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Retinal Microvascular Changes in Subtypes of Ischemic Stroke

Aims: Retinal microvasculature shares prominent similarities with the brain vasculature. We aimed to assess the association between retinal microvasculature and subtypes of ischemic stroke. Method: We consecutively enrolled ischemic stroke patients within 7 days of onset, who met the criteria of sub...

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Autores principales: Zhao, Ying, Yang, Bing, Xu, An-Ding, Ruan, Yi-Wen, Xu, Ying, Hu, Hui-Ling, Tan, Ze-Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7873353/
https://www.ncbi.nlm.nih.gov/pubmed/33584518
http://dx.doi.org/10.3389/fneur.2020.619554
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author Zhao, Ying
Yang, Bing
Xu, An-Ding
Ruan, Yi-Wen
Xu, Ying
Hu, Hui-Ling
Tan, Ze-Feng
author_facet Zhao, Ying
Yang, Bing
Xu, An-Ding
Ruan, Yi-Wen
Xu, Ying
Hu, Hui-Ling
Tan, Ze-Feng
author_sort Zhao, Ying
collection PubMed
description Aims: Retinal microvasculature shares prominent similarities with the brain vasculature. We aimed to assess the association between retinal microvasculature and subtypes of ischemic stroke. Method: We consecutively enrolled ischemic stroke patients within 7 days of onset, who met the criteria of subtype of atherothrombosis (AT), small artery disease (SAD), or cardioembolism (CE) according to a modified version of the Trial of Org 10172 in Acute Stroke Treatment (NEW-TOAST). Digital fundus photographs were taken within 72 h of hospital admission using a digital camera (Topcon TRC-50DX), and fundus photographs were semi-automatically measured by software (Canvus 14 and NeuroLucida) for retinal vasculature parameters. Results: A total of 141 patients were enrolled, including 72 with AT, 54 with SAD, and 15 with CE. AT subtype patients had the widest mean venular diameter within 0.5–1.0 disk diameter (MVD(0.5−1.0DD)) followed by SAD and CE subtypes (86.37 ± 13.49 vs. 83.55 ± 11.54 vs. 77.90 ± 8.50, respectively, P = 0.047); CE subtype patients had the highest mean arteriovenous ratio within 0.5–1.0 disk diameter (MAVR(0.5−1.0DD)) followed by the AT and SAD subtype groups (0.97 ± 0.03 vs. 0.89 ± 0.99 vs. 0.89 ± 0.11, respectively, P = 0.010); SAD subtype patients were found with the highest mean venular tortuosity within 0.0–2.0 disk diameter (MVT(0.0−2.0DD)) followed by the AT and CE subtypes (1.0294 ± 0.0081 vs. 1.0259 ± 0.0084 vs. 1.0243 ± 0.0066, respectively, P = 0.024). After adjusting for clinic characteristics, MVD(0.5−1.0DD) was significantly different among AT, SAD, and CE subtypes (P = 0.033). By receiver operating characteristic curve analysis, MVD(0.5−1.0DD) predicted the AT subtype (area 0.690, 95% confidence interval, 0.566–0.815), with a cutoff value of 82.23 μm (sensitivity 61.1%, specificity 73.3%). Conclusion: Retinal MVD(0.5−1.0DD) (>82.23 μm) might be associated with the AT stroke subtype; however, we need large-scale prospective studies in future to explore the underlying mechanism and causal explanation for this finding.
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spelling pubmed-78733532021-02-11 Retinal Microvascular Changes in Subtypes of Ischemic Stroke Zhao, Ying Yang, Bing Xu, An-Ding Ruan, Yi-Wen Xu, Ying Hu, Hui-Ling Tan, Ze-Feng Front Neurol Neurology Aims: Retinal microvasculature shares prominent similarities with the brain vasculature. We aimed to assess the association between retinal microvasculature and subtypes of ischemic stroke. Method: We consecutively enrolled ischemic stroke patients within 7 days of onset, who met the criteria of subtype of atherothrombosis (AT), small artery disease (SAD), or cardioembolism (CE) according to a modified version of the Trial of Org 10172 in Acute Stroke Treatment (NEW-TOAST). Digital fundus photographs were taken within 72 h of hospital admission using a digital camera (Topcon TRC-50DX), and fundus photographs were semi-automatically measured by software (Canvus 14 and NeuroLucida) for retinal vasculature parameters. Results: A total of 141 patients were enrolled, including 72 with AT, 54 with SAD, and 15 with CE. AT subtype patients had the widest mean venular diameter within 0.5–1.0 disk diameter (MVD(0.5−1.0DD)) followed by SAD and CE subtypes (86.37 ± 13.49 vs. 83.55 ± 11.54 vs. 77.90 ± 8.50, respectively, P = 0.047); CE subtype patients had the highest mean arteriovenous ratio within 0.5–1.0 disk diameter (MAVR(0.5−1.0DD)) followed by the AT and SAD subtype groups (0.97 ± 0.03 vs. 0.89 ± 0.99 vs. 0.89 ± 0.11, respectively, P = 0.010); SAD subtype patients were found with the highest mean venular tortuosity within 0.0–2.0 disk diameter (MVT(0.0−2.0DD)) followed by the AT and CE subtypes (1.0294 ± 0.0081 vs. 1.0259 ± 0.0084 vs. 1.0243 ± 0.0066, respectively, P = 0.024). After adjusting for clinic characteristics, MVD(0.5−1.0DD) was significantly different among AT, SAD, and CE subtypes (P = 0.033). By receiver operating characteristic curve analysis, MVD(0.5−1.0DD) predicted the AT subtype (area 0.690, 95% confidence interval, 0.566–0.815), with a cutoff value of 82.23 μm (sensitivity 61.1%, specificity 73.3%). Conclusion: Retinal MVD(0.5−1.0DD) (>82.23 μm) might be associated with the AT stroke subtype; however, we need large-scale prospective studies in future to explore the underlying mechanism and causal explanation for this finding. Frontiers Media S.A. 2021-01-27 /pmc/articles/PMC7873353/ /pubmed/33584518 http://dx.doi.org/10.3389/fneur.2020.619554 Text en Copyright © 2021 Zhao, Yang, Xu, Ruan, Xu, Hu and Tan. http://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 Neurology
Zhao, Ying
Yang, Bing
Xu, An-Ding
Ruan, Yi-Wen
Xu, Ying
Hu, Hui-Ling
Tan, Ze-Feng
Retinal Microvascular Changes in Subtypes of Ischemic Stroke
title Retinal Microvascular Changes in Subtypes of Ischemic Stroke
title_full Retinal Microvascular Changes in Subtypes of Ischemic Stroke
title_fullStr Retinal Microvascular Changes in Subtypes of Ischemic Stroke
title_full_unstemmed Retinal Microvascular Changes in Subtypes of Ischemic Stroke
title_short Retinal Microvascular Changes in Subtypes of Ischemic Stroke
title_sort retinal microvascular changes in subtypes of ischemic stroke
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7873353/
https://www.ncbi.nlm.nih.gov/pubmed/33584518
http://dx.doi.org/10.3389/fneur.2020.619554
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