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Retinal vascular assessment in psoriatic patients with and without metabolic syndrome using optical coherence tomography angiography

To evaluate the retinal vasculature in psoriasis patients and detect if metabolic syndrome is an additional risk factor. This cross-sectional analytic study was carried out on 80 eyes of 80 subjects; 28 eyes with psoriasis only (PS group), 12 eyes with additional metabolic syndrome to psoriasis (PMS...

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Autores principales: Tolba, Doaa Ahmed, Amin, Rana Hussein, Alorbani, Aya Magdi, Mamdouh Esmat, Sara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9537140/
https://www.ncbi.nlm.nih.gov/pubmed/36202827
http://dx.doi.org/10.1038/s41598-022-20307-3
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author Tolba, Doaa Ahmed
Amin, Rana Hussein
Alorbani, Aya Magdi
Mamdouh Esmat, Sara
author_facet Tolba, Doaa Ahmed
Amin, Rana Hussein
Alorbani, Aya Magdi
Mamdouh Esmat, Sara
author_sort Tolba, Doaa Ahmed
collection PubMed
description To evaluate the retinal vasculature in psoriasis patients and detect if metabolic syndrome is an additional risk factor. This cross-sectional analytic study was carried out on 80 eyes of 80 subjects; 28 eyes with psoriasis only (PS group), 12 eyes with additional metabolic syndrome to psoriasis (PMS group) and 40 eyes healthy controls (HS). The retinal capillary plexuses were evaluated by OCTA. The disease activity was evaluated by the Psoriasis Area and Severity Index (PASI) score and extent. The superficial capillary plexus (SCP) vascular density was significantly lower in PS group than HS while in PMS it was significantly lower only in whole image and superior and temporal perifoveal areas (p-value = 0.020, 0.030, 0.001 respectively). The changes correlated with the disease duration. The vascular density of the deep capillary plexus (DCP) was significantly lower in both PS and PMS groups (p-value < 0.001). Psoriatic patients are at a higher risk of developing retinal vascular complications even without evident clinical ocular disease. It was noted that the presence of metabolic syndrome contributes as an additional risk factor in possible visual loss secondary to ischemic changes that are likely to start in the DCP and progress to involve all levels.
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spelling pubmed-95371402022-10-08 Retinal vascular assessment in psoriatic patients with and without metabolic syndrome using optical coherence tomography angiography Tolba, Doaa Ahmed Amin, Rana Hussein Alorbani, Aya Magdi Mamdouh Esmat, Sara Sci Rep Article To evaluate the retinal vasculature in psoriasis patients and detect if metabolic syndrome is an additional risk factor. This cross-sectional analytic study was carried out on 80 eyes of 80 subjects; 28 eyes with psoriasis only (PS group), 12 eyes with additional metabolic syndrome to psoriasis (PMS group) and 40 eyes healthy controls (HS). The retinal capillary plexuses were evaluated by OCTA. The disease activity was evaluated by the Psoriasis Area and Severity Index (PASI) score and extent. The superficial capillary plexus (SCP) vascular density was significantly lower in PS group than HS while in PMS it was significantly lower only in whole image and superior and temporal perifoveal areas (p-value = 0.020, 0.030, 0.001 respectively). The changes correlated with the disease duration. The vascular density of the deep capillary plexus (DCP) was significantly lower in both PS and PMS groups (p-value < 0.001). Psoriatic patients are at a higher risk of developing retinal vascular complications even without evident clinical ocular disease. It was noted that the presence of metabolic syndrome contributes as an additional risk factor in possible visual loss secondary to ischemic changes that are likely to start in the DCP and progress to involve all levels. Nature Publishing Group UK 2022-10-06 /pmc/articles/PMC9537140/ /pubmed/36202827 http://dx.doi.org/10.1038/s41598-022-20307-3 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
Tolba, Doaa Ahmed
Amin, Rana Hussein
Alorbani, Aya Magdi
Mamdouh Esmat, Sara
Retinal vascular assessment in psoriatic patients with and without metabolic syndrome using optical coherence tomography angiography
title Retinal vascular assessment in psoriatic patients with and without metabolic syndrome using optical coherence tomography angiography
title_full Retinal vascular assessment in psoriatic patients with and without metabolic syndrome using optical coherence tomography angiography
title_fullStr Retinal vascular assessment in psoriatic patients with and without metabolic syndrome using optical coherence tomography angiography
title_full_unstemmed Retinal vascular assessment in psoriatic patients with and without metabolic syndrome using optical coherence tomography angiography
title_short Retinal vascular assessment in psoriatic patients with and without metabolic syndrome using optical coherence tomography angiography
title_sort retinal vascular assessment in psoriatic patients with and without metabolic syndrome using optical coherence tomography angiography
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9537140/
https://www.ncbi.nlm.nih.gov/pubmed/36202827
http://dx.doi.org/10.1038/s41598-022-20307-3
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