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• W2103941977 abstract "To investigate the influence of the Factor H (CFH) Tyr⁴⁰²His polymorphism on the plasma levels of the alternative pathway proteins CFH, C3, Factor B (FB), Factor D (FD), and Factor I (FI) and the inflammatory marker C-reactive protein (CRP) in 119 patients with age-related macular degeneration (AMD) and 152 unrelated control individuals.Patients with AMD and the control group were separated according to CFH polymorphism, age, and gender. Plasma complement proteins and CRP concentrations were determined with enzyme-linked immunosorbent assay, immunodiffusion, or nephelometry.Significant differences in the concentrations of FD and FI were observed between the patients with AMD and the control individuals. We observed significantly reduced FD plasma levels in patients with AMD. We also identified a significant decrease in CFH plasma levels in female patients with AMD in relation to female controls. Plasma FI levels were significantly increased in patients with AMD compared to the control group. Regarding gender, a significant increase in FI plasma levels was observed in male patients. Finally, we found no significant correlation between the CFH Tyr(402)His polymorphism and the CFH, C3, FB, FD, FI, and CRP plasma levels.Patients with AMD present altered levels of FD and FI in a manner independent of this CFH polymorphism, and gender apparently contributes to the plasma levels of these two proteins in patients with AMD and control individuals." @default.
• W2103941977 created "2016-06-24" @default.
• W2103941977 creator A5011693299 @default.
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• W2103941977 creator A5085474741 @default.
• W2103941977 date "2012-01-01" @default.
• W2103941977 modified "2023-09-26" @default.
• W2103941977 title "Plasma levels of complement proteins from the alternative pathway in patients with age-related macular degeneration are independent of Complement Factor H Tyr⁴⁰²His polymorphism." @default.
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• W2103941977 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3436886" @default.
• W2103941977 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/22969267" @default.
• W2103941977 hasPublicationYear "2012" @default.
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