2011
DOI: 10.1136/bjo.2010.193680
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CFH,VEGFandHTRA1promoter genotype may influence the response to intravitreal ranibizumab therapy for neovascular age-related macular degeneration

Abstract: This study reports preliminary evidence suggesting that the higher AMD risk genotypes in CFH, VEGF and HTRA1 may influence the short-term response to treatment with ranibizumab for neovascular AMD.

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Cited by 95 publications
(89 citation statements)
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References 28 publications
(26 reference statements)
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“…Risk factors for AMD include age, smoking, systemic arterial hypertension (SAH), high serum cholesterol, and substantial alcohol consumption. In addition, studies have provided evidence indicating the important role of genetic factors in the physiopathology of AMD (7) . Recently, a number of studies have evaluated the relationship between vascular endothelial growth factor (VEGF) polymorphisms and AMD genetic susceptibility variants (4) .…”
Section: Introductionmentioning
confidence: 99%
“…Risk factors for AMD include age, smoking, systemic arterial hypertension (SAH), high serum cholesterol, and substantial alcohol consumption. In addition, studies have provided evidence indicating the important role of genetic factors in the physiopathology of AMD (7) . Recently, a number of studies have evaluated the relationship between vascular endothelial growth factor (VEGF) polymorphisms and AMD genetic susceptibility variants (4) .…”
Section: Introductionmentioning
confidence: 99%
“…Thereby, gene polymophisms of the VEGF-A (rs3025000), complement factor H (rs1061170), age-related macular susceptibility 2 (rs10490924), and high-temperature requirement A-1 (rs11200638) were determined to influence the therapeutic outcome. 16,[39][40][41] Likewise, the gene polymorphisms rs12913832 and rs1129038 were identified to influence the iris color. 42 The interaction of gene polymorphisms associated to iris color and the anti-VEGF responsiveness has not been investigated yet.…”
Section: Discussionmentioning
confidence: 99%
“…[11][12][13] In this context, predictive baseline characteristics such as visual acuity, central retinal thickness, lesion size, choroidal neovascularization type, duration of symptoms, genotype, and coincidental systemic factors were identified. [14][15][16][17] However, taking known influencing parameters into account by adapting therapy regimes individually, the diversity of the outcome after anti-VEGF therapy is still remarkable. 18,19 Accordingly, the purpose of this study was to investigate the influence of seasonal sunlight intensity and patients' iris color on the visual recovery after initial anti-VEGF therapy with ranibizumab or bevacizumab for neovascular AMD.…”
Section: Introductionmentioning
confidence: 99%
“…The genotypes of rs1413711 were found to be indicators of anti-VEGF response in a UK study by McKibbin group (McKibbin et al, 2012), but other studies did not find this to be the case (Boltz et al, 2012;Yuan et al, 2013;Fauser and Lambrou, 2014). In the UK study, the presence of a C nucleotide at rs1413711 was associated with a marked improvement in visual acuity (McKibbin et al, 2012) and it had a maximum followup time of six months, whereas some of the other studies had longer durations. It is then possible that there is a statistically significant effect at month six of treatment, which decreases to a non-significant level by month twelve or month fifteen (Fauser and Lambrou, 2014).…”
Section: Association Of Vegf Polymorphisms With Disease Riskmentioning
confidence: 99%