Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/106226
DC FieldValueLanguage
dc.contributor.authorMarques, Inês P.-
dc.contributor.authorAlves, Dalila-
dc.contributor.authorSantos, Torcato-
dc.contributor.authorMendes, Luís-
dc.contributor.authorLobo, Conceição-
dc.contributor.authorSantos, Ana Rita-
dc.contributor.authorDurbin, Mary-
dc.contributor.authorCunha-Vaz, José-
dc.date.accessioned2023-03-27T09:54:43Z-
dc.date.available2023-03-27T09:54:43Z-
dc.date.issued2020-03-09-
dc.identifier.issn1552-5783pt
dc.identifier.urihttps://hdl.handle.net/10316/106226-
dc.description.abstractPURPOSE. To characterize 2-year changes occurring in neurodegeneration, edema, and capillary dropout in nonproliferative diabetic retinopathy. METHODS. Two-year prospective longitudinal observational cohort of eyes/patients with type 2 diabetes using spectral domain optical coherence tomography (SD-OCT) and optical coherence tomography angiography (OCTA). Eyes were examined three times with intervals of 1 year. Thickness of the full retina and layer-by-layer measurements were used to identify edema or neurodegeneration. OCTA vessel density maps of the retina were used to identify capillary dropout. Early Treatment Diabetic Retinopathy Study (ETDRS) classification was performed using the seven-field ETDRS protocol. RESULTS. A total of 62 eyes from 62 patients with diabetes were followed for 2 years. After verification for image quality, a total of 44 eyes from 44 patients (30% women) aged 52 to 80 years were retained for data analysis. There were 18 eyes with ETDRS grades 10 to 20, 17 eyes with ETDRS grade 35, and 9 eyes with ETDRS grades 43 to 47. During the 2-year follow-up period, there was a progressive increase in capillary dropout, whereas edema and neurodegeneration remained stable. In multivariate analysis, considering a model adjusted for age, sex, hemoglobin A1C, visual acuity, and diabetes duration, vessel density remained significantly different between Diabetic Retinopathy Severity Scale groups (Wilks’ λ = 0.707; P = 0.015) showing association with disease progression. CONCLUSIONS. Capillary dropout increased in a period of 2 years in eyes with minimal, mild, and moderate diabetic retinopathy, whereas the presence of edema and neurodegeneration remained stable.pt
dc.language.isoengpt
dc.publisherAssociation for Research in Vision and Ophthalmologypt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectdiabetic retinopathypt
dc.subjectoptical coherence tomographypt
dc.subjectbiomarkerpt
dc.subjectprogressionpt
dc.subject.meshAgedpt
dc.subject.meshAged, 80 and overpt
dc.subject.meshCapillariespt
dc.subject.meshCase-Control Studiespt
dc.subject.meshDiabetes Mellitus, Type 2pt
dc.subject.meshDiabetic Retinopathypt
dc.subject.meshDisease Progressionpt
dc.subject.meshFemalept
dc.subject.meshHumanspt
dc.subject.meshLongitudinal Studiespt
dc.subject.meshMacular Edemapt
dc.subject.meshMalept
dc.subject.meshMiddle Agedpt
dc.subject.meshNerve Degenerationpt
dc.subject.meshRetinapt
dc.subject.meshRetinal Vesselspt
dc.subject.meshSeverity of Illness Indexpt
dc.subject.meshTomography, Optical Coherencept
dc.titleCharacterization of Disease Progression in the Initial Stages of Retinopathy in Type 2 Diabetes: A 2-Year Longitudinal Studypt
dc.typearticle-
degois.publication.firstPage20pt
degois.publication.issue3pt
degois.publication.titleInvestigative Ophthalmology and Visual Sciencept
dc.peerreviewedyespt
dc.identifier.doi10.1167/iovs.61.3.20pt
degois.publication.volume61pt
dc.date.embargo2020-03-09*
uc.date.periodoEmbargo0pt
item.grantfulltextopen-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextCom Texto completo-
crisitem.author.researchunitICBR Coimbra Institute for Clinical and Biomedical Research-
crisitem.author.researchunitCIBIT - Coimbra Institute for Biomedical Imaging and Translational Research-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.parentresearchunitFaculty of Medicine-
crisitem.author.orcid0000-0001-9170-6997-
crisitem.author.orcid0000-0003-3296-179X-
crisitem.author.orcid0000-0003-3761-3292-
crisitem.author.orcid0000-0002-0947-9850-
Appears in Collections:I&D CIBIT - Artigos em Revistas Internacionais
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