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Effect of Artificial Tear Formulations on the Metabolic Activity of Human Corneal Epithelial Cells after Exposure to Desiccation
Published on: May 2, 2020
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Tear Mediators in Corneal Ectatic Disorders.
Dorottya Pásztor1, Bence Lajos Kolozsvári1, Adrienne Csutak1
1Department of Ophthalmology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Plos One
|April 14, 2016
Summary
This study found matrix metalloproteinase-9 (MMP-9) levels differ between pellucid marginal degeneration (PMD) and keratoconus (KC) patients. These findings highlight biochemical distinctions in corneal ectasias.
Area of Science:
- Ophthalmology
- Biochemistry
- Corneal Diseases
Background:
- Pellucid marginal degeneration (PMD) and keratoconus (KC) are distinct corneal ectatic disorders.
- Biochemical differences between PMD and KC are not well-established.
- Tear mediators may offer insights into the pathogenesis of these conditions.
Purpose of the Study:
- To compare tear mediator concentrations between PMD and KC.
- To identify biochemical differences between these two corneal diseases.
Main Methods:
- A cross-sectional study enrolled patients with corneal ectasia diagnosed via slit-lamp biomicroscopy and Pentacam HR.
- Tear samples were collected from 9 eyes of 7 PMD patients, 55 eyes of 55 KC patients, and 24 healthy controls.
- Concentrations of 11 tear mediators, including matrix metalloproteinase-9 (MMP-9) and tissue inhibitor of metalloproteinases (TIMP)-1, were measured using Cytometric Bead Array.
Main Results:
- Matrix metalloproteinase-9 (MMP-9) was the sole mediator showing significant variance between PMD and KC groups (p = 0.005).
- The ratios of MMP-9 to TIMP-1 were 2.45 in PMD, 0.40 in KC, and 0.23 in controls.
Conclusions:
- This is the first study to investigate biochemical differences between PMD and KC using tear mediators.
- Matrix metalloproteinase-9 (MMP-9) may serve as a potential biomarker differentiating PMD from KC.
- Further research with larger cohorts is needed to validate these findings and explore the molecular alterations in PMD.
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