Recent developments in the management of dry age-related macular degeneration.

Clin Ophthalmol

Ospedale Oftalmico, Ophthalmic Section, Department of Clinical Pathophysiology, University of Turin, Turin, Italy.

Published: April 2015

AI Article Synopsis

  • Dry age-related macular degeneration (AMD) is a common eye condition that leads to the deterioration of parts of the retina, accounting for 80% of advanced cases, and poses significant treatment challenges due to the lack of effective therapies.
  • Management strategies include lifestyle changes, vitamin supplements, and support for severe stages, with research indicating that antioxidants and omega-3 fatty acids may slow progression.
  • Current research efforts focus on various approaches, such as reducing inflammation, blocking harmful by-products, and exploring advanced treatments like stem cell therapy and gene therapy to treat or repair damage from AMD.

Article Abstract

Dry age-related macular degeneration (AMD), also called geographic atrophy, is characterized by the atrophy of outer retinal layers and retinal pigment epithelium (RPE) cells. Dry AMD accounts for 80% of all intermediate and advanced forms of the disease. Although vision loss is mainly due to the neovascular form (75%), dry AMD remains a challenge for ophthalmologists because of the lack of effective therapies. Actual management consists of lifestyle modification, vitamin supplements, and supportive measures in the advanced stages. The Age-Related Eye Disease Study demonstrated a statistically significant protective effect of dietary supplementation of antioxidants (vitamin C, vitamin E, beta-carotene, zinc, and copper) on dry AMD progression rate. It was also stated that the consumption of omega-3 polyunsaturated fatty acids, such as docosahexaenoic acid and eicosapentaenoic acid, has protective effects. Other antioxidants, vitamins, and minerals (such as crocetin, curcumin, and vitamins B9, B12, and B6) are under evaluation, but the results are still uncertain. New strategies aim to 1) reduce or block drusen formation, 2) reduce or eliminate inflammation, 3) lower the accumulation of toxic by-products from the visual cycle, 4) reduce or eliminate retinal oxidative stress, 5) improve choroidal perfusion, 6) replace/repair or regenerate lost RPE cells and photoreceptors with stem cell therapy, and 7) develop a target gene therapy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4388086PMC
http://dx.doi.org/10.2147/OPTH.S59724DOI Listing

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