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Alzheimer's Lesions Found In The Retina

Date:
October 22, 2009
Source:
University of California - Irvine
Summary:
The eyes may be the windows to the soul, but new research indicates they also may mirror a brain ravaged by Alzheimer's disease.

UCI neuroscientist Zhiqun Tan lead research that found the retinas of mice may mirror the brain ravaged by Alzheimer's disease.
Credit: Photo by Daniel A. Anderson / University Communications

The eyes may be the windows to the soul, but new research indicates they also may mirror a brain ravaged by Alzheimer's disease.

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UC Irvine neuroscientists have found that retinas in mice genetically altered to have Alzheimer's undergo changes similar to those that occur in the brain -- most notably the accumulation of amyloid plaque lesions.

In addition, the scientists discovered that when Alzheimer's therapies are tested in such mice, retinal changes that result might predict how the treatments will work in humans better than changes in mouse brain tissue.

These findings are key to developing retinal imaging technology that may help diagnose and treat people with Alzheimer's, which afflicts 5.3 million people in the U.S. and is the leading cause of elderly dementia. Brain imaging techniques are being tested, but retinal imaging could be less invasive, less expensive and easier to perform.

"It's important to discover the pathological changes before an Alzheimer's patient dies," said Zhiqun Tan, a UCI neuroscientist leading the research. "Brain tissue isn't transparent, but retinas are. I hope in the future we'll be able to diagnose the disease and track its progress by looking into the eyes."

For a study appearing in the November issue of The American Journal of Pathology, Tan and colleagues analyzed the retinas of Alzheimer's mice that had been treated with immunotherapy.

Vaccinated mice performed better on learning and memory tests than untreated mice, and their brains had fewer plaque lesions. Similarly, retinas in the treated mice had fewer lesions than in untreated mice. However, the treated mice's retinas had worse inflammation and vascular changes associated with Alzheimer's than did their brains.

When immunotherapy was tested in humans, inflammation of brain tissue occurred similar to that observed in the mice retinas. "This tells us the retina may be more sensitive at reflecting changes in the human brain," Tan said.

UCI researchers, including Dr. Steven Schreiber, neurology professor and interim chair, are working on retinal imaging technology for Alzheimer's patients.

"New ways to view various body parts with high resolution are being invented at a rapid pace," Schreiber said. "I expect the imaging field will continue improving as we progress in developing our retinal technique."

In addition to Tan and Schreiber, UCI's Bingqian Liu, Suhail Rasool and Charles Glabe contributed to the study, along with Zhikuan Yang and Jian Ge of the Zhongshan Ophthalmic Center in China. Liu also is affiliated with the center. The UCI scientists are from the departments of neurology, molecular biology & biochemistry, and anatomy & neurobiology, as well as the Institute for Memory Impairments and Neurological Disorders, or UCI MIND.

The research was supported by the Alzheimer's Drug Discovery Foundation, the National Basic Research Program of China, the UC Discovery Grant Program, and the Larry L. Hillblom Foundation.


Story Source:

The above story is based on materials provided by University of California - Irvine. Note: Materials may be edited for content and length.


Cite This Page:

University of California - Irvine. "Alzheimer's Lesions Found In The Retina." ScienceDaily. ScienceDaily, 22 October 2009. <www.sciencedaily.com/releases/2009/10/091021125139.htm>.
University of California - Irvine. (2009, October 22). Alzheimer's Lesions Found In The Retina. ScienceDaily. Retrieved October 30, 2014 from www.sciencedaily.com/releases/2009/10/091021125139.htm
University of California - Irvine. "Alzheimer's Lesions Found In The Retina." ScienceDaily. www.sciencedaily.com/releases/2009/10/091021125139.htm (accessed October 30, 2014).

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