4.5 Article

Parallel findings in age-related macular degeneration and Alzheimer's disease

期刊

PROGRESS IN RETINAL AND EYE RESEARCH
卷 30, 期 4, 页码 217-238

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.preteyeres.2011.02.004

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Age-related macular degeneration; Alzheimer's disease; Drusen; Amyloid beta; Senile plaque; Complement activation

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Age is a common risk factor for Alzheimer's disease (AD) and age-related macular degeneration (AMD). Because of the increasing age of the population, these two age-related diseases have recently received a great deal of attention. In addition to age as a risk factor, AD and AMD have many characteristics in common. An important characteristic common to both diseases is the presence of amyloid beta (A beta) in the senile plaques of the AD brain and in the drusen of AMD patients. We have focused on the role of A beta as a key regulator of the progression from drusen to AMD, and our results have shown that A beta causes an imbalance of angiogenesis-related factors in the retinal pigment epithelial (RPE) cells. Mice that lack the A beta-degrading enzyme neprilysin develop RPE degeneration, and the sub-RPE deposits that are formed have features similar to those of AMD in humans. These data suggest that a common pathogenic mechanism might exist between AMD and AD. Thus, therapeutic approaches that have targeted A beta in patients with AD can also be applied to AMD. In this review, we summarise recent findings on the shared characteristics and perspectives between AMD and AD, beginning with the mechanism of A beta deposition and including a discussion of A beta-targeted therapeutic approaches for both AD and AMD. (C) 2011 Elsevier Ltd. All rights reserved.

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