Voxel-wise analysis of [123I]β-CIT SPECT differentiates the Parkinson variant of multiple system atrophy from idiopathic Parkinson's disease

To investigate the cerebral dopamine transporter status in the early stages of the parkinson-variant of multiple system atrophy (MSA-P), 15 patients with MSA-P and a disease duration up to 3 years were studied with [123I]β-CIT single photon emission computed tomography (SPECT). Data were compared wi...

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Veröffentlicht in:Brain (London, England : 1878) England : 1878), 2005-07, Vol.128 (7), p.1605-1612
Hauptverfasser: Scherfler, Christoph, Seppi, Klaus, Donnemiller, Eveline, Goebel, Georg, Brenneis, Christian, Virgolini, Irene, Wenning, Gregor K., Poewe, Werner
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container_title Brain (London, England : 1878)
container_volume 128
creator Scherfler, Christoph
Seppi, Klaus
Donnemiller, Eveline
Goebel, Georg
Brenneis, Christian
Virgolini, Irene
Wenning, Gregor K.
Poewe, Werner
description To investigate the cerebral dopamine transporter status in the early stages of the parkinson-variant of multiple system atrophy (MSA-P), 15 patients with MSA-P and a disease duration up to 3 years were studied with [123I]β-CIT single photon emission computed tomography (SPECT). Data were compared with 13 age-matched healthy control subjects and 15 patients with idiopathic Parkinson's disease (IPD), matched for age and disease duration. Parametric SPECT images of the specific-to-nondisplaceable equilibrium partition coefficient (V3″), which is proportional to the receptor density (Bmax) have been generated. To objectively localize focal changes in dopaminergic function throughout the entire brain volume without having to make an a priori hypothesis as to their location, statistical parametric mapping (SPM) was applied to our [123I]β-CIT SPECT study. Both MSA-P and IPD patients showed significant decreases in striatal [123I]β-CIT SPECT uptake. However, in MSA-P patients an additional reduction in midbrain [123I]β-CIT signal was localized with SPM compared with control subjects (MSA-P, V3″: 0.89 ± 0.37 versus controls V3″: 1.81 ± 0.38; P < 0.001) and patients with IPD (V3″: 1.84 ± 0.26; P < 0.001). Stepwise linear discriminant analysis of mean [123I]β-CIT uptake in the putamen, caudate and midbrain identified the caudate and midbrain as indices to classify correctly 95.2% of subjects as either normal, patients with MSA-P or IPD. Voxel-wise analysis of [123I]β-CIT SPECT revealed more widespread decline of monoaminergic transporter availability in MSA-P compared with IPD, matching the underlying pathological features. We suggest that the quantification of midbrain DAT signal should be included in the routine clinical analysis of [123I]β-CIT SPECT in patients with uncertain parkinsonism.
doi_str_mv 10.1093/brain/awh485
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Data were compared with 13 age-matched healthy control subjects and 15 patients with idiopathic Parkinson's disease (IPD), matched for age and disease duration. Parametric SPECT images of the specific-to-nondisplaceable equilibrium partition coefficient (V3″), which is proportional to the receptor density (Bmax) have been generated. To objectively localize focal changes in dopaminergic function throughout the entire brain volume without having to make an a priori hypothesis as to their location, statistical parametric mapping (SPM) was applied to our [123I]β-CIT SPECT study. Both MSA-P and IPD patients showed significant decreases in striatal [123I]β-CIT SPECT uptake. However, in MSA-P patients an additional reduction in midbrain [123I]β-CIT signal was localized with SPM compared with control subjects (MSA-P, V3″: 0.89 ± 0.37 versus controls V3″: 1.81 ± 0.38; P &lt; 0.001) and patients with IPD (V3″: 1.84 ± 0.26; P &lt; 0.001). Stepwise linear discriminant analysis of mean [123I]β-CIT uptake in the putamen, caudate and midbrain identified the caudate and midbrain as indices to classify correctly 95.2% of subjects as either normal, patients with MSA-P or IPD. Voxel-wise analysis of [123I]β-CIT SPECT revealed more widespread decline of monoaminergic transporter availability in MSA-P compared with IPD, matching the underlying pathological features. We suggest that the quantification of midbrain DAT signal should be included in the routine clinical analysis of [123I]β-CIT SPECT in patients with uncertain parkinsonism.</description><identifier>ISSN: 0006-8950</identifier><identifier>EISSN: 1460-2156</identifier><identifier>DOI: 10.1093/brain/awh485</identifier><identifier>PMID: 15817519</identifier><identifier>CODEN: BRAIAK</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>[123I]β-CIT = [123I]-2β-carbomethoxy-3β-(4-iodophenyl)tropane ; [123I]β-CIT SPECT ; Aged ; AI = asymmetry index ; Biological and medical sciences ; Case-Control Studies ; Caudate Nucleus - metabolism ; CI = confidence interval ; Cocaine - analogs &amp; derivatives ; Corpus Striatum - metabolism ; DAT = dopamine transporter ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Diagnosis, Differential ; Discriminant Analysis ; Dopamine - metabolism ; Dopamine Plasma Membrane Transport Proteins ; FDG = fluorodesoxyglucose ; Female ; FWHM = full width at half maximum ; H&amp;Y = Hoehn and Yahr ; Humans ; idiopathic Parkinson's disease ; IPD = idiopathic Parkinson's disease ; Linear Models ; Male ; Medical sciences ; Membrane Glycoproteins - metabolism ; Membrane Transport Proteins - metabolism ; Mesencephalon - metabolism ; Middle Aged ; MNI = Montreal Neurological Institute ; MSA-P = parkinsonian-variant of MSA ; Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis ; multiple system atrophy ; Multiple System Atrophy - diagnostic imaging ; Multiple System Atrophy - metabolism ; NAT = noradrenergic transporter ; Nerve Tissue Proteins - metabolism ; Neurology ; Parkinson Disease - diagnostic imaging ; Parkinson Disease - metabolism ; PET = positron emission tomography ; Radiopharmaceuticals ; Receptors, Dopamine D2 - metabolism ; ROI = region of interest ; SERT = serotonin transporter ; SPECT = single photon emission computed tomography ; SPM = statistical parametric mapping ; statistical parametric mapping ; Tomography, Emission-Computed, Single-Photon ; UPDRS = Unified Parkinson's Disease Rating Scale ; V3″ = specific-to-nondisplaceable equilibrium partition coefficient</subject><ispartof>Brain (London, England : 1878), 2005-07, Vol.128 (7), p.1605-1612</ispartof><rights>2005 INIST-CNRS</rights><rights>Copyright Oxford University Press(England) Jul 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c415t-6b2c4322a0428191cb43be66d0abdd4534ea7867ec79df9a03872e888c5f5f753</citedby><cites>FETCH-LOGICAL-c415t-6b2c4322a0428191cb43be66d0abdd4534ea7867ec79df9a03872e888c5f5f753</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=16941208$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15817519$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Scherfler, Christoph</creatorcontrib><creatorcontrib>Seppi, Klaus</creatorcontrib><creatorcontrib>Donnemiller, Eveline</creatorcontrib><creatorcontrib>Goebel, Georg</creatorcontrib><creatorcontrib>Brenneis, Christian</creatorcontrib><creatorcontrib>Virgolini, Irene</creatorcontrib><creatorcontrib>Wenning, Gregor K.</creatorcontrib><creatorcontrib>Poewe, Werner</creatorcontrib><title>Voxel-wise analysis of [123I]β-CIT SPECT differentiates the Parkinson variant of multiple system atrophy from idiopathic Parkinson's disease</title><title>Brain (London, England : 1878)</title><addtitle>Brain</addtitle><description>To investigate the cerebral dopamine transporter status in the early stages of the parkinson-variant of multiple system atrophy (MSA-P), 15 patients with MSA-P and a disease duration up to 3 years were studied with [123I]β-CIT single photon emission computed tomography (SPECT). Data were compared with 13 age-matched healthy control subjects and 15 patients with idiopathic Parkinson's disease (IPD), matched for age and disease duration. Parametric SPECT images of the specific-to-nondisplaceable equilibrium partition coefficient (V3″), which is proportional to the receptor density (Bmax) have been generated. To objectively localize focal changes in dopaminergic function throughout the entire brain volume without having to make an a priori hypothesis as to their location, statistical parametric mapping (SPM) was applied to our [123I]β-CIT SPECT study. Both MSA-P and IPD patients showed significant decreases in striatal [123I]β-CIT SPECT uptake. However, in MSA-P patients an additional reduction in midbrain [123I]β-CIT signal was localized with SPM compared with control subjects (MSA-P, V3″: 0.89 ± 0.37 versus controls V3″: 1.81 ± 0.38; P &lt; 0.001) and patients with IPD (V3″: 1.84 ± 0.26; P &lt; 0.001). Stepwise linear discriminant analysis of mean [123I]β-CIT uptake in the putamen, caudate and midbrain identified the caudate and midbrain as indices to classify correctly 95.2% of subjects as either normal, patients with MSA-P or IPD. Voxel-wise analysis of [123I]β-CIT SPECT revealed more widespread decline of monoaminergic transporter availability in MSA-P compared with IPD, matching the underlying pathological features. We suggest that the quantification of midbrain DAT signal should be included in the routine clinical analysis of [123I]β-CIT SPECT in patients with uncertain parkinsonism.</description><subject>[123I]β-CIT = [123I]-2β-carbomethoxy-3β-(4-iodophenyl)tropane</subject><subject>[123I]β-CIT SPECT</subject><subject>Aged</subject><subject>AI = asymmetry index</subject><subject>Biological and medical sciences</subject><subject>Case-Control Studies</subject><subject>Caudate Nucleus - metabolism</subject><subject>CI = confidence interval</subject><subject>Cocaine - analogs &amp; derivatives</subject><subject>Corpus Striatum - metabolism</subject><subject>DAT = dopamine transporter</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Diagnosis, Differential</subject><subject>Discriminant Analysis</subject><subject>Dopamine - metabolism</subject><subject>Dopamine Plasma Membrane Transport Proteins</subject><subject>FDG = fluorodesoxyglucose</subject><subject>Female</subject><subject>FWHM = full width at half maximum</subject><subject>H&amp;Y = Hoehn and Yahr</subject><subject>Humans</subject><subject>idiopathic Parkinson's disease</subject><subject>IPD = idiopathic Parkinson's disease</subject><subject>Linear Models</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Membrane Glycoproteins - metabolism</subject><subject>Membrane Transport Proteins - metabolism</subject><subject>Mesencephalon - metabolism</subject><subject>Middle Aged</subject><subject>MNI = Montreal Neurological Institute</subject><subject>MSA-P = parkinsonian-variant of MSA</subject><subject>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</subject><subject>multiple system atrophy</subject><subject>Multiple System Atrophy - diagnostic imaging</subject><subject>Multiple System Atrophy - metabolism</subject><subject>NAT = noradrenergic transporter</subject><subject>Nerve Tissue Proteins - metabolism</subject><subject>Neurology</subject><subject>Parkinson Disease - diagnostic imaging</subject><subject>Parkinson Disease - metabolism</subject><subject>PET = positron emission tomography</subject><subject>Radiopharmaceuticals</subject><subject>Receptors, Dopamine D2 - metabolism</subject><subject>ROI = region of interest</subject><subject>SERT = serotonin transporter</subject><subject>SPECT = single photon emission computed tomography</subject><subject>SPM = statistical parametric mapping</subject><subject>statistical parametric mapping</subject><subject>Tomography, Emission-Computed, Single-Photon</subject><subject>UPDRS = Unified Parkinson's Disease Rating Scale</subject><subject>V3″ = specific-to-nondisplaceable equilibrium partition coefficient</subject><issn>0006-8950</issn><issn>1460-2156</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0d-K1DAUBvAiijuu3nktQVBvrJuk-Xu5DOvOLCsuOIooUk7TlMnaNjVp3Z2H8GV8EJ_JjDM44I1XucjvfHDOl2WPCX5FsC5OqgCuP4GbNVP8TjYjTOCcEi7uZjOMsciV5vgoexDjNcaEFVTcz44IV0RyomfZjw_-1rb5jYsWQQ_tJrqIfIM-E1osv_z6mc-XK_Tu6my-QrVrGhtsPzoYbUTj2qIrCF9dH32PvkNw0I_b0W5qRze0FsVNHG2HYAx-WG9QE3yHXO38AOPamcPwi5iyo4VoH2b3GmijfbR_j7P3r89W80V--fZ8OT-9zA0jfMxFRU3ahAJmVBFNTMWKygpRY6jqmvGCWZBKSGukrhsNuFCSWqWU4Q1vJC-Os-e73CH4b5ONY9m5aGzbQm_9FEshtWSUqv9CooWWSskEn_4Dr_0U0kG3hjOq0_ETerlDJvgYg23KIbgOwqYkuNyWWf4ps9yVmfiTfeZUdbY-4H17CTzbA4gG2iZAb1w8OKEZoXi7Rb5zLhVy-_c_3T9tWkheLj5-KqV6c35xwRelLH4DvJO5kg</recordid><startdate>20050701</startdate><enddate>20050701</enddate><creator>Scherfler, Christoph</creator><creator>Seppi, Klaus</creator><creator>Donnemiller, Eveline</creator><creator>Goebel, Georg</creator><creator>Brenneis, Christian</creator><creator>Virgolini, Irene</creator><creator>Wenning, Gregor K.</creator><creator>Poewe, Werner</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20050701</creationdate><title>Voxel-wise analysis of [123I]β-CIT SPECT differentiates the Parkinson variant of multiple system atrophy from idiopathic Parkinson's disease</title><author>Scherfler, Christoph ; Seppi, Klaus ; Donnemiller, Eveline ; Goebel, Georg ; Brenneis, Christian ; Virgolini, Irene ; Wenning, Gregor K. ; Poewe, Werner</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-6b2c4322a0428191cb43be66d0abdd4534ea7867ec79df9a03872e888c5f5f753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>[123I]β-CIT = [123I]-2β-carbomethoxy-3β-(4-iodophenyl)tropane</topic><topic>[123I]β-CIT SPECT</topic><topic>Aged</topic><topic>AI = asymmetry index</topic><topic>Biological and medical sciences</topic><topic>Case-Control Studies</topic><topic>Caudate Nucleus - metabolism</topic><topic>CI = confidence interval</topic><topic>Cocaine - analogs &amp; derivatives</topic><topic>Corpus Striatum - metabolism</topic><topic>DAT = dopamine transporter</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Diagnosis, Differential</topic><topic>Discriminant Analysis</topic><topic>Dopamine - metabolism</topic><topic>Dopamine Plasma Membrane Transport Proteins</topic><topic>FDG = fluorodesoxyglucose</topic><topic>Female</topic><topic>FWHM = full width at half maximum</topic><topic>H&amp;Y = Hoehn and Yahr</topic><topic>Humans</topic><topic>idiopathic Parkinson's disease</topic><topic>IPD = idiopathic Parkinson's disease</topic><topic>Linear Models</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Membrane Glycoproteins - metabolism</topic><topic>Membrane Transport Proteins - metabolism</topic><topic>Mesencephalon - metabolism</topic><topic>Middle Aged</topic><topic>MNI = Montreal Neurological Institute</topic><topic>MSA-P = parkinsonian-variant of MSA</topic><topic>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</topic><topic>multiple system atrophy</topic><topic>Multiple System Atrophy - diagnostic imaging</topic><topic>Multiple System Atrophy - metabolism</topic><topic>NAT = noradrenergic transporter</topic><topic>Nerve Tissue Proteins - metabolism</topic><topic>Neurology</topic><topic>Parkinson Disease - diagnostic imaging</topic><topic>Parkinson Disease - metabolism</topic><topic>PET = positron emission tomography</topic><topic>Radiopharmaceuticals</topic><topic>Receptors, Dopamine D2 - metabolism</topic><topic>ROI = region of interest</topic><topic>SERT = serotonin transporter</topic><topic>SPECT = single photon emission computed tomography</topic><topic>SPM = statistical parametric mapping</topic><topic>statistical parametric mapping</topic><topic>Tomography, Emission-Computed, Single-Photon</topic><topic>UPDRS = Unified Parkinson's Disease Rating Scale</topic><topic>V3″ = specific-to-nondisplaceable equilibrium partition coefficient</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Scherfler, Christoph</creatorcontrib><creatorcontrib>Seppi, Klaus</creatorcontrib><creatorcontrib>Donnemiller, Eveline</creatorcontrib><creatorcontrib>Goebel, Georg</creatorcontrib><creatorcontrib>Brenneis, Christian</creatorcontrib><creatorcontrib>Virgolini, Irene</creatorcontrib><creatorcontrib>Wenning, Gregor K.</creatorcontrib><creatorcontrib>Poewe, Werner</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Brain (London, England : 1878)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Scherfler, Christoph</au><au>Seppi, Klaus</au><au>Donnemiller, Eveline</au><au>Goebel, Georg</au><au>Brenneis, Christian</au><au>Virgolini, Irene</au><au>Wenning, Gregor K.</au><au>Poewe, Werner</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Voxel-wise analysis of [123I]β-CIT SPECT differentiates the Parkinson variant of multiple system atrophy from idiopathic Parkinson's disease</atitle><jtitle>Brain (London, England : 1878)</jtitle><addtitle>Brain</addtitle><date>2005-07-01</date><risdate>2005</risdate><volume>128</volume><issue>7</issue><spage>1605</spage><epage>1612</epage><pages>1605-1612</pages><issn>0006-8950</issn><eissn>1460-2156</eissn><coden>BRAIAK</coden><abstract>To investigate the cerebral dopamine transporter status in the early stages of the parkinson-variant of multiple system atrophy (MSA-P), 15 patients with MSA-P and a disease duration up to 3 years were studied with [123I]β-CIT single photon emission computed tomography (SPECT). Data were compared with 13 age-matched healthy control subjects and 15 patients with idiopathic Parkinson's disease (IPD), matched for age and disease duration. Parametric SPECT images of the specific-to-nondisplaceable equilibrium partition coefficient (V3″), which is proportional to the receptor density (Bmax) have been generated. To objectively localize focal changes in dopaminergic function throughout the entire brain volume without having to make an a priori hypothesis as to their location, statistical parametric mapping (SPM) was applied to our [123I]β-CIT SPECT study. Both MSA-P and IPD patients showed significant decreases in striatal [123I]β-CIT SPECT uptake. However, in MSA-P patients an additional reduction in midbrain [123I]β-CIT signal was localized with SPM compared with control subjects (MSA-P, V3″: 0.89 ± 0.37 versus controls V3″: 1.81 ± 0.38; P &lt; 0.001) and patients with IPD (V3″: 1.84 ± 0.26; P &lt; 0.001). Stepwise linear discriminant analysis of mean [123I]β-CIT uptake in the putamen, caudate and midbrain identified the caudate and midbrain as indices to classify correctly 95.2% of subjects as either normal, patients with MSA-P or IPD. Voxel-wise analysis of [123I]β-CIT SPECT revealed more widespread decline of monoaminergic transporter availability in MSA-P compared with IPD, matching the underlying pathological features. We suggest that the quantification of midbrain DAT signal should be included in the routine clinical analysis of [123I]β-CIT SPECT in patients with uncertain parkinsonism.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>15817519</pmid><doi>10.1093/brain/awh485</doi><tpages>8</tpages></addata></record>
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1460-2156
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source Oxford University Press Journals All Titles (1996-Current); MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects [123I]β-CIT = [123I]-2β-carbomethoxy-3β-(4-iodophenyl)tropane
[123I]β-CIT SPECT
Aged
AI = asymmetry index
Biological and medical sciences
Case-Control Studies
Caudate Nucleus - metabolism
CI = confidence interval
Cocaine - analogs & derivatives
Corpus Striatum - metabolism
DAT = dopamine transporter
Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
Diagnosis, Differential
Discriminant Analysis
Dopamine - metabolism
Dopamine Plasma Membrane Transport Proteins
FDG = fluorodesoxyglucose
Female
FWHM = full width at half maximum
H&Y = Hoehn and Yahr
Humans
idiopathic Parkinson's disease
IPD = idiopathic Parkinson's disease
Linear Models
Male
Medical sciences
Membrane Glycoproteins - metabolism
Membrane Transport Proteins - metabolism
Mesencephalon - metabolism
Middle Aged
MNI = Montreal Neurological Institute
MSA-P = parkinsonian-variant of MSA
Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis
multiple system atrophy
Multiple System Atrophy - diagnostic imaging
Multiple System Atrophy - metabolism
NAT = noradrenergic transporter
Nerve Tissue Proteins - metabolism
Neurology
Parkinson Disease - diagnostic imaging
Parkinson Disease - metabolism
PET = positron emission tomography
Radiopharmaceuticals
Receptors, Dopamine D2 - metabolism
ROI = region of interest
SERT = serotonin transporter
SPECT = single photon emission computed tomography
SPM = statistical parametric mapping
statistical parametric mapping
Tomography, Emission-Computed, Single-Photon
UPDRS = Unified Parkinson's Disease Rating Scale
V3″ = specific-to-nondisplaceable equilibrium partition coefficient
title Voxel-wise analysis of [123I]β-CIT SPECT differentiates the Parkinson variant of multiple system atrophy from idiopathic Parkinson's disease
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