Iron homeostasis and eye disease

Biochim Biophys Acta. 2009 Jul;1790(7):637-49. doi: 10.1016/j.bbagen.2008.11.001. Epub 2008 Nov 14.

Abstract

Background: Iron is necessary for life, but excess iron can be toxic to tissues. Iron is thought to damage tissues primarily by generating oxygen free radicals through the Fenton reaction.

Methods: We present an overview of the evidence supporting iron's potential contribution to a broad range of eye disease using an anatomical approach.

Results: Iron can be visualized in the cornea as iron lines in the normal aging cornea as well as in diseases like keratoconus and pterygium. In the lens, we present the evidence for the role of oxidative damage in cataractogenesis. Also, we review the evidence that iron may play a role in the pathogenesis of the retinal disease age-related macular degeneration. Although currently there is no direct link between excess iron and development of optic neuropathies, ferrous iron's ability to form highly reactive oxygen species may play a role in optic nerve pathology. Lastly, we discuss recent advances in prevention and therapeutics for eye disease with antioxidants and iron chelators.

General significance: Iron homeostasis is important for ocular health.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Antioxidants / therapeutic use
  • Cataract / etiology
  • Corneal Diseases / chemically induced
  • Corneal Diseases / etiology
  • Eye Diseases / physiopathology*
  • Eye Diseases / prevention & control
  • Homeostasis
  • Humans
  • Iron / metabolism*
  • Iron Chelating Agents / therapeutic use
  • Iron Overload / physiopathology*
  • Keratoconus / pathology
  • Macular Degeneration / physiopathology
  • Optic Nerve Diseases / physiopathology
  • Optic Nerve Injuries / physiopathology
  • Pterygium / pathology
  • Reactive Oxygen Species

Substances

  • Antioxidants
  • Iron Chelating Agents
  • Reactive Oxygen Species
  • Iron