Chromatic and luminance contrast sensitivities in asymptomatic carriers from a large Brazilian pedigree of 11778 Leber hereditary optic neuropathy

Detalhes bibliográficos
Autor(a) principal: Ventura, D. F.
Data de Publicação: 2005
Outros Autores: 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.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/handle/11600/28566
http://dx.doi.org/10.1167/iovs.05-0455
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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spelling Ventura, 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.Universidade de São Paulo (USP)Univ So CalifUniv BolognaUniversidade Federal de São Paulo (UNIFESP)Osped S Giovanni EvangelistaAzienda Osped San Camillo Forlanini2016-01-24T12:38:11Z2016-01-24T12:38:11Z2005-12-01Investigative Ophthalmology & Visual Science. Rockville: Assoc Research Vision Ophthalmology Inc, v. 46, n. 12, p. 4809-4814, 2005.0146-0404http://repositorio.unifesp.br/handle/11600/28566http://dx.doi.org/10.1167/iovs.05-045510.1167/iovs.05-0455WOS:000233578600065PURPOSE. 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 Science4809-4814engAssoc Research Vision Ophthalmology IncInvestigative Ophthalmology & Visual ScienceChromatic and luminance contrast sensitivities in asymptomatic carriers from a large Brazilian pedigree of 11778 Leber hereditary optic neuropathyinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP11600/285662023-02-14 13:42:51.303metadata only accessoai:repositorio.unifesp.br:11600/28566Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652023-05-25T12:30:02.971432Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.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.institution.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.issued.fl_str_mv 2005-12-01
dc.date.accessioned.fl_str_mv 2016-01-24T12:38:11Z
dc.date.available.fl_str_mv 2016-01-24T12:38:11Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.citation.fl_str_mv Investigative Ophthalmology & Visual Science. Rockville: Assoc Research Vision Ophthalmology Inc, v. 46, n. 12, p. 4809-4814, 2005.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/handle/11600/28566
http://dx.doi.org/10.1167/iovs.05-0455
dc.identifier.issn.none.fl_str_mv 0146-0404
dc.identifier.doi.none.fl_str_mv 10.1167/iovs.05-0455
dc.identifier.wos.none.fl_str_mv WOS:000233578600065
identifier_str_mv Investigative Ophthalmology & Visual Science. Rockville: Assoc Research Vision Ophthalmology Inc, v. 46, n. 12, p. 4809-4814, 2005.
0146-0404
10.1167/iovs.05-0455
WOS:000233578600065
url http://repositorio.unifesp.br/handle/11600/28566
http://dx.doi.org/10.1167/iovs.05-0455
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.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
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