Differences in pupillary light reflex between optic neuritis and ischemic optic neuropathy
To determine the differences in pupillary light reflex (PLR) between the acute and chronic phases of optic neuritis (ON) and nonarteritic anterior ischemic optic neuropathy (NAION). The study included 30 patients with ON and 22 patients with NAION whose PLR were measured by a dynamic pupillometer (P...
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description | To determine the differences in pupillary light reflex (PLR) between the acute and chronic phases of optic neuritis (ON) and nonarteritic anterior ischemic optic neuropathy (NAION).
The study included 30 patients with ON and 22 patients with NAION whose PLR were measured by a dynamic pupillometer (PLR-200; NeurOptics Inc., Irvine, USA). Age-matched controls included 58 healthy individuals with normal vision and optic nerve function. Pupil diameters, latency, constriction ratio, constriction velocity and dilation velocity were noted. The differences in PLR measurements were compared among the acute and chronic phases of ON and NAION, and in age-matched controls. Regression analysis determined factors associated with PLR measurements, including visual acuity, color vision defect, visual field defects and retinal nerve fiber layer thickness measurements on optical coherence tomography.
Pupillary constriction velocity, constriction ratio and latency were all significantly decreased in the acute phase of ON and NAION. ON showed significantly delayed constriction latency compared to NAION (P = 0.047). Pupillary constriction velocity, constriction ratio and latency were recovered in the chronic phase of ON (P = 0.038, 0.018, and 0.045), however, these parameters were not recovered in NAION (P = 0.693, 0.173 and 0.994).
Pupillary constriction velocity, constriction ratio, and latency were significantly decreased in the acute phase of ON and NAION compared to normal controls. ON showed delayed constriction latency compared to NAION. Decreased PLR were recovered in the chronic phase of ON, but not in NAION. |
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The study included 30 patients with ON and 22 patients with NAION whose PLR were measured by a dynamic pupillometer (PLR-200; NeurOptics Inc., Irvine, USA). Age-matched controls included 58 healthy individuals with normal vision and optic nerve function. Pupil diameters, latency, constriction ratio, constriction velocity and dilation velocity were noted. The differences in PLR measurements were compared among the acute and chronic phases of ON and NAION, and in age-matched controls. Regression analysis determined factors associated with PLR measurements, including visual acuity, color vision defect, visual field defects and retinal nerve fiber layer thickness measurements on optical coherence tomography.
Pupillary constriction velocity, constriction ratio and latency were all significantly decreased in the acute phase of ON and NAION. ON showed significantly delayed constriction latency compared to NAION (P = 0.047). Pupillary constriction velocity, constriction ratio and latency were recovered in the chronic phase of ON (P = 0.038, 0.018, and 0.045), however, these parameters were not recovered in NAION (P = 0.693, 0.173 and 0.994).
Pupillary constriction velocity, constriction ratio, and latency were significantly decreased in the acute phase of ON and NAION compared to normal controls. ON showed delayed constriction latency compared to NAION. Decreased PLR were recovered in the chronic phase of ON, but not in NAION.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0186741</identifier><identifier>PMID: 29049405</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Acuity ; Adult ; Age ; Biology and Life Sciences ; Color vision ; Comparative analysis ; Constrictions ; Defects ; Development and progression ; Edema ; Female ; Hospitals ; Humans ; Ischemia ; Latency ; Light ; Male ; Medicine and Health Sciences ; Middle Aged ; Multiple sclerosis ; Nerve conduction ; Neuritis ; Neuropathy ; Optic nerve ; Optic neuritis ; Optic Neuritis - physiopathology ; Optic neuropathy ; Optic Neuropathy, Ischemic - physiopathology ; Optical Coherence Tomography ; Patients ; Pupil - physiology ; Regression analysis ; Retina ; Retrospective Studies ; Social Sciences ; Thickness measurement ; Velocity ; Vision ; Visual acuity ; Visual field ; Visual fields ; Young Adult</subject><ispartof>PloS one, 2017-10, Vol.12 (10), p.e0186741-e0186741</ispartof><rights>COPYRIGHT 2017 Public Library of Science</rights><rights>2017 Yoo et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (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>2017 Yoo et al 2017 Yoo et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-993f00c40089c66c99c70e71b01ea4cfa7a3519ba6f56353fc0b46e949449b993</citedby><cites>FETCH-LOGICAL-c692t-993f00c40089c66c99c70e71b01ea4cfa7a3519ba6f56353fc0b46e949449b993</cites><orcidid>0000-0003-0837-2864 ; 0000-0002-1140-6036</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5648212/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5648212/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2100,2926,23865,27923,27924,53790,53792,79371,79372</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29049405$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Bhattacharya, Sanjoy</contributor><creatorcontrib>Yoo, Yung Ju</creatorcontrib><creatorcontrib>Hwang, Jeong-Min</creatorcontrib><creatorcontrib>Yang, Hee Kyung</creatorcontrib><title>Differences in pupillary light reflex between optic neuritis and ischemic optic neuropathy</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>To determine the differences in pupillary light reflex (PLR) between the acute and chronic phases of optic neuritis (ON) and nonarteritic anterior ischemic optic neuropathy (NAION).
The study included 30 patients with ON and 22 patients with NAION whose PLR were measured by a dynamic pupillometer (PLR-200; NeurOptics Inc., Irvine, USA). Age-matched controls included 58 healthy individuals with normal vision and optic nerve function. Pupil diameters, latency, constriction ratio, constriction velocity and dilation velocity were noted. The differences in PLR measurements were compared among the acute and chronic phases of ON and NAION, and in age-matched controls. Regression analysis determined factors associated with PLR measurements, including visual acuity, color vision defect, visual field defects and retinal nerve fiber layer thickness measurements on optical coherence tomography.
Pupillary constriction velocity, constriction ratio and latency were all significantly decreased in the acute phase of ON and NAION. ON showed significantly delayed constriction latency compared to NAION (P = 0.047). Pupillary constriction velocity, constriction ratio and latency were recovered in the chronic phase of ON (P = 0.038, 0.018, and 0.045), however, these parameters were not recovered in NAION (P = 0.693, 0.173 and 0.994).
Pupillary constriction velocity, constriction ratio, and latency were significantly decreased in the acute phase of ON and NAION compared to normal controls. ON showed delayed constriction latency compared to NAION. Decreased PLR were recovered in the chronic phase of ON, but not in NAION.</description><subject>Acuity</subject><subject>Adult</subject><subject>Age</subject><subject>Biology and Life Sciences</subject><subject>Color vision</subject><subject>Comparative analysis</subject><subject>Constrictions</subject><subject>Defects</subject><subject>Development and progression</subject><subject>Edema</subject><subject>Female</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Ischemia</subject><subject>Latency</subject><subject>Light</subject><subject>Male</subject><subject>Medicine and Health Sciences</subject><subject>Middle Aged</subject><subject>Multiple sclerosis</subject><subject>Nerve conduction</subject><subject>Neuritis</subject><subject>Neuropathy</subject><subject>Optic nerve</subject><subject>Optic neuritis</subject><subject>Optic Neuritis - physiopathology</subject><subject>Optic neuropathy</subject><subject>Optic Neuropathy, Ischemic - physiopathology</subject><subject>Optical Coherence Tomography</subject><subject>Patients</subject><subject>Pupil - physiology</subject><subject>Regression analysis</subject><subject>Retina</subject><subject>Retrospective Studies</subject><subject>Social Sciences</subject><subject>Thickness measurement</subject><subject>Velocity</subject><subject>Vision</subject><subject>Visual acuity</subject><subject>Visual field</subject><subject>Visual fields</subject><subject>Young Adult</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNqNk01v1DAQhiMEoqXwDxBEQkJw2MWOHSe-IFXla6VKlfg6cLEcZ7zxKmsH24H23-PtpmWDekA5OBo_89rzeibLnmK0xKTCbzZu9Fb2y8FZWCJcs4rie9kx5qRYsAKR-wf_R9mjEDYIlaRm7GF2VHBEOUXlcfbjndEaPFgFITc2H8bB9L30V3lv1l3MPegeLvMG4m8Am7shGpVbGL2JJuTStrkJqoNtiv7dc4OM3dXj7IGWfYAn03qSffvw_uvZp8X5xcfV2en5QjFexAXnRCOkKEI1V4wpzlWFoMINwiCp0rKSpMS8kUyXjJREK9RQBjwVQHmTsk-y53vdoXdBTLYEgXlJcFlRThKx2hOtkxsxeLNNBQonjbgOOL8W0qfL9yAazUoiQbaSMwqsbBRGCLUV061GWNGk9XY6bWy20Cqw0ct-JjrfsaYTa_dLlIzWBS6SwKtJwLufI4QotslCSKZbcOP1vSlihGCU0Bf_oHdXN1FrmQowVrt0rtqJitMSI4oJretELe-g0tfuHi_1kDYpPkt4PUtITITLuJZjCGL15fP_sxff5-zLA7YD2ccuuH6MxtkwB-keVN6FkBrx1mSMxG4EbtwQuxEQ0wiktGeHD3SbdNPz5A_cPgFt</recordid><startdate>20171019</startdate><enddate>20171019</enddate><creator>Yoo, Yung Ju</creator><creator>Hwang, Jeong-Min</creator><creator>Yang, Hee Kyung</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>IOV</scope><scope>ISR</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>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-0837-2864</orcidid><orcidid>https://orcid.org/0000-0002-1140-6036</orcidid></search><sort><creationdate>20171019</creationdate><title>Differences in pupillary light reflex between optic neuritis and ischemic optic neuropathy</title><author>Yoo, Yung Ju ; Hwang, Jeong-Min ; Yang, Hee Kyung</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-993f00c40089c66c99c70e71b01ea4cfa7a3519ba6f56353fc0b46e949449b993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Acuity</topic><topic>Adult</topic><topic>Age</topic><topic>Biology and Life Sciences</topic><topic>Color vision</topic><topic>Comparative analysis</topic><topic>Constrictions</topic><topic>Defects</topic><topic>Development and progression</topic><topic>Edema</topic><topic>Female</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Ischemia</topic><topic>Latency</topic><topic>Light</topic><topic>Male</topic><topic>Medicine and Health Sciences</topic><topic>Middle Aged</topic><topic>Multiple sclerosis</topic><topic>Nerve conduction</topic><topic>Neuritis</topic><topic>Neuropathy</topic><topic>Optic nerve</topic><topic>Optic neuritis</topic><topic>Optic Neuritis - physiopathology</topic><topic>Optic neuropathy</topic><topic>Optic Neuropathy, Ischemic - physiopathology</topic><topic>Optical Coherence Tomography</topic><topic>Patients</topic><topic>Pupil - physiology</topic><topic>Regression analysis</topic><topic>Retina</topic><topic>Retrospective Studies</topic><topic>Social Sciences</topic><topic>Thickness measurement</topic><topic>Velocity</topic><topic>Vision</topic><topic>Visual acuity</topic><topic>Visual field</topic><topic>Visual fields</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yoo, Yung Ju</creatorcontrib><creatorcontrib>Hwang, Jeong-Min</creatorcontrib><creatorcontrib>Yang, Hee Kyung</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale in Context : Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>ProQuest Health and Medical</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 & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & 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 & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - 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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>Yoo, Yung Ju</au><au>Hwang, Jeong-Min</au><au>Yang, Hee Kyung</au><au>Bhattacharya, Sanjoy</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differences in pupillary light reflex between optic neuritis and ischemic optic neuropathy</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2017-10-19</date><risdate>2017</risdate><volume>12</volume><issue>10</issue><spage>e0186741</spage><epage>e0186741</epage><pages>e0186741-e0186741</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>To determine the differences in pupillary light reflex (PLR) between the acute and chronic phases of optic neuritis (ON) and nonarteritic anterior ischemic optic neuropathy (NAION).
The study included 30 patients with ON and 22 patients with NAION whose PLR were measured by a dynamic pupillometer (PLR-200; NeurOptics Inc., Irvine, USA). Age-matched controls included 58 healthy individuals with normal vision and optic nerve function. Pupil diameters, latency, constriction ratio, constriction velocity and dilation velocity were noted. The differences in PLR measurements were compared among the acute and chronic phases of ON and NAION, and in age-matched controls. Regression analysis determined factors associated with PLR measurements, including visual acuity, color vision defect, visual field defects and retinal nerve fiber layer thickness measurements on optical coherence tomography.
Pupillary constriction velocity, constriction ratio and latency were all significantly decreased in the acute phase of ON and NAION. ON showed significantly delayed constriction latency compared to NAION (P = 0.047). Pupillary constriction velocity, constriction ratio and latency were recovered in the chronic phase of ON (P = 0.038, 0.018, and 0.045), however, these parameters were not recovered in NAION (P = 0.693, 0.173 and 0.994).
Pupillary constriction velocity, constriction ratio, and latency were significantly decreased in the acute phase of ON and NAION compared to normal controls. ON showed delayed constriction latency compared to NAION. Decreased PLR were recovered in the chronic phase of ON, but not in NAION.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>29049405</pmid><doi>10.1371/journal.pone.0186741</doi><tpages>e0186741</tpages><orcidid>https://orcid.org/0000-0003-0837-2864</orcidid><orcidid>https://orcid.org/0000-0002-1140-6036</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acuity Adult Age Biology and Life Sciences Color vision Comparative analysis Constrictions Defects Development and progression Edema Female Hospitals Humans Ischemia Latency Light Male Medicine and Health Sciences Middle Aged Multiple sclerosis Nerve conduction Neuritis Neuropathy Optic nerve Optic neuritis Optic Neuritis - physiopathology Optic neuropathy Optic Neuropathy, Ischemic - physiopathology Optical Coherence Tomography Patients Pupil - physiology Regression analysis Retina Retrospective Studies Social Sciences Thickness measurement Velocity Vision Visual acuity Visual field Visual fields Young Adult |
title | Differences in pupillary light reflex between optic neuritis and ischemic optic neuropathy |
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