Publication
Characterization of one-year progression of risk phenotypes of diabetic retinopathy
dc.contributor.author | Ribeiro, Luísa | |
dc.contributor.author | Marques, Inês P. | |
dc.contributor.author | Coimbra, Rita | |
dc.contributor.author | Santos, Torcato | |
dc.contributor.author | Madeira, Maria H. | |
dc.contributor.author | Santos, Ana Rita | |
dc.contributor.author | Barreto, Patrícia | |
dc.contributor.author | Lobo, Conceição | |
dc.contributor.author | Cunha-Vaz, José | |
dc.date.accessioned | 2023-01-31T15:34:36Z | |
dc.date.available | 2023-01-31T15:34:36Z | |
dc.date.issued | 2022 | |
dc.description.abstract | We characterized the progression of different diabetic retinopathy (DR) phenotypes in type 2 diabetes (T2D). A prospective longitudinal cohort study (CORDIS, NCT03696810) was conducted with three visits (baseline, 6 months, and 1 year). Demographic and systemic data included age, sex, diabetes duration, lipid profile, and hemoglobin A1c (HbA1c). Ophthalmological examinations included best-corrected visual acuity (BCVA), color fundus photography (CFP), and optical coherence tomography (OCT and OCTA). Phenotype classification was performed at the 6-month visit based on microaneurysm turnover (MAT, on CFP) and central retinal thickness (CRT, on OCT). Only risk phenotypes B (MAT < 6 and increased CRT) and C (MAT ≥ 6 with or without increased CRT) were included. ETDRS grading was performed at the baseline visit based on seven-field CFP.A total of 133 T2D individuals were included in the study; 81 (60%) eyes were classified as phenotype B and 52 (40%) eyes as phenotype C. Of these, 128 completed the 1-year follow-up. At baseline, eyes with phenotype C showed greater capillary closure (superior capillary plexus, deep capillary plexus, and full retina, p < 0.001) and increased foveal avascular zone (FAZ) area (p < 0.001), indicating more advanced microvascular disease. Neurodegeneration represented by thinning of the ganglion cell layer + inner plexiform layer (GCL + IPL) was present in both phenotypes. When analyzing the 1-year progression of each phenotype, only phenotype C revealed a significant decrease in BCVA (p = 0.02) and enlargement of the FAZ (p = 0.03). A significant progressive decrease in the vessel density of the deep capillary layer and in MAT occurred in both phenotypes, but these changes were particularly relevant in phenotype C and ETDRS grades 43–47. During the 1-year period, both phenotypes B and C showed progression in GCL + IPL thinning (p < 0.001). In the 1-year period of follow-up, both phenotypes B and C showed progression in retinal neurodegeneration, whereas phenotype C showed more marked disease progression at the microvascular level. | pt_PT |
dc.description.version | info:eu-repo/semantics/publishedVersion | pt_PT |
dc.identifier.citation | Ribeiro, L., Marques, I.P., Coimbra, R. et al. Characterization of One-Year Progression of Risk Phenotypes of Diabetic Retinopathy. Ophthalmol Ther 11, 333–345 (2022). https://doi.org/10.1007/s40123-021-00437-z | pt_PT |
dc.identifier.doi | 10.1007/s40123-021-00437-z | pt_PT |
dc.identifier.eissn | 2193-6528 | |
dc.identifier.issn | 2193-8245 | |
dc.identifier.uri | http://hdl.handle.net/10400.22/22039 | |
dc.language.iso | eng | pt_PT |
dc.peerreviewed | yes | pt_PT |
dc.publisher | Springer | pt_PT |
dc.relation.publisherversion | https://link.springer.com/article/10.1007/s40123-021-00437-z | pt_PT |
dc.rights.uri | http://creativecommons.org/licenses/by-nc/4.0/ | pt_PT |
dc.subject | Diabetes | pt_PT |
dc.subject | Retinopathy | pt_PT |
dc.subject | Capillary closure | pt_PT |
dc.subject | Neurodegeneration | pt_PT |
dc.title | Characterization of one-year progression of risk phenotypes of diabetic retinopathy | pt_PT |
dc.type | journal article | |
dspace.entity.type | Publication | |
oaire.citation.endPage | 345 | pt_PT |
oaire.citation.startPage | 333 | pt_PT |
oaire.citation.title | Ophthalmology and Therapy | pt_PT |
oaire.citation.volume | 11 | pt_PT |
person.familyName | Santos | |
person.givenName | Ana Rita | |
person.identifier.ciencia-id | 0911-4138-0C3A | |
person.identifier.orcid | 0000-0003-0139-0285 | |
rcaap.rights | openAccess | pt_PT |
rcaap.type | article | pt_PT |
relation.isAuthorOfPublication | d71931b8-d869-4334-993c-ba14ad713f01 | |
relation.isAuthorOfPublication.latestForDiscovery | d71931b8-d869-4334-993c-ba14ad713f01 |