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Short Term Stress Can Affect Learning and Memory Print
Monday, 17 March 2008

Short-term stress lasting as little as a few hours can impair brain-cell communication in areas associated with learning and memory, University of California, Irvine researchers have found.

It has been known that severe stress lasting weeks or months can impair cell communication in the brain’s learning and memory region, but this study provides the first evidence that short-term stress has the same effect. The study appears in the March 12 edition of the Journal of Neuroscience.

“Stress is a constant in our lives and cannot be avoided,” said Dr. Tallie Z. Baram, the Danette Shepard Chair in Neurological Sciences in the UC Irvine School of Medicine and study leader. “Our findings can play an important role in the current development of drugs that might prevent these undesirable effects and offer insights into why some people are forgetful or have difficulty retaining information during stressful situations.”

In their study, Baram and her UC Irvine colleagues identified a novel process by which stress caused these effects. They found that rather than involving the widely known stress hormone cortisol, which circulates throughout the body, acute stress activated selective molecules called corticotropin releasing hormones, which disrupted the process by which the brain collects and stores memories.

Learning and memory take place at synapses, which are junctions through which brain cells communicate. These synapses reside on specialized branchlike protrusions on neurons called dendritic spines.

Read more...
 
Emory Begins Testing New Alzheimer's Vaccine Print
Thursday, 28 February 2008

Doctors at Emory University will begin testing a vaccine designed to slow the accumulation of amyloid plaques in the brains of patients with Alzheimer's disease.
Alzheimer's affects more than 4.5 million Americans and is marked by gradual nerve cell death and a progressive loss of memory and mental functioning. All of the medications now available aim to improve the functioning of the nerve cells that remain alive.

Several still-experimental vaccines or immunotherapies take a different approach. They target beta-amyloid, a naturally occurring protein that clumps together and forms plaques in the brains of Alzheimer's patients. The clumps appear to damage brain cells.

The study's main purpose is to evaluate the vaccine's safety, possible side effects and how well it stimulates the immune system.

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New Study From Rhode Island Hospital Confirms Previous Reports and Raises New Questions Print
Wednesday, 23 January 2008

A new study by researchers at Rhode Island Hospital and Brown University finds that people with Alzheimer's Disease (AD) experienced more accidents and performed more poorly on road tests compared to drivers without cognitive impairment. The study is published in the January 23 edition of Neurology, the medical journal of the American Academy of Neurology.


While the study does confirm previous reports of potentially hazardous driving in persons with early AD, it also indicates that some individuals with very mild dementia can continue to drive safety for extended periods of time. The study included 128 individuals—84 with early AD and 44 age-matched control subjects without cognitive impairments. Drivers with early AD were enrolled in this study and followed every six months over two to three years.


Under the direction of principal investigator Brian Ott, M.D., director of the Alzheimer’s Disease and Memory Disorders Center at Rhode Island Hospital and professor at The Warren Alpert Medical School of Brown University, the study looked at driving abilities through self-reports, family reports and a standardized road test.


The study results indicate that people with early AD experienced more accidents and performed more poorly on road tests when compared to participants without cognitive impairments. “We also found that people with what is defined as mild dementia were significantly more likely to fail a road test than those defined with very mild dementia.”


Ott says, “Our findings showed that people with mild dementia were nearly four times more likely to fail a road test than those with very mild dementia, indicating that people with very mild dementia may be able to drive safely for longer periods of time.”


Ott notes, “It is clear, however, that driving ability declines fairly rapidly among patients with dementia, and therefore, regular follow-up assessments are warranted in these people with very mild dementia.” Currently, the American Academy of Neurology Guideline on Risk of Driving and Alzheimer’s Disease recommends a reassessment every six months for those patients diagnosed with very mild dementia who continue to drive.


The study also found increased age as well as lower education can impact driving abilities. Ott comments, “The odds of failing a road test increased by about six percent for every year exceeding the age of 75.” The study found that drivers who lagged behind the average education experience within the study group were likely to fail a road test; failure was 10 percent more likely for each year in which they lagged behind the average education experience of 14 years.


Of interest, the frequency of motor vehicle accidents in the AD drivers declined during the study. Overall, Ott says, “The results suggest that a regular driving assessment program may actually reduce the frequency of motor vehicle accidents in drivers with mild dementia by increasing awareness among the driver and caregivers. This, however, may also result in premature termination of driving privileges for some persons with dementia.” The researchers note that this is a major challenge facing clinicians: to develop valid and reliable office screening tools, which can assist the clinician with making driving assessment referrals and recommendations regarding driving safety for those with early AD.


The study was funded by a grant from the National Institute on Aging. The researchers recently announced the grant has been renewed to fund the study for another four years.

Source: Lifespan

 
Portable Device Quickly Detects Early Alzheimer's Print
Friday, 18 January 2008

ATLANTA (January 16, 2008) — The latest medications can delay the onset of Alzheimer’s disease, but none are able to reverse its devastating effects. This limitation often makes early detection the key to Alzheimer’s patients maintaining a good quality of life for as long as possible.tsh99291.jpg
Now, a new device developed by the Georgia Institute of Technology and Emory University may allow patients to take a brief, inexpensive test that could be administered as part of a routine yearly checkup at a doctor’s office to detect mild cognitive impairment (MCI) — often the earliest stage of Alzheimer’s. The device is expected to be commercialized later this year.

Current assessment tests capable of detecting early Alzheimer’s typically are taken with a pen and paper or at a computer terminal and last about an hour and a half. They must be given by a trained technician in a quiet environment, because any distractions can influence the patient’s score and reduce the test’s effectiveness. Because of their length and expense, the tests are not used as regular screening tools and typically are given only after there is obvious cognitive impairment such as forgetfulness or unsafe behavior.

Read more...
 
Applied NeuroSolutions’ Test is a Significant Predictor Print
Wednesday, 02 January 2008
Study Shows Applied NeuroSolutions’ Test is a Significant Predictor of the Decline from Mild Cognitive Impairment to Alzheimer’s Disease


Vernon Hills, IL December 18, 2007 – Applied NeuroSolutions, Inc. (OTC BB:APNS, www.appliedneurosolutions.com), a Company focused on the development of an integrated portfolio of products for the treatment and diagnosis of Alzheimer’s disease (AD), today reported that a peer-reviewed paper, "Multicenter assessment of CSF-phosphorylated tau for the prediction of conversion of MCI,” is highlighted as a featured study in the December 11, 2007 issue of  the print edition of Neurology.  APNS’s p-tau 231 biomarker (p-tau 231) was utilized in an international, multicenter study, led by Dr. Harald Hampel, and shown to be a significant predictor of conversion in the transition from mild cognitive impairment (MCI) to Alzheimer's disease in a relatively short and clinically relevant observation interval.

Mild cognitive impairment is a predementia risk state for the possible development of Alzheimer's disease. Research literature indicates that approximately 16% of individuals with MCI develop AD annually, however the conversion rate may be as high as 41% after one year and 64% after two years while some patients may never convert to Alzheimer's disease and some may return to normal.....

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Protein 'fingerprint' in spinal fluid could spot Alzheimer's Disease Print
Monday, 24 December 2007

23-protein screen is highly accurate and first to be validated

ITHACA, N.Y. -- Scientists collaborating at Cornell University in Ithaca and Weill Cornell Medical College in New York City have identified a panel of 23 protein biomarkers in cerebrospinal fluid that acts as a neurochemical "fingerprint," which doctors might use someday to identify patients living with Alzheimer's disease.The research will be published in the December online-edition of the journal Annals of Neurology.

Right now, physicians rely on their clinical judgment to decide whether a particular patient has Alzheimer's rather than some other form of dementia. In many cases, the diagnosis remains uncertain until brain tissue is examined at autopsy.

"Our study is the first to use sophisticated proteomic methods to hone in on a group of cerebrospinal fluid biomarkers that are specific to autopsy-proven Alzheimer's disease. Those postmortem tests confirmed that the panel is over 90 percent sensitive in identifying people with Alzheimer's disease," says Kelvin Lee, the Samuel C. and Nancy M. Fleming Professor of Molecular and Cell Biology and associate professor of chemical and biomolecular engineering at Cornell.

Researchers at a variety of centers have long sought biomarkers in blood or cerebrospinal fluid that identify the presence of Alzheimer's pathology and distinguish it from other conditions that cause dementia.

"Some of these studies have met with limited success, but most have correlated their findings with patient's clinical symptoms rather than working with the gold-standard of autopsy-proven Alzheimer's," notes Norman Relkin, M.D., associate professor of clinical neurology and neuroscience at Weill Cornell and director of the Memory Disorders Program at NewYork-Presbyterian Hospital/Weill Cornell Medical Center.
Read more...
 
Third Party Japanese Study Suggests Drug Improves Memory Print
Monday, 17 December 2007
Sarasota's Roskamp Institute Highlights Positive Japanese Data that Validates its Ongoing Alzheimer's Disease Research

Sarasota, Fla. The Roskamp Institute announced December 14th that its promising new drug application for the treatment of Alzheimer's disease has received positive validation from an independent human clinical study conducted at the Tokyo Medical University in Japan. The study, which suggests the drug, Nilvadipine, can prevent the onset of Alzheimer's disease in patients with memory problems, is detailed in the International Journal of Geriatric Psychiatry, a highly prestigious medical research journal.

The Japanese study was conducted over the course of a 20-month period, where a group of 15 amnestic mild cognitive impairment (MCI) patients with essential hypertension were divided into two groups. A group of eight participants were randomly allocated to take the drug Nilvadipine, while the other seven remaining participants were designated to take the drug Amlodipine.
 
The study found that the group treated with Nilvadipine had stabilized their decline in memory over the 20 months; whereas, the group treated with Amlodipine had continued to suffer loss of cognitive function, which was double that of the small decline in the Nilvadipine controlled group. 
Read more...
 
Dementia screening in primary care: Is it time? Print
Tuesday, 11 December 2007

INDIANAPOLIS -- Primary care physicians should focus on "dementia red flags" rather than routinely screening individuals with no dementia symptoms just because they've reached a certain age, writes Dr. Malaz Boustani of the Indiana University School of Medicine and the Regenstrief Institute, Inc. and colleagues from the University of Kent and the University of Cambridge in the United Kingdom in a commentary published in the Nov. 28 issue of the Journal of the American Medical Association.

"To screen without symptoms, unless there is a suspicion of a problem, either by the individual, caregivers or a physician, may led to negative consequences for the person and for society," says Boustani, who is a geriatrician.

"There currently is no accurate screening test, and we would be faced with an unacceptable number of false positives and false negatives. If we focus on dementia red flags, we will be identifying individuals who will have a very high probability of having dementia and be able to focus our resources, including diagnostic testing, on these people," Boustani says.....read more


Read more...
 
Visiting Aging Parents Over the Holidays: Elder Care Expert Encourages Boomers to Move Beyond Denial Print
Sunday, 02 December 2007
With the Holiday season upon us, Boomers will be spending more time with their aging parents. Elder care expert Esther Koch encourages Boomers to be more aware of their parents' needs.

San Mateo, CA (PRWEB) -- With the primary family get-together season upon us, now is the perfect time for Boomers to become more attuned to the potentially increasing needs of their aging parents.

"Caring for aging parents and becoming their advocate may be one of the most important and challenging roles that a Boomer will assume during their lifetime", states elder care expert, Esther Koch who has also been the primary caregiver to her mother over the last ten years. "Admitting that the parent who once kissed the hurts away now needs you can be emotionally overwhelming," emphasizes Koch.

To be sensitive to a parent's needs, Boomers need to get beyond their own denial of their parent's aging and perhaps their parent's denial too. Koch continues, "All denial does is reduce options. The opportunity cost of that denial, in financial and emotional terms, is far too great."

Thanksgiving probably provided some clues to a parent's changing condition and increasing needs. Koch suggests being honest with your answers to the following questions:
  • Did you notice a decline in physical abilities?
  • Did your parent seem less stable on their feet or did they recently fall?
  • Did you notice a decline in short-term memory?
  • Were there stacks of unopened mail or cancellation notices triggered by unpaid bills?
  • Did your parent or their home seem unusually unkempt?
  • Is the refrigerator supplied with nutritious foods or evidence of their lack?
  • Has your parent lost weight?
  • Did you have any questions about your parent's medications?
  • Did you question your parent's driving ability?

"Any one of these changes can be a tell tale sign," says Koch. "Remember, if something doesn't seem right, it probably isn't."

"If you didn't focus on these things over Thanksgiving, make sure you do during the upcoming holidays," encourages Koch. "Sooner or later, your parents will need your help, reminds Koch.
 
"Being there from the beginning will more positively impact everyone's lives."

About Esther Koch
: Esther Koch is a gerontologist and elder care advisor. Her firm, Encore Management, provides personal and corporate advisory services and seminars that assist Boomers with the range of issues associated with caring for an aging parent and their own aging. Her media interviews and articles have appeared on television, radio and in print. 



 
 
Dementia screening in primary care: Is it time? Print
Friday, 30 November 2007

INDIANAPOLIS -- Primary care physicians should focus on "dementia red flags" rather than routinely screening individuals with no dementia symptoms just because they've reached a certain age, writes Dr. Malaz Boustani of the Indiana University School of Medicine and the Regenstrief Institute, Inc. and colleagues from the University of Kent and the University of Cambridge in the United Kingdom in a commentary published in the Nov. 28 issue of the Journal of the American Medical Association.

"To screen without symptoms, unless there is a suspicion of a problem, either by the individual, caregivers or a physician, may led to negative consequences for the person and for society," says Boustani, who is a geriatrician.

"There currently is no accurate screening test, and we would be faced with an unacceptable number of false positives and false negatives. If we focus on dementia red flags, we will be identifying individuals who will have a very high probability of having dementia and be able to focus our resources, including diagnostic testing, on these people," Boustani says.

Dementia red flags include medication adherence problems, more than seven prescribed medications, agitation, multiple falls, and more than two hospitalizations or emergency department visits in the past year. Boustani, who says the healthcare system in the United States misses between 60 percent and 80 percent of individuals with dementia, is currently testing ways to help physicians identify dementia red flags in their patients so these missed individuals can be helped.

Someone in the United States develops Alzheimer's disease every 72 seconds, according to the Alzheimer's Association. The average primary care physician sees 2,000 patients per year of whom 300 are aged 65 or older. Of these 24 will develop dementia.

Despite this burden of disease, the benefit-harm ratio of conducting general population-based screening has not yet reached the point where the benefit outweighs the harm, the commentary maintains. Potential harms include possible stigma, loss of long term care insurance, emotional dislocation for both the individual and family, and resources' shifting from other health problems.


Boustani is the author of a 2003 report evaluating the wisdom of routine screening for dementia in primary care settings. The report, prepared for the U.S Preventative Services Task Force, found that while two-thirds of dementia cases are undetected by the patient's primary care physician, insufficient data exists to indicate whether or not it is a good idea to administer dementia screening tests to patients who do not have symptoms of memory loss or confusion.

"Pressures to institute screening of unproven benefit could divert much needed resources from the health and social care systems and have an overall negative impact on care for patients with dementia and other illnesses, ultimately delaying the point when dementia screening becomes indicated," the commentary concludes. "The goal should continue to be the best possible care for the most patients, which currently does not include screening for dementia."


From Indiana University

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