The Pupil Light Reflex in Leber's Hereditary Optic Neuropathy: Evidence for Preservation of Melanopsin-Expressing Retinal Ganglion Cells
Autor(a) principal: | |
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Data de Publicação: | 2013 |
Outros Autores: | , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1167/iovs.12-11137 http://repositorio.unifesp.br/handle/11600/36454 |
Resumo: | PURPOSE. To investigate the pupillary light reflex (PLR) of patients with severe loss of vision due to Leber's Hereditary Optic Neuropathy (LHON) in the context of a proposed preservation of melanopsin-expressing retinal ganglion cells (mRGCs).METHODS. Ten LHON patients (7 males; 51.6 +/- 14.1 years), with visual acuities ranging from 20/400 to hand motion perception and severe visual field losses, were tested and compared with 16 healthy subjects (7 males; 42.15 +/- 15.4 years) tested as controls. PLR was measured with an eye tracker and the stimuli were controlled with a Ganzfeld system. Pupil responses were measured monocularly, to 1 second of blue (470 nm) and red (640 nm) flashes with 1, 10, 100, and 250 cd/m(2) luminances. the normalized amplitude of peak of the transient PLR and the amplitude of the sustained PLR at 6 seconds after the flash offset were measured. in addition, optical coherence topography (OCT) scans of the peripapillary retinal nerve fiber layer were obtained.RESULTS. the patient's peak PLR responses were on average 15% smaller than controls (P < 0.05), but 5 out of 10 patients had amplitudes within the range of controls. the patients' sustained PLRs were comparable with controls at lower flash intensities, but on average, 27% smaller to the 250 cd/m(2) blue light, although there was considerable overlap with the PLR amplitudes of control. All patients had severe visual field losses and the retinal nerve fiber layer thickness was reduced to a minimum around the optic disc in 8 of the 10 patients.CONCLUSIONS. the PLR is maintained overall in LHON patients despite the severity of optic atrophy. These results are consistent with previous evidence of selective preservation of mRGCs. |
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The Pupil Light Reflex in Leber's Hereditary Optic Neuropathy: Evidence for Preservation of Melanopsin-Expressing Retinal Ganglion Cellspupillometrymelanopsinganglion cellsLHONOCTPURPOSE. To investigate the pupillary light reflex (PLR) of patients with severe loss of vision due to Leber's Hereditary Optic Neuropathy (LHON) in the context of a proposed preservation of melanopsin-expressing retinal ganglion cells (mRGCs).METHODS. Ten LHON patients (7 males; 51.6 +/- 14.1 years), with visual acuities ranging from 20/400 to hand motion perception and severe visual field losses, were tested and compared with 16 healthy subjects (7 males; 42.15 +/- 15.4 years) tested as controls. PLR was measured with an eye tracker and the stimuli were controlled with a Ganzfeld system. Pupil responses were measured monocularly, to 1 second of blue (470 nm) and red (640 nm) flashes with 1, 10, 100, and 250 cd/m(2) luminances. the normalized amplitude of peak of the transient PLR and the amplitude of the sustained PLR at 6 seconds after the flash offset were measured. in addition, optical coherence topography (OCT) scans of the peripapillary retinal nerve fiber layer were obtained.RESULTS. the patient's peak PLR responses were on average 15% smaller than controls (P < 0.05), but 5 out of 10 patients had amplitudes within the range of controls. the patients' sustained PLRs were comparable with controls at lower flash intensities, but on average, 27% smaller to the 250 cd/m(2) blue light, although there was considerable overlap with the PLR amplitudes of control. All patients had severe visual field losses and the retinal nerve fiber layer thickness was reduced to a minimum around the optic disc in 8 of the 10 patients.CONCLUSIONS. the PLR is maintained overall in LHON patients despite the severity of optic atrophy. These results are consistent with previous evidence of selective preservation of mRGCs.Univ São Paulo, Inst Psicol, São Paulo, BrazilUniv São Paulo, Nucleo Neurociencias & Comportamento, São Paulo, BrazilBudapest Univ Technol & Econ, Dept Mech Opt & Eng Informat, Budapest, HungaryIRCCS Ist Sci Neurol Bologna, Bologna, ItalyUniv Bologna, Dept Biomed & Neuromotor Sci DIBINEM, Bologna, ItalyStudio Oculist Azeglio, Bologna, ItalyUniversidade Federal de São Paulo UNIFESP, Escola Paulista Med, Dept Oftalmol, São Paulo, BrazilUniv So Calif, Keck Sch Med, Dept Ophthalmol, Doheny Eye Inst, Los Angeles, CA 90033 USAColumbia Univ, Dept Psychol, New York, NY 10027 USAColumbia Univ, Dept Ophthalmol, New York, NY 10027 USAUniversidade Federal de São Paulo UNIFESP, Escola Paulista Med, Dept Oftalmol, São Paulo, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)International Foundation for Optic Nerve DiseaseFAPESP: 08/58731-2Assoc Research Vision Ophthalmology IncUniversidade de São Paulo (USP)Budapest Univ Technol & EconIRCCS Ist Sci Neurol BolognaUniv BolognaStudio Oculist AzeglioUniversidade Federal de São Paulo (UNIFESP)Univ So CalifColumbia UnivMoura, Ana Laura A.Nagy, Balazs V.La Morgia, ChiaraBarboni, PieroOliveira, Andre Gustavo FernandesSalomão, Solange Rios [UNIFESP]Berezovsky, Adriana [UNIFESP]Moraes-Filho, Milton Nunes de [UNIFESP]Chicani, Carlos FilipeBelfort, Rubens Junior [UNIFESP]Carelli, ValerioSadun, Alfredo A.Hood, Donald C.Ventura, Dora Fix2016-01-24T14:31:55Z2016-01-24T14:31:55Z2013-07-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion4471-4477http://dx.doi.org/10.1167/iovs.12-11137Investigative Ophthalmology & Visual Science. Rockville: Assoc Research Vision Ophthalmology Inc, v. 54, n. 7, p. 4471-4477, 2013.10.1167/iovs.12-111370146-0404http://repositorio.unifesp.br/handle/11600/36454WOS:000322637000008engInvestigative Ophthalmology & Visual Scienceinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2022-02-07T21:52:44Zoai:repositorio.unifesp.br/:11600/36454Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652022-02-07T21:52:44Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
The Pupil Light Reflex in Leber's Hereditary Optic Neuropathy: Evidence for Preservation of Melanopsin-Expressing Retinal Ganglion Cells |
title |
The Pupil Light Reflex in Leber's Hereditary Optic Neuropathy: Evidence for Preservation of Melanopsin-Expressing Retinal Ganglion Cells |
spellingShingle |
The Pupil Light Reflex in Leber's Hereditary Optic Neuropathy: Evidence for Preservation of Melanopsin-Expressing Retinal Ganglion Cells Moura, Ana Laura A. pupillometry melanopsin ganglion cells LHON OCT |
title_short |
The Pupil Light Reflex in Leber's Hereditary Optic Neuropathy: Evidence for Preservation of Melanopsin-Expressing Retinal Ganglion Cells |
title_full |
The Pupil Light Reflex in Leber's Hereditary Optic Neuropathy: Evidence for Preservation of Melanopsin-Expressing Retinal Ganglion Cells |
title_fullStr |
The Pupil Light Reflex in Leber's Hereditary Optic Neuropathy: Evidence for Preservation of Melanopsin-Expressing Retinal Ganglion Cells |
title_full_unstemmed |
The Pupil Light Reflex in Leber's Hereditary Optic Neuropathy: Evidence for Preservation of Melanopsin-Expressing Retinal Ganglion Cells |
title_sort |
The Pupil Light Reflex in Leber's Hereditary Optic Neuropathy: Evidence for Preservation of Melanopsin-Expressing Retinal Ganglion Cells |
author |
Moura, Ana Laura A. |
author_facet |
Moura, Ana Laura A. Nagy, Balazs V. La Morgia, Chiara Barboni, Piero Oliveira, Andre Gustavo Fernandes Salomão, Solange Rios [UNIFESP] Berezovsky, Adriana [UNIFESP] Moraes-Filho, Milton Nunes de [UNIFESP] Chicani, Carlos Filipe Belfort, Rubens Junior [UNIFESP] Carelli, Valerio Sadun, Alfredo A. Hood, Donald C. Ventura, Dora Fix |
author_role |
author |
author2 |
Nagy, Balazs V. La Morgia, Chiara Barboni, Piero Oliveira, Andre Gustavo Fernandes Salomão, Solange Rios [UNIFESP] Berezovsky, Adriana [UNIFESP] Moraes-Filho, Milton Nunes de [UNIFESP] Chicani, Carlos Filipe Belfort, Rubens Junior [UNIFESP] Carelli, Valerio Sadun, Alfredo A. Hood, Donald C. Ventura, Dora Fix |
author2_role |
author author author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade de São Paulo (USP) Budapest Univ Technol & Econ IRCCS Ist Sci Neurol Bologna Univ Bologna Studio Oculist Azeglio Universidade Federal de São Paulo (UNIFESP) Univ So Calif Columbia Univ |
dc.contributor.author.fl_str_mv |
Moura, Ana Laura A. Nagy, Balazs V. La Morgia, Chiara Barboni, Piero Oliveira, Andre Gustavo Fernandes Salomão, Solange Rios [UNIFESP] Berezovsky, Adriana [UNIFESP] Moraes-Filho, Milton Nunes de [UNIFESP] Chicani, Carlos Filipe Belfort, Rubens Junior [UNIFESP] Carelli, Valerio Sadun, Alfredo A. Hood, Donald C. Ventura, Dora Fix |
dc.subject.por.fl_str_mv |
pupillometry melanopsin ganglion cells LHON OCT |
topic |
pupillometry melanopsin ganglion cells LHON OCT |
description |
PURPOSE. To investigate the pupillary light reflex (PLR) of patients with severe loss of vision due to Leber's Hereditary Optic Neuropathy (LHON) in the context of a proposed preservation of melanopsin-expressing retinal ganglion cells (mRGCs).METHODS. Ten LHON patients (7 males; 51.6 +/- 14.1 years), with visual acuities ranging from 20/400 to hand motion perception and severe visual field losses, were tested and compared with 16 healthy subjects (7 males; 42.15 +/- 15.4 years) tested as controls. PLR was measured with an eye tracker and the stimuli were controlled with a Ganzfeld system. Pupil responses were measured monocularly, to 1 second of blue (470 nm) and red (640 nm) flashes with 1, 10, 100, and 250 cd/m(2) luminances. the normalized amplitude of peak of the transient PLR and the amplitude of the sustained PLR at 6 seconds after the flash offset were measured. in addition, optical coherence topography (OCT) scans of the peripapillary retinal nerve fiber layer were obtained.RESULTS. the patient's peak PLR responses were on average 15% smaller than controls (P < 0.05), but 5 out of 10 patients had amplitudes within the range of controls. the patients' sustained PLRs were comparable with controls at lower flash intensities, but on average, 27% smaller to the 250 cd/m(2) blue light, although there was considerable overlap with the PLR amplitudes of control. All patients had severe visual field losses and the retinal nerve fiber layer thickness was reduced to a minimum around the optic disc in 8 of the 10 patients.CONCLUSIONS. the PLR is maintained overall in LHON patients despite the severity of optic atrophy. These results are consistent with previous evidence of selective preservation of mRGCs. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-07-01 2016-01-24T14:31:55Z 2016-01-24T14:31:55Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1167/iovs.12-11137 Investigative Ophthalmology & Visual Science. Rockville: Assoc Research Vision Ophthalmology Inc, v. 54, n. 7, p. 4471-4477, 2013. 10.1167/iovs.12-11137 0146-0404 http://repositorio.unifesp.br/handle/11600/36454 WOS:000322637000008 |
url |
http://dx.doi.org/10.1167/iovs.12-11137 http://repositorio.unifesp.br/handle/11600/36454 |
identifier_str_mv |
Investigative Ophthalmology & Visual Science. Rockville: Assoc Research Vision Ophthalmology Inc, v. 54, n. 7, p. 4471-4477, 2013. 10.1167/iovs.12-11137 0146-0404 WOS:000322637000008 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Investigative Ophthalmology & Visual Science |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
4471-4477 |
dc.publisher.none.fl_str_mv |
Assoc Research Vision Ophthalmology Inc |
publisher.none.fl_str_mv |
Assoc Research Vision Ophthalmology Inc |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1814268330786160640 |