Chromatic and luminance contrast sensitivities in asymptomatic carriers from a large Brazilian pedigree of 11778 Leber hereditary optic neuropathy
Autor(a) principal: | |
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Data de Publicação: | 2005 |
Outros Autores: | , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1167/iovs.05-0455 http://repositorio.unifesp.br/handle/11600/28566 |
Resumo: | PURPOSE. To determine whether asymptomatic 11778 LHON carriers demonstrated impairments in ( 1) chromatic red/green (R/G) and blue/yellow (B/Y) contrast sensitivity functions (CSF) and in ( 2) luminance contrast sensitivity functions in the spatial CSF (SCSF) and temporal CSF ( TCSF) domains.METHODS. Twenty-five carriers ( 8 male, 17 female; 34.1 +/- 15.1 years of age) of homoplasmic 11778 LHON from the same well-described family and 30 age-matched controls ( 17 male, 13 female; 29.2 +/- 7.1 years of age) were tested in one eye, randomly selected. of the 25 eyes tested, 18 had normal fundus, 5 had swelling and microangiopathy, and 2 had temporal pallor. the R/G and B/Y CSFs were obtained after equiluminance correction with bichromatic horizontal sinusoidal gratings at 0.3, 0.7, and 2 cycles per degree (cpd); the SCSFs were obtained with achromatic gratings at 0.3, 2, 6, and 12 cpd; and the TCSFs were obtained at 2, 10, 20, and 33 Hz with sinusoidal modulation of a 2.7 field with a superimposed spatial Gabor function.RESULTS. Differences between carriers and controls were statistically significant for all spatial frequencies of chromatic and luminance SCSFs, but not for the TCSFs. R/G equiluminance settings of carriers differed from those of controls ( P < 0.001), requiring higher luminance in the green; B/Y equiluminance settings were not statistically different in carriers and controls. Fundus findings did not correlate with CS results.CONCLUSIONS. Luminance and chromatic spatial CS losses that affected all tested spatial frequencies, are reported in LHON asymptomatic carriers with the mtDNA 11778 mutation. No losses were found in the temporal CSF. An intriguing finding is that the blue system is substantially spared in this LHON family. These represent subclinical visual impairments in otherwise asymptomatic LHON carriers. |
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Repositório Institucional da UNIFESP |
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3465 |
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Chromatic and luminance contrast sensitivities in asymptomatic carriers from a large Brazilian pedigree of 11778 Leber hereditary optic neuropathyPURPOSE. To determine whether asymptomatic 11778 LHON carriers demonstrated impairments in ( 1) chromatic red/green (R/G) and blue/yellow (B/Y) contrast sensitivity functions (CSF) and in ( 2) luminance contrast sensitivity functions in the spatial CSF (SCSF) and temporal CSF ( TCSF) domains.METHODS. Twenty-five carriers ( 8 male, 17 female; 34.1 +/- 15.1 years of age) of homoplasmic 11778 LHON from the same well-described family and 30 age-matched controls ( 17 male, 13 female; 29.2 +/- 7.1 years of age) were tested in one eye, randomly selected. of the 25 eyes tested, 18 had normal fundus, 5 had swelling and microangiopathy, and 2 had temporal pallor. the R/G and B/Y CSFs were obtained after equiluminance correction with bichromatic horizontal sinusoidal gratings at 0.3, 0.7, and 2 cycles per degree (cpd); the SCSFs were obtained with achromatic gratings at 0.3, 2, 6, and 12 cpd; and the TCSFs were obtained at 2, 10, 20, and 33 Hz with sinusoidal modulation of a 2.7 field with a superimposed spatial Gabor function.RESULTS. Differences between carriers and controls were statistically significant for all spatial frequencies of chromatic and luminance SCSFs, but not for the TCSFs. R/G equiluminance settings of carriers differed from those of controls ( P < 0.001), requiring higher luminance in the green; B/Y equiluminance settings were not statistically different in carriers and controls. Fundus findings did not correlate with CS results.CONCLUSIONS. Luminance and chromatic spatial CS losses that affected all tested spatial frequencies, are reported in LHON asymptomatic carriers with the mtDNA 11778 mutation. No losses were found in the temporal CSF. An intriguing finding is that the blue system is substantially spared in this LHON family. These represent subclinical visual impairments in otherwise asymptomatic LHON carriers.Univ São Paulo, Inst Psicol, Dept Expt Psychol, BR-05508900 São Paulo, BrazilUniv So Calif, Keck Sch Med, Los Angeles, CA USAUniv Bologna, Bologna, ItalyUniversidade Federal de São Paulo, São Paulo, BrazilOsped S Giovanni Evangelista, Rome, ItalyAzienda Osped San Camillo Forlanini, Rome, ItalyUniversidade Federal de São Paulo, EPM, São Paulo, BrazilWeb of ScienceAssoc Research Vision Ophthalmology IncUniversidade de São Paulo (USP)Univ So CalifUniv BolognaUniversidade Federal de São Paulo (UNIFESP)Osped S Giovanni EvangelistaAzienda Osped San Camillo ForlaniniVentura, D. F.Quiros, P.Carelli, VSalomão, Solange Rios [UNIFESP]Gualtieri, M.Oliveira, AGFCosta, M. F.Berezovsky, Adriana [UNIFESP]Sadun, F.Negri, A. M. deSadun, A. A.2016-01-24T12:38:11Z2016-01-24T12:38:11Z2005-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion4809-4814http://dx.doi.org/10.1167/iovs.05-0455Investigative Ophthalmology & Visual Science. Rockville: Assoc Research Vision Ophthalmology Inc, v. 46, n. 12, p. 4809-4814, 2005.10.1167/iovs.05-04550146-0404http://repositorio.unifesp.br/handle/11600/28566WOS:000233578600065engInvestigative Ophthalmology & Visual Scienceinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2023-02-14T13:42:51Zoai:repositorio.unifesp.br/:11600/28566Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652023-02-14T13:42:51Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Chromatic and luminance contrast sensitivities in asymptomatic carriers from a large Brazilian pedigree of 11778 Leber hereditary optic neuropathy |
title |
Chromatic and luminance contrast sensitivities in asymptomatic carriers from a large Brazilian pedigree of 11778 Leber hereditary optic neuropathy |
spellingShingle |
Chromatic and luminance contrast sensitivities in asymptomatic carriers from a large Brazilian pedigree of 11778 Leber hereditary optic neuropathy Ventura, D. F. |
title_short |
Chromatic and luminance contrast sensitivities in asymptomatic carriers from a large Brazilian pedigree of 11778 Leber hereditary optic neuropathy |
title_full |
Chromatic and luminance contrast sensitivities in asymptomatic carriers from a large Brazilian pedigree of 11778 Leber hereditary optic neuropathy |
title_fullStr |
Chromatic and luminance contrast sensitivities in asymptomatic carriers from a large Brazilian pedigree of 11778 Leber hereditary optic neuropathy |
title_full_unstemmed |
Chromatic and luminance contrast sensitivities in asymptomatic carriers from a large Brazilian pedigree of 11778 Leber hereditary optic neuropathy |
title_sort |
Chromatic and luminance contrast sensitivities in asymptomatic carriers from a large Brazilian pedigree of 11778 Leber hereditary optic neuropathy |
author |
Ventura, D. F. |
author_facet |
Ventura, D. F. Quiros, P. Carelli, V Salomão, Solange Rios [UNIFESP] Gualtieri, M. Oliveira, AGF Costa, M. F. Berezovsky, Adriana [UNIFESP] Sadun, F. Negri, A. M. de Sadun, A. A. |
author_role |
author |
author2 |
Quiros, P. Carelli, V Salomão, Solange Rios [UNIFESP] Gualtieri, M. Oliveira, AGF Costa, M. F. Berezovsky, Adriana [UNIFESP] Sadun, F. Negri, A. M. de Sadun, A. A. |
author2_role |
author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade de São Paulo (USP) Univ So Calif Univ Bologna Universidade Federal de São Paulo (UNIFESP) Osped S Giovanni Evangelista Azienda Osped San Camillo Forlanini |
dc.contributor.author.fl_str_mv |
Ventura, D. F. Quiros, P. Carelli, V Salomão, Solange Rios [UNIFESP] Gualtieri, M. Oliveira, AGF Costa, M. F. Berezovsky, Adriana [UNIFESP] Sadun, F. Negri, A. M. de Sadun, A. A. |
description |
PURPOSE. To determine whether asymptomatic 11778 LHON carriers demonstrated impairments in ( 1) chromatic red/green (R/G) and blue/yellow (B/Y) contrast sensitivity functions (CSF) and in ( 2) luminance contrast sensitivity functions in the spatial CSF (SCSF) and temporal CSF ( TCSF) domains.METHODS. Twenty-five carriers ( 8 male, 17 female; 34.1 +/- 15.1 years of age) of homoplasmic 11778 LHON from the same well-described family and 30 age-matched controls ( 17 male, 13 female; 29.2 +/- 7.1 years of age) were tested in one eye, randomly selected. of the 25 eyes tested, 18 had normal fundus, 5 had swelling and microangiopathy, and 2 had temporal pallor. the R/G and B/Y CSFs were obtained after equiluminance correction with bichromatic horizontal sinusoidal gratings at 0.3, 0.7, and 2 cycles per degree (cpd); the SCSFs were obtained with achromatic gratings at 0.3, 2, 6, and 12 cpd; and the TCSFs were obtained at 2, 10, 20, and 33 Hz with sinusoidal modulation of a 2.7 field with a superimposed spatial Gabor function.RESULTS. Differences between carriers and controls were statistically significant for all spatial frequencies of chromatic and luminance SCSFs, but not for the TCSFs. R/G equiluminance settings of carriers differed from those of controls ( P < 0.001), requiring higher luminance in the green; B/Y equiluminance settings were not statistically different in carriers and controls. Fundus findings did not correlate with CS results.CONCLUSIONS. Luminance and chromatic spatial CS losses that affected all tested spatial frequencies, are reported in LHON asymptomatic carriers with the mtDNA 11778 mutation. No losses were found in the temporal CSF. An intriguing finding is that the blue system is substantially spared in this LHON family. These represent subclinical visual impairments in otherwise asymptomatic LHON carriers. |
publishDate |
2005 |
dc.date.none.fl_str_mv |
2005-12-01 2016-01-24T12:38:11Z 2016-01-24T12:38:11Z |
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.05-0455 Investigative Ophthalmology & Visual Science. Rockville: Assoc Research Vision Ophthalmology Inc, v. 46, n. 12, p. 4809-4814, 2005. 10.1167/iovs.05-0455 0146-0404 http://repositorio.unifesp.br/handle/11600/28566 WOS:000233578600065 |
url |
http://dx.doi.org/10.1167/iovs.05-0455 http://repositorio.unifesp.br/handle/11600/28566 |
identifier_str_mv |
Investigative Ophthalmology & Visual Science. Rockville: Assoc Research Vision Ophthalmology Inc, v. 46, n. 12, p. 4809-4814, 2005. 10.1167/iovs.05-0455 0146-0404 WOS:000233578600065 |
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 |
4809-4814 |
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_ |
1814268326935789568 |