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      Optimization of supervised cluster analysis for extracting reference tissue input curves in ( R)-[ 11C]PK11195 brain PET studies

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          Abstract

          Performance of two supervised cluster analysis (SVCA) algorithms for extracting reference tissue curves was evaluated to improve quantification of dynamic (R)-[ 11C]PK11195 brain positron emission tomography (PET) studies. Reference tissues were extracted from images using both a manually defined cerebellum and SVCA algorithms based on either four (SVCA4) or six (SVCA6) kinetic classes. Data from controls, mild cognitive impairment patients, and patients with Alzheimer's disease were analyzed using various kinetic models including plasma input, the simplified reference tissue model (RPM) and RPM with vascular correction (RPM V b ). In all subject groups, SVCA-based reference tissue curves showed lower blood volume fractions ( V b ) and volume of distributions than those based on cerebellum time-activity curve. Probably resulting from the presence of specific signal from the vessel walls that contains in normal condition a significant concentration of the 18 kDa translocation protein. Best contrast between subject groups was seen using SVCA4-based reference tissues as the result of a lower number of kinetic classes and the prior removal of extracerebral tissues. In addition, incorporation of V b in RPM improved both parametric images and binding potential contrast between groups. Incorporation of V b within RPM, together with SVCA4, appears to be the method of choice for analyzing cerebral (R)-[ 11C]PK11195 neurodegeneration studies.

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          Most cited references14

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          Parametric imaging of ligand-receptor binding in PET using a simplified reference region model.

          A method is presented for the generation of parametric images of radioligand-receptor binding using PET. The method is based on a simplified reference region compartmental model, which requires no arterial blood sampling, and gives parametric images of both the binding potential of the radioligand and its local rate of delivery relative to the reference region. The technique presented for the estimation of parameters in the model employs a set of basis functions which enables the incorporation of parameter bounds. This basis function method (BFM) is compared with conventional nonlinear least squares estimation of parameters (NLM), using both simulated and real data. BFM is shown to be more stable than NLM at the voxel level and is computationally much faster. Application of the technique is illustrated for three radiotracers: [11C]raclopride (a marker of the D2 receptor), [11C]SCH 23390 (a marker of the D1 receptor) in human studies, and [11C]CFT (a marker of the dopamine transporter) in rats. The assumptions implicit in the model and its implementation using BFM are discussed. Copyright 1997 Academic Press.
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            Microglia activation in recent-onset schizophrenia: a quantitative (R)-[11C]PK11195 positron emission tomography study.

            Schizophrenia is a brain disease involving progressive loss of gray matter of unknown cause. Most likely, this loss reflects neuronal damage, which should, in turn, be accompanied by microglia activation. Microglia activation can be quantified in vivo using (R)-[(11)C]PK11195 and positron emission tomography (PET). The purpose of this study was to investigate whether microglia activation occurs in patients with recent-onset schizophrenia. Ten patients with recent-onset schizophrenia and 10 age-matched healthy control subjects were included. A fully quantitative (R)-[(11)C]PK11195 PET scan was performed on all subjects, including arterial sampling to generate a metabolite-corrected input curve. Compared with control subjects, binding potential of (R)-[(11)C]PK11195 in total gray matter was increased in patients with schizophrenia. There were no differences in other PET parameters. Activated microglia are present in schizophrenia patients within the first 5 years of disease onset. This suggests that, in this period, neuronal injury is present and that neuronal damage may be involved in the loss of gray matter associated with this disease. Microglia may form a novel target for neuroprotective therapies in schizophrenia.
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              Positron emission tomography compartmental models.

              The current article presents theory for compartmental models used in positron emission tomography (PET). Both plasma input models and reference tissue input models are considered. General theory is derived and the systems are characterized in terms of their impulse response functions. The theory shows that the macro parameters of the system may be determined simply from the coefficients of the impulse response functions. These results are discussed in the context of radioligand binding studies. It is shown that binding potential is simply related to the integral of the impulse response functions for all plasma and reference tissue input models currently used in PET. This article also introduces a general compartmental description for the behavior of the tracer in blood, which then allows for the blood volume-induced bias in reference tissue input models to be assessed.
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                Author and article information

                Journal
                J Cereb Blood Flow Metab
                J. Cereb. Blood Flow Metab
                Journal of Cerebral Blood Flow & Metabolism
                Nature Publishing Group
                0271-678X
                1559-7016
                August 2012
                16 May 2012
                1 August 2012
                : 32
                : 8
                : 1600-1608
                Affiliations
                [1 ]simpleDepartment of Nuclear Medicine and PET Research, VU University Medical Center , Amsterdam, The Netherlands
                [2 ]simpleDepartment of Neurology and Alzheimer Center, VU University Medical Center , Amsterdam, The Netherlands
                [3 ]simpleWolfson Molecular Imaging Centre, University of Manchester , Manchester, UK
                [4 ]simpleDivision of Experimental Medicine, Imperial College London , London, UK
                [5 ]simpleDepartment of Diagnostic Radiology, Yale University , New Haven, Connecticut, USA
                Author notes
                [* ]simpleDepartment of Nuclear Medicine and PET Research, VU University Medical Center, PO Box 7057 , 1007 MB Amsterdam, The Netherlands. E-mail: Maqsood.Yaqub@ 123456VUmc.nl
                Article
                jcbfm201259
                10.1038/jcbfm.2012.59
                3421099
                22588187
                d8ebac2a-fc73-496c-b698-2fed6aba8aeb
                Copyright © 2012 International Society for Cerebral Blood Flow & Metabolism, Inc.

                This work is licensed under the Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/

                History
                : 31 January 2012
                : 28 March 2012
                : 07 April 2012
                Categories
                Original Article

                Neurosciences
                reference tissue,(r)-[11c]pk11195,parametric analysis,clustering
                Neurosciences
                reference tissue, (r)-[11c]pk11195, parametric analysis, clustering

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