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Comparison of matrix metallopeptidase-9 expression following cyclosporine and diquafosol treatment in dry eye
PURPOSE: We sought to evaluate the expression of matrix metalloproteinase-9 (MMP-9) in dry eyes treated with 0.05% cyclosporin A and 3.0% diquafosol tetrasodium. METHODS: One-hundred ninety-five eyes of 195 patients with dry eye were divided into three groups as follows: group 1, cyclosporin group (...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10291919/ https://www.ncbi.nlm.nih.gov/pubmed/37354028 http://dx.doi.org/10.1080/07853890.2023.2228192 |
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author | So, Ha Rim Baek, Jiwon Lee, Ji Young Kim, Hyun Seung Kim, Man Soo Kim, Eun Chul |
author_facet | So, Ha Rim Baek, Jiwon Lee, Ji Young Kim, Hyun Seung Kim, Man Soo Kim, Eun Chul |
author_sort | So, Ha Rim |
collection | PubMed |
description | PURPOSE: We sought to evaluate the expression of matrix metalloproteinase-9 (MMP-9) in dry eyes treated with 0.05% cyclosporin A and 3.0% diquafosol tetrasodium. METHODS: One-hundred ninety-five eyes of 195 patients with dry eye were divided into three groups as follows: group 1, cyclosporin group (n = 69); group 2, diquafosol group (n = 59); and group 3, artificial tears eyes (n = 67). All eyes were treated and followed up for three months. Schirmer I Test, corneal staining, tear-film break-up time (TBUT), and tear-film MMP-9 content were measured at three months and compared between groups. The expression of MMP-9 was confirmed using a point-of-care test device (InflammaDry®; RPS Diagnostics, Sarasota, FL, USA) and graded as zero to four points. RESULTS: At the third month, MMP-9 expression was lower in group 1 as compared with in groups 2 and 3 (p = 0.020 and 0.006, respectively). The mean MMP-9 grade according to point-of-care testing was also lower in group 1 than in groups 2 or 3 (p = 0.002 and 0.038, respectively). MMP-9 showed a correlation with corneal staining in both groups 1 and 2 (all p < 0.001) and with Schirmer I Test and TBUT in group 1 (p = 0.018 and 0.015, respectively). CONCLUSIONS: MMP-9 expression and grade were lower after treatment with cyclosporin than after treatment with diquafosol in the dry eye disease. Anti-inflammatory treatment can decrease ocular MMP-9 levels in dry eye disease. |
format | Online Article Text |
id | pubmed-10291919 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-102919192023-06-27 Comparison of matrix metallopeptidase-9 expression following cyclosporine and diquafosol treatment in dry eye So, Ha Rim Baek, Jiwon Lee, Ji Young Kim, Hyun Seung Kim, Man Soo Kim, Eun Chul Ann Med Ophthalmology PURPOSE: We sought to evaluate the expression of matrix metalloproteinase-9 (MMP-9) in dry eyes treated with 0.05% cyclosporin A and 3.0% diquafosol tetrasodium. METHODS: One-hundred ninety-five eyes of 195 patients with dry eye were divided into three groups as follows: group 1, cyclosporin group (n = 69); group 2, diquafosol group (n = 59); and group 3, artificial tears eyes (n = 67). All eyes were treated and followed up for three months. Schirmer I Test, corneal staining, tear-film break-up time (TBUT), and tear-film MMP-9 content were measured at three months and compared between groups. The expression of MMP-9 was confirmed using a point-of-care test device (InflammaDry®; RPS Diagnostics, Sarasota, FL, USA) and graded as zero to four points. RESULTS: At the third month, MMP-9 expression was lower in group 1 as compared with in groups 2 and 3 (p = 0.020 and 0.006, respectively). The mean MMP-9 grade according to point-of-care testing was also lower in group 1 than in groups 2 or 3 (p = 0.002 and 0.038, respectively). MMP-9 showed a correlation with corneal staining in both groups 1 and 2 (all p < 0.001) and with Schirmer I Test and TBUT in group 1 (p = 0.018 and 0.015, respectively). CONCLUSIONS: MMP-9 expression and grade were lower after treatment with cyclosporin than after treatment with diquafosol in the dry eye disease. Anti-inflammatory treatment can decrease ocular MMP-9 levels in dry eye disease. Taylor & Francis 2023-06-24 /pmc/articles/PMC10291919/ /pubmed/37354028 http://dx.doi.org/10.1080/07853890.2023.2228192 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent. |
spellingShingle | Ophthalmology So, Ha Rim Baek, Jiwon Lee, Ji Young Kim, Hyun Seung Kim, Man Soo Kim, Eun Chul Comparison of matrix metallopeptidase-9 expression following cyclosporine and diquafosol treatment in dry eye |
title | Comparison of matrix metallopeptidase-9 expression following cyclosporine and diquafosol treatment in dry eye |
title_full | Comparison of matrix metallopeptidase-9 expression following cyclosporine and diquafosol treatment in dry eye |
title_fullStr | Comparison of matrix metallopeptidase-9 expression following cyclosporine and diquafosol treatment in dry eye |
title_full_unstemmed | Comparison of matrix metallopeptidase-9 expression following cyclosporine and diquafosol treatment in dry eye |
title_short | Comparison of matrix metallopeptidase-9 expression following cyclosporine and diquafosol treatment in dry eye |
title_sort | comparison of matrix metallopeptidase-9 expression following cyclosporine and diquafosol treatment in dry eye |
topic | Ophthalmology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10291919/ https://www.ncbi.nlm.nih.gov/pubmed/37354028 http://dx.doi.org/10.1080/07853890.2023.2228192 |
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