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      Diabetic retinopathy: current understanding, mechanisms, and treatment strategies

      review-article
      1 , , 2 , 3
      JCI Insight
      American Society for Clinical Investigation

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          Abstract

          Diabetic retinopathy (DR) causes significant visual loss on a global scale. Treatments for the vision-threatening complications of diabetic macular edema (DME) and proliferative diabetic retinopathy (PDR) have greatly improved over the past decade. However, additional therapeutic options are needed that take into account pathology associated with vascular, glial, and neuronal components of the diabetic retina. Recent work indicates that diabetes markedly impacts the retinal neurovascular unit and its interdependent vascular, neuronal, glial, and immune cells. This knowledge is leading to identification of new targets and therapeutic strategies for preventing or reversing retinal neuronal dysfunction, vascular leakage, ischemia, and pathologic angiogenesis. These advances, together with approaches embracing the potential of preventative or regenerative medicine, could provide the means to better manage DR, including treatment at earlier stages and more precise tailoring of treatments based on individual patient variations.

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          Author and article information

          Contributors
          Journal
          JCI Insight
          JCI Insight
          JCI Insight
          JCI Insight
          American Society for Clinical Investigation
          2379-3708
          20 July 2017
          20 July 2017
          20 July 2017
          : 2
          : 14
          : e93751
          Affiliations
          [1 ]Wilmer Ophthalmologic Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
          [2 ]Joslin Diabetes Center, Harvard Medical School, Boston, Massachusetts, USA.
          [3 ]Centre for Experimental Medicine, Queen’s University Belfast, Northern Ireland, United Kingdom.
          Author notes
          Address correspondence to: Elia Duh, Department of Ophthalmology, Wilmer Ophthalmologic Institute, Johns Hopkins University School of Medicine, 400 N. Broadway, Room 3011, Baltimore, Maryland 21287, USA. Phone:1.410.614.3388; Email: eduh@ 123456jhmi.edu . Or to: Alan Stitt, Centre for Experimental Medicine, Queen’s University Belfast, Belfast, BT9 7BL, Northern Ireland, United Kingdom. Phone: 44.28.9097.5375; Email: a.stitt@ 123456qub.ac.uk .
          Article
          PMC5518557 PMC5518557 5518557 93751
          10.1172/jci.insight.93751
          5518557
          28724805
          97601246-f2ab-4bcf-9e54-4edd3200b75f
          Copyright © 2017, American Society for Clinical Investigation
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