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Length of optic nerve double inversion recovery hypersignal is associated with retinal axonal loss
Objectives: To assess the association between optic nerve double inversion recovery (DIR) hypersignal length and retinal axonal loss in neuroinflammatory diseases affecting optic nerves. Methods: We recruited patients previously affected (> 6 months) by a clinical episode of optic neuritis (ON)....
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Published in: | Multiple sclerosis 2016-04, Vol.22 (5), p.649-658 |
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container_title | Multiple sclerosis |
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creator | Hadhoum, N Hodel, J Defoort-Dhellemmes, S Duhamel, A Drumez, E Zéphir, H Pruvo, JP Leclerc, X Vermersch, P Outteryck, O |
description | Objectives:
To assess the association between optic nerve double inversion recovery (DIR) hypersignal length and retinal axonal loss in neuroinflammatory diseases affecting optic nerves.
Methods:
We recruited patients previously affected (> 6 months) by a clinical episode of optic neuritis (ON). We had 25 multiple sclerosis (MS) patients, eight neuromyelitis optica spectrum disorder (NMOSD) patients and two patients suffering from idiopathic caused ON undergo brain magnetic resonance imaging (MRI); including a 3-dimensional (3D) DIR sequence, optical coherence tomography (OCT) examination and visual disability evaluation. Evaluation criteria were retinal thickness/volume, optic nerve DIR hypersignal length and high/low contrast vision acuity.
Results:
In the whole cohort, we found good associations (< 0.0001) between optic nerve DIR hypersignal length, peripapillary retinal nerve fiber layer thickness, inner macular layers volumes, and visual disability. We found subclinical radiological optic nerve involvement in 38.5% of non-ON MS eyes.
Conclusions:
Optic nerve DIR hypersignal length may be a biomarker for retinal axonal loss, easily applicable in routine and research on new anti-inflammatory or neuroprotective drug evaluation. Detection of subclinical ON with 3D-DIR in a non-negligible proportion of MS patients argues in favor of optic nerve imaging in future OCT MS studies, in order to achieve a better understanding of retinal axonal loss in non-ON eyes. |
doi_str_mv | 10.1177/1352458515598021 |
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To assess the association between optic nerve double inversion recovery (DIR) hypersignal length and retinal axonal loss in neuroinflammatory diseases affecting optic nerves.
Methods:
We recruited patients previously affected (> 6 months) by a clinical episode of optic neuritis (ON). We had 25 multiple sclerosis (MS) patients, eight neuromyelitis optica spectrum disorder (NMOSD) patients and two patients suffering from idiopathic caused ON undergo brain magnetic resonance imaging (MRI); including a 3-dimensional (3D) DIR sequence, optical coherence tomography (OCT) examination and visual disability evaluation. Evaluation criteria were retinal thickness/volume, optic nerve DIR hypersignal length and high/low contrast vision acuity.
Results:
In the whole cohort, we found good associations (< 0.0001) between optic nerve DIR hypersignal length, peripapillary retinal nerve fiber layer thickness, inner macular layers volumes, and visual disability. We found subclinical radiological optic nerve involvement in 38.5% of non-ON MS eyes.
Conclusions:
Optic nerve DIR hypersignal length may be a biomarker for retinal axonal loss, easily applicable in routine and research on new anti-inflammatory or neuroprotective drug evaluation. Detection of subclinical ON with 3D-DIR in a non-negligible proportion of MS patients argues in favor of optic nerve imaging in future OCT MS studies, in order to achieve a better understanding of retinal axonal loss in non-ON eyes.</description><identifier>ISSN: 1352-4585</identifier><identifier>EISSN: 1477-0970</identifier><identifier>DOI: 10.1177/1352458515598021</identifier><identifier>PMID: 26227005</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Acuity ; Adult ; Female ; Humans ; Inflammation ; Magnetic resonance imaging ; Male ; Medical imaging ; Middle Aged ; Multiple sclerosis ; Multiple Sclerosis - pathology ; Nerve Fibers - pathology ; Neuritis ; Neuroimaging ; Neuromyelitis ; Neuromyelitis Optica - pathology ; Neuroprotection ; NMR ; Nuclear magnetic resonance ; Optic nerve ; Optic Nerve - pathology ; Optic neuritis ; Optic Neuritis - diagnosis ; Optic Neuritis - pathology ; Retina ; Retina - pathology ; Retinal Ganglion Cells - pathology ; Tomography, Optical Coherence - methods</subject><ispartof>Multiple sclerosis, 2016-04, Vol.22 (5), p.649-658</ispartof><rights>The Author(s), 2015</rights><rights>The Author(s), 2015.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c398t-f74adea05bdc089fc165dd841a1b43e8d6c96057204effd0c30f451d542dd8fb3</citedby><cites>FETCH-LOGICAL-c398t-f74adea05bdc089fc165dd841a1b43e8d6c96057204effd0c30f451d542dd8fb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925,79236</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26227005$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hadhoum, N</creatorcontrib><creatorcontrib>Hodel, J</creatorcontrib><creatorcontrib>Defoort-Dhellemmes, S</creatorcontrib><creatorcontrib>Duhamel, A</creatorcontrib><creatorcontrib>Drumez, E</creatorcontrib><creatorcontrib>Zéphir, H</creatorcontrib><creatorcontrib>Pruvo, JP</creatorcontrib><creatorcontrib>Leclerc, X</creatorcontrib><creatorcontrib>Vermersch, P</creatorcontrib><creatorcontrib>Outteryck, O</creatorcontrib><title>Length of optic nerve double inversion recovery hypersignal is associated with retinal axonal loss</title><title>Multiple sclerosis</title><addtitle>Mult Scler</addtitle><description>Objectives:
To assess the association between optic nerve double inversion recovery (DIR) hypersignal length and retinal axonal loss in neuroinflammatory diseases affecting optic nerves.
Methods:
We recruited patients previously affected (> 6 months) by a clinical episode of optic neuritis (ON). We had 25 multiple sclerosis (MS) patients, eight neuromyelitis optica spectrum disorder (NMOSD) patients and two patients suffering from idiopathic caused ON undergo brain magnetic resonance imaging (MRI); including a 3-dimensional (3D) DIR sequence, optical coherence tomography (OCT) examination and visual disability evaluation. Evaluation criteria were retinal thickness/volume, optic nerve DIR hypersignal length and high/low contrast vision acuity.
Results:
In the whole cohort, we found good associations (< 0.0001) between optic nerve DIR hypersignal length, peripapillary retinal nerve fiber layer thickness, inner macular layers volumes, and visual disability. We found subclinical radiological optic nerve involvement in 38.5% of non-ON MS eyes.
Conclusions:
Optic nerve DIR hypersignal length may be a biomarker for retinal axonal loss, easily applicable in routine and research on new anti-inflammatory or neuroprotective drug evaluation. Detection of subclinical ON with 3D-DIR in a non-negligible proportion of MS patients argues in favor of optic nerve imaging in future OCT MS studies, in order to achieve a better understanding of retinal axonal loss in non-ON eyes.</description><subject>Acuity</subject><subject>Adult</subject><subject>Female</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Magnetic resonance imaging</subject><subject>Male</subject><subject>Medical imaging</subject><subject>Middle Aged</subject><subject>Multiple sclerosis</subject><subject>Multiple Sclerosis - pathology</subject><subject>Nerve Fibers - pathology</subject><subject>Neuritis</subject><subject>Neuroimaging</subject><subject>Neuromyelitis</subject><subject>Neuromyelitis Optica - pathology</subject><subject>Neuroprotection</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Optic nerve</subject><subject>Optic Nerve - pathology</subject><subject>Optic neuritis</subject><subject>Optic Neuritis - diagnosis</subject><subject>Optic Neuritis - pathology</subject><subject>Retina</subject><subject>Retina - pathology</subject><subject>Retinal Ganglion Cells - pathology</subject><subject>Tomography, Optical Coherence - methods</subject><issn>1352-4585</issn><issn>1477-0970</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqNkc1r3DAQxUVJaD7ae05F0EsubkeyZMnHEvIFC700ZyNLo42C19pKdpr97yuzSSiBQk4zzPvNG4ZHyBmDb4wp9Z3VkgupJZOy1cDZB3LMhFIVtAoOSl_katGPyEnODwCgVC0_kiPecK4A5DHpVziup3saPY3bKVg6YnpE6uLcD0jD-IgphzjShDaWfkfvd9tltB7NQEOmJudog5nQ0T-h-CScwiKZp7iUIeb8iRx6M2T8_FxPyd3V5a-Lm2r18_r24seqsnWrp8orYRwakL2zoFtvWSOd04IZ1osatWts24BUHAR678DW4IVkTgpeMN_Xp-R877tN8feMeeo2IVscBjNinHPHlAbJpWzad6CqAd1oXhf06xv0Ic6p_FaoFloua61FoWBP2VQ-Tui7bQobk3Ydg26JqnsbVVn58mw89xt0rwsv2RSg2gPZrPGfq_8z_Av2c5u1</recordid><startdate>201604</startdate><enddate>201604</enddate><creator>Hadhoum, N</creator><creator>Hodel, J</creator><creator>Defoort-Dhellemmes, S</creator><creator>Duhamel, A</creator><creator>Drumez, E</creator><creator>Zéphir, H</creator><creator>Pruvo, JP</creator><creator>Leclerc, X</creator><creator>Vermersch, P</creator><creator>Outteryck, O</creator><general>SAGE Publications</general><general>Sage Publications Ltd</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>7T5</scope><scope>7TK</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201604</creationdate><title>Length of optic nerve double inversion recovery hypersignal is associated with retinal axonal loss</title><author>Hadhoum, N ; Hodel, J ; Defoort-Dhellemmes, S ; Duhamel, A ; Drumez, E ; Zéphir, H ; Pruvo, JP ; Leclerc, X ; Vermersch, P ; Outteryck, O</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c398t-f74adea05bdc089fc165dd841a1b43e8d6c96057204effd0c30f451d542dd8fb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Acuity</topic><topic>Adult</topic><topic>Female</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Magnetic resonance imaging</topic><topic>Male</topic><topic>Medical imaging</topic><topic>Middle Aged</topic><topic>Multiple sclerosis</topic><topic>Multiple Sclerosis - pathology</topic><topic>Nerve Fibers - pathology</topic><topic>Neuritis</topic><topic>Neuroimaging</topic><topic>Neuromyelitis</topic><topic>Neuromyelitis Optica - pathology</topic><topic>Neuroprotection</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Optic nerve</topic><topic>Optic Nerve - pathology</topic><topic>Optic neuritis</topic><topic>Optic Neuritis - diagnosis</topic><topic>Optic Neuritis - pathology</topic><topic>Retina</topic><topic>Retina - pathology</topic><topic>Retinal Ganglion Cells - pathology</topic><topic>Tomography, Optical Coherence - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hadhoum, N</creatorcontrib><creatorcontrib>Hodel, J</creatorcontrib><creatorcontrib>Defoort-Dhellemmes, S</creatorcontrib><creatorcontrib>Duhamel, A</creatorcontrib><creatorcontrib>Drumez, E</creatorcontrib><creatorcontrib>Zéphir, H</creatorcontrib><creatorcontrib>Pruvo, JP</creatorcontrib><creatorcontrib>Leclerc, X</creatorcontrib><creatorcontrib>Vermersch, P</creatorcontrib><creatorcontrib>Outteryck, O</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Multiple sclerosis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hadhoum, N</au><au>Hodel, J</au><au>Defoort-Dhellemmes, S</au><au>Duhamel, A</au><au>Drumez, E</au><au>Zéphir, H</au><au>Pruvo, JP</au><au>Leclerc, X</au><au>Vermersch, P</au><au>Outteryck, O</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Length of optic nerve double inversion recovery hypersignal is associated with retinal axonal loss</atitle><jtitle>Multiple sclerosis</jtitle><addtitle>Mult Scler</addtitle><date>2016-04</date><risdate>2016</risdate><volume>22</volume><issue>5</issue><spage>649</spage><epage>658</epage><pages>649-658</pages><issn>1352-4585</issn><eissn>1477-0970</eissn><abstract>Objectives:
To assess the association between optic nerve double inversion recovery (DIR) hypersignal length and retinal axonal loss in neuroinflammatory diseases affecting optic nerves.
Methods:
We recruited patients previously affected (> 6 months) by a clinical episode of optic neuritis (ON). We had 25 multiple sclerosis (MS) patients, eight neuromyelitis optica spectrum disorder (NMOSD) patients and two patients suffering from idiopathic caused ON undergo brain magnetic resonance imaging (MRI); including a 3-dimensional (3D) DIR sequence, optical coherence tomography (OCT) examination and visual disability evaluation. Evaluation criteria were retinal thickness/volume, optic nerve DIR hypersignal length and high/low contrast vision acuity.
Results:
In the whole cohort, we found good associations (< 0.0001) between optic nerve DIR hypersignal length, peripapillary retinal nerve fiber layer thickness, inner macular layers volumes, and visual disability. We found subclinical radiological optic nerve involvement in 38.5% of non-ON MS eyes.
Conclusions:
Optic nerve DIR hypersignal length may be a biomarker for retinal axonal loss, easily applicable in routine and research on new anti-inflammatory or neuroprotective drug evaluation. Detection of subclinical ON with 3D-DIR in a non-negligible proportion of MS patients argues in favor of optic nerve imaging in future OCT MS studies, in order to achieve a better understanding of retinal axonal loss in non-ON eyes.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>26227005</pmid><doi>10.1177/1352458515598021</doi><tpages>10</tpages></addata></record> |
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subjects | Acuity Adult Female Humans Inflammation Magnetic resonance imaging Male Medical imaging Middle Aged Multiple sclerosis Multiple Sclerosis - pathology Nerve Fibers - pathology Neuritis Neuroimaging Neuromyelitis Neuromyelitis Optica - pathology Neuroprotection NMR Nuclear magnetic resonance Optic nerve Optic Nerve - pathology Optic neuritis Optic Neuritis - diagnosis Optic Neuritis - pathology Retina Retina - pathology Retinal Ganglion Cells - pathology Tomography, Optical Coherence - methods |
title | Length of optic nerve double inversion recovery hypersignal is associated with retinal axonal loss |
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