Elevated VEGF-A Levels in the Aqueous Humor of Patients With Primary Open Angle Glaucoma

The purpose of the current study was to compare the vascular endothelial growth factor-A (VEGF-A) levels in the aqueous humor of patients with primary open angle glaucoma (POAG) and non-glaucomatous eyes and reveal any potential statistically significant correlations. This was an observational cross...

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Veröffentlicht in:In vivo (Athens) 2024-07, Vol.38 (4), p.1875-1881
Hauptverfasser: Dimtsas, Georgios S, Ieronymaki, Alexandra, Chatzistefanou, Klio I, Siasos, Gerasimos, Krassas, Augustinos, Moschos, Marilita M
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Sprache:eng
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Zusammenfassung:The purpose of the current study was to compare the vascular endothelial growth factor-A (VEGF-A) levels in the aqueous humor of patients with primary open angle glaucoma (POAG) and non-glaucomatous eyes and reveal any potential statistically significant correlations. This was an observational cross-sectional study. Aqueous humor samples (50-100 μl) were collected under aseptic conditions, from the anterior chamber at the start of glaucoma or cataract surgery. The levels of VEGF-A were measured using a multiplex bead-based immunoassay. Aqueous humor samples were obtained from 76 participants: 39 with POAG and 36 with age-related cataracts as controls. VEGF-A levels were significantly elevated in the POAG group (166.37±110.04 pg/ml, p=0.011) compared to the control group (119.02±49.09 pg/ml). The receiver operating characteristic (ROC) analysis showed that VEGF-A had significant prognostic ability for POAG (AUC=0.67; p=0.006). An optimal cut-off for VEGF-A was found to be 148.5 pg/ml with a sensitivity of 54%, specificity of 81.1%, positive prognostic value (PPV) of 75% and negative prognostic value (NPV) of 62.5%. Logistic regression analysis showed that after adjusting for sex and age, patients with VEGF-A higher than 148.5 pg/ml had almost 10 times greater likelihood for POAG. VEGF-A is elevated in patients with POAG and can potentially have a prognostic ability for these patients.
ISSN:0258-851X
1791-7549
1791-7549
DOI:10.21873/invivo.13642