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Research ArticleAdult Brain
Open Access

Clinical Applications of Simultaneous PET/MR Imaging Using (R)-[11C]-Verapamil with Cyclosporin A: Preliminary Results on a Surrogate Marker of Drug-Resistant Epilepsy

J.-W. Shin, K. Chu, S.A. Shin, K.-H. Jung, S.-T. Lee, Y.-S. Lee, J. Moon, D.Y. Lee, J.S. Lee, D.S. Lee and S.K. Lee
American Journal of Neuroradiology November 2015, DOI: https://doi.org/10.3174/ajnr.A4566
J.-W. Shin
From the Department of Neurology (J.-W.S., K.C., K.-H.J., S.-T.L., J.M., D.Y.L., S.K.L.), Comprehensive Epilepsy Center, Laboratory for Neurotherapeutics, Biomedical Research Institute; and Department of Nuclear Medicine (S.A.S., Y.-S.L., J.S.L., D.S.L.); and Department of Biomedical Sciences (S.A.S., J.S.L.), Seoul National University Hospital, Seoul National University College of Medicine, Seoul, South Korea; Department of Neurology (J.-W.S.), CHA Bundang Medical Center, CHA University, Seongnam, Korea; and Department of Molecular Medicine and Biopharmaceutical Sciences (Y.-S.L., D.S.L.), Graduate School of Convergence Science and Technology, Kyunggi, South Korea.
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K. Chu
From the Department of Neurology (J.-W.S., K.C., K.-H.J., S.-T.L., J.M., D.Y.L., S.K.L.), Comprehensive Epilepsy Center, Laboratory for Neurotherapeutics, Biomedical Research Institute; and Department of Nuclear Medicine (S.A.S., Y.-S.L., J.S.L., D.S.L.); and Department of Biomedical Sciences (S.A.S., J.S.L.), Seoul National University Hospital, Seoul National University College of Medicine, Seoul, South Korea; Department of Neurology (J.-W.S.), CHA Bundang Medical Center, CHA University, Seongnam, Korea; and Department of Molecular Medicine and Biopharmaceutical Sciences (Y.-S.L., D.S.L.), Graduate School of Convergence Science and Technology, Kyunggi, South Korea.
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S.A. Shin
From the Department of Neurology (J.-W.S., K.C., K.-H.J., S.-T.L., J.M., D.Y.L., S.K.L.), Comprehensive Epilepsy Center, Laboratory for Neurotherapeutics, Biomedical Research Institute; and Department of Nuclear Medicine (S.A.S., Y.-S.L., J.S.L., D.S.L.); and Department of Biomedical Sciences (S.A.S., J.S.L.), Seoul National University Hospital, Seoul National University College of Medicine, Seoul, South Korea; Department of Neurology (J.-W.S.), CHA Bundang Medical Center, CHA University, Seongnam, Korea; and Department of Molecular Medicine and Biopharmaceutical Sciences (Y.-S.L., D.S.L.), Graduate School of Convergence Science and Technology, Kyunggi, South Korea.
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K.-H. Jung
From the Department of Neurology (J.-W.S., K.C., K.-H.J., S.-T.L., J.M., D.Y.L., S.K.L.), Comprehensive Epilepsy Center, Laboratory for Neurotherapeutics, Biomedical Research Institute; and Department of Nuclear Medicine (S.A.S., Y.-S.L., J.S.L., D.S.L.); and Department of Biomedical Sciences (S.A.S., J.S.L.), Seoul National University Hospital, Seoul National University College of Medicine, Seoul, South Korea; Department of Neurology (J.-W.S.), CHA Bundang Medical Center, CHA University, Seongnam, Korea; and Department of Molecular Medicine and Biopharmaceutical Sciences (Y.-S.L., D.S.L.), Graduate School of Convergence Science and Technology, Kyunggi, South Korea.
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S.-T. Lee
From the Department of Neurology (J.-W.S., K.C., K.-H.J., S.-T.L., J.M., D.Y.L., S.K.L.), Comprehensive Epilepsy Center, Laboratory for Neurotherapeutics, Biomedical Research Institute; and Department of Nuclear Medicine (S.A.S., Y.-S.L., J.S.L., D.S.L.); and Department of Biomedical Sciences (S.A.S., J.S.L.), Seoul National University Hospital, Seoul National University College of Medicine, Seoul, South Korea; Department of Neurology (J.-W.S.), CHA Bundang Medical Center, CHA University, Seongnam, Korea; and Department of Molecular Medicine and Biopharmaceutical Sciences (Y.-S.L., D.S.L.), Graduate School of Convergence Science and Technology, Kyunggi, South Korea.
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Y.-S. Lee
From the Department of Neurology (J.-W.S., K.C., K.-H.J., S.-T.L., J.M., D.Y.L., S.K.L.), Comprehensive Epilepsy Center, Laboratory for Neurotherapeutics, Biomedical Research Institute; and Department of Nuclear Medicine (S.A.S., Y.-S.L., J.S.L., D.S.L.); and Department of Biomedical Sciences (S.A.S., J.S.L.), Seoul National University Hospital, Seoul National University College of Medicine, Seoul, South Korea; Department of Neurology (J.-W.S.), CHA Bundang Medical Center, CHA University, Seongnam, Korea; and Department of Molecular Medicine and Biopharmaceutical Sciences (Y.-S.L., D.S.L.), Graduate School of Convergence Science and Technology, Kyunggi, South Korea.
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J. Moon
From the Department of Neurology (J.-W.S., K.C., K.-H.J., S.-T.L., J.M., D.Y.L., S.K.L.), Comprehensive Epilepsy Center, Laboratory for Neurotherapeutics, Biomedical Research Institute; and Department of Nuclear Medicine (S.A.S., Y.-S.L., J.S.L., D.S.L.); and Department of Biomedical Sciences (S.A.S., J.S.L.), Seoul National University Hospital, Seoul National University College of Medicine, Seoul, South Korea; Department of Neurology (J.-W.S.), CHA Bundang Medical Center, CHA University, Seongnam, Korea; and Department of Molecular Medicine and Biopharmaceutical Sciences (Y.-S.L., D.S.L.), Graduate School of Convergence Science and Technology, Kyunggi, South Korea.
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D.Y. Lee
From the Department of Neurology (J.-W.S., K.C., K.-H.J., S.-T.L., J.M., D.Y.L., S.K.L.), Comprehensive Epilepsy Center, Laboratory for Neurotherapeutics, Biomedical Research Institute; and Department of Nuclear Medicine (S.A.S., Y.-S.L., J.S.L., D.S.L.); and Department of Biomedical Sciences (S.A.S., J.S.L.), Seoul National University Hospital, Seoul National University College of Medicine, Seoul, South Korea; Department of Neurology (J.-W.S.), CHA Bundang Medical Center, CHA University, Seongnam, Korea; and Department of Molecular Medicine and Biopharmaceutical Sciences (Y.-S.L., D.S.L.), Graduate School of Convergence Science and Technology, Kyunggi, South Korea.
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J.S. Lee
From the Department of Neurology (J.-W.S., K.C., K.-H.J., S.-T.L., J.M., D.Y.L., S.K.L.), Comprehensive Epilepsy Center, Laboratory for Neurotherapeutics, Biomedical Research Institute; and Department of Nuclear Medicine (S.A.S., Y.-S.L., J.S.L., D.S.L.); and Department of Biomedical Sciences (S.A.S., J.S.L.), Seoul National University Hospital, Seoul National University College of Medicine, Seoul, South Korea; Department of Neurology (J.-W.S.), CHA Bundang Medical Center, CHA University, Seongnam, Korea; and Department of Molecular Medicine and Biopharmaceutical Sciences (Y.-S.L., D.S.L.), Graduate School of Convergence Science and Technology, Kyunggi, South Korea.
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D.S. Lee
From the Department of Neurology (J.-W.S., K.C., K.-H.J., S.-T.L., J.M., D.Y.L., S.K.L.), Comprehensive Epilepsy Center, Laboratory for Neurotherapeutics, Biomedical Research Institute; and Department of Nuclear Medicine (S.A.S., Y.-S.L., J.S.L., D.S.L.); and Department of Biomedical Sciences (S.A.S., J.S.L.), Seoul National University Hospital, Seoul National University College of Medicine, Seoul, South Korea; Department of Neurology (J.-W.S.), CHA Bundang Medical Center, CHA University, Seongnam, Korea; and Department of Molecular Medicine and Biopharmaceutical Sciences (Y.-S.L., D.S.L.), Graduate School of Convergence Science and Technology, Kyunggi, South Korea.
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S.K. Lee
From the Department of Neurology (J.-W.S., K.C., K.-H.J., S.-T.L., J.M., D.Y.L., S.K.L.), Comprehensive Epilepsy Center, Laboratory for Neurotherapeutics, Biomedical Research Institute; and Department of Nuclear Medicine (S.A.S., Y.-S.L., J.S.L., D.S.L.); and Department of Biomedical Sciences (S.A.S., J.S.L.), Seoul National University Hospital, Seoul National University College of Medicine, Seoul, South Korea; Department of Neurology (J.-W.S.), CHA Bundang Medical Center, CHA University, Seongnam, Korea; and Department of Molecular Medicine and Biopharmaceutical Sciences (Y.-S.L., D.S.L.), Graduate School of Convergence Science and Technology, Kyunggi, South Korea.
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Abstract

BACKGROUND AND PURPOSE: The development of resistance to antiepileptic drugs is explained well by the transporter hypothesis, which suggests that drug resistance is caused by inadequate penetration of drugs into the brain barrier as a result of increased levels of efflux transporter such as p-glycoprotein. To evaluate the brain expression of p-glycoprotein in patients with drug-resistant epilepsy, including neocortical epilepsy, we developed a noninvsive quantitative analysis including asymmetry indices based on (R)-[11C]-verapamil PET/MR imaging with cyclosporin A, a p-glycoprotein inhibitor.

MATERIALS AND METHODS: Six patients with drug-resistant epilepsy, 5 patients with drug-sensitive epilepsy, and 8 healthy controls underwent dynamic (R)-[11C]-verapamil PET/MR imaging with an intravenous infusion of cyclosporin A. Asymmetry indices [(Right Region - Left Region)/(Right Region + Left Region) × 200%] of the standard uptake values in each of the paired lobes were calculated.

RESULTS: All patients with drug-resistant epilepsy had significantly different asymmetry from the healthy controls, whereas all patients with drug-sensitive epilepsy had asymmetry similar to that in healthy controls. In the temporal lobe, the asymmetry indices of patients with left temporal lobe drug-resistant epilepsy were more positive than those of healthy controls (healthy controls: 4.0413 ± 1.7452; patients: 7.2184 ± 1.8237; P = .048), and those of patients with right temporal drug-resistant epilepsy were more negative (patients: -1.6496 ± 3.4136; P = .044). In addition, specific regions that had significant asymmetry were different between the lateral and medial temporal lobe epilepsy groups. In the frontal lobe, the asymmetry index of patients with right frontal lobe drug-resistant epilepsy was more negative than that in healthy controls.

CONCLUSIONS: We confirmed that statistical parametric mapping analysis by using asymmetry indices of (R)-[11C]-verapamil PET/MR imaging with cyclosporin A could be used as a surrogate marker for drug-resistant epilepsy, and this approach might be helpful for localizing or lateralizing the epileptic zone.

Abbreviations

AI
asymmetry index
CS
cyclosporin A
DRE
drug-resistant epilepsy
DSE
seizure-free drug-sensitive epilepsy
Pgp
p-glycoprotein
SPAM
statistical probabilistic anatomic mapping
SUV
standard uptake value
TLE
temporal lobe epilepsy
VPM-PET/MR-CS
(R)-[11C]-verapamil PET and MR imaging with intravenous infusion of cyclosporin A without serial arterial sampling

Footnotes

  • J.-W.S. and K.C. contributed equally to this work.

  • © 2016 American Society of Neuroradiology

Indicates open access to non-subscribers at www.ajnr.org

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Cite this article
J.-W. Shin, K. Chu, S.A. Shin, K.-H. Jung, S.-T. Lee, Y.-S. Lee, J. Moon, D.Y. Lee, J.S. Lee, D.S. Lee, S.K. Lee
Clinical Applications of Simultaneous PET/MR Imaging Using (R)-[11C]-Verapamil with Cyclosporin A: Preliminary Results on a Surrogate Marker of Drug-Resistant Epilepsy
American Journal of Neuroradiology Nov 2015, DOI: 10.3174/ajnr.A4566

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Clinical Applications of Simultaneous PET/MR Imaging Using (R)-[11C]-Verapamil with Cyclosporin A: Preliminary Results on a Surrogate Marker of Drug-Resistant Epilepsy
J.-W. Shin, K. Chu, S.A. Shin, K.-H. Jung, S.-T. Lee, Y.-S. Lee, J. Moon, D.Y. Lee, J.S. Lee, D.S. Lee, S.K. Lee
American Journal of Neuroradiology Nov 2015, DOI: 10.3174/ajnr.A4566
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