Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/12610
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dc.contributor.authorMaia-Lopes, Susana-
dc.contributor.authorSilva, Eduardo Duarte-
dc.contributor.authorReis, Aldina-
dc.contributor.authorSilva, Maria Fátima-
dc.contributor.authorMateus, Catarina-
dc.contributor.authorCastelo-Branco, Miguel-
dc.date.accessioned2010-02-26T09:14:36Z-
dc.date.available2010-02-26T09:14:36Z-
dc.date.issued2008-12-
dc.identifier.citationInvestigative Ophthalmology & Visual Science. 49:12(2008) 5553-5560en_US
dc.identifier.issn0146-0404-
dc.identifier.urihttps://hdl.handle.net/10316/12610-
dc.description.abstractPURPOSE: To establish structure-function correlations across the visual field, to investigate disease progression in Best macular dystrophy (BMD), by correlating structural damage with retinal function as assessed by the combination of psychophysics and multifocal electrophysiology. METHODS: Spatial achromatic and chromatic contrast sensitivities (probing red-green and blue-yellow pathways) were assessed using custom-made psychophysical software to evaluate retinal damage in BMD and age-matched control eyes (n = 19 and n = 22, respectively). Neurosensory retinal dysfunction was also evaluated by means of multifocal electroretinography (mfERG). Correlation analysis was performed between functional parameters in BMD, clinical measures, and morphologic data obtained by optical coherence tomography (OCT). RESULTS: Significant peripheral impairment of retinal function, as measured by mfERG and spatial achromatic contrast sensitivity (CS) methods, was found in BMD. Furthermore, changes in thickness of the neurosensory retina, as measured by OCT, and reduced mfERG responses were also indicators of early loss in BMD and often occurred even with preserved visual acuity. Disease duration was significantly correlated with psychophysical deterioration in chromatic and achromatic tasks but not with mfERG measures. Interestingly, partial correlation analysis revealed a significant independent correlation with our CS measures. CONCLUSIONS: Novel topographic achromatic and chromatic CS methods can detect and quantify functional impairment in early stages of BMD, including the involvement of the peripheral retina and the central chromatic pathway, and can provide new pathophysiological information with added value in relation to electrophysiological and structural measures of damageen_US
dc.language.isoengen_US
dc.publisherAssociation for Research in Vision and Ophthalmologyen_US
dc.rightsopenAccessen_US
dc.titleRetinal function in best macular dystrophy: relationship between electrophysiological, psychophysical, and structural measures of damageen_US
dc.typearticleen_US
dc.identifier.doi10.1167/iovs.08-2093-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypearticle-
item.cerifentitytypePublications-
item.grantfulltextopen-
item.fulltextCom Texto completo-
item.languageiso639-1en-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCIBIT - Coimbra Institute for Biomedical Imaging and Translational Research-
crisitem.author.orcid0000-0002-2739-9854-
crisitem.author.orcid0000-0001-7598-8736-
crisitem.author.orcid0000-0002-3270-7575-
crisitem.author.orcid0000-0003-4364-6373-
Appears in Collections:FMUC Medicina - Artigos em Revistas Internacionais
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