Alzheimer’s disease is the leading cause of dementia in the U.S., with approximately 5.4 million currently affected and an estimated 16 million by 2050. Damage to the brain from Alzheimer’s disease occurs years before patients exhibit symptoms. Attempted therapies have been unsuccessful largely because there is no measurable indicator — or biomarker — for Alzheimer’s disease before it is already symptomatic and advanced.
The eye’s retina is considered the developmental extension of the brain and can be accessed non-invasively. In a recently published study in the ACS Chemical Neuroscience journal, University of Minnesota Professors Robert Vince and Swati More researched a promising retinal biomarker using a hyperspectral imaging technique for early Alzheimer’s disease detection. The hyperspectral imaging technique allows for the analysis of a wide spectrum of light outside of — but not excluding — primary colors that detect the biomarker of Alzheimer’s disease.
The research team examined the potential of retinal hyperspectral imaging to detect biochemical changes present at the early stages of Alzheimer’s disease. Specifically, the technique characterizes light scatter changes in the retina of Alzheimer’s disease patients when compared with healthy participants.
The process, which has been used in preclinical trials and a human pilot study, scans a patient’s eye to detect small quantities of a protein long before they collect in large enough clusters to form plaques in the brain — a biological sign of Alzheimer’s disease progression. The test is non-invasive and is conducted in less than 10 minutes.
For the study, nineteen Alzheimer’s disease patients who had memory scores ranging from mild cognitive impairment (MCI) to advanced Alzheimer’s disease were scanned and compared to non-Alzheimer’s disease participants of the same age. Light scatter changes were recorded from the patients’ different retinal areas (e.g., optic disc, nerve fiber layer of the peripapillary retina, perifoveal retina and the central retina) using a specialized camera coupled to a custom designed spectral imaging system.
An analysis of the retinal hyperspectral imaging (rHSI) data displayed that:
“The preliminary results from this study are promising and have laid the foundation for next steps involving rigorous validation of the technique in a clinical setting,” said Swati More, an associate professor in the Center for Drug Design, College of Pharmacy. “In the future, the rHSI-based retinal biomarker screening could be part of an annual eye exam, with results potentially dictating follow-up evaluations or therapeutic intervention.”
“While Alzheimer’s disease cannot yet be treated with the intent to cure, early diagnosis with retinal screening can facilitate interventions with available therapeutics,” said Robert Vince, director of the Center for Drug Design. “This could add years of productive, quality time to the patient’s lifespan. The rHSI technique has shown promise and could be particularly valuable for identifying high-risk individuals for Alzheimer’s disease by starting periodic retinal screening at an early age.”
“In collaboration with our industry partner, RetiSpec, we hope to accelerate clinical development of this early detection technique and provide existing or new treatments the best chance for success,” added Vince.
This study was funded by the Center for Drug Design endowment at the University of Minnesota Twin Cities.
Robert Vince invented the anti-HIV drug, Abacavir (Ziagen®), which is currently marketed for clinical use by GlaxoSmithKline®. A portion of the royalty revenue from the commercialization of this drug helped to establish the Center for Drug Design. His current research is focused on the development of therapeutics and diagnostics for Alzheimer’s disease, antiviral and anticancer drug design.
Swati More’s expertise is in solving biological problems through chemical means, design and successful development of novel chemical or biological therapeutics and diagnostic tools being the end-goals. Currently, she studies the biochemistry of oxidative stress, drug transport mechanisms, and applies the insights gained to the development of imaging and diagnostic tools.
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