WASHINGTON, Mar 2: Scientists have for the first time found that an abnormal protein whose accumulation in the brain is a hallmark of Alzheimer’s disease starts building up inside neurons of people as young as 20.
It has long been known that amyloid accumulates and forms clumps of plaque outside neurons in ageing adults and in Alzheimer’s but this is the first time amyloid accumulation has been shown in such young human brains, researchers said.
“Discovering that amyloid begins to accumulate so early in life is unprecedented,” said lead investigator Changiz Geula, research professor at the Cognitive Neurology and Alzheimer’s Disease Center at Northwestern University Feinberg School of Medicine.
“This is very significant. We know that amyloid, when present for long periods of time, is bad for you,” Geula said.
In the study, scientists examined basal forebrain cholinergic neurons to try to understand why they are damaged early and are among the first to die in normal ageing and in Alzheimer’s.
These vulnerable neurons are closely involved in memory and attention.
Geula and colleagues examined these neurons from the brains of three groups of deceased individuals: 13 cognitively normal young individuals, ages 20 to 66; 16 non-demented old individuals, ages 70 to 99; and 21 individuals with Alzheimer’s ages 60 to 95.
Scientists found amyloid molecules began accumulating inside these neurons in young adulthood and continued throughout the lifespan.
Nerve cells in other areas of the brain did not show the same extent of amyloid accumulation. The amyloid molecules in these cells formed small toxic clumps, amyloid oligomers, which were present even in individuals in their 20’s and other normal young individuals.
The size of the clumps grew larger in older individuals and those with Alzheimer’s.
“This points to why these neurons die early,” Geula said.
“The small clumps of amyloid may be a key reason. The lifelong accumulation of amyloid in these neurons likely contributes to the vulnerability of these cells to pathology in ageing and loss in Alzheimer’s,” Geula said.
The growing clumps likely damage and eventually kill the neurons. It’s known that when neurons are exposed to these clumps, they trigger an excess of calcium leaking into the cell, which can cause their death.
The clumps may also cause damage by secreting amyloid outside the cell, contributing to the formation of the large amyloid plaques found in Alzheimer’s.
The study is published in the journal Brain. (PTI)
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