The simplified reference tissue model with 18F-fallypride positron emission tomography: choice of reference region
- PMID: 24447617
- PMCID: PMC4103900
- DOI: 10.2310/7290.2013.00065
The simplified reference tissue model with 18F-fallypride positron emission tomography: choice of reference region
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 (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.
Figures



Similar articles
-
Surrogate markers for cerebral blood flow correlate with [¹⁸F]-fallypride binding potential at dopamine D(2/3) receptors in human striatum.Synapse. 2013 Apr;67(4):199-203. doi: 10.1002/syn.21630. Epub 2013 Jan 12. Synapse. 2013. PMID: 23239525
-
Preliminary assessment of extrastriatal dopamine D-2 receptor binding in the rodent and nonhuman primate brains using the high affinity radioligand, 18F-fallypride.Nucl Med Biol. 1999 Jul;26(5):519-27. doi: 10.1016/s0969-8051(99)00012-8. Nucl Med Biol. 1999. PMID: 10473190
-
Quantification of dopamine D(2/3) receptors in rat brain using factor analysis corrected [18F]Fallypride images.Neuroimage. 2012 Sep;62(3):1455-68. doi: 10.1016/j.neuroimage.2012.05.075. Epub 2012 Jun 1. Neuroimage. 2012. PMID: 22659483
-
Challenges in the development of dopamine D2- and D3-selective radiotracers for PET imaging studies.J Labelled Comp Radiopharm. 2018 Mar;61(3):291-298. doi: 10.1002/jlcr.3558. Epub 2017 Sep 26. J Labelled Comp Radiopharm. 2018. PMID: 28857231 Review.
-
Selectivity of probes for PET imaging of dopamine D3 receptors.Neurosci Lett. 2019 Jan 19;691:18-25. doi: 10.1016/j.neulet.2018.03.006. Epub 2018 Mar 5. Neurosci Lett. 2019. PMID: 29518538 Free PMC article. Review.
Cited by
-
Individual time course of pre- and postsynaptic PET imaging may improve differential diagnosis of Parkinson's disease and multiple system atrophy: a case report.BMC Res Notes. 2015 Sep 29;8:496. doi: 10.1186/s13104-015-1522-0. BMC Res Notes. 2015. PMID: 26419749 Free PMC article.
-
Striatal D1- and D2-type dopamine receptors are linked to motor response inhibition in human subjects.J Neurosci. 2015 Apr 15;35(15):5990-7. doi: 10.1523/JNEUROSCI.4850-14.2015. J Neurosci. 2015. PMID: 25878272 Free PMC article.
-
Feasibility study of a SiPM-fiber detector for non-invasive measurement of arterial input function for preclinical and clinical positron emission tomography.EJNMMI Phys. 2024 Jan 31;11(1):12. doi: 10.1186/s40658-024-00618-2. EJNMMI Phys. 2024. PMID: 38291187 Free PMC article.
-
Stressful life events are associated with striatal dopamine receptor availability in alcohol dependence.J Neural Transm (Vienna). 2019 Sep;126(9):1127-1134. doi: 10.1007/s00702-019-01985-2. Epub 2019 Feb 12. J Neural Transm (Vienna). 2019. PMID: 30747311 Clinical Trial.
-
Quantification of Positron Emission Tomography Data Using Simultaneous Estimation of the Input Function: Validation with Venous Blood and Replication of Clinical Studies.Mol Imaging Biol. 2019 Oct;21(5):926-934. doi: 10.1007/s11307-018-1300-1. Mol Imaging Biol. 2019. PMID: 30535672 Free PMC article. Clinical Trial.
References
-
- Cunningham VJ, Jones T. Spectral analysis of dynamic PET studies. J Cereb Blood Flow Metab. 1993;13:15–23. - PubMed
-
- Hume SP, Myers R, Bloomfield PM, et al. Quantitation of carbon-11-labeled raclopride in rat striatum using positron emission tomography. Synapse. 1992;12:47–54. - PubMed
-
- Lammertsma AA, Bench CJ, Hume SP, et al. Comparison of methods for analysis of clinical [11C]raclopride studies. J Cereb Blood Flow Metab. 1996;16:42–52. - PubMed
-
- Lammertsma AA, Hume SP. Simplified reference tissue model for PET receptor studies. Neuroimage. 1996;4:153–158. - PubMed
-
- Slifstein M, Laruelle M. Effects of statistical noise on graphic analysis of PET neuroreceptor studies. J Nucl Med. 2000;41:2083–2088. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials