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Clinical significance of metabolic quantification for retinal nonperfusion in diabetic retinopathy
Diabetic retinopathy (DR) is characterized by microvascular changes including ischemia. Degradation and metabolic changes of various retinal cells occur during ischemia. Ischemic region containing more cells will lead to greater metabolic impairment. We analyzed the non-perfusion region (NPR) by int...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9167306/ https://www.ncbi.nlm.nih.gov/pubmed/35665762 http://dx.doi.org/10.1038/s41598-022-13439-z |
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author | Jeong, Areum Yao, Xue van Hemert, Jano Sagong, Min |
author_facet | Jeong, Areum Yao, Xue van Hemert, Jano Sagong, Min |
author_sort | Jeong, Areum |
collection | PubMed |
description | Diabetic retinopathy (DR) is characterized by microvascular changes including ischemia. Degradation and metabolic changes of various retinal cells occur during ischemia. Ischemic region containing more cells will lead to greater metabolic impairment. We analyzed the non-perfusion region (NPR) by integrating histologic mapping with ultra-widefield fluorescein angiography (UWF FA) images. We also investigated the correlations of the weighted ischemic index (ISI) considering the regional distribution of retinal cells with cytokines, macular edema (ME), and neovascularization (NV). In this study, 32 patients with treatment-naïve DR and 21 age-matched control participants were included. The difference between the non-weighted and weighted ISI of NPR with leakage was greatest at the posterior region. The weighted ISI of NPR with leakage was correlated with MCP-1, IL-8, IL-6, PlGF, and VEGF-A levels, while the non-weighted ISI of NPR with leakage was correlated with IL-8 and IL-6 levels. The presence of baseline ME or NV in patients with DR was associated with the weighted ISI, with a stronger association when cones and rods were weighted. The weighted ISI reflecting both metabolic activity and cell distribution demonstrated a better correlation with clinical features and was more valuable in NPR with leakage than non-weighted ISI, which previous studies conventionally used. |
format | Online Article Text |
id | pubmed-9167306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91673062022-06-06 Clinical significance of metabolic quantification for retinal nonperfusion in diabetic retinopathy Jeong, Areum Yao, Xue van Hemert, Jano Sagong, Min Sci Rep Article Diabetic retinopathy (DR) is characterized by microvascular changes including ischemia. Degradation and metabolic changes of various retinal cells occur during ischemia. Ischemic region containing more cells will lead to greater metabolic impairment. We analyzed the non-perfusion region (NPR) by integrating histologic mapping with ultra-widefield fluorescein angiography (UWF FA) images. We also investigated the correlations of the weighted ischemic index (ISI) considering the regional distribution of retinal cells with cytokines, macular edema (ME), and neovascularization (NV). In this study, 32 patients with treatment-naïve DR and 21 age-matched control participants were included. The difference between the non-weighted and weighted ISI of NPR with leakage was greatest at the posterior region. The weighted ISI of NPR with leakage was correlated with MCP-1, IL-8, IL-6, PlGF, and VEGF-A levels, while the non-weighted ISI of NPR with leakage was correlated with IL-8 and IL-6 levels. The presence of baseline ME or NV in patients with DR was associated with the weighted ISI, with a stronger association when cones and rods were weighted. The weighted ISI reflecting both metabolic activity and cell distribution demonstrated a better correlation with clinical features and was more valuable in NPR with leakage than non-weighted ISI, which previous studies conventionally used. Nature Publishing Group UK 2022-06-04 /pmc/articles/PMC9167306/ /pubmed/35665762 http://dx.doi.org/10.1038/s41598-022-13439-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Jeong, Areum Yao, Xue van Hemert, Jano Sagong, Min Clinical significance of metabolic quantification for retinal nonperfusion in diabetic retinopathy |
title | Clinical significance of metabolic quantification for retinal nonperfusion in diabetic retinopathy |
title_full | Clinical significance of metabolic quantification for retinal nonperfusion in diabetic retinopathy |
title_fullStr | Clinical significance of metabolic quantification for retinal nonperfusion in diabetic retinopathy |
title_full_unstemmed | Clinical significance of metabolic quantification for retinal nonperfusion in diabetic retinopathy |
title_short | Clinical significance of metabolic quantification for retinal nonperfusion in diabetic retinopathy |
title_sort | clinical significance of metabolic quantification for retinal nonperfusion in diabetic retinopathy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9167306/ https://www.ncbi.nlm.nih.gov/pubmed/35665762 http://dx.doi.org/10.1038/s41598-022-13439-z |
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