Noninvasive Relative Quantification of [11C]ABP688 PET Imaging in Mice Versus an Input Function Measured Over an Arteriovenous Shunt

Impairment of the metabotropic glutamate receptor 5 (mGluR5) has been implicated with various neurologic disorders. Although mGluR5 density can be quantified with the PET radiotracer [ C]ABP688, the methods for reproducible quantification of [ C]ABP688 PET imaging in mice have not been thoroughly in...

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Published inFrontiers in neurology Vol. 9; p. 516
Main Authors Verhaeghe, Jeroen, Bertoglio, Daniele, Kosten, Lauren, Thomae, David, Verhoye, Marleen, Van Der Linden, Annemie, Wyffels, Leonie, Stroobants, Sigrid, Wityak, John, Dominguez, Celia, Mrzljak, Ladislav, Staelens, Steven
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LanguageEnglish
Published Switzerland Frontiers Media S.A 29.06.2018
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Abstract Impairment of the metabotropic glutamate receptor 5 (mGluR5) has been implicated with various neurologic disorders. Although mGluR5 density can be quantified with the PET radiotracer [ C]ABP688, the methods for reproducible quantification of [ C]ABP688 PET imaging in mice have not been thoroughly investigated yet. Thus, this study aimed to assess and validate cerebellum as reference region for simplified reference tissue model (SRTM), investigate the feasibility of a noninvasive cardiac image-derived input function (IDIF) for relative quantification, to validate the use of a PET template instead of an MRI template for spatial normalization, and to determine the reproducibility and within-subject variability of [ C]ABP688 PET imaging in mice. Blocking with the mGluR5 antagonist MPEP resulted in a reduction of [ C]ABP688 binding of 41% in striatum ( < 0.0001), while no significant effect could be found in cerebellum (-4.8%, > 0.99) indicating cerebellum as suitable reference region for mice. DVR-1 calculated using a noninvasive IDIF and an arteriovenous input function correlated significantly when considering the cerebellum as the reference region (striatum: DVR-1, = 0.978, < 0.0001). Additionally, strong correlations between binding potential calculated from SRTM (BP ) with DVR-1 based on IDIF (striatum: = 0.980, < 0.0001) and AV shunt (striatum: = 0.987, < 0.0001). BP displayed higher discrimination power than V values in determining differences between wild-types and heterozygous Q175 mice, an animal model of Huntington's disease. Furthermore, we showed high agreement between PET- and MRI-based spatial normalization approaches (striatum: = 0.989, < 0.0001). Finally, both spatial normalization approaches did not reveal any significant bias between test-retest scans, with a relative difference below 5%. This study indicates that noninvasive quantification of [ C]ABP688 PET imaging is reproducible and cerebellum can be used as reference region in mice.
AbstractList Impairment of the metabotropic glutamate receptor 5 (mGluR5) has been implicated with various neurologic disorders. Although mGluR5 density can be quantified with the PET radiotracer [11C]ABP688, the methods for reproducible quantification of [11C]ABP688 PET imaging in mice have not been thoroughly investigated yet. Thus, this study aimed to assess and validate cerebellum as reference region for simplified reference tissue model (SRTM), investigate the feasibility of a noninvasive cardiac image-derived input function (IDIF) for relative quantification, to validate the use of a PET template instead of an MRI template for spatial normalization, and to determine the reproducibility and within-subject variability of [11C]ABP688 PET imaging in mice. Blocking with the mGluR5 antagonist MPEP resulted in a reduction of [11C]ABP688 binding of 41% in striatum (p < 0.0001), while no significant effect could be found in cerebellum (−4.8%, p > 0.99) indicating cerebellum as suitable reference region for mice. DVR-1 calculated using a noninvasive IDIF and an arteriovenous input function correlated significantly when considering the cerebellum as the reference region (striatum: DVR-1, r = 0.978, p < 0.0001). Additionally, strong correlations between binding potential calculated from SRTM (BPND) with DVR-1 based on IDIF (striatum: r = 0.980, p < 0.0001) and AV shunt (striatum: r = 0.987, p < 0.0001). BPND displayed higher discrimination power than VT values in determining differences between wild-types and heterozygous Q175 mice, an animal model of Huntington's disease. Furthermore, we showed high agreement between PET- and MRI-based spatial normalization approaches (striatum: r = 0.989, p < 0.0001). Finally, both spatial normalization approaches did not reveal any significant bias between test-retest scans, with a relative difference below 5%. This study indicates that noninvasive quantification of [11C]ABP688 PET imaging is reproducible and cerebellum can be used as reference region in mice.
Impairment of the metabotropic glutamate receptor 5 (mGluR5) has been implicated with various neurologic disorders. Although mGluR5 density can be quantified with the PET radiotracer [ 11 C]ABP688, the methods for reproducible quantification of [ 11 C]ABP688 PET imaging in mice have not been thoroughly investigated yet. Thus, this study aimed to assess and validate cerebellum as reference region for simplified reference tissue model (SRTM), investigate the feasibility of a noninvasive cardiac image-derived input function (IDIF) for relative quantification, to validate the use of a PET template instead of an MRI template for spatial normalization, and to determine the reproducibility and within-subject variability of [ 11 C]ABP688 PET imaging in mice. Blocking with the mGluR5 antagonist MPEP resulted in a reduction of [ 11 C]ABP688 binding of 41% in striatum ( p < 0.0001), while no significant effect could be found in cerebellum (−4.8%, p > 0.99) indicating cerebellum as suitable reference region for mice. DVR-1 calculated using a noninvasive IDIF and an arteriovenous input function correlated significantly when considering the cerebellum as the reference region (striatum: DVR-1, r = 0.978, p < 0.0001). Additionally, strong correlations between binding potential calculated from SRTM (BP ND ) with DVR-1 based on IDIF (striatum: r = 0.980, p < 0.0001) and AV shunt (striatum: r = 0.987, p < 0.0001). BP ND displayed higher discrimination power than V T values in determining differences between wild-types and heterozygous Q175 mice, an animal model of Huntington's disease. Furthermore, we showed high agreement between PET- and MRI-based spatial normalization approaches (striatum: r = 0.989, p < 0.0001). Finally, both spatial normalization approaches did not reveal any significant bias between test-retest scans, with a relative difference below 5%. This study indicates that noninvasive quantification of [ 11 C]ABP688 PET imaging is reproducible and cerebellum can be used as reference region in mice.
Impairment of the metabotropic glutamate receptor 5 (mGluR5) has been implicated with various neurologic disorders. Although mGluR5 density can be quantified with the PET radiotracer [ C]ABP688, the methods for reproducible quantification of [ C]ABP688 PET imaging in mice have not been thoroughly investigated yet. Thus, this study aimed to assess and validate cerebellum as reference region for simplified reference tissue model (SRTM), investigate the feasibility of a noninvasive cardiac image-derived input function (IDIF) for relative quantification, to validate the use of a PET template instead of an MRI template for spatial normalization, and to determine the reproducibility and within-subject variability of [ C]ABP688 PET imaging in mice. Blocking with the mGluR5 antagonist MPEP resulted in a reduction of [ C]ABP688 binding of 41% in striatum ( < 0.0001), while no significant effect could be found in cerebellum (-4.8%, > 0.99) indicating cerebellum as suitable reference region for mice. DVR-1 calculated using a noninvasive IDIF and an arteriovenous input function correlated significantly when considering the cerebellum as the reference region (striatum: DVR-1, = 0.978, < 0.0001). Additionally, strong correlations between binding potential calculated from SRTM (BP ) with DVR-1 based on IDIF (striatum: = 0.980, < 0.0001) and AV shunt (striatum: = 0.987, < 0.0001). BP displayed higher discrimination power than V values in determining differences between wild-types and heterozygous Q175 mice, an animal model of Huntington's disease. Furthermore, we showed high agreement between PET- and MRI-based spatial normalization approaches (striatum: = 0.989, < 0.0001). Finally, both spatial normalization approaches did not reveal any significant bias between test-retest scans, with a relative difference below 5%. This study indicates that noninvasive quantification of [ C]ABP688 PET imaging is reproducible and cerebellum can be used as reference region in mice.
Author Dominguez, Celia
Stroobants, Sigrid
Mrzljak, Ladislav
Wityak, John
Verhoye, Marleen
Wyffels, Leonie
Verhaeghe, Jeroen
Staelens, Steven
Van Der Linden, Annemie
Thomae, David
Bertoglio, Daniele
Kosten, Lauren
AuthorAffiliation 2 Department of Nuclear Medicine, Antwerp University Hospital , Edegem , Belgium
4 CHDI Foundation , Princeton, NJ , United States
3 Bio-Imaging Lab, University of Antwerp , Wilrijk , Belgium
1 Molecular Imaging Center Antwerp, University of Antwerp , Wilrijk , Belgium
AuthorAffiliation_xml – name: 2 Department of Nuclear Medicine, Antwerp University Hospital , Edegem , Belgium
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/30013509$$D View this record in MEDLINE/PubMed
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Copyright Copyright © 2018 Verhaeghe, Bertoglio, Kosten, Thomae, Verhoye, Van Der Linden, Wyffels, Stroobants, Wityak, Dominguez, Mrzljak and Staelens. 2018 Verhaeghe, Bertoglio, Kosten, Thomae, Verhoye, Van Der Linden, Wyffels, Stroobants, Wityak, Dominguez, Mrzljak and Staelens
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Keywords input function
[11C]ABP688
PET imaging
mGluR5
test-retest
Language English
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Snippet Impairment of the metabotropic glutamate receptor 5 (mGluR5) has been implicated with various neurologic disorders. Although mGluR5 density can be quantified...
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StartPage 516
SubjectTerms [11C]ABP688
input function
mGluR5
Neurology
PET imaging
test-retest
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Title Noninvasive Relative Quantification of [11C]ABP688 PET Imaging in Mice Versus an Input Function Measured Over an Arteriovenous Shunt
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https://pubmed.ncbi.nlm.nih.gov/PMC6036254
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