High resolution spectral domain optical coherence tomography (SD-OCT) in multiple sclerosis: the first follow up study over two years

"Non-invasive, faster and less expensive than MRI" and "the eye is a window to the brain" are recent slogans promoting optical coherence tomography (OCT) as a new surrogate marker in multiple sclerosis (MS). Indeed, OCT allows for the first time a non-invasive visualization of ax...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:PloS one 2011-05, Vol.6 (5), p.e19843-e19843
Hauptverfasser: Serbecic, Nermin, Aboul-Enein, Fahmy, Beutelspacher, Sven C, Vass, Clemens, Kristoferitsch, Wolfgang, Lassmann, Hans, Reitner, Andreas, Schmidt-Erfurth, Ursula
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page e19843
container_issue 5
container_start_page e19843
container_title PloS one
container_volume 6
creator Serbecic, Nermin
Aboul-Enein, Fahmy
Beutelspacher, Sven C
Vass, Clemens
Kristoferitsch, Wolfgang
Lassmann, Hans
Reitner, Andreas
Schmidt-Erfurth, Ursula
description "Non-invasive, faster and less expensive than MRI" and "the eye is a window to the brain" are recent slogans promoting optical coherence tomography (OCT) as a new surrogate marker in multiple sclerosis (MS). Indeed, OCT allows for the first time a non-invasive visualization of axons of the central nervous system (CNS). Reduction of retina nerve fibre layer (RNFL) thickness was suggested to correlate with disease activity and duration. However, several issues are unclear: Do a few million axons, which build up both optic nerves, really resemble billions of CNS neurons? Does global CNS damage really result in global RNFL reduction? And if so, does global RNFL reduction really exist in all MS patients, and follow a slowly but steadily ongoing pattern? How can these (hypothesized) subtle global RNFL changes be reliably measured and separated from the rather gross RNFL changes caused by optic neuritis? Before generally being accepted, this interpretation needs further critical and objective validation. We prospectively studied 37 MS patients with relapsing remitting (n = 27) and secondary progressive (n = 10) course on two occasions with a median interval of 22.4±0.5 months [range 19-27]. We used the high resolution spectral domain (SD-)OCT with the Spectralis 3.5 mm circle scan protocol with locked reference images and eye tracking mode. Patients with an attack of optic neuritis within 12 months prior to the onset of the study were excluded. Although the disease was highly active over the observation period in more than half of the included relapsing remitting MS patients (19 patients/32 relapses) and the initial RNFL pattern showed a broad range, from normal to markedly reduced thickness, no significant changes between baseline and follow-up examinations could be detected. These results show that caution is required when using OCT for monitoring disease activity and global axonal injury in MS.
doi_str_mv 10.1371/journal.pone.0019843
format Article
fullrecord <record><control><sourceid>gale_plos_</sourceid><recordid>TN_cdi_plos_journals_1299027193</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A476891544</galeid><doaj_id>oai_doaj_org_article_4b2e5cf113b6442c899b43764512a137</doaj_id><sourcerecordid>A476891544</sourcerecordid><originalsourceid>FETCH-LOGICAL-c592t-da491fb8469d725268c48afd7b9ac69cf6b80b8e8a286dad9995c64333acd1033</originalsourceid><addsrcrecordid>eNptUstu1DAUjRCIlsIfILDEAljM4FccmwVSNTxaqVIXlLXlOE7GIydObafVfAD_jaeTVh1UeeHXOedeH5-ieIvgEpEKfdn4KQzKLUc_mCWESHBKnhXHSBC8YBiS54_WR8WrGDcQloQz9rI4woghlBnHxd8z261BMNG7KVk_gDganYJyoPG9sgPwY7I6b7Vfm2AGbUDyve-CGtdb8On398Xl6uozyMB-csmOzoConQk-2vgVpLUBrQ0xgdY752_BNIKYpmYL_I0JIN16sDUqxNfFi1a5aN7M80nx5-ePq9XZ4uLy1_nq9GKhS4HTolFUoLbmlImmwiVmXFOu2qaqhdJM6JbVHNbccIU5a1QjhCg1o4QQpRsECTkp3u91R-ejnB2MEmEhIK6yXRlxvkc0Xm3kGGyvwlZ6ZeXdgQ-dVCE74oykNTalbhEiNaMUay5ETUnFaImwyl-Utb7N1aa6N402w87YA9HDm8GuZedvJIGCZcks8HEWCP56MjHJ3kZtnFOD8VOUnPGKccJYRn74D_n042ZUp3L_dmh9Lqt3mvKUZiWByruqyydQeTSmtzqnrbX5_IBA9wSdvz0G0z48EUG5y-p9M3KXVTlnNdPePbbngXQfTvIPyJfnxQ</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1299027193</pqid></control><display><type>article</type><title>High resolution spectral domain optical coherence tomography (SD-OCT) in multiple sclerosis: the first follow up study over two years</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><source>Public Library of Science (PLoS)</source><creator>Serbecic, Nermin ; Aboul-Enein, Fahmy ; Beutelspacher, Sven C ; Vass, Clemens ; Kristoferitsch, Wolfgang ; Lassmann, Hans ; Reitner, Andreas ; Schmidt-Erfurth, Ursula</creator><creatorcontrib>Serbecic, Nermin ; Aboul-Enein, Fahmy ; Beutelspacher, Sven C ; Vass, Clemens ; Kristoferitsch, Wolfgang ; Lassmann, Hans ; Reitner, Andreas ; Schmidt-Erfurth, Ursula</creatorcontrib><description>"Non-invasive, faster and less expensive than MRI" and "the eye is a window to the brain" are recent slogans promoting optical coherence tomography (OCT) as a new surrogate marker in multiple sclerosis (MS). Indeed, OCT allows for the first time a non-invasive visualization of axons of the central nervous system (CNS). Reduction of retina nerve fibre layer (RNFL) thickness was suggested to correlate with disease activity and duration. However, several issues are unclear: Do a few million axons, which build up both optic nerves, really resemble billions of CNS neurons? Does global CNS damage really result in global RNFL reduction? And if so, does global RNFL reduction really exist in all MS patients, and follow a slowly but steadily ongoing pattern? How can these (hypothesized) subtle global RNFL changes be reliably measured and separated from the rather gross RNFL changes caused by optic neuritis? Before generally being accepted, this interpretation needs further critical and objective validation. We prospectively studied 37 MS patients with relapsing remitting (n = 27) and secondary progressive (n = 10) course on two occasions with a median interval of 22.4±0.5 months [range 19-27]. We used the high resolution spectral domain (SD-)OCT with the Spectralis 3.5 mm circle scan protocol with locked reference images and eye tracking mode. Patients with an attack of optic neuritis within 12 months prior to the onset of the study were excluded. Although the disease was highly active over the observation period in more than half of the included relapsing remitting MS patients (19 patients/32 relapses) and the initial RNFL pattern showed a broad range, from normal to markedly reduced thickness, no significant changes between baseline and follow-up examinations could be detected. These results show that caution is required when using OCT for monitoring disease activity and global axonal injury in MS.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0019843</identifier><identifier>PMID: 21611198</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adolescent ; Adult ; Aquaporins ; Axons ; Biology ; Brain ; Central nervous system ; Coherence ; Demography ; Epidemiology ; Eye ; Eye injuries ; Follow-Up Studies ; Glaucoma ; High resolution ; Humans ; Magnetic resonance imaging ; Medicine ; Middle Aged ; Multiple sclerosis ; Multiple Sclerosis - diagnosis ; Nerve Fibers - pathology ; Nerves ; Neuritis ; Neurology ; Optic neuritis ; Optical Coherence Tomography ; Optics ; Pathology ; Patients ; Reduction ; Retina ; Retina - pathology ; Spectra ; Thickness ; Tomography ; Tomography, Optical Coherence - methods ; Young Adult</subject><ispartof>PloS one, 2011-05, Vol.6 (5), p.e19843-e19843</ispartof><rights>COPYRIGHT 2011 Public Library of Science</rights><rights>2011 Serbecic et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Serbecic et al. 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c592t-da491fb8469d725268c48afd7b9ac69cf6b80b8e8a286dad9995c64333acd1033</citedby><cites>FETCH-LOGICAL-c592t-da491fb8469d725268c48afd7b9ac69cf6b80b8e8a286dad9995c64333acd1033</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3096644/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3096644/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79342,79343</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21611198$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Serbecic, Nermin</creatorcontrib><creatorcontrib>Aboul-Enein, Fahmy</creatorcontrib><creatorcontrib>Beutelspacher, Sven C</creatorcontrib><creatorcontrib>Vass, Clemens</creatorcontrib><creatorcontrib>Kristoferitsch, Wolfgang</creatorcontrib><creatorcontrib>Lassmann, Hans</creatorcontrib><creatorcontrib>Reitner, Andreas</creatorcontrib><creatorcontrib>Schmidt-Erfurth, Ursula</creatorcontrib><title>High resolution spectral domain optical coherence tomography (SD-OCT) in multiple sclerosis: the first follow up study over two years</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>"Non-invasive, faster and less expensive than MRI" and "the eye is a window to the brain" are recent slogans promoting optical coherence tomography (OCT) as a new surrogate marker in multiple sclerosis (MS). Indeed, OCT allows for the first time a non-invasive visualization of axons of the central nervous system (CNS). Reduction of retina nerve fibre layer (RNFL) thickness was suggested to correlate with disease activity and duration. However, several issues are unclear: Do a few million axons, which build up both optic nerves, really resemble billions of CNS neurons? Does global CNS damage really result in global RNFL reduction? And if so, does global RNFL reduction really exist in all MS patients, and follow a slowly but steadily ongoing pattern? How can these (hypothesized) subtle global RNFL changes be reliably measured and separated from the rather gross RNFL changes caused by optic neuritis? Before generally being accepted, this interpretation needs further critical and objective validation. We prospectively studied 37 MS patients with relapsing remitting (n = 27) and secondary progressive (n = 10) course on two occasions with a median interval of 22.4±0.5 months [range 19-27]. We used the high resolution spectral domain (SD-)OCT with the Spectralis 3.5 mm circle scan protocol with locked reference images and eye tracking mode. Patients with an attack of optic neuritis within 12 months prior to the onset of the study were excluded. Although the disease was highly active over the observation period in more than half of the included relapsing remitting MS patients (19 patients/32 relapses) and the initial RNFL pattern showed a broad range, from normal to markedly reduced thickness, no significant changes between baseline and follow-up examinations could be detected. These results show that caution is required when using OCT for monitoring disease activity and global axonal injury in MS.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aquaporins</subject><subject>Axons</subject><subject>Biology</subject><subject>Brain</subject><subject>Central nervous system</subject><subject>Coherence</subject><subject>Demography</subject><subject>Epidemiology</subject><subject>Eye</subject><subject>Eye injuries</subject><subject>Follow-Up Studies</subject><subject>Glaucoma</subject><subject>High resolution</subject><subject>Humans</subject><subject>Magnetic resonance imaging</subject><subject>Medicine</subject><subject>Middle Aged</subject><subject>Multiple sclerosis</subject><subject>Multiple Sclerosis - diagnosis</subject><subject>Nerve Fibers - pathology</subject><subject>Nerves</subject><subject>Neuritis</subject><subject>Neurology</subject><subject>Optic neuritis</subject><subject>Optical Coherence Tomography</subject><subject>Optics</subject><subject>Pathology</subject><subject>Patients</subject><subject>Reduction</subject><subject>Retina</subject><subject>Retina - pathology</subject><subject>Spectra</subject><subject>Thickness</subject><subject>Tomography</subject><subject>Tomography, Optical Coherence - methods</subject><subject>Young Adult</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNptUstu1DAUjRCIlsIfILDEAljM4FccmwVSNTxaqVIXlLXlOE7GIydObafVfAD_jaeTVh1UeeHXOedeH5-ieIvgEpEKfdn4KQzKLUc_mCWESHBKnhXHSBC8YBiS54_WR8WrGDcQloQz9rI4woghlBnHxd8z261BMNG7KVk_gDganYJyoPG9sgPwY7I6b7Vfm2AGbUDyve-CGtdb8On398Xl6uozyMB-csmOzoConQk-2vgVpLUBrQ0xgdY752_BNIKYpmYL_I0JIN16sDUqxNfFi1a5aN7M80nx5-ePq9XZ4uLy1_nq9GKhS4HTolFUoLbmlImmwiVmXFOu2qaqhdJM6JbVHNbccIU5a1QjhCg1o4QQpRsECTkp3u91R-ejnB2MEmEhIK6yXRlxvkc0Xm3kGGyvwlZ6ZeXdgQ-dVCE74oykNTalbhEiNaMUay5ETUnFaImwyl-Utb7N1aa6N402w87YA9HDm8GuZedvJIGCZcks8HEWCP56MjHJ3kZtnFOD8VOUnPGKccJYRn74D_n042ZUp3L_dmh9Lqt3mvKUZiWByruqyydQeTSmtzqnrbX5_IBA9wSdvz0G0z48EUG5y-p9M3KXVTlnNdPePbbngXQfTvIPyJfnxQ</recordid><startdate>20110517</startdate><enddate>20110517</enddate><creator>Serbecic, Nermin</creator><creator>Aboul-Enein, Fahmy</creator><creator>Beutelspacher, Sven C</creator><creator>Vass, Clemens</creator><creator>Kristoferitsch, Wolfgang</creator><creator>Lassmann, Hans</creator><creator>Reitner, Andreas</creator><creator>Schmidt-Erfurth, Ursula</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20110517</creationdate><title>High resolution spectral domain optical coherence tomography (SD-OCT) in multiple sclerosis: the first follow up study over two years</title><author>Serbecic, Nermin ; Aboul-Enein, Fahmy ; Beutelspacher, Sven C ; Vass, Clemens ; Kristoferitsch, Wolfgang ; Lassmann, Hans ; Reitner, Andreas ; Schmidt-Erfurth, Ursula</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c592t-da491fb8469d725268c48afd7b9ac69cf6b80b8e8a286dad9995c64333acd1033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aquaporins</topic><topic>Axons</topic><topic>Biology</topic><topic>Brain</topic><topic>Central nervous system</topic><topic>Coherence</topic><topic>Demography</topic><topic>Epidemiology</topic><topic>Eye</topic><topic>Eye injuries</topic><topic>Follow-Up Studies</topic><topic>Glaucoma</topic><topic>High resolution</topic><topic>Humans</topic><topic>Magnetic resonance imaging</topic><topic>Medicine</topic><topic>Middle Aged</topic><topic>Multiple sclerosis</topic><topic>Multiple Sclerosis - diagnosis</topic><topic>Nerve Fibers - pathology</topic><topic>Nerves</topic><topic>Neuritis</topic><topic>Neurology</topic><topic>Optic neuritis</topic><topic>Optical Coherence Tomography</topic><topic>Optics</topic><topic>Pathology</topic><topic>Patients</topic><topic>Reduction</topic><topic>Retina</topic><topic>Retina - pathology</topic><topic>Spectra</topic><topic>Thickness</topic><topic>Tomography</topic><topic>Tomography, Optical Coherence - methods</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Serbecic, Nermin</creatorcontrib><creatorcontrib>Aboul-Enein, Fahmy</creatorcontrib><creatorcontrib>Beutelspacher, Sven C</creatorcontrib><creatorcontrib>Vass, Clemens</creatorcontrib><creatorcontrib>Kristoferitsch, Wolfgang</creatorcontrib><creatorcontrib>Lassmann, Hans</creatorcontrib><creatorcontrib>Reitner, Andreas</creatorcontrib><creatorcontrib>Schmidt-Erfurth, Ursula</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological &amp; Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies &amp; Aerospace Collection</collection><collection>Agricultural &amp; Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</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>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Meteorological &amp; Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</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>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Serbecic, Nermin</au><au>Aboul-Enein, Fahmy</au><au>Beutelspacher, Sven C</au><au>Vass, Clemens</au><au>Kristoferitsch, Wolfgang</au><au>Lassmann, Hans</au><au>Reitner, Andreas</au><au>Schmidt-Erfurth, Ursula</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High resolution spectral domain optical coherence tomography (SD-OCT) in multiple sclerosis: the first follow up study over two years</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2011-05-17</date><risdate>2011</risdate><volume>6</volume><issue>5</issue><spage>e19843</spage><epage>e19843</epage><pages>e19843-e19843</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>"Non-invasive, faster and less expensive than MRI" and "the eye is a window to the brain" are recent slogans promoting optical coherence tomography (OCT) as a new surrogate marker in multiple sclerosis (MS). Indeed, OCT allows for the first time a non-invasive visualization of axons of the central nervous system (CNS). Reduction of retina nerve fibre layer (RNFL) thickness was suggested to correlate with disease activity and duration. However, several issues are unclear: Do a few million axons, which build up both optic nerves, really resemble billions of CNS neurons? Does global CNS damage really result in global RNFL reduction? And if so, does global RNFL reduction really exist in all MS patients, and follow a slowly but steadily ongoing pattern? How can these (hypothesized) subtle global RNFL changes be reliably measured and separated from the rather gross RNFL changes caused by optic neuritis? Before generally being accepted, this interpretation needs further critical and objective validation. We prospectively studied 37 MS patients with relapsing remitting (n = 27) and secondary progressive (n = 10) course on two occasions with a median interval of 22.4±0.5 months [range 19-27]. We used the high resolution spectral domain (SD-)OCT with the Spectralis 3.5 mm circle scan protocol with locked reference images and eye tracking mode. Patients with an attack of optic neuritis within 12 months prior to the onset of the study were excluded. Although the disease was highly active over the observation period in more than half of the included relapsing remitting MS patients (19 patients/32 relapses) and the initial RNFL pattern showed a broad range, from normal to markedly reduced thickness, no significant changes between baseline and follow-up examinations could be detected. These results show that caution is required when using OCT for monitoring disease activity and global axonal injury in MS.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>21611198</pmid><doi>10.1371/journal.pone.0019843</doi><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1932-6203
ispartof PloS one, 2011-05, Vol.6 (5), p.e19843-e19843
issn 1932-6203
1932-6203
language eng
recordid cdi_plos_journals_1299027193
source MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Free Full-Text Journals in Chemistry; Public Library of Science (PLoS)
subjects Adolescent
Adult
Aquaporins
Axons
Biology
Brain
Central nervous system
Coherence
Demography
Epidemiology
Eye
Eye injuries
Follow-Up Studies
Glaucoma
High resolution
Humans
Magnetic resonance imaging
Medicine
Middle Aged
Multiple sclerosis
Multiple Sclerosis - diagnosis
Nerve Fibers - pathology
Nerves
Neuritis
Neurology
Optic neuritis
Optical Coherence Tomography
Optics
Pathology
Patients
Reduction
Retina
Retina - pathology
Spectra
Thickness
Tomography
Tomography, Optical Coherence - methods
Young Adult
title High resolution spectral domain optical coherence tomography (SD-OCT) in multiple sclerosis: the first follow up study over two years
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T13%3A41%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=High%20resolution%20spectral%20domain%20optical%20coherence%20tomography%20(SD-OCT)%20in%20multiple%20sclerosis:%20the%20first%20follow%20up%20study%20over%20two%20years&rft.jtitle=PloS%20one&rft.au=Serbecic,%20Nermin&rft.date=2011-05-17&rft.volume=6&rft.issue=5&rft.spage=e19843&rft.epage=e19843&rft.pages=e19843-e19843&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0019843&rft_dat=%3Cgale_plos_%3EA476891544%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1299027193&rft_id=info:pmid/21611198&rft_galeid=A476891544&rft_doaj_id=oai_doaj_org_article_4b2e5cf113b6442c899b43764512a137&rfr_iscdi=true