A new study has found that children who have a gene known to increase the risk of Alzheimer's disease already display signs of reduced cognitive function. Researchers at the Oregon Health & Science University study found that 7- to 10-year-olds with a member of a family of genes implicated in development, nerve cell regeneration and neuroprotection exhibit reduced spatial learning and memory, associated with later-life cognitive impairments.
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.
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.