Children with Alzheimer’s risk gene display reduced cognitive functionNovember 14th, 2007 - 8:32 am ICT by admin
According to researchers, their findings imply that changes predisposing a person to Alzheimer’s and other forms of dementia might occur much sooner in the brain than previously thought.
“One of our questions has been is this a risk that only happens with age, or is it already - early on - the cause of differences in performance. This study suggests there already are cognitive differences very early on in life,” said study co-author Jacob Raber, Ph.D., associate professor of behavioural neuroscience and neurology in the OHSU School of Medicine.
He added that the results also point out that therapeutic interventions that delay the effects of cognitive decline may be possible at a much younger age.
Previous studies have shown that a member of the apolipoprotein E gene family, apoE4, increases a person’s risk of age-related cognitive decline and cognitive injury from such “environmental” challenges as brain trauma. Half of all people with Alzheimer’s disease carry apoE4, Raber said.
“When we looked at non-demented healthy elderly, we saw the clear effect of apoE4. So it’s not just Alzheimer’s disease. ApoE4 carriers generally do worse in our tests. Among the nondemented oldest old, where the mean age is 82, those who have apoE4 do less well on cognitive tests,” he said.
In their study on children, Raber and colleagues examined 55 healthy boys and girls ages 7 to 10. Among them were eight girls and six boys who carried the apoE4 gene, and 17 girls and 24 boys who didn’t.
The children were assessed using a combination of paper- and computer-based tests, including a 3-dimensional, virtual reality program called “Memory Island” that assesses spatial learning and memory. “Memory Island” immerses participants in a simulated world in which they must navigate to a location marked with a flag that’s adjacent to the target in each of four quadrants. The participants are given several tries to navigate back to the targets based on memory.
The computer program mimics the Morris water maze, a standard scientific tool for testing memory in rodents by training them to swim to a platform based on visual cues.
Raber and colleagues found that apoE4 carriers scored lower in location recognition tests, and non-apoE4 carriers outperformed apoE4 carriers in the “Memory Island” test by navigating closer to the visible target location. Also, non-apoE4 carriers showed spatial memory retention when a target wasn’t present and searched more frequently for the targets in the appropriate quadrants while apoE4 carriers did not.
In all, 75.6 percent non-apoE4 carriers showed target preference compared with only 43 percent of apoE4 carriers. (ANI)
- 'Bad' neighbourhood linked to worse cognitive function in some older adults - Mar 08, 2011
- How diets high in fish oil fight Alzheimer's - Feb 16, 2011
- Drug reversing Alzheimer's symptoms found - Feb 12, 2012
- Study predicts risk of memory loss in healthy, older adults - Jan 20, 2011
- Drug reverses Alzheimer's symptoms in mice: Study - Feb 10, 2012
- A gene for Alzheimer's sharpens young minds - Feb 16, 2010
- Study explains why humans outlive apes - Jan 27, 2010
- Alzheimer's hits women more severely than men - Aug 26, 2012
- Key Alzheimer's risk gene causes alterations in shapes of brain protein deposits - Jul 15, 2010
- Gene harms brain decades before Alzheimer's outbreak - May 15, 2011
- Study: Low Testosterone linked to Alzheimer's disease - Oct 07, 2010
- Low testosterone levels could lead to Alzheimer's - Oct 06, 2010
- Super-early signs of Alzheimer's revealed - Dec 17, 2010
- Earliest brain changes linked to genetic risk of Alzheimer's identified - Dec 01, 2010
- Why do humans outlive chimps? - Dec 03, 2009
Tags: alzheimer, apolipoprotein e, behavioural neuroscience, brain trauma, cell regeneration, cognitive decline, cognitive differences, cognitive function, cognitive impairments, cognitive tests, dementia, environmental challenges, gene family, girls, learning and memory, ohsu school, raber, risk, therapeutic interventions