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• W2022704784 abstract "Recently, eotaxin–CCR3 was reported to play an important role in choroidal neovascularization (CNV) development and was documented to be superior than vascular endothelial growth factor-A treatment when tested in CNV animals. As eotaxin studies are lacking in the human age-related macular degeneration (AMD) patients, we sought to determine whether eotaxin-2 (CCL24) has any association with inflammatory processes that occur in CNV. CCL24 levels were determined by enzyme linked immunosorbant assay (ELISA) after normalization to total serum protein and levels of ELISA were correlated to various risk factors in about 133 AMD patients and 80 healthy controls. The CCL24 levels were significantly higher in wet AMD patients as compared with dry AMD and normal controls. There was a significant difference when compared among wet AMD patients (i.e., minimally classic, predominantly classic, and occult). We also report significant difference in the CCL24 levels of Avastin-treated and untreated AMD patients. This study shows that CCL24 levels were found to be significantly increased in AMD patients despite Avastin treatment as compared with normal controls and those without Avastin, indicating that CCL24 may have an association with CNV and may be an important target to validate future therapeutic approaches in AMD in tandem with Avastin treatment. Eotaxin-2 (CCL24), the activating ligand for G-coupled protein receptor CCR3, levels are elevated in samples derived from age-related macular degeneration patients despite treatment with anti-angiogenic therapy. The study is consistent with an angiogenic role for eotaxin-2 in the neovascularization in the wet form of the disease." @default.
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• W2022704784 date "2012-11-01" @default.
• W2022704784 modified "2023-10-01" @default.
• W2022704784 title "New Biomarker for Neovascular Age-Related Macular Degeneration: Eotaxin-2" @default.
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• W2022704784 doi "https://doi.org/10.1089/dna.2012.1786" @default.
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