from Part V - Bionics
Published online by Cambridge University Press: 05 September 2015
Introduction
Age-related macular degeneration (AMD) is one of the leading causes ofblindness in the developed world, with an incidence of 1:500 in patientsaged 55–64, and 1:8 in patients over 85 [1]. Retinitis pigmentosa(RP) is an inherited disease blinding about 1 in every 4000 individuals muchearlier in life [2]. In both of these conditions the photoreceptor layerdegenerates, while the inner retinal neurons survive to a large extent[3–5]. Electrically activating these neurons provides an alternativeroute for visual information and raises hope for the restoration of sight tothe blind.
In a normal retina, photoreceptors convert light into neural signals that areprocessed by inner retinal neurons, leading to generation of actionpotentials in the retinal ganglion cells (RGCs). These signals travel to thebrain through the optic nerve and serve as the basis for visual perception.Electrical stimulation of the retina with microelectrodes can also produceaction potentials in RGCs, creating spatially patterned percepts of lightcalled phosphenes. Indeed, recent clinical trials with retinal prostheticelectrode arrays have restored visual acuity to subjects blinded by retinaldegeneration up to 20/1200 using epiretinal placement (facing theganglion cell side) [6], and up to 20/550 with subretinalimplantation [7]. While this serves as an important proof of concept withclinically useful implications, existing retinal prosthesis designs have anumber of shortcomings.
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