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      Nanosecond laser therapy reverses pathologic and molecular changes in age-related macular degeneration without retinal damage.

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          Abstract

          Age-related macular degeneration (AMD) is a leading cause of vision loss, characterized by drusen deposits and thickened Bruch's membrane (BM). This study details the capacity of nanosecond laser treatment to reduce drusen and thin BM while maintaining retinal structure. Fifty patients with AMD had a single nanosecond laser treatment session and after 2 yr, change in drusen area was compared with an untreated cohort of patients. The retinal effect of the laser was determined in human and mouse eyes using immunohistochemistry and compared with untreated eyes. In a mouse with thickened BM (ApoEnull), the effect of laser treatment was quantified using electron microscopy and quantitative PCR. In patients with AMD, nanosecond laser treatment reduced drusen load at 2 yr. Retinal structure was not compromised in human and mouse retina after laser treatment, with only a discrete retinal pigment epithelium (RPE) injury, and limited mononuclear cell response observed. BM was thinned in the ApoEnull mouse 3 mo after treatment (ApoEnull treated 683 ± 38 nm, ApoEnull untreated 890 ± 60 nm, C57Bl6J 606 ± 43 nm), with the expression of matrix metalloproteinase-2 and -3 increased (>260%). Nanosecond laser resolved drusen independent of retinal damage and improved BM structure, suggesting this treatment has the potential to reduce AMD progression.

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          Author and article information

          Journal
          FASEB J.
          FASEB journal : official publication of the Federation of American Societies for Experimental Biology
          FASEB
          1530-6860
          0892-6638
          Feb 2015
          : 29
          : 2
          Affiliations
          [1 ] Department of Anatomy and Neuroscience, The University of Melbourne, Victoria, Australia;
          [2 ] Centre for Eye Research Australia, University of Melbourne, Royal Victorian Eye and Ear Hospital, Victoria, Australia; and.
          [3 ] Ellex R&D Pty Ltd, Adelaide, Australia.
          [4 ] Department of Anatomy and Neuroscience, The University of Melbourne, Victoria, Australia; elf@unimelb.edu.au.
          Article
          fj.14-262444
          10.1096/fj.14-262444
          25392267
          75ccf90a-1435-4eef-a369-6c3098d2cc03
          History

          Bruch’s membrane,drusen,matrix metalloproteinase,vision loss

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