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Postoperative proliferative vitreoretinopathy development is linked to vitreal CXCL5 concentrations
The specific changes linked to de novo development of postoperative PVR have remained elusive and were the object of the underlying study. Vitreous fluid (VF) was obtained at the beginning of vitrectomy from 65 eyes that underwent vitrectomy for primary rhegmatogenous retinal detachment (RRD) withou...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8671512/ https://www.ncbi.nlm.nih.gov/pubmed/34907233 http://dx.doi.org/10.1038/s41598-021-03294-9 |
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author | Zandi, Souska Pfister, Isabel B. Garweg, Justus G. |
author_facet | Zandi, Souska Pfister, Isabel B. Garweg, Justus G. |
author_sort | Zandi, Souska |
collection | PubMed |
description | The specific changes linked to de novo development of postoperative PVR have remained elusive and were the object of the underlying study. Vitreous fluid (VF) was obtained at the beginning of vitrectomy from 65 eyes that underwent vitrectomy for primary rhegmatogenous retinal detachment (RRD) without preoperative PVR. Eyes developing postoperative PVR within 6 months after re-attachment surgery were compared to those which did not regarding the preoperative concentrations of 43 cytokines and chemokines in the VF, using multiplex beads analysis. For all comparisons Holm’s correction was applied in order to control for multiple comparisons. Twelve out of 65 eyes (18.5%) developed PVR postoperatively. While 12 of the chemokines and cytokines presented concentration differences on a statistical level of p < 0.05 (CXCL5, CCL11, CCL24, CCL26, GM-CSF, IFN-γ, CCL8, CCL7, MIF, MIG/CXCL9, CCL19, and CCL25), CXCL5 was the only cytokine with sufficiently robust difference in its VF concentrations to achieve significance in eyes developing postoperative PVR compared to eyes without PVR. CXCL5 may represent a potent biomarker for the de novo development of postoperative PVR. In line with its pathophysiological role in the development of PVR, it might serve as a basis for the development of urgently needed preventive options. |
format | Online Article Text |
id | pubmed-8671512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86715122021-12-16 Postoperative proliferative vitreoretinopathy development is linked to vitreal CXCL5 concentrations Zandi, Souska Pfister, Isabel B. Garweg, Justus G. Sci Rep Article The specific changes linked to de novo development of postoperative PVR have remained elusive and were the object of the underlying study. Vitreous fluid (VF) was obtained at the beginning of vitrectomy from 65 eyes that underwent vitrectomy for primary rhegmatogenous retinal detachment (RRD) without preoperative PVR. Eyes developing postoperative PVR within 6 months after re-attachment surgery were compared to those which did not regarding the preoperative concentrations of 43 cytokines and chemokines in the VF, using multiplex beads analysis. For all comparisons Holm’s correction was applied in order to control for multiple comparisons. Twelve out of 65 eyes (18.5%) developed PVR postoperatively. While 12 of the chemokines and cytokines presented concentration differences on a statistical level of p < 0.05 (CXCL5, CCL11, CCL24, CCL26, GM-CSF, IFN-γ, CCL8, CCL7, MIF, MIG/CXCL9, CCL19, and CCL25), CXCL5 was the only cytokine with sufficiently robust difference in its VF concentrations to achieve significance in eyes developing postoperative PVR compared to eyes without PVR. CXCL5 may represent a potent biomarker for the de novo development of postoperative PVR. In line with its pathophysiological role in the development of PVR, it might serve as a basis for the development of urgently needed preventive options. Nature Publishing Group UK 2021-12-14 /pmc/articles/PMC8671512/ /pubmed/34907233 http://dx.doi.org/10.1038/s41598-021-03294-9 Text en © The Author(s) 2021 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 Zandi, Souska Pfister, Isabel B. Garweg, Justus G. Postoperative proliferative vitreoretinopathy development is linked to vitreal CXCL5 concentrations |
title | Postoperative proliferative vitreoretinopathy development is linked to vitreal CXCL5 concentrations |
title_full | Postoperative proliferative vitreoretinopathy development is linked to vitreal CXCL5 concentrations |
title_fullStr | Postoperative proliferative vitreoretinopathy development is linked to vitreal CXCL5 concentrations |
title_full_unstemmed | Postoperative proliferative vitreoretinopathy development is linked to vitreal CXCL5 concentrations |
title_short | Postoperative proliferative vitreoretinopathy development is linked to vitreal CXCL5 concentrations |
title_sort | postoperative proliferative vitreoretinopathy development is linked to vitreal cxcl5 concentrations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8671512/ https://www.ncbi.nlm.nih.gov/pubmed/34907233 http://dx.doi.org/10.1038/s41598-021-03294-9 |
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