2008
DOI: 10.1167/iovs.07-1654
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Coagulation Gene Predictors of Photodynamic Therapy for Occult Choroidal Neovascularization in Age-Related Macular Degeneration

Abstract: These data provide evidence of the presence of a pharmacogenetic relationship between peculiar coagulation-balance genetic backgrounds and different levels of PDT-V effectiveness in patients with AMD with occult CNV.

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Cited by 38 publications
(50 citation statements)
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References 60 publications
(58 reference statements)
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“…Unlike many previous studies [10][11][12][13][14], we classified PDT responders and nonresponders based on objective findings including fundus photography, FA and OCT. The classifications between "PDT-responder" and "nonresponder" according with objective (anatomical) findings are also seen in recent publications [25,26].…”
Section: Discussionmentioning
confidence: 85%
“…Unlike many previous studies [10][11][12][13][14], we classified PDT responders and nonresponders based on objective findings including fundus photography, FA and OCT. The classifications between "PDT-responder" and "nonresponder" according with objective (anatomical) findings are also seen in recent publications [25,26].…”
Section: Discussionmentioning
confidence: 85%
“…Of six gene polymorphisms genotyped, thrombophilic factor V G1691A, factor XIII-A G185T, methionine synthase A2756G, methionine synthase reductase A66G, methylenetetrahydrofolate reductase C677T and prothrombin G20210A, the latter two were identified to be more prevalent within responders. Hyperfibrinolytic factor XIII-A G185T was clearly overrepresented in the nonresponder fraction [176,177].…”
Section: Genetic Studiesmentioning
confidence: 91%
“…Variants in genes predisposing to hypercoagulability, including prothrombin 20210A and factor V 1691A alleles, have been associated with improved responses to therapy, and the C677T polymorphism in the gene for methylenetetrahydrofolate reductase associates with increased responses in classic CNV. 95,96 Rather unsurprisingly, variations predisposing to increased fibrinolysis, notably the G185T mutation of factor XIII-A, have been linked to nonresponse to treatment. 95,96 Dry Age-Related Macular Degeneration…”
Section: Photodynamic Therapymentioning
confidence: 99%
“…95,96 Rather unsurprisingly, variations predisposing to increased fibrinolysis, notably the G185T mutation of factor XIII-A, have been linked to nonresponse to treatment. 95,96 Dry Age-Related Macular Degeneration…”
Section: Photodynamic Therapymentioning
confidence: 99%