Researchers at Karolinska Institutet in Sweden have studied the incidence and regional distribution of Alzheimer’s disease biomarkers in the brains of people with Down’s syndrome. The results can bring new possibilities for earlier diagnosis and preventive treatment of dementia. The study is published in Molecular Neurodegeneration.
While medical advances and improvements of life quality have increased the life expectancy of people with Down’s syndrome to an average of 60 years, up to 90 percent develop Alzheimer’s disease if they live long enough.
In Alzheimer’s disease, clumps of amyloid form plaques around the neurons of the brain, while another protein, tau, accumulates inside the nerve cells in what are referred to as tangles. Plaque and tangles appear first in one region of the brain and then spread, causing gradually deteriorating functional impairment.
People with Down’s syndrome have an extra copy of chromosome 21. One reason for the high incidence of Alzheimer’s disease in people with Down’s syndrome is that the gene coding for the production of amyloid is located on chromosome 21, which can cause an accumulation of amyloid in the brain already in childhood.
“Previous studies of Down’s syndrome by our group and others have been able to demonstrate that pathological forms of amyloid and tau can appear years before someone shows signs of dementia,” says Lotta Granholm, professor at Karolinska Institutet and the University of Denver, and one of the paper’s principal authors.
In the current study, the researchers studied the extent and distribution of tau and amyloid in the brain tissue of people with Down’s syndrome with or without an Alzheimer’s diagnosis, and of people who had died with Alzheimer’s disease but without any other functional disability.
Their analyses showed that the incidence of tau in the brain tissue of people with Down’s syndrome and Alzheimer’s disease was higher than in people with Alzheimer’s but without Down’s syndrome, suggesting that tau is an early change in Down’s syndrome.
“Apart from a high level of tau, we also measured a different regional distribution of tau in the brains of people with Down’s syndrome and Alzheimer’s disease compared to the control group,” says the paper’s first author Laetitia Lemoine, assistant professor at the Department of Neurobiology, Care Sciences and Society, Karolinska Institutet.
Traces of tau were also detected in the brain tissue of fetuses with Down’s syndrome. Early prophylactic measures against tau accumulation could prevent the development of Alzheimer pathology in childhood for this patient group, the researchers believe.
“Our studies support the need for continued research on the progress and incidence of amyloid plaque and tau in the brain by imaging the brains of live individuals with Down’s syndrome,” says Agneta Nordberg, professor at the Department of Neurobiology, Care Sciences and Society, and the paper’s second principal author. “Our aim is a better understanding of how we can take early steps to discover pathological changes that produce cognitive symptoms and begin medication that helps to improve life quality.”
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The study was financed by grants from the National Institute on Aging, the Bright Focus Foundation, the Swedish Foundation for Strategic Research, the Swedish Research Council, Region Stockholm, Karolinska Institutet, the Swedish Brain Fund, the Swedish Alzheimer’s Foundation, the foundation for old servants, the Gun and Bertil Stohne Foundation, the Gunvor and Josef Anér Foundation, the Loo and Hans Osterman Foundation for Medical Research, the Dementia Research Fund and the Croatian Science Foundation. There are no reported conflicts of interest.
Publication: “Regional binding of tau and amyloid PET tracers in Down syndrome autopsy brain tissue.” L Lemoine, A Ledreux, EJ Mufson, SE Perez, G Simic, E Doran, I Lott, S Carroll, K Bharani, S Thomas, A Gilmore, ED Hamlett, A Nordberg, AC Granholm. Molecular Neurodegeneration, 23 November 2020, doi: 10.1186/s13024-020-00414-3.
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