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      Changing vision: a review of pharmacogenetic studies for treatment response in age-related macular degeneration patients.

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          Abstract

          Nonresponsiveness to age-related macular degeneration (AMD) treatments has become a growing concern in ophthalmology. Disparity among publications that have assessed pharmacogenetic (PGx) connections between AMD disease genes and treatments has delayed the implementation of PGx testing in AMD. We assessed all AMD PGx publications to identify the degree of agreement for publications within similar ethnic cohorts and worldwide, and the causes for differences in study outcomes. There are no accepted genotype-phenotype correlations, either within similar ethnic cohorts or worldwide. The diversity of measured outcomes, treatment protocols and statistical methods used may be causing this discrepancy. A universally accepted treatment protocol and the creation of agreed response group classification may bridge the gap between AMD PGx publications.

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          Author and article information

          Journal
          Pharmacogenomics
          Pharmacogenomics
          Future Medicine Ltd
          1744-8042
          1462-2416
          April 2018
          : 19
          : 5
          Affiliations
          [1 ] Department of Surgery (Ophthalmology), Centre for Eye Research Australia, University of Melbourne, Royal Victorian Eye & Ear Hospital, East Melbourne, Victoria, 3002, Australia.
          Article
          10.2217/pgs-2017-0183
          29577807
          466514dc-2801-4267-8a8d-840a919fb0b1
          History

          DNA,age-related macular degeration,personalized medicine,pharmacogenetics,pharmacogenomics,treatment response

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