Structure-function correlations in Retinitis Pigmentosa patients with partially preserved vision: a voxel-based morphometry study

Detalhes bibliográficos
Autor(a) principal: Machado, Ana Rita
Data de Publicação: 2017
Outros Autores: Pereira, Andreia Carvalho, Ferreira, Fábio, Ferreira, Sónia, Quendera, Bruno, Silva, Eduardo, Castelo-Branco, Miguel
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/108383
https://doi.org/10.1038/s41598-017-11317-7
Resumo: Retinitis Pigmentosa is a group of hereditary retinal dystrophy disorders associated with progressive peripheral visual field loss. The impact of this retinal loss in cortical gray matter volume has not been addressed before in Retinitis Pigmentosa patients with low vision. Voxel-based morphometry was applied to study whole brain gray matter volume changes in 27 Retinitis Pigmentosa patients with partially preserved vision and 38 age- and gender-matched normally sighted controls to determine whether peripheral visual loss can lead to changes in gray matter volume. We found significant reductions in gray matter volume that were restricted to the occipital cortex of patients. The anteromedial pattern of reduced gray matter volume in visual primary and association cortices was significantly correlated with the extent of the peripheral visual field deficit in this cohort. Moreover, this pattern was found to be associated with the extent of visual field loss. In summary, we found specific visual cortical gray matter loss in Retinitis Pigmentosa patients associated with their visual function profile. The spatial pattern of gray matter loss is consistent with disuse-driven neuronal atrophy which may have clinical implications for disease management, including prosthetic restoration strategies.
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spelling Structure-function correlations in Retinitis Pigmentosa patients with partially preserved vision: a voxel-based morphometry studyAdultAgedFemaleGray MatterHumansMagnetic Resonance ImagingMaleMiddle AgedOrgan SizeRetinaRetinitis PigmentosaVision TestsVision, LowVisual AcuityVisual Field TestsVisual FieldsYoung AdultRetinitis Pigmentosa is a group of hereditary retinal dystrophy disorders associated with progressive peripheral visual field loss. The impact of this retinal loss in cortical gray matter volume has not been addressed before in Retinitis Pigmentosa patients with low vision. Voxel-based morphometry was applied to study whole brain gray matter volume changes in 27 Retinitis Pigmentosa patients with partially preserved vision and 38 age- and gender-matched normally sighted controls to determine whether peripheral visual loss can lead to changes in gray matter volume. We found significant reductions in gray matter volume that were restricted to the occipital cortex of patients. The anteromedial pattern of reduced gray matter volume in visual primary and association cortices was significantly correlated with the extent of the peripheral visual field deficit in this cohort. Moreover, this pattern was found to be associated with the extent of visual field loss. In summary, we found specific visual cortical gray matter loss in Retinitis Pigmentosa patients associated with their visual function profile. The spatial pattern of gray matter loss is consistent with disuse-driven neuronal atrophy which may have clinical implications for disease management, including prosthetic restoration strategies.Springer Nature2017-09-12info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/108383http://hdl.handle.net/10316/108383https://doi.org/10.1038/s41598-017-11317-7eng2045-2322Machado, Ana RitaPereira, Andreia CarvalhoFerreira, FábioFerreira, SóniaQuendera, BrunoSilva, EduardoCastelo-Branco, Miguelinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-08-28T09:55:46Zoai:estudogeral.uc.pt:10316/108383Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:24:41.051001Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Structure-function correlations in Retinitis Pigmentosa patients with partially preserved vision: a voxel-based morphometry study
title Structure-function correlations in Retinitis Pigmentosa patients with partially preserved vision: a voxel-based morphometry study
spellingShingle Structure-function correlations in Retinitis Pigmentosa patients with partially preserved vision: a voxel-based morphometry study
Machado, Ana Rita
Adult
Aged
Female
Gray Matter
Humans
Magnetic Resonance Imaging
Male
Middle Aged
Organ Size
Retina
Retinitis Pigmentosa
Vision Tests
Vision, Low
Visual Acuity
Visual Field Tests
Visual Fields
Young Adult
title_short Structure-function correlations in Retinitis Pigmentosa patients with partially preserved vision: a voxel-based morphometry study
title_full Structure-function correlations in Retinitis Pigmentosa patients with partially preserved vision: a voxel-based morphometry study
title_fullStr Structure-function correlations in Retinitis Pigmentosa patients with partially preserved vision: a voxel-based morphometry study
title_full_unstemmed Structure-function correlations in Retinitis Pigmentosa patients with partially preserved vision: a voxel-based morphometry study
title_sort Structure-function correlations in Retinitis Pigmentosa patients with partially preserved vision: a voxel-based morphometry study
author Machado, Ana Rita
author_facet Machado, Ana Rita
Pereira, Andreia Carvalho
Ferreira, Fábio
Ferreira, Sónia
Quendera, Bruno
Silva, Eduardo
Castelo-Branco, Miguel
author_role author
author2 Pereira, Andreia Carvalho
Ferreira, Fábio
Ferreira, Sónia
Quendera, Bruno
Silva, Eduardo
Castelo-Branco, Miguel
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Machado, Ana Rita
Pereira, Andreia Carvalho
Ferreira, Fábio
Ferreira, Sónia
Quendera, Bruno
Silva, Eduardo
Castelo-Branco, Miguel
dc.subject.por.fl_str_mv Adult
Aged
Female
Gray Matter
Humans
Magnetic Resonance Imaging
Male
Middle Aged
Organ Size
Retina
Retinitis Pigmentosa
Vision Tests
Vision, Low
Visual Acuity
Visual Field Tests
Visual Fields
Young Adult
topic Adult
Aged
Female
Gray Matter
Humans
Magnetic Resonance Imaging
Male
Middle Aged
Organ Size
Retina
Retinitis Pigmentosa
Vision Tests
Vision, Low
Visual Acuity
Visual Field Tests
Visual Fields
Young Adult
description Retinitis Pigmentosa is a group of hereditary retinal dystrophy disorders associated with progressive peripheral visual field loss. The impact of this retinal loss in cortical gray matter volume has not been addressed before in Retinitis Pigmentosa patients with low vision. Voxel-based morphometry was applied to study whole brain gray matter volume changes in 27 Retinitis Pigmentosa patients with partially preserved vision and 38 age- and gender-matched normally sighted controls to determine whether peripheral visual loss can lead to changes in gray matter volume. We found significant reductions in gray matter volume that were restricted to the occipital cortex of patients. The anteromedial pattern of reduced gray matter volume in visual primary and association cortices was significantly correlated with the extent of the peripheral visual field deficit in this cohort. Moreover, this pattern was found to be associated with the extent of visual field loss. In summary, we found specific visual cortical gray matter loss in Retinitis Pigmentosa patients associated with their visual function profile. The spatial pattern of gray matter loss is consistent with disuse-driven neuronal atrophy which may have clinical implications for disease management, including prosthetic restoration strategies.
publishDate 2017
dc.date.none.fl_str_mv 2017-09-12
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.uri.fl_str_mv http://hdl.handle.net/10316/108383
http://hdl.handle.net/10316/108383
https://doi.org/10.1038/s41598-017-11317-7
url http://hdl.handle.net/10316/108383
https://doi.org/10.1038/s41598-017-11317-7
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 2045-2322
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.publisher.none.fl_str_mv Springer Nature
publisher.none.fl_str_mv Springer Nature
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
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