Showing posts with label Amyloid brain plaques. Show all posts
Showing posts with label Amyloid brain plaques. Show all posts

Wednesday, July 21, 2010

Dementia May Differ in Those With and Without Diabetes

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(HealthDay News) -- Vascular disease, which affects blood flow in brain vessels, appears to be a common cause of dementia in some people with diabetes, new study findings suggest.

That's in contrast to dementia in people without diabetes, which the researchers say is more likely to be linked to the brain plaque deposits commonly seen in people with Alzheimer's disease.

The findings come from researchers at the Mayo Clinic's Florida campus and the University of California, San Francisco, who compared the ratios of two different types of amyloid beta proteins in blood samples from 211 people with dementia and 403 others without dementia.

"This helps in understanding diabetes and dementia. It suggests that the vascular dementia seen in diabetics, which appears to be related to small blood vessel disease and strokes, can potentially be averted if development of diabetes is prevented," neurologist Dr. Neill Graff-Radford said in a Mayo Clinic news release.

The study findings were slated for presentation July 14 at the Alzheimer's Association International Conference on Alzheimer's Disease meeting, in Hawaii.

The findings support previous autopsy studies on people with diabetes and dementia, which found vascular abnormalities were related to dementia but not to the plaques and tangles characteristic of Alzheimer's disease, the authors noted in the news release.

More information

The U.S. National Institute of Neurological Disorders and Stroke has more about dementia.

Friday, October 16, 2009

Skills tests like 'connect the dots' may be early Alzheimer's indicator

Here is a great dementia resource for caregivers and healthcare professinals,

Here is information on being the best caregiver you can be

Here are more interesting dementia brain boosting activities

Washington University News

By Michael Purdy

A study of mental decline in the years prior to diagnosis of Alzheimer's disease suggests that changing the focus of testing may allow physicians to detect signs of the disease three years earlier.

Current cognitive testing typically focuses on episodic memory, or the ability to remember things like word lists or information from a reading. But scientists at Washington University School of Medicine in St. Louis found that another class of mental abilities known as visuospatial skills begins to deteriorate up to three years prior to diagnosis. These skills are tested with tasks such as connecting the dots or using a guide to build a structure with blocks.

"We may need to rethink what we look for as the earliest signs of mental change associated with Alzheimer's disease," says senior author James Galvin, M.D., a Washington University neurologist who is also on staff at Barnes-Jewish Hospital. "If we can better recognize the first signs of disease, we can start treating patients earlier and hopefully with new treatments we can slow or perhaps even stop their progress into dementia."

The results are published in the October issue of Archives of Neurology.

Galvin and his coauthors analyzed long-term data from volunteers at the Memory and Aging Project at Washington University's Alzheimer's Disease Research Center (ADRC). For three decades, researchers have been regularly conducting extensive testing of volunteers to uncover the factors associated with the normal, healthy retention of mental function in seniors. The new study analyzes data on 444 volunteers aged 60 to 101 that were gathered between 1979 and 2006.

Scientists categorized cognitive testing results into a global measure of cognitive abilities as well as three specific types of mental skills: episodic memory, visuospatial skills and working memory, which assesses the ability to manipulate facts from memory, such as repeating a list of numbers backwards.

Declines in episodic memory and working memory became discernible a year before volunteers were diagnosed with Alzheimer's disease. Losses in the composite assessment of cognitive abilities were detectable two years prior to diagnosis, and visuospatial skills began to decay three years earlier. According to Galvin, the losses in visuospatial skills were particularly noticeable if testing tasks were timed.

Researchers also analyzed the data using a new model that not only tracks the speed of decline in a mental ability but also the acceleration of the decline. Episodic memory's decline accelerated more slowly than that of both visuospatial skills and working memory, which declined fastest.

The new perspective may allow doctors to detect signs of Alzheimer's earlier, but more information will be needed to make a firm diagnosis. To make that possible, researchers at the ADRC are trying to take what they've learned in the new study and correlate it with biomarkers, which are physical changes associated with preclinical Alzheimer's disease. These include such tests as scanning the brain for amyloid plaques or analyzing the levels of proteins in the cerebrospinal fluid.

Amyloid brain plaques, a primary characteristic of Alzheimer's disease, can begin building in patients 10 years or more before clinical symptoms become apparent, Galvin notes.

"The new findings raise the question of what changes are occurring in the brain during the one- to three-year period prior to diagnosis," Galvin says. "Patients have had plaques in their brain for years, and suddenly their cognitive abilities begin to deteriorate. Is a threshold being crossed where brain cell death begins to occur or really starts to pick up speed?"

Galvin and his coauthors also plan to apply their new approach for assessing mental decline to other dementias including Lewy body dementia and the form of dementia associated with Parkinson's disease.
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