Pilot Study That Investigates the Potential of Using OCT (Optical Coherence Tomography) Measurements of the Thickness of the Retinal Nerve Fiber Layer as a Biomarker for the Early Detection of Alzheimer's Disease.

Alzheimer's Disease (AD) is a degenerative neurological disorder characterized by the insidious onset of a progressive decline in cognitive function. It is the most common form of dementia affecting an estimated 26 million people worldwide in 2006, a number that is expected to quadruple by 2050 due to the anticipated increase in life expectancy. Difficulty remembering names and recent events is often an early clinical symptom as is apathy and depression. Later symptoms include impaired judgment, disorientation, confusion, behavior changes and difficulty in swallowing and walking.

New criteria and guidelines for diagnosing Alzheimer's published in 2011 recommend that it be considered a disease that begins well before the development of symptoms. Brain changes in individuals with Alzheimer's are thought to begin 10 years or more before symptoms such as memory loss occur - the asymptomatic preclinical phase of AD. Researchers believe that treatment to slow down or stop progression of Alzheimer's and preserve brain function will be most effective when administered early in the course of the disease. The pursuit of biomarkers to detect asymptomatic preclinical AD is a current issue and potential biomarkers such as: brain volume, level of glucose metabolism in the brain, levels of beta-amyloid and tau in the CSF, detection of apoptosing retinal cells (DARC), are being investigated. In this study we would like to propose the measurement of retinal nerve fiber layer thickness as a potential key biomarker for the detection of asymptomatic preclinical Alzheimer's and Mild Cognitive Impairment (MCI).

The eye can be considered a window to the brain and the retina exists as an extension of the CNS. Changes that occur in the retina can be visualized non-invasively and directly with increasingly sophisticated imaging techniques. It is now possible to detect changes in single neurons in the eye. Historically the visual symptoms that have been reported in AD patients have been attributed to neuronal damage to the visual pathways in the brain rather than the retina. However there is increasing evidence that shows that the specific pathological findings in the brain occur in the retina also.

The ocular manifestations in AD were first documented by Cogan in 1985, who documented deficits in visual acuity, contrast sensitivity, colour vision and motion perception. In more recent studies using optical coherence tomography (OCT), peripapillary thinning of the retinal nerve fiber layer (RNFL) has been demonstrated, occurring initially superiorly and causing inferior visual field loss.

The use of OCT as a non-invasive optical imaging technique has become an accepted method for assessing the thickness of the RNFL due to its reproducibility and accuracy. Blanks et al. provided ultrastructural studies that showed retinal ganglion cell degeneration in post mortem retinas of patients with AD. He demonstrated that in AD extensive neuronal loss was seen throughout the retina but most pronounced in superior and inferior quadrant and loss in the central retina, the greatest decrease of neurons being in the temporal foveal region.