Value of the central vein sign at 3T to differentiate MS from seropositive NMOSD

OBJECTIVETo assess the value of the central vein sign (CVS) on a clinical 3T scanner to distinguish between multiple sclerosis (MS) and neuromyelitis optica spectrum disorder (NMOSD). METHODSEighteen aquaporin-4-antibody-positive patients with NMOSD, 18 patients with relapsing-remitting MS, and 25 h...

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Veröffentlicht in:Neurology 2018-04, Vol.90 (14), p.e1183-e1190
Hauptverfasser: Cortese, Rosa, Magnollay, Lise, Tur, Carmen, Abdel-Aziz, Khaled, Jacob, Anu, De Angelis, Floriana, Yiannakas, Marios C, Prados, Ferran, Ourselin, Sebastien, Yousry, Tarek A, Barkhof, Frederik, Ciccarelli, Olga
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container_end_page e1190
container_issue 14
container_start_page e1183
container_title Neurology
container_volume 90
creator Cortese, Rosa
Magnollay, Lise
Tur, Carmen
Abdel-Aziz, Khaled
Jacob, Anu
De Angelis, Floriana
Yiannakas, Marios C
Prados, Ferran
Ourselin, Sebastien
Yousry, Tarek A
Barkhof, Frederik
Ciccarelli, Olga
description OBJECTIVETo assess the value of the central vein sign (CVS) on a clinical 3T scanner to distinguish between multiple sclerosis (MS) and neuromyelitis optica spectrum disorder (NMOSD). METHODSEighteen aquaporin-4-antibody-positive patients with NMOSD, 18 patients with relapsing-remitting MS, and 25 healthy controls underwent 3T MRI. The presence of a central vein in white matter lesions on susceptibility-weighted imaging, defined as a thin hypointense line or a small dot, was recorded. RESULTSThe proportion of lesions with the CVS was higher in MS than NMOSD (80% vs 32%, p < 0.001). A greater proportion of lesions with the CVS predicted the diagnosis of MS, rather than NMOSD (odds ratio 1.10, 95% confidence interval [CI] 1.04 to 1.16, p = 0.001), suggesting that each percent unit increase in the proportion of lesions with the CVS in an individual patient was associated with a 10% increase in the risk of the same patient having MS. If more than 54% of the lesions on any given scan show the CVS, then the patient can be given a diagnosis of MS with an accuracy of 94% (95% CIs 81.34, 99.32, p < 0.001, sensitivity/specificity 90%/100%). CONCLUSIONThe clinical value of the CVS in the context of the differential diagnosis between MS and NMOSD, previously suggested using 7T scanners, is now extended to clinical 3T scanners, thereby making a step towards the use of CVS in clinical practice. CLASSIFICATION OF EVIDENCEThis study provides Class III evidence that the CVS on 3T MRI accurately distinguishes patients with MS from those with seropositive NMOSD.
doi_str_mv 10.1212/WNL.0000000000005256
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METHODSEighteen aquaporin-4-antibody-positive patients with NMOSD, 18 patients with relapsing-remitting MS, and 25 healthy controls underwent 3T MRI. The presence of a central vein in white matter lesions on susceptibility-weighted imaging, defined as a thin hypointense line or a small dot, was recorded. RESULTSThe proportion of lesions with the CVS was higher in MS than NMOSD (80% vs 32%, p &lt; 0.001). A greater proportion of lesions with the CVS predicted the diagnosis of MS, rather than NMOSD (odds ratio 1.10, 95% confidence interval [CI] 1.04 to 1.16, p = 0.001), suggesting that each percent unit increase in the proportion of lesions with the CVS in an individual patient was associated with a 10% increase in the risk of the same patient having MS. If more than 54% of the lesions on any given scan show the CVS, then the patient can be given a diagnosis of MS with an accuracy of 94% (95% CIs 81.34, 99.32, p &lt; 0.001, sensitivity/specificity 90%/100%). CONCLUSIONThe clinical value of the CVS in the context of the differential diagnosis between MS and NMOSD, previously suggested using 7T scanners, is now extended to clinical 3T scanners, thereby making a step towards the use of CVS in clinical practice. CLASSIFICATION OF EVIDENCEThis study provides Class III evidence that the CVS on 3T MRI accurately distinguishes patients with MS from those with seropositive NMOSD.</description><identifier>ISSN: 0028-3878</identifier><identifier>EISSN: 1526-632X</identifier><identifier>DOI: 10.1212/WNL.0000000000005256</identifier><identifier>PMID: 29514948</identifier><language>eng</language><publisher>United States: American Academy of Neurology</publisher><subject>Adult ; Aquaporin 4 - immunology ; Autoantibodies - blood ; Diagnosis, Differential ; Female ; Humans ; Image Interpretation, Computer-Assisted ; Magnetic Resonance Imaging - methods ; Male ; Middle Aged ; Multiple Sclerosis, Relapsing-Remitting - diagnostic imaging ; Neuromyelitis Optica - blood ; Neuromyelitis Optica - diagnostic imaging ; Neuromyelitis Optica - immunology ; Prospective Studies ; White Matter - diagnostic imaging</subject><ispartof>Neurology, 2018-04, Vol.90 (14), p.e1183-e1190</ispartof><rights>2018 American Academy of Neurology</rights><rights>2018 American Academy of Neurology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4026-dd9200ef98340dd583bfed34b2c989f8a0ce77af005faabfb3acd58a1095dd303</citedby><cites>FETCH-LOGICAL-c4026-dd9200ef98340dd583bfed34b2c989f8a0ce77af005faabfb3acd58a1095dd303</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,27931,27932</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29514948$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cortese, Rosa</creatorcontrib><creatorcontrib>Magnollay, Lise</creatorcontrib><creatorcontrib>Tur, Carmen</creatorcontrib><creatorcontrib>Abdel-Aziz, Khaled</creatorcontrib><creatorcontrib>Jacob, Anu</creatorcontrib><creatorcontrib>De Angelis, Floriana</creatorcontrib><creatorcontrib>Yiannakas, Marios C</creatorcontrib><creatorcontrib>Prados, Ferran</creatorcontrib><creatorcontrib>Ourselin, Sebastien</creatorcontrib><creatorcontrib>Yousry, Tarek A</creatorcontrib><creatorcontrib>Barkhof, Frederik</creatorcontrib><creatorcontrib>Ciccarelli, Olga</creatorcontrib><title>Value of the central vein sign at 3T to differentiate MS from seropositive NMOSD</title><title>Neurology</title><addtitle>Neurology</addtitle><description>OBJECTIVETo assess the value of the central vein sign (CVS) on a clinical 3T scanner to distinguish between multiple sclerosis (MS) and neuromyelitis optica spectrum disorder (NMOSD). METHODSEighteen aquaporin-4-antibody-positive patients with NMOSD, 18 patients with relapsing-remitting MS, and 25 healthy controls underwent 3T MRI. The presence of a central vein in white matter lesions on susceptibility-weighted imaging, defined as a thin hypointense line or a small dot, was recorded. RESULTSThe proportion of lesions with the CVS was higher in MS than NMOSD (80% vs 32%, p &lt; 0.001). A greater proportion of lesions with the CVS predicted the diagnosis of MS, rather than NMOSD (odds ratio 1.10, 95% confidence interval [CI] 1.04 to 1.16, p = 0.001), suggesting that each percent unit increase in the proportion of lesions with the CVS in an individual patient was associated with a 10% increase in the risk of the same patient having MS. If more than 54% of the lesions on any given scan show the CVS, then the patient can be given a diagnosis of MS with an accuracy of 94% (95% CIs 81.34, 99.32, p &lt; 0.001, sensitivity/specificity 90%/100%). CONCLUSIONThe clinical value of the CVS in the context of the differential diagnosis between MS and NMOSD, previously suggested using 7T scanners, is now extended to clinical 3T scanners, thereby making a step towards the use of CVS in clinical practice. CLASSIFICATION OF EVIDENCEThis study provides Class III evidence that the CVS on 3T MRI accurately distinguishes patients with MS from those with seropositive NMOSD.</description><subject>Adult</subject><subject>Aquaporin 4 - immunology</subject><subject>Autoantibodies - blood</subject><subject>Diagnosis, Differential</subject><subject>Female</subject><subject>Humans</subject><subject>Image Interpretation, Computer-Assisted</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Multiple Sclerosis, Relapsing-Remitting - diagnostic imaging</subject><subject>Neuromyelitis Optica - blood</subject><subject>Neuromyelitis Optica - diagnostic imaging</subject><subject>Neuromyelitis Optica - immunology</subject><subject>Prospective Studies</subject><subject>White Matter - diagnostic imaging</subject><issn>0028-3878</issn><issn>1526-632X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMlOwzAQQC0EoqXwBwj5yCXFSxbniNilLkgtyy1y4jENpHWxnVb8PUYtCHFgLnOYN9tD6JiSPmWUnT2NBn3yKxKWpDuoSxOWRilnz7uoSwgTEReZ6KAD514JCcUs30cdlic0zmPRRfePsmkBG439DHAFC29lg1dQL7CrXxZYesyn2Busaq3BhnotPeDhBGtr5tiBNUvjal-vAI-G48nlIdrTsnFwtM099HB9Nb24jQbjm7uL80FUxSRcqFTOCAGdCx4TpRLBSw2KxyWrcpFrIUkFWSZ1-EtLWeqSyypQkpI8UYoT3kOnm7lLa95bcL6Y166CppELMK0rGAmWaJbSNKDxBq2scc6CLpa2nkv7UVBSfLksgsvir8vQdrLd0JZzUD9N3_ICIDbA2jQerHtr2jXYYgay8bP_Z38CQ-Z_1g</recordid><startdate>20180403</startdate><enddate>20180403</enddate><creator>Cortese, Rosa</creator><creator>Magnollay, Lise</creator><creator>Tur, Carmen</creator><creator>Abdel-Aziz, Khaled</creator><creator>Jacob, Anu</creator><creator>De Angelis, Floriana</creator><creator>Yiannakas, Marios C</creator><creator>Prados, Ferran</creator><creator>Ourselin, Sebastien</creator><creator>Yousry, Tarek A</creator><creator>Barkhof, Frederik</creator><creator>Ciccarelli, Olga</creator><general>American Academy of Neurology</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>7X8</scope></search><sort><creationdate>20180403</creationdate><title>Value of the central vein sign at 3T to differentiate MS from seropositive NMOSD</title><author>Cortese, Rosa ; Magnollay, Lise ; Tur, Carmen ; Abdel-Aziz, Khaled ; Jacob, Anu ; De Angelis, Floriana ; Yiannakas, Marios C ; Prados, Ferran ; Ourselin, Sebastien ; Yousry, Tarek A ; Barkhof, Frederik ; Ciccarelli, Olga</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4026-dd9200ef98340dd583bfed34b2c989f8a0ce77af005faabfb3acd58a1095dd303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adult</topic><topic>Aquaporin 4 - immunology</topic><topic>Autoantibodies - blood</topic><topic>Diagnosis, Differential</topic><topic>Female</topic><topic>Humans</topic><topic>Image Interpretation, Computer-Assisted</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Multiple Sclerosis, Relapsing-Remitting - diagnostic imaging</topic><topic>Neuromyelitis Optica - blood</topic><topic>Neuromyelitis Optica - diagnostic imaging</topic><topic>Neuromyelitis Optica - immunology</topic><topic>Prospective Studies</topic><topic>White Matter - diagnostic imaging</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cortese, Rosa</creatorcontrib><creatorcontrib>Magnollay, Lise</creatorcontrib><creatorcontrib>Tur, Carmen</creatorcontrib><creatorcontrib>Abdel-Aziz, Khaled</creatorcontrib><creatorcontrib>Jacob, Anu</creatorcontrib><creatorcontrib>De Angelis, Floriana</creatorcontrib><creatorcontrib>Yiannakas, Marios C</creatorcontrib><creatorcontrib>Prados, Ferran</creatorcontrib><creatorcontrib>Ourselin, Sebastien</creatorcontrib><creatorcontrib>Yousry, Tarek A</creatorcontrib><creatorcontrib>Barkhof, Frederik</creatorcontrib><creatorcontrib>Ciccarelli, Olga</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cortese, Rosa</au><au>Magnollay, Lise</au><au>Tur, Carmen</au><au>Abdel-Aziz, Khaled</au><au>Jacob, Anu</au><au>De Angelis, Floriana</au><au>Yiannakas, Marios C</au><au>Prados, Ferran</au><au>Ourselin, Sebastien</au><au>Yousry, Tarek A</au><au>Barkhof, Frederik</au><au>Ciccarelli, Olga</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Value of the central vein sign at 3T to differentiate MS from seropositive NMOSD</atitle><jtitle>Neurology</jtitle><addtitle>Neurology</addtitle><date>2018-04-03</date><risdate>2018</risdate><volume>90</volume><issue>14</issue><spage>e1183</spage><epage>e1190</epage><pages>e1183-e1190</pages><issn>0028-3878</issn><eissn>1526-632X</eissn><abstract>OBJECTIVETo assess the value of the central vein sign (CVS) on a clinical 3T scanner to distinguish between multiple sclerosis (MS) and neuromyelitis optica spectrum disorder (NMOSD). METHODSEighteen aquaporin-4-antibody-positive patients with NMOSD, 18 patients with relapsing-remitting MS, and 25 healthy controls underwent 3T MRI. The presence of a central vein in white matter lesions on susceptibility-weighted imaging, defined as a thin hypointense line or a small dot, was recorded. RESULTSThe proportion of lesions with the CVS was higher in MS than NMOSD (80% vs 32%, p &lt; 0.001). A greater proportion of lesions with the CVS predicted the diagnosis of MS, rather than NMOSD (odds ratio 1.10, 95% confidence interval [CI] 1.04 to 1.16, p = 0.001), suggesting that each percent unit increase in the proportion of lesions with the CVS in an individual patient was associated with a 10% increase in the risk of the same patient having MS. If more than 54% of the lesions on any given scan show the CVS, then the patient can be given a diagnosis of MS with an accuracy of 94% (95% CIs 81.34, 99.32, p &lt; 0.001, sensitivity/specificity 90%/100%). CONCLUSIONThe clinical value of the CVS in the context of the differential diagnosis between MS and NMOSD, previously suggested using 7T scanners, is now extended to clinical 3T scanners, thereby making a step towards the use of CVS in clinical practice. CLASSIFICATION OF EVIDENCEThis study provides Class III evidence that the CVS on 3T MRI accurately distinguishes patients with MS from those with seropositive NMOSD.</abstract><cop>United States</cop><pub>American Academy of Neurology</pub><pmid>29514948</pmid><doi>10.1212/WNL.0000000000005256</doi><oa>free_for_read</oa></addata></record>
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source MEDLINE; Journals@Ovid Complete; Alma/SFX Local Collection
subjects Adult
Aquaporin 4 - immunology
Autoantibodies - blood
Diagnosis, Differential
Female
Humans
Image Interpretation, Computer-Assisted
Magnetic Resonance Imaging - methods
Male
Middle Aged
Multiple Sclerosis, Relapsing-Remitting - diagnostic imaging
Neuromyelitis Optica - blood
Neuromyelitis Optica - diagnostic imaging
Neuromyelitis Optica - immunology
Prospective Studies
White Matter - diagnostic imaging
title Value of the central vein sign at 3T to differentiate MS from seropositive NMOSD
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