hyperPET) in an Osteomyelitis Pig Model: A Pilot Study. IEEE Transactions on Radiation and Plasma Medical Sciences, 1(2), [164-167]. https://doi.org/10.1109/TNS.2016.2642478

Vancouver

Rahbek S, Gutte H, Johannesen HH, Koch J, Jensen LK, Dich-Jørgensen K et al. Hyperpolarized 13C-MRSI and PET (hyperPET) in an Osteomyelitis Pig Model: A Pilot Study. IEEE Transactions on Radiation and Plasma Medical Sciences. 2017 Mar;1(2). 164-167. https://doi.org/10.1109/TNS.2016.2642478

Author

Rahbek, Sofie ; Gutte, Henrik ; Johannesen, Helle H ; Koch, Janne ; Jensen, Louise Kruse ; Dich-Jørgensen, Kristine ; Jensen, Henrik Elvang ; Hansen, Adam E ; Kjær, Andreas. / Hyperpolarized 13C-MRSI and PET (hyperPET) in an Osteomyelitis Pig Model : A Pilot Study. In: IEEE Transactions on Radiation and Plasma Medical Sciences. 2017 ; Vol. 1, No. 2.

Bibtex

@article{279abf1dde74486595291a3737c6e9d0,
title = "Hyperpolarized 13C-MRSI and PET (hyperPET) in an Osteomyelitis Pig Model: A Pilot Study",
abstract = "Abstract:AIM: Hyperpolarized 13C-pyruvate magnetic resonance spectroscopic imaging (MRSI) is a real-time metabolic imaging technique, which can be combined with positron emission tomography (PET). In this pilot study, we explore the potential of combined hyperpolarized 13C-MRSI and FDG-PET for imaging of infection. METHODS: Three pigs were inoculated with S. aureusbacteria in the right tibia and saline in the left tibial bone. FDG-PET, 1H-MRI and 13C-MRSI was performed using a clinical whole-body PET/MR system (Siemens Biograph mMR, Erlangen, Germany). Hyperpolarized13C-pyruvate was prepared using a SpinLab System (GE Healthcare, Pittsburgh, PA, USA). 13C-lactate to 13C-pyruvate ratio and FDG SUV was reported in anatomical regions of interest covering bone and regions of inflammation and abscess defined on 1H-MRI. Histopathological examination was performed of both legs. RESULTS: An abscess was observed outside the right (infected bone) on 1H-MRI and confirmed by histopathology. In the abscess the 13C-lactate to 13C-pyruvate ratio was increased as compared to the inflammatory region of the control leg. 18F-FDG uptake showed no clear trend when comparing abscess versus inflammation, but showed an increase considering the infected bone versus the control. In the abscess, the FDG-PET signal distribution had highest intensity in the abscess membrane, whereas the maximum of the13C lactate ratio appears in the abscess cavity. DISCUSSION: The apparent different spatial enhancement pattern of FDG uptake and 13C lactate ratio in abscess suggests that they are independent biomarkers and that hyperpolarized 13C-MRSI is a method with potential for clinical imaging of infection and treatment response.",
author = "Sofie Rahbek and Henrik Gutte and Johannesen, {Helle H} and Janne Koch and Jensen, {Louise Kruse} and Kristine Dich-J{\o}rgensen and Jensen, {Henrik Elvang} and Hansen, {Adam E} and Andreas Kj{\ae}r",
year = "2017",
month = mar,
doi = "10.1109/TNS.2016.2642478",
language = "English",
volume = "1",
journal = "IEEE Transactions on Radiation and Plasma Medical Sciences",
issn = "2469-7303",
publisher = "IEEE",
number = "2",

}

RIS

TY - JOUR

T1 - Hyperpolarized 13C-MRSI and PET (hyperPET) in an Osteomyelitis Pig Model

T2 - A Pilot Study

AU - Rahbek, Sofie

AU - Gutte, Henrik

AU - Johannesen, Helle H

AU - Koch, Janne

AU - Jensen, Louise Kruse

AU - Dich-Jørgensen, Kristine

AU - Jensen, Henrik Elvang

AU - Hansen, Adam E

AU - Kjær, Andreas

PY - 2017/3

Y1 - 2017/3

N2 - Abstract:AIM: Hyperpolarized 13C-pyruvate magnetic resonance spectroscopic imaging (MRSI) is a real-time metabolic imaging technique, which can be combined with positron emission tomography (PET). In this pilot study, we explore the potential of combined hyperpolarized 13C-MRSI and FDG-PET for imaging of infection. METHODS: Three pigs were inoculated with S. aureusbacteria in the right tibia and saline in the left tibial bone. FDG-PET, 1H-MRI and 13C-MRSI was performed using a clinical whole-body PET/MR system (Siemens Biograph mMR, Erlangen, Germany). Hyperpolarized13C-pyruvate was prepared using a SpinLab System (GE Healthcare, Pittsburgh, PA, USA). 13C-lactate to 13C-pyruvate ratio and FDG SUV was reported in anatomical regions of interest covering bone and regions of inflammation and abscess defined on 1H-MRI. Histopathological examination was performed of both legs. RESULTS: An abscess was observed outside the right (infected bone) on 1H-MRI and confirmed by histopathology. In the abscess the 13C-lactate to 13C-pyruvate ratio was increased as compared to the inflammatory region of the control leg. 18F-FDG uptake showed no clear trend when comparing abscess versus inflammation, but showed an increase considering the infected bone versus the control. In the abscess, the FDG-PET signal distribution had highest intensity in the abscess membrane, whereas the maximum of the13C lactate ratio appears in the abscess cavity. DISCUSSION: The apparent different spatial enhancement pattern of FDG uptake and 13C lactate ratio in abscess suggests that they are independent biomarkers and that hyperpolarized 13C-MRSI is a method with potential for clinical imaging of infection and treatment response.

AB - Abstract:AIM: Hyperpolarized 13C-pyruvate magnetic resonance spectroscopic imaging (MRSI) is a real-time metabolic imaging technique, which can be combined with positron emission tomography (PET). In this pilot study, we explore the potential of combined hyperpolarized 13C-MRSI and FDG-PET for imaging of infection. METHODS: Three pigs were inoculated with S. aureusbacteria in the right tibia and saline in the left tibial bone. FDG-PET, 1H-MRI and 13C-MRSI was performed using a clinical whole-body PET/MR system (Siemens Biograph mMR, Erlangen, Germany). Hyperpolarized13C-pyruvate was prepared using a SpinLab System (GE Healthcare, Pittsburgh, PA, USA). 13C-lactate to 13C-pyruvate ratio and FDG SUV was reported in anatomical regions of interest covering bone and regions of inflammation and abscess defined on 1H-MRI. Histopathological examination was performed of both legs. RESULTS: An abscess was observed outside the right (infected bone) on 1H-MRI and confirmed by histopathology. In the abscess the 13C-lactate to 13C-pyruvate ratio was increased as compared to the inflammatory region of the control leg. 18F-FDG uptake showed no clear trend when comparing abscess versus inflammation, but showed an increase considering the infected bone versus the control. In the abscess, the FDG-PET signal distribution had highest intensity in the abscess membrane, whereas the maximum of the13C lactate ratio appears in the abscess cavity. DISCUSSION: The apparent different spatial enhancement pattern of FDG uptake and 13C lactate ratio in abscess suggests that they are independent biomarkers and that hyperpolarized 13C-MRSI is a method with potential for clinical imaging of infection and treatment response.

U2 - 10.1109/TNS.2016.2642478

DO - 10.1109/TNS.2016.2642478

M3 - Journal article

VL - 1

JO - IEEE Transactions on Radiation and Plasma Medical Sciences

JF - IEEE Transactions on Radiation and Plasma Medical Sciences

SN - 2469-7303

IS - 2

M1 - 164-167

ER -

ID: 179666848