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Thickness of retinal nerve fiber layer correlates with disease duration in parallel with corticospinal tract dysfunction in untreated multiple sclerosis
Optical coherence tomography (OCT) is an emerging clinical and research measure of retinal nerve fiber layer (RNFL) loss in multiple sclerosis (MS) and may reflect neurodegeneration. Few studies capture the effect of disease duration on the RNFL in subjects without exposure to disease-modulating the...
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Published in: | Journal of rehabilitation research and development 2009-01, Vol.46 (5), p.633-642 |
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creator | Spain, Rebecca I Maltenfort, Mitchell Sergott, Robert C Leist, Thomas P |
description | Optical coherence tomography (OCT) is an emerging clinical and research measure of retinal nerve fiber layer (RNFL) loss in multiple sclerosis (MS) and may reflect neurodegeneration. Few studies capture the effect of disease duration on the RNFL in subjects without exposure to disease-modulating therapies.We assessed the relationship of RNFL loss with disease duration in subjects with untreated MS and determined if such loss paralleled corticospinal tract dysfunction in MS.Subjects underwent OCT (n = 52) and visual testing (n = 60). Either they were either examined or they participated in a validated telephone interview so we could determine their Expanded Disability Status Scale (EDSS) scores.Both RNFL thickness (Spearman r(s) = -0.47, p < 0.001) and EDSS scores ( r(s) = 0.51, p < 0.001) correlated with disease duration. RNFL thickness correlated with EDSS scores (r(s) = -0.43, p < 0.001).In conclusion, RNFL loss correlates with disease duration and EDSS scores in subjects with untreated MS, indicating that OCT may capture neurodegeneration. |
doi_str_mv | 10.1682/JRRD.2008.11.0156 |
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Few studies capture the effect of disease duration on the RNFL in subjects without exposure to disease-modulating therapies.We assessed the relationship of RNFL loss with disease duration in subjects with untreated MS and determined if such loss paralleled corticospinal tract dysfunction in MS.Subjects underwent OCT (n = 52) and visual testing (n = 60). Either they were either examined or they participated in a validated telephone interview so we could determine their Expanded Disability Status Scale (EDSS) scores.Both RNFL thickness (Spearman r(s) = -0.47, p < 0.001) and EDSS scores ( r(s) = 0.51, p < 0.001) correlated with disease duration. RNFL thickness correlated with EDSS scores (r(s) = -0.43, p < 0.001).In conclusion, RNFL loss correlates with disease duration and EDSS scores in subjects with untreated MS, indicating that OCT may capture neurodegeneration.</description><identifier>ISSN: 0748-7711</identifier><identifier>EISSN: 1938-1352</identifier><identifier>DOI: 10.1682/JRRD.2008.11.0156</identifier><identifier>PMID: 19882496</identifier><identifier>CODEN: JRRDDB</identifier><language>eng</language><publisher>United States: Department of Veterans Affairs</publisher><subject>Adult ; Aged ; Clinical trials ; Complications and side effects ; CT imaging ; Degeneration ; Disease ; Disease Progression ; Female ; Humans ; Male ; Medical imaging ; Middle Aged ; Multiple sclerosis ; Multiple Sclerosis - diagnosis ; Multiple Sclerosis - physiopathology ; Nervous system ; Neurofibrils ; Optic Nerve - pathology ; Optic Nerve - physiopathology ; Physiological aspects ; Pyramidal Tracts - physiopathology ; Sample size ; Studies ; Time Factors ; Tomography, Optical Coherence ; Young Adult</subject><ispartof>Journal of rehabilitation research and development, 2009-01, Vol.46 (5), p.633-642</ispartof><rights>COPYRIGHT 2009 Department of Veterans Affairs</rights><rights>Copyright Superintendent of Documents 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19882496$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Spain, Rebecca I</creatorcontrib><creatorcontrib>Maltenfort, Mitchell</creatorcontrib><creatorcontrib>Sergott, Robert C</creatorcontrib><creatorcontrib>Leist, Thomas P</creatorcontrib><title>Thickness of retinal nerve fiber layer correlates with disease duration in parallel with corticospinal tract dysfunction in untreated multiple sclerosis</title><title>Journal of rehabilitation research and development</title><addtitle>J Rehabil Res Dev</addtitle><description>Optical coherence tomography (OCT) is an emerging clinical and research measure of retinal nerve fiber layer (RNFL) loss in multiple sclerosis (MS) and may reflect neurodegeneration. Few studies capture the effect of disease duration on the RNFL in subjects without exposure to disease-modulating therapies.We assessed the relationship of RNFL loss with disease duration in subjects with untreated MS and determined if such loss paralleled corticospinal tract dysfunction in MS.Subjects underwent OCT (n = 52) and visual testing (n = 60). Either they were either examined or they participated in a validated telephone interview so we could determine their Expanded Disability Status Scale (EDSS) scores.Both RNFL thickness (Spearman r(s) = -0.47, p < 0.001) and EDSS scores ( r(s) = 0.51, p < 0.001) correlated with disease duration. RNFL thickness correlated with EDSS scores (r(s) = -0.43, p < 0.001).In conclusion, RNFL loss correlates with disease duration and EDSS scores in subjects with untreated MS, indicating that OCT may capture neurodegeneration.</description><subject>Adult</subject><subject>Aged</subject><subject>Clinical trials</subject><subject>Complications and side effects</subject><subject>CT imaging</subject><subject>Degeneration</subject><subject>Disease</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Medical imaging</subject><subject>Middle Aged</subject><subject>Multiple sclerosis</subject><subject>Multiple Sclerosis - diagnosis</subject><subject>Multiple Sclerosis - physiopathology</subject><subject>Nervous system</subject><subject>Neurofibrils</subject><subject>Optic Nerve - pathology</subject><subject>Optic Nerve - physiopathology</subject><subject>Physiological aspects</subject><subject>Pyramidal Tracts - physiopathology</subject><subject>Sample size</subject><subject>Studies</subject><subject>Time Factors</subject><subject>Tomography, Optical Coherence</subject><subject>Young Adult</subject><issn>0748-7711</issn><issn>1938-1352</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp9kU1rFTEUhoMo9lr9AW4kuNDVjDnJZDJZltZPCkKp6yE3OdOmZjLXJKPcf-LPNdfbblxIIIHD8z5w3hDyElgL_cDffbm6umg5Y0ML0DKQ_SOyAS2GBoTkj8mGqW5olAI4Ic9yvmOMccHhKTkBPQy80_2G_L6-9fZ7xJzpMtGExUcTaMT0E-nkt5hoMPt62yUlDKZgpr98uaXOZzQZqVuTKX6J1Ee6M8mEgOFI1ETxdsm7v8aSjC3U7fO0RvsQWGNJWJ2OzmsofheQZhswLdnn5-TJZELGF_fvKfn24f31-afm8uvHz-dnl82NYKo02FttZN1KdwPvldDKQr-1kxuUUWiZQ-5k7zrBNbdcVkJaxSZrtdSdUVtxSt4evbu0_Fgxl3H22WIIJuKy5lGJDkBzrSr55r8kB-hVx2UFX_8D3i1rqi0cGMkHCR2vUHuEbkzA0cdpOVRUj8O51hZx8nV-xqEDJkAerK_uret2Rjfukp9N2o8Pfyn-AFrRo-A</recordid><startdate>20090101</startdate><enddate>20090101</enddate><creator>Spain, Rebecca I</creator><creator>Maltenfort, Mitchell</creator><creator>Sergott, Robert C</creator><creator>Leist, Thomas P</creator><general>Department of Veterans Affairs</general><general>Superintendent of Documents</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>4T-</scope><scope>7QO</scope><scope>7RV</scope><scope>7TK</scope><scope>7TS</scope><scope>7X7</scope><scope>7XB</scope><scope>88C</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope></search><sort><creationdate>20090101</creationdate><title>Thickness of retinal nerve fiber layer correlates with disease duration in parallel with corticospinal tract dysfunction in untreated multiple sclerosis</title><author>Spain, Rebecca I ; Maltenfort, Mitchell ; Sergott, Robert C ; Leist, Thomas P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g307t-e6c9a5321948267397c16bcfd87a7ec0de2d56d43292c256735c70fcc9594a7b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Clinical trials</topic><topic>Complications and side effects</topic><topic>CT imaging</topic><topic>Degeneration</topic><topic>Disease</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Medical imaging</topic><topic>Middle Aged</topic><topic>Multiple sclerosis</topic><topic>Multiple Sclerosis - diagnosis</topic><topic>Multiple Sclerosis - physiopathology</topic><topic>Nervous system</topic><topic>Neurofibrils</topic><topic>Optic Nerve - pathology</topic><topic>Optic Nerve - physiopathology</topic><topic>Physiological aspects</topic><topic>Pyramidal Tracts - physiopathology</topic><topic>Sample size</topic><topic>Studies</topic><topic>Time Factors</topic><topic>Tomography, Optical Coherence</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Spain, Rebecca I</creatorcontrib><creatorcontrib>Maltenfort, Mitchell</creatorcontrib><creatorcontrib>Sergott, Robert C</creatorcontrib><creatorcontrib>Leist, Thomas P</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Physical Education Index</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>eLibrary</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>Research Library (ProQuest Database)</collection><collection>Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of rehabilitation research and development</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Spain, Rebecca I</au><au>Maltenfort, Mitchell</au><au>Sergott, Robert C</au><au>Leist, Thomas P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Thickness of retinal nerve fiber layer correlates with disease duration in parallel with corticospinal tract dysfunction in untreated multiple sclerosis</atitle><jtitle>Journal of rehabilitation research and development</jtitle><addtitle>J Rehabil Res Dev</addtitle><date>2009-01-01</date><risdate>2009</risdate><volume>46</volume><issue>5</issue><spage>633</spage><epage>642</epage><pages>633-642</pages><issn>0748-7711</issn><eissn>1938-1352</eissn><coden>JRRDDB</coden><abstract>Optical coherence tomography (OCT) is an emerging clinical and research measure of retinal nerve fiber layer (RNFL) loss in multiple sclerosis (MS) and may reflect neurodegeneration. Few studies capture the effect of disease duration on the RNFL in subjects without exposure to disease-modulating therapies.We assessed the relationship of RNFL loss with disease duration in subjects with untreated MS and determined if such loss paralleled corticospinal tract dysfunction in MS.Subjects underwent OCT (n = 52) and visual testing (n = 60). Either they were either examined or they participated in a validated telephone interview so we could determine their Expanded Disability Status Scale (EDSS) scores.Both RNFL thickness (Spearman r(s) = -0.47, p < 0.001) and EDSS scores ( r(s) = 0.51, p < 0.001) correlated with disease duration. RNFL thickness correlated with EDSS scores (r(s) = -0.43, p < 0.001).In conclusion, RNFL loss correlates with disease duration and EDSS scores in subjects with untreated MS, indicating that OCT may capture neurodegeneration.</abstract><cop>United States</cop><pub>Department of Veterans Affairs</pub><pmid>19882496</pmid><doi>10.1682/JRRD.2008.11.0156</doi><tpages>10</tpages></addata></record> |
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subjects | Adult Aged Clinical trials Complications and side effects CT imaging Degeneration Disease Disease Progression Female Humans Male Medical imaging Middle Aged Multiple sclerosis Multiple Sclerosis - diagnosis Multiple Sclerosis - physiopathology Nervous system Neurofibrils Optic Nerve - pathology Optic Nerve - physiopathology Physiological aspects Pyramidal Tracts - physiopathology Sample size Studies Time Factors Tomography, Optical Coherence Young Adult |
title | Thickness of retinal nerve fiber layer correlates with disease duration in parallel with corticospinal tract dysfunction in untreated multiple sclerosis |
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