Dopamine transporter SPECT imaging in corticobasal syndrome: A peak into the underlying pathology?
Background Multiple pathologies may underlie corticobasal syndrome (CBS), including Alzheimer's disease (AD). Dopamine transporter density imaging with Ioflupane 123 I SPECT (DaTscan) may be normal in CBS. No studies to date have examined the relationship between DaTscan status and underlying p...
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Veröffentlicht in: | Acta neurologica Scandinavica 2022-06, Vol.145 (6), p.762-769 |
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creator | Constantinides, Vasilios C. Souvatzoglou, Michail Paraskevas, George P. Chalioti, Maria Boufidou, Fotini Stefanis, Leonidas Kapaki, Elisabeth |
description | Background
Multiple pathologies may underlie corticobasal syndrome (CBS), including Alzheimer's disease (AD). Dopamine transporter density imaging with Ioflupane 123 I SPECT (DaTscan) may be normal in CBS. No studies to date have examined the relationship between DaTscan status and underlying pathology in CBS.
Objectives
The main objective of the study was to test whether a normal DaTscan in CBS patients is indicative of an underlying AD pathology, as determined by cerebrospinal fluid (CSF) biomarkers.
Methods
Eighteen CBS patients were included. They were divided into patients with an AD and a non‐AD disease pathology, based on their cerebrospinal fluid biochemical profile. A typical AD CSF profile was defined as an increase in total and phosphorylated at threonine 181 tau protein in addition to a decrease in amyloid‐beta with 42 amino acids. DaTscan data were compared in these two groups.
Results
Eight of the 18 CBS patients (44%) had a normal DaTscan. Seven of the 18 CBS patients (39%) had an AD cerebrospinal fluid biochemical profile. Two of seven CBS patients with AD biomarker profile had abnormal DaTscans. Three of 11 CBS patients with a non‐AD biomarker profile had normal DaTscans. A normal DaTscan was indicative of AD pathology with suboptimal (~70%) sensitivity and specificity. Semi‐quantitative DaTscan analysis did not differentiate between AD from non‐AD CSF biomarker profile in CBS.
Conclusion
A normal DaTscan is indicative of AD in CBS, but the sensitivity and specificity of DaTscan as an in vivo marker of AD pathology is suboptimal. |
doi_str_mv | 10.1111/ane.13614 |
format | Article |
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Multiple pathologies may underlie corticobasal syndrome (CBS), including Alzheimer's disease (AD). Dopamine transporter density imaging with Ioflupane 123 I SPECT (DaTscan) may be normal in CBS. No studies to date have examined the relationship between DaTscan status and underlying pathology in CBS.
Objectives
The main objective of the study was to test whether a normal DaTscan in CBS patients is indicative of an underlying AD pathology, as determined by cerebrospinal fluid (CSF) biomarkers.
Methods
Eighteen CBS patients were included. They were divided into patients with an AD and a non‐AD disease pathology, based on their cerebrospinal fluid biochemical profile. A typical AD CSF profile was defined as an increase in total and phosphorylated at threonine 181 tau protein in addition to a decrease in amyloid‐beta with 42 amino acids. DaTscan data were compared in these two groups.
Results
Eight of the 18 CBS patients (44%) had a normal DaTscan. Seven of the 18 CBS patients (39%) had an AD cerebrospinal fluid biochemical profile. Two of seven CBS patients with AD biomarker profile had abnormal DaTscans. Three of 11 CBS patients with a non‐AD biomarker profile had normal DaTscans. A normal DaTscan was indicative of AD pathology with suboptimal (~70%) sensitivity and specificity. Semi‐quantitative DaTscan analysis did not differentiate between AD from non‐AD CSF biomarker profile in CBS.
Conclusion
A normal DaTscan is indicative of AD in CBS, but the sensitivity and specificity of DaTscan as an in vivo marker of AD pathology is suboptimal.</description><identifier>ISSN: 0001-6314</identifier><identifier>EISSN: 1600-0404</identifier><identifier>DOI: 10.1111/ane.13614</identifier><identifier>PMID: 35307816</identifier><language>eng</language><publisher>Denmark: Hindawi Limited</publisher><subject>Alzheimer Disease - diagnostic imaging ; Alzheimer Disease - pathology ; Alzheimer's disease ; Amyloid beta-Peptides - cerebrospinal fluid ; beta‐amyloid ; Biomarkers ; Biomarkers - cerebrospinal fluid ; Cerebrospinal fluid ; Corticobasal Degeneration ; corticobasal syndrome ; Dopamine ; Dopamine Plasma Membrane Transport Proteins ; Dopamine transporter ; dopamine transporter imaging ; Humans ; Neurodegenerative diseases ; Pathology ; Peptide Fragments ; Single photon emission computed tomography ; Tau protein ; tau Proteins - cerebrospinal fluid ; Threonine ; Tomography, Emission-Computed, Single-Photon</subject><ispartof>Acta neurologica Scandinavica, 2022-06, Vol.145 (6), p.762-769</ispartof><rights>2022 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><rights>2022 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</rights><rights>Copyright © 2022 John Wiley & Sons A/S</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3534-bc2b4b22ae9c8f4973842c5f5e1c8c57c731ba18221eeb09f7c90d0bbe22c8503</citedby><cites>FETCH-LOGICAL-c3534-bc2b4b22ae9c8f4973842c5f5e1c8c57c731ba18221eeb09f7c90d0bbe22c8503</cites><orcidid>0000-0001-7432-5009</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fane.13614$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fane.13614$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35307816$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Constantinides, Vasilios C.</creatorcontrib><creatorcontrib>Souvatzoglou, Michail</creatorcontrib><creatorcontrib>Paraskevas, George P.</creatorcontrib><creatorcontrib>Chalioti, Maria</creatorcontrib><creatorcontrib>Boufidou, Fotini</creatorcontrib><creatorcontrib>Stefanis, Leonidas</creatorcontrib><creatorcontrib>Kapaki, Elisabeth</creatorcontrib><title>Dopamine transporter SPECT imaging in corticobasal syndrome: A peak into the underlying pathology?</title><title>Acta neurologica Scandinavica</title><addtitle>Acta Neurol Scand</addtitle><description>Background
Multiple pathologies may underlie corticobasal syndrome (CBS), including Alzheimer's disease (AD). Dopamine transporter density imaging with Ioflupane 123 I SPECT (DaTscan) may be normal in CBS. No studies to date have examined the relationship between DaTscan status and underlying pathology in CBS.
Objectives
The main objective of the study was to test whether a normal DaTscan in CBS patients is indicative of an underlying AD pathology, as determined by cerebrospinal fluid (CSF) biomarkers.
Methods
Eighteen CBS patients were included. They were divided into patients with an AD and a non‐AD disease pathology, based on their cerebrospinal fluid biochemical profile. A typical AD CSF profile was defined as an increase in total and phosphorylated at threonine 181 tau protein in addition to a decrease in amyloid‐beta with 42 amino acids. DaTscan data were compared in these two groups.
Results
Eight of the 18 CBS patients (44%) had a normal DaTscan. Seven of the 18 CBS patients (39%) had an AD cerebrospinal fluid biochemical profile. Two of seven CBS patients with AD biomarker profile had abnormal DaTscans. Three of 11 CBS patients with a non‐AD biomarker profile had normal DaTscans. A normal DaTscan was indicative of AD pathology with suboptimal (~70%) sensitivity and specificity. Semi‐quantitative DaTscan analysis did not differentiate between AD from non‐AD CSF biomarker profile in CBS.
Conclusion
A normal DaTscan is indicative of AD in CBS, but the sensitivity and specificity of DaTscan as an in vivo marker of AD pathology is suboptimal.</description><subject>Alzheimer Disease - diagnostic imaging</subject><subject>Alzheimer Disease - pathology</subject><subject>Alzheimer's disease</subject><subject>Amyloid beta-Peptides - cerebrospinal fluid</subject><subject>beta‐amyloid</subject><subject>Biomarkers</subject><subject>Biomarkers - cerebrospinal fluid</subject><subject>Cerebrospinal fluid</subject><subject>Corticobasal Degeneration</subject><subject>corticobasal syndrome</subject><subject>Dopamine</subject><subject>Dopamine Plasma Membrane Transport Proteins</subject><subject>Dopamine transporter</subject><subject>dopamine transporter imaging</subject><subject>Humans</subject><subject>Neurodegenerative diseases</subject><subject>Pathology</subject><subject>Peptide Fragments</subject><subject>Single photon emission computed tomography</subject><subject>Tau protein</subject><subject>tau Proteins - cerebrospinal fluid</subject><subject>Threonine</subject><subject>Tomography, Emission-Computed, Single-Photon</subject><issn>0001-6314</issn><issn>1600-0404</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE1LwzAYgIMobk4P_gEJeNFDZ5KmX15kzPkBQwXnuSTZ262zbWrSIv33ZnZ6EMwl5OXJw8uD0CklY-rOlahgTP2Q8j00pCEhHuGE76MhIYR6oU_5AB1Zu3EvFnF-iAZ-4JMopuEQyVtdizKvADdGVLbWpgGDX19m0wXOS7HKqxXOK6zcPFdaCisKbLtqaXQJ13iCaxDvDmg0btaA22oJpui2n2rRrHWhV93NMTrIRGHhZHeP0NvdbDF98ObP94_TydxTbh3uScUkl4wJSFSc8STyY85UkAVAVayCSEU-lYLGjFEASZIsUglZEimBMRUHxB-hi95bG_3Rgm3SMrcKisLl0a1NWchpQHjIY4ee_0E3ujWV285RQUJYEga-oy57ShltrYEsrY1rYrqUknQbPnXm9Du8Y892xlaWsPwlf0o74KoHPvMCuv9N6eRp1iu_AKODjBU</recordid><startdate>202206</startdate><enddate>202206</enddate><creator>Constantinides, Vasilios C.</creator><creator>Souvatzoglou, Michail</creator><creator>Paraskevas, George P.</creator><creator>Chalioti, Maria</creator><creator>Boufidou, Fotini</creator><creator>Stefanis, Leonidas</creator><creator>Kapaki, Elisabeth</creator><general>Hindawi Limited</general><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>7TK</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-7432-5009</orcidid></search><sort><creationdate>202206</creationdate><title>Dopamine transporter SPECT imaging in corticobasal syndrome: A peak into the underlying pathology?</title><author>Constantinides, Vasilios C. ; Souvatzoglou, Michail ; Paraskevas, George P. ; Chalioti, Maria ; Boufidou, Fotini ; Stefanis, Leonidas ; Kapaki, Elisabeth</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3534-bc2b4b22ae9c8f4973842c5f5e1c8c57c731ba18221eeb09f7c90d0bbe22c8503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Alzheimer Disease - diagnostic imaging</topic><topic>Alzheimer Disease - pathology</topic><topic>Alzheimer's disease</topic><topic>Amyloid beta-Peptides - cerebrospinal fluid</topic><topic>beta‐amyloid</topic><topic>Biomarkers</topic><topic>Biomarkers - cerebrospinal fluid</topic><topic>Cerebrospinal fluid</topic><topic>Corticobasal Degeneration</topic><topic>corticobasal syndrome</topic><topic>Dopamine</topic><topic>Dopamine Plasma Membrane Transport Proteins</topic><topic>Dopamine transporter</topic><topic>dopamine transporter imaging</topic><topic>Humans</topic><topic>Neurodegenerative diseases</topic><topic>Pathology</topic><topic>Peptide Fragments</topic><topic>Single photon emission computed tomography</topic><topic>Tau protein</topic><topic>tau Proteins - cerebrospinal fluid</topic><topic>Threonine</topic><topic>Tomography, Emission-Computed, Single-Photon</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Constantinides, Vasilios C.</creatorcontrib><creatorcontrib>Souvatzoglou, Michail</creatorcontrib><creatorcontrib>Paraskevas, George P.</creatorcontrib><creatorcontrib>Chalioti, Maria</creatorcontrib><creatorcontrib>Boufidou, Fotini</creatorcontrib><creatorcontrib>Stefanis, Leonidas</creatorcontrib><creatorcontrib>Kapaki, Elisabeth</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Acta neurologica Scandinavica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Constantinides, Vasilios C.</au><au>Souvatzoglou, Michail</au><au>Paraskevas, George P.</au><au>Chalioti, Maria</au><au>Boufidou, Fotini</au><au>Stefanis, Leonidas</au><au>Kapaki, Elisabeth</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dopamine transporter SPECT imaging in corticobasal syndrome: A peak into the underlying pathology?</atitle><jtitle>Acta neurologica Scandinavica</jtitle><addtitle>Acta Neurol Scand</addtitle><date>2022-06</date><risdate>2022</risdate><volume>145</volume><issue>6</issue><spage>762</spage><epage>769</epage><pages>762-769</pages><issn>0001-6314</issn><eissn>1600-0404</eissn><abstract>Background
Multiple pathologies may underlie corticobasal syndrome (CBS), including Alzheimer's disease (AD). Dopamine transporter density imaging with Ioflupane 123 I SPECT (DaTscan) may be normal in CBS. No studies to date have examined the relationship between DaTscan status and underlying pathology in CBS.
Objectives
The main objective of the study was to test whether a normal DaTscan in CBS patients is indicative of an underlying AD pathology, as determined by cerebrospinal fluid (CSF) biomarkers.
Methods
Eighteen CBS patients were included. They were divided into patients with an AD and a non‐AD disease pathology, based on their cerebrospinal fluid biochemical profile. A typical AD CSF profile was defined as an increase in total and phosphorylated at threonine 181 tau protein in addition to a decrease in amyloid‐beta with 42 amino acids. DaTscan data were compared in these two groups.
Results
Eight of the 18 CBS patients (44%) had a normal DaTscan. Seven of the 18 CBS patients (39%) had an AD cerebrospinal fluid biochemical profile. Two of seven CBS patients with AD biomarker profile had abnormal DaTscans. Three of 11 CBS patients with a non‐AD biomarker profile had normal DaTscans. A normal DaTscan was indicative of AD pathology with suboptimal (~70%) sensitivity and specificity. Semi‐quantitative DaTscan analysis did not differentiate between AD from non‐AD CSF biomarker profile in CBS.
Conclusion
A normal DaTscan is indicative of AD in CBS, but the sensitivity and specificity of DaTscan as an in vivo marker of AD pathology is suboptimal.</abstract><cop>Denmark</cop><pub>Hindawi Limited</pub><pmid>35307816</pmid><doi>10.1111/ane.13614</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-7432-5009</orcidid></addata></record> |
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subjects | Alzheimer Disease - diagnostic imaging Alzheimer Disease - pathology Alzheimer's disease Amyloid beta-Peptides - cerebrospinal fluid beta‐amyloid Biomarkers Biomarkers - cerebrospinal fluid Cerebrospinal fluid Corticobasal Degeneration corticobasal syndrome Dopamine Dopamine Plasma Membrane Transport Proteins Dopamine transporter dopamine transporter imaging Humans Neurodegenerative diseases Pathology Peptide Fragments Single photon emission computed tomography Tau protein tau Proteins - cerebrospinal fluid Threonine Tomography, Emission-Computed, Single-Photon |
title | Dopamine transporter SPECT imaging in corticobasal syndrome: A peak into the underlying pathology? |
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