The Simplified Reference Tissue Model with 18F-Fallypride Positron Emission Tomography: Choice of Reference Region
The development of high-affinity radiotracers for positron emission tomography (PET) has allowed for quantification of dopamine receptors in extrastriatal and striatal regions of the brain. As these new radiotracers have distinctly different kinetic properties than their predecessors, it is importan...
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Published in | Molecular imaging Vol. 12; no. 8 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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Los Angeles, CA
SAGE Publications
01.11.2013
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ISSN | 1536-0121 1536-0121 |
DOI | 10.2310/7290.2013.00065 |
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Abstract | The development of high-affinity radiotracers for positron emission tomography (PET) has allowed for quantification of dopamine receptors in extrastriatal and striatal regions of the brain. As these new radiotracers have distinctly different kinetic properties than their predecessors, it is important to examine the suitability of kinetic models to represent their uptake, distribution, and in vivo washout. Using the simplified reference tissue model, we investigated the influence of reference region choice on the striatal binding potential of 18F-fallypride, a high-affinity dopamine D2/D3 receptor ligand. We compared the use of the visual cortex and a white matter region (superior longitudinal fasciculus) to the cerebellum, a commonly used reference tissue, in a PET-fallypride study of healthy and methamphetamine-dependent subjects. Compared to the cerebellum, use of the visual cortex produced significantly greater sample variance in binding potential relative to nondisplaceable uptake (BPND). Use of the white matter region was associated with BPND values and sample variance similar to those obtained with the cerebellum and a larger effect size for the group differences in striatal BPND between healthy and methamphetamine-dependent subjects. Our results do not support the use of the visual cortex as a reference region in 18F-fallypride studies and suggest that white matter may be a reasonable alternative to the cerebellum as it displays similar statistical and kinetic properties. |
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AbstractList | The development of high-affinity radiotracers for positron emission tomography (PET) has allowed for quantification of dopamine receptors in extrastriatal and striatal regions of the brain. As these new radiotracers have distinctly different kinetic properties than their predecessors, it is important to examine the suitability of kinetic models to represent their uptake, distribution, and in vivo washout. Using the simplified reference tissue model, we investigated the influence of reference region choice on the striatal binding potential of 18F-fallypride, a high-affinity dopamine D2/D3 receptor ligand. We compared the use of the visual cortex and a white matter region (superior longitudinal fasciculus) to the cerebellum, a commonly used reference tissue, in a PET-fallypride study of healthy and methamphetamine-dependent subjects. Compared to the cerebellum, use of the visual cortex produced significantly greater sample variance in binding potential relative to nondisplaceable uptake (BP(ND)). Use of the white matter region was associated with BP(ND) values and sample variance similar to those obtained with the cerebellum and a larger effect size for the group differences in striatal BP(ND) between healthy and methamphetamine-dependent subjects. Our results do not support the use of the visual cortex as a reference region in 18F-fallypride studies and suggest that white matter may be a reasonable alternative to the cerebellum as it displays similar statistical and kinetic properties. The development of high-affinity radiotracers for positron emission tomography (PET) has allowed for quantification of dopamine receptors in extrastriatal and striatal regions of the brain. As these new radiotracers have distinctly different kinetic properties than their predecessors, it is important to examine the suitability of kinetic models to represent their uptake, distribution, and in vivo washout. Using the simplified reference tissue model, we investigated the influence of reference region choice on the striatal binding potential of 18F-fallypride, a high-affinity dopamine D2/D3 receptor ligand. We compared the use of the visual cortex and a white matter region (superior longitudinal fasciculus) to the cerebellum, a commonly used reference tissue, in a PET-fallypride study of healthy and methamphetamine-dependent subjects. Compared to the cerebellum, use of the visual cortex produced significantly greater sample variance in binding potential relative to nondisplaceable uptake (BPND). Use of the white matter region was associated with BPND values and sample variance similar to those obtained with the cerebellum and a larger effect size for the group differences in striatal BPND between healthy and methamphetamine-dependent subjects. Our results do not support the use of the visual cortex as a reference region in 18F-fallypride studies and suggest that white matter may be a reasonable alternative to the cerebellum as it displays similar statistical and kinetic properties. The development of high-affinity radiotracers for positron emission tomography (PET) has allowed for quantification of dopamine receptors in extrastriatal and striatal regions of the brain. As these new radiotracers have distinctly different kinetic properties than their predecessors, it is important to examine the suitability of kinetic models to represent their uptake, distribution, and in vivo washout. Using the simplified reference tissue model, we investigated the influence of reference region choice on the striatal binding potential of 18F-fallypride, a high-affinity dopamine D2/D3 receptor ligand. We compared the use of the visual cortex and a white matter region (superior longitudinal fasciculus) to the cerebellum, a commonly used reference tissue, in a PET-fallypride study of healthy and methamphetamine-dependent subjects. Compared to the cerebellum, use of the visual cortex produced significantly greater sample variance in binding potential relative to nondisplaceable uptake (BP(ND)). Use of the white matter region was associated with BP(ND) values and sample variance similar to those obtained with the cerebellum and a larger effect size for the group differences in striatal BP(ND) between healthy and methamphetamine-dependent subjects. Our results do not support the use of the visual cortex as a reference region in 18F-fallypride studies and suggest that white matter may be a reasonable alternative to the cerebellum as it displays similar statistical and kinetic properties.The development of high-affinity radiotracers for positron emission tomography (PET) has allowed for quantification of dopamine receptors in extrastriatal and striatal regions of the brain. As these new radiotracers have distinctly different kinetic properties than their predecessors, it is important to examine the suitability of kinetic models to represent their uptake, distribution, and in vivo washout. Using the simplified reference tissue model, we investigated the influence of reference region choice on the striatal binding potential of 18F-fallypride, a high-affinity dopamine D2/D3 receptor ligand. We compared the use of the visual cortex and a white matter region (superior longitudinal fasciculus) to the cerebellum, a commonly used reference tissue, in a PET-fallypride study of healthy and methamphetamine-dependent subjects. Compared to the cerebellum, use of the visual cortex produced significantly greater sample variance in binding potential relative to nondisplaceable uptake (BP(ND)). Use of the white matter region was associated with BP(ND) values and sample variance similar to those obtained with the cerebellum and a larger effect size for the group differences in striatal BP(ND) between healthy and methamphetamine-dependent subjects. Our results do not support the use of the visual cortex as a reference region in 18F-fallypride studies and suggest that white matter may be a reasonable alternative to the cerebellum as it displays similar statistical and kinetic properties. |
Author | Ishibashi, Kenji Mandelkern, Mark A. Morgan, Andrew T. London, Edythe D. Robertson, Chelsea L. |
Author_xml | – sequence: 1 givenname: Kenji surname: Ishibashi fullname: Ishibashi, Kenji organization: From the Department of Psychiatry and Biobehavioral Sciences, Department of Molecular and Medical Pharmacology, and Brain Research Institute, David Geffen School of Medicine, University of California-Los Angeles, Los Angeles, CA; Department of Physics, University of California-Irvine, Irvine, CA; and Veterans Administration of Greater Los Angeles Health System, Los Angeles, CA – sequence: 2 givenname: Chelsea L. surname: Robertson fullname: Robertson, Chelsea L. organization: From the Department of Psychiatry and Biobehavioral Sciences, Department of Molecular and Medical Pharmacology, and Brain Research Institute, David Geffen School of Medicine, University of California-Los Angeles, Los Angeles, CA; Department of Physics, University of California-Irvine, Irvine, CA; and Veterans Administration of Greater Los Angeles Health System, Los Angeles, CA – sequence: 3 givenname: Mark A. surname: Mandelkern fullname: Mandelkern, Mark A. organization: From the Department of Psychiatry and Biobehavioral Sciences, Department of Molecular and Medical Pharmacology, and Brain Research Institute, David Geffen School of Medicine, University of California-Los Angeles, Los Angeles, CA; Department of Physics, University of California-Irvine, Irvine, CA; and Veterans Administration of Greater Los Angeles Health System, Los Angeles, CA – sequence: 4 givenname: Andrew T. surname: Morgan fullname: Morgan, Andrew T. organization: From the Department of Psychiatry and Biobehavioral Sciences, Department of Molecular and Medical Pharmacology, and Brain Research Institute, David Geffen School of Medicine, University of California-Los Angeles, Los Angeles, CA; Department of Physics, University of California-Irvine, Irvine, CA; and Veterans Administration of Greater Los Angeles Health System, Los Angeles, CA – sequence: 5 givenname: Edythe D. surname: London fullname: London, Edythe D. email: elondon@mednet.ucla.edu organization: From the Department of Psychiatry and Biobehavioral Sciences, Department of Molecular and Medical Pharmacology, and Brain Research Institute, David Geffen School of Medicine, University of California-Los Angeles, Los Angeles, CA; Department of Physics, University of California-Irvine, Irvine, CA; and Veterans Administration of Greater Los Angeles Health System, Los Angeles, CA |
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SubjectTerms | Adult Amphetamine-Related Disorders - diagnostic imaging Amphetamine-Related Disorders - metabolism Benzamides - pharmacokinetics Cerebellum - diagnostic imaging Fluorine Radioisotopes - pharmacokinetics Humans Methamphetamine - pharmacology Positron-Emission Tomography Receptors, Dopamine - metabolism Receptors, Dopamine D2 - metabolism Receptors, Dopamine D3 - metabolism Visual Cortex - diagnostic imaging Visual Cortex - metabolism |
Title | The Simplified Reference Tissue Model with 18F-Fallypride Positron Emission Tomography: Choice of Reference Region |
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