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A team of researchers has found a link between strains of misshapen and fast-replicating tau protein and accelerated cognitive decline -- a critical result that could help lead to more precise diagnoses and targeted therapies.
The research has been published in the 'Science Translational Medicine Journal'. Such work could lead to changes in Alzheimer's care, possibly giving patients and families more accurate prognoses. "For the first time, we established the link between the behaviour of tau protein in the test tube and the clinical duration of the disease in patients," said Jiri Safar, a professor in the departments of pathology, neurology, and neurosciences at the Case Western Reserve School of Medicine. "What the research says, in general, is that Alzheimer's is not a single disease. There is a spectrum, and different cases have distinct biological drivers of the progression -- and they should be handled as separate diseases," Safar added. "We have to understand the disease and then sort it out into the different subsets or categories, and that's effectively where we are now with Alzheimer's disease," Safar said. Safar's co-authors included CWRU colleagues Alan Lerner, a professor of neurology, and Mark Cohen, a professor of pathology and neurology; David Westaway, a professor in the Department of Medicine at University of Alberta and director of its Centre for Prions and Protein Folding Diseases; and Rohan de Silva, a professor of molecular neuroscience at University College London's Queen Square Institute of Neurology. Safar hopes the research will help dispel the public perception that people with Alzheimer's disease will likely decline slowly over eight to 10 years; 10 per cent to 30 per cent have the rapidly progressing form of the disease. "We're talking about 600,000 to 1.8 million patients in the United States alone," he said. "So now we can think about it in the same way we clinically handle malignancies like breast cancer or pulmonary cancer -- that different cancers have very different prognoses and therapeutic strategies," he added. The next step is to translate the tools used in the study to clinical practice and identify people at high risk for rapid disease progression and then tailor treatments to the diagnosis. The Alzheimer's disease research followed Safar's ground-breaking work involving prion proteins. He and colleagues discovered that when prions became misfolded they can replicate and damage the brain. They used concepts and tools developed in the prion work to investigate the mechanisms of misfolded proteins and applied them to tau protein and Alzheimer's disease. The prion research helped create a new paradigm for understanding Alzheimer's disease, Parkinson's disease, Amyotrophic Lateral Sclerosis, and other neurodegenerative conditions. They knew that genetic and environmental factors linked to the increased risk of developing Alzheimer's disease explained about 30 per cent of cases. In the recent research, they sought to understand the other 70 per cent. The scientists examined brain samples from 40 people who died of Alzheimer's disease -- roughly half had lost cognitive functions slowly over years and the rest declined quickly and died in less than three years. The researchers found that in rapidly progressing cases, the cores of tau protein particles were shaped differently, meaning they had different structural organizations. Moreover, using processes they previously developed, they found that these misfolded tau species -- like prions -- can replicate more rapidly in test tubes. They also deepened their understanding of the impacts of different structures and characteristics of abnormal tau and determined the attributes that predicted the speed of replication. (ANI)
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