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 in | Frontiers in neurology Vol. 9; p. 516 |
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Main Authors | , , , , , , , , , , , |
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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 – name: 3 Bio-Imaging Lab, University of Antwerp , Wilrijk , Belgium – name: 4 CHDI Foundation , Princeton, NJ , United States – name: 1 Molecular Imaging Center Antwerp, University of Antwerp , Wilrijk , Belgium |
Author_xml | – sequence: 1 givenname: Jeroen surname: Verhaeghe fullname: Verhaeghe, Jeroen – sequence: 2 givenname: Daniele surname: Bertoglio fullname: Bertoglio, Daniele – sequence: 3 givenname: Lauren surname: Kosten fullname: Kosten, Lauren – sequence: 4 givenname: David surname: Thomae fullname: Thomae, David – sequence: 5 givenname: Marleen surname: Verhoye fullname: Verhoye, Marleen – sequence: 6 givenname: Annemie surname: Van Der Linden fullname: Van Der Linden, Annemie – sequence: 7 givenname: Leonie surname: Wyffels fullname: Wyffels, Leonie – sequence: 8 givenname: Sigrid surname: Stroobants fullname: Stroobants, Sigrid – sequence: 9 givenname: John surname: Wityak fullname: Wityak, John – sequence: 10 givenname: Celia surname: Dominguez fullname: Dominguez, Celia – sequence: 11 givenname: Ladislav surname: Mrzljak fullname: Mrzljak, Ladislav – sequence: 12 givenname: Steven surname: Staelens fullname: Staelens, Steven |
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 |
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Notes | Reviewed by: Christine DeLorenzo, Stony Brook University, United States; Adriaan Anthonius Lammertsma, VU University Medical Center, Netherlands This article was submitted to Applied Neuroimaging, a section of the journal Frontiers in Neurology Edited by: Freimut Dankwart Juengling, St. Claraspital Basel, Switzerland |
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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 |
URI | https://www.ncbi.nlm.nih.gov/pubmed/30013509 https://pubmed.ncbi.nlm.nih.gov/PMC6036254 https://doaj.org/article/a37fe964a9284659b7c8cdb502919689 |
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