Cargando…
Retinal Neurodegeneration in Different Risk Phenotypes of Diabetic Retinal Disease
Diabetic retinopathy (DR) has been considered a microvascular disease, but it has become evident that neurodegeneration also plays a key role in this complex pathology. Indeed, this complexity is reflected in its progression which occurs at different rates in different type 2 diabetic (T2D) individu...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9231566/ https://www.ncbi.nlm.nih.gov/pubmed/35757010 http://dx.doi.org/10.3389/fnins.2021.800004 |
_version_ | 1784735373113425920 |
---|---|
author | Madeira, Maria H. Marques, Inês P. Ferreira, Sónia Tavares, Diana Santos, Torcato Santos, Ana Rita Figueira, João Lobo, Conceição Cunha-Vaz, José |
author_facet | Madeira, Maria H. Marques, Inês P. Ferreira, Sónia Tavares, Diana Santos, Torcato Santos, Ana Rita Figueira, João Lobo, Conceição Cunha-Vaz, José |
author_sort | Madeira, Maria H. |
collection | PubMed |
description | Diabetic retinopathy (DR) has been considered a microvascular disease, but it has become evident that neurodegeneration also plays a key role in this complex pathology. Indeed, this complexity is reflected in its progression which occurs at different rates in different type 2 diabetic (T2D) individuals. Based on this concept, our group has identified three DR progression phenotypes that might reflect the interindividual differences: phenotype A, characterized by low microaneurysm turnover (MAT <6), phenotype B, low MAT (<6) and increased central retinal thickness (CRT); and phenotype C, with high MAT (≥6). In this study, we evaluated the progression of DR neurodegeneration, considering ganglion cell+inner plexiform layers (GCL+IPL) thinning, in 170 T2D individuals followed for a period of 5 years, to explore associations with disease progression or risk phenotypes. Ophthalmological examinations were performed at baseline, first 6 months, and annually. GCL+IPL average thickness was evaluated by optical coherence tomography (OCT). Microaneurysm turnover (MAT) was evaluated using the RetMarkerDR. ETDRS level and severity progression were assessed in seven-field color fundus photography. In the overall population there was a significant loss in GCL+IPL (−0.147 μm/year), independently of glycated hemoglobin, age, sex, and duration of diabetes. Interestingly, this progressive thinning in GCL + IPL reached higher values in phenotypes B and C (−0.249 and −0.238 μm/year, respectively), whereas phenotype A remained relatively stable. The presence of neurodegeneration in all phenotypes suggests that it is the retinal vascular response to the early neurodegenerative changes that determines the course of the retinopathy in each individual. Therefore, classification of different DR phenotypes appears to offer relevant clarification of DR disease progression and an opportunity for improved management of each T2D individual with DR, thus playing a valuable role for the implementation of personalized medicine in DR. |
format | Online Article Text |
id | pubmed-9231566 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92315662022-06-25 Retinal Neurodegeneration in Different Risk Phenotypes of Diabetic Retinal Disease Madeira, Maria H. Marques, Inês P. Ferreira, Sónia Tavares, Diana Santos, Torcato Santos, Ana Rita Figueira, João Lobo, Conceição Cunha-Vaz, José Front Neurosci Neuroscience Diabetic retinopathy (DR) has been considered a microvascular disease, but it has become evident that neurodegeneration also plays a key role in this complex pathology. Indeed, this complexity is reflected in its progression which occurs at different rates in different type 2 diabetic (T2D) individuals. Based on this concept, our group has identified three DR progression phenotypes that might reflect the interindividual differences: phenotype A, characterized by low microaneurysm turnover (MAT <6), phenotype B, low MAT (<6) and increased central retinal thickness (CRT); and phenotype C, with high MAT (≥6). In this study, we evaluated the progression of DR neurodegeneration, considering ganglion cell+inner plexiform layers (GCL+IPL) thinning, in 170 T2D individuals followed for a period of 5 years, to explore associations with disease progression or risk phenotypes. Ophthalmological examinations were performed at baseline, first 6 months, and annually. GCL+IPL average thickness was evaluated by optical coherence tomography (OCT). Microaneurysm turnover (MAT) was evaluated using the RetMarkerDR. ETDRS level and severity progression were assessed in seven-field color fundus photography. In the overall population there was a significant loss in GCL+IPL (−0.147 μm/year), independently of glycated hemoglobin, age, sex, and duration of diabetes. Interestingly, this progressive thinning in GCL + IPL reached higher values in phenotypes B and C (−0.249 and −0.238 μm/year, respectively), whereas phenotype A remained relatively stable. The presence of neurodegeneration in all phenotypes suggests that it is the retinal vascular response to the early neurodegenerative changes that determines the course of the retinopathy in each individual. Therefore, classification of different DR phenotypes appears to offer relevant clarification of DR disease progression and an opportunity for improved management of each T2D individual with DR, thus playing a valuable role for the implementation of personalized medicine in DR. Frontiers Media S.A. 2021-12-21 /pmc/articles/PMC9231566/ /pubmed/35757010 http://dx.doi.org/10.3389/fnins.2021.800004 Text en Copyright © 2021 Madeira, Marques, Ferreira, Tavares, Santos, Santos, Figueira, Lobo and Cunha-Vaz. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Madeira, Maria H. Marques, Inês P. Ferreira, Sónia Tavares, Diana Santos, Torcato Santos, Ana Rita Figueira, João Lobo, Conceição Cunha-Vaz, José Retinal Neurodegeneration in Different Risk Phenotypes of Diabetic Retinal Disease |
title | Retinal Neurodegeneration in Different Risk Phenotypes of Diabetic Retinal Disease |
title_full | Retinal Neurodegeneration in Different Risk Phenotypes of Diabetic Retinal Disease |
title_fullStr | Retinal Neurodegeneration in Different Risk Phenotypes of Diabetic Retinal Disease |
title_full_unstemmed | Retinal Neurodegeneration in Different Risk Phenotypes of Diabetic Retinal Disease |
title_short | Retinal Neurodegeneration in Different Risk Phenotypes of Diabetic Retinal Disease |
title_sort | retinal neurodegeneration in different risk phenotypes of diabetic retinal disease |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9231566/ https://www.ncbi.nlm.nih.gov/pubmed/35757010 http://dx.doi.org/10.3389/fnins.2021.800004 |
work_keys_str_mv | AT madeiramariah retinalneurodegenerationindifferentriskphenotypesofdiabeticretinaldisease AT marquesinesp retinalneurodegenerationindifferentriskphenotypesofdiabeticretinaldisease AT ferreirasonia retinalneurodegenerationindifferentriskphenotypesofdiabeticretinaldisease AT tavaresdiana retinalneurodegenerationindifferentriskphenotypesofdiabeticretinaldisease AT santostorcato retinalneurodegenerationindifferentriskphenotypesofdiabeticretinaldisease AT santosanarita retinalneurodegenerationindifferentriskphenotypesofdiabeticretinaldisease AT figueirajoao retinalneurodegenerationindifferentriskphenotypesofdiabeticretinaldisease AT loboconceicao retinalneurodegenerationindifferentriskphenotypesofdiabeticretinaldisease AT cunhavazjose retinalneurodegenerationindifferentriskphenotypesofdiabeticretinaldisease |