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Updated: May 24, 2026

Assessing Early Stage Open-Angle Glaucoma in Patients by Isolated-Check Visual Evoked Potential
Published on: May 25, 2020
Endothelin-1 plasma levels and vascular endothelial dysfunction in primary open angle glaucoma.
Mauro Cellini1, Ernesto Strobbe, Corrado Gizzi
1Department of Specialistic Surgery and Anesthesiology Science-Ophthalmology, Service, University of Bologna, Italy. mauro.cellini@unibo.it
Primary open-angle glaucoma (POAG) patients show elevated endothelin 1 (ET-1) and vascular dysfunction, linked to sub-clinical inflammation. These factors may drive progressive visual field damage even with controlled intraocular pressure.
Area of Science:
- Ophthalmology
- Vascular Biology
- Immunology
Background:
- Primary open-angle glaucoma (POAG) is a leading cause of irreversible blindness.
- Endothelial dysfunction and inflammation are implicated in glaucoma pathogenesis.
- Endothelin 1 (ET-1) is a potent vasoconstrictor with potential roles in ocular vascular diseases.
Purpose of the Study:
- To investigate the association between endothelial dysfunction, ET-1 plasma levels, and subclinical intraocular inflammation in POAG patients.
- To determine if these markers correlate with progressive visual field damage in POAG.
- To explore the relationship between ET-1, vascular function, and inflammation in POAG.
Main Methods:
- Forty POAG patients with progressive visual field damage and controlled intraocular pressure (IOP) were compared to age- and sex-matched healthy controls.
- Ophthalmological examination, standard achromatic perimetry (SAP), and anterior chamber cellularity (FLARE) assessment were performed.
- Blood samples for ET-1 plasma levels and brachial artery flow-mediated dilation (FMD) using ultrasonography were measured.
Main Results:
- POAG patients exhibited significantly higher ET-1 plasma levels (2.83 vs. 1.75 pg/ml) and increased FLARE (9.98 vs. 5.87 photons/ms) compared to controls.
- POAG patients demonstrated significantly lower FMD values (4.46% vs. 13.18%), indicating endothelial dysfunction.
- Follow-up revealed a further increase in ET-1 and decrease in FMD in POAG patients over one year.
Conclusions:
- Elevated ET-1 levels in POAG are strongly correlated with vascular dysfunction (r=0.942, p=0.001).
- Vascular dysfunction is significantly associated with sub-clinical intraocular inflammation (r=0.968, p=0.001).
- ET-1 and vascular dysfunction, driven by sub-clinical inflammation, may be critical in the progression of visual field damage in POAG with controlled IOP.
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