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Association of OCT biomarkers and visual impairment in patients with diabetic macular oedema with vitreomacular adhesion
BACKGROUND: To analyse the distribution of spectral domain optical coherence tomography (SD-OCT) biomarkers in different types of vitreomacular adhesion (VMA) associated visual impairment in diabetic macular oedema. METHODS: A total of 317 eyes of 202 patients were enrolled. Cases were divided into...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10353796/ https://www.ncbi.nlm.nih.gov/pubmed/37463157 http://dx.doi.org/10.1371/journal.pone.0288879 |
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author | Subramanian, Brughanya Devishamani, Chitralekha Raman, Rajiv Ratra, Dhanashree |
author_facet | Subramanian, Brughanya Devishamani, Chitralekha Raman, Rajiv Ratra, Dhanashree |
author_sort | Subramanian, Brughanya |
collection | PubMed |
description | BACKGROUND: To analyse the distribution of spectral domain optical coherence tomography (SD-OCT) biomarkers in different types of vitreomacular adhesion (VMA) associated visual impairment in diabetic macular oedema. METHODS: A total of 317 eyes of 202 patients were enrolled. Cases were divided into two groups focal VMA and broad VMA and subjects with no VMA were enrolled as controls. A grading platform was used for evaluating the morphology of diabetic macular oedema (DME), using good-quality SD-OCT images. Grading was done for VMA and the biomarkers. Best corrected visual acuity (BCVA), central retinal thickness (CRT) and central subfield thickness (CSFT) was also recorded. RESULTS: The CRT (p = <0.001) and CSFT (p = <0.001) values were statistically significant between the groups. Except for Inner Nuclear Layer Cysts (p = <0.001), absence of Bridging Tissue that is composed of muller cell fibers and bipolar cells (p<0.001), and Hyper Reflective Dots (HRD) in cyst (p = 0.006) there were no significant differences in the distribution of OCT biomarkers among the 3 groups (focal VMA, broad VMA and no VMA). Only Disorganization of Retinal Inner Layers (DRIL) (p = 0.044) showed significant association with vision impairment in all the 3 groups. CONCLUSION: The distribution of OCT biomarkers was similar across all eyes of cases and controls. However, they were more likely to be associated with visual impairment in the presence of VMA than no VMA. |
format | Online Article Text |
id | pubmed-10353796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-103537962023-07-19 Association of OCT biomarkers and visual impairment in patients with diabetic macular oedema with vitreomacular adhesion Subramanian, Brughanya Devishamani, Chitralekha Raman, Rajiv Ratra, Dhanashree PLoS One Research Article BACKGROUND: To analyse the distribution of spectral domain optical coherence tomography (SD-OCT) biomarkers in different types of vitreomacular adhesion (VMA) associated visual impairment in diabetic macular oedema. METHODS: A total of 317 eyes of 202 patients were enrolled. Cases were divided into two groups focal VMA and broad VMA and subjects with no VMA were enrolled as controls. A grading platform was used for evaluating the morphology of diabetic macular oedema (DME), using good-quality SD-OCT images. Grading was done for VMA and the biomarkers. Best corrected visual acuity (BCVA), central retinal thickness (CRT) and central subfield thickness (CSFT) was also recorded. RESULTS: The CRT (p = <0.001) and CSFT (p = <0.001) values were statistically significant between the groups. Except for Inner Nuclear Layer Cysts (p = <0.001), absence of Bridging Tissue that is composed of muller cell fibers and bipolar cells (p<0.001), and Hyper Reflective Dots (HRD) in cyst (p = 0.006) there were no significant differences in the distribution of OCT biomarkers among the 3 groups (focal VMA, broad VMA and no VMA). Only Disorganization of Retinal Inner Layers (DRIL) (p = 0.044) showed significant association with vision impairment in all the 3 groups. CONCLUSION: The distribution of OCT biomarkers was similar across all eyes of cases and controls. However, they were more likely to be associated with visual impairment in the presence of VMA than no VMA. Public Library of Science 2023-07-18 /pmc/articles/PMC10353796/ /pubmed/37463157 http://dx.doi.org/10.1371/journal.pone.0288879 Text en © 2023 Subramanian et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Subramanian, Brughanya Devishamani, Chitralekha Raman, Rajiv Ratra, Dhanashree Association of OCT biomarkers and visual impairment in patients with diabetic macular oedema with vitreomacular adhesion |
title | Association of OCT biomarkers and visual impairment in patients with diabetic macular oedema with vitreomacular adhesion |
title_full | Association of OCT biomarkers and visual impairment in patients with diabetic macular oedema with vitreomacular adhesion |
title_fullStr | Association of OCT biomarkers and visual impairment in patients with diabetic macular oedema with vitreomacular adhesion |
title_full_unstemmed | Association of OCT biomarkers and visual impairment in patients with diabetic macular oedema with vitreomacular adhesion |
title_short | Association of OCT biomarkers and visual impairment in patients with diabetic macular oedema with vitreomacular adhesion |
title_sort | association of oct biomarkers and visual impairment in patients with diabetic macular oedema with vitreomacular adhesion |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10353796/ https://www.ncbi.nlm.nih.gov/pubmed/37463157 http://dx.doi.org/10.1371/journal.pone.0288879 |
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