Blood Test Predicts Alzheimer's Symptom Onset Within Three to Four Years
Researchers at Washington University School of Medicine developed a blood test-based method to predict when Alzheimer's symptoms will begin, with accuracy within three to four years, using plasma p-tau217 protein levels.
Researchers at Washington University School of Medicine in St. Louis have developed a method to predict when someone is likely to develop symptoms of Alzheimer's disease using a single blood test. In a study published in Nature Medicine, the researchers demonstrated that their models predicted the onset of Alzheimer's symptoms within a margin of three to four years.
The models use a protein called p-tau217 in an individual's plasma, the liquid part of the blood, to estimate the age when they will begin experiencing symptoms of the neurodegenerative disease. The scientists found that the ratio of phosphorylated to non-phosphorylated tau at position 217 ("%p-tau217") could predict the arrival of Alzheimer's symptoms within three and four years.
The study was part of a project developed and launched by the Foundation for the National Institutes of Health Biomarkers Consortium, a public–private partnership of which WashU Medicine is a member. Researchers analyzed data from volunteers in two independent long-running Alzheimer's research initiatives: the WashU Medicine Knight Alzheimer Disease Research Center (Knight ADRC) and the Alzheimer's Disease Neuroimaging Initiative (ADNI), based at multiple sites in the U.S. The participants included 603 older adults who lived independently in the community.
Plasma p-tau217 was measured with PrecivityAD2, a clinically available diagnostic blood test for Alzheimer's disease from C2N Diagnostics. Plasma p-tau217 was also measured in the ADNI cohort using blood tests from other companies, including one cleared by the U.S. Food and Drug Administration.
Plasma p-tau217 has previously been shown to correlate strongly with the accumulation of amyloid and tau in the brain as shown on PET scans. The key hallmarks of Alzheimer's disease, amyloid and tau are misfolded proteins that begin building up in the brain many years before Alzheimer's symptoms develop. Tau is what neurofibrillary tangles are composed of, and neurofibrillary tangles are one of two key components of Alzheimer's disease.
"Amyloid and tau levels are similar to tree rings—if we know how many rings a tree has, we know how many years old it is," said lead author Kellen K. Petersen, an instructor in neurology at WashU Medicine. "It turns out that amyloid and tau also accumulate in a consistent pattern and the age they become positive strongly predicts when someone is going to develop Alzheimer's symptoms. We found this is also true of plasma p-tau217, which reflects both amyloid and tau levels."
Older individuals had a shorter time from when elevated p-tau217 appeared to the start of symptoms as compared to younger participants, suggesting that younger people's brains may be more resilient to neurodegeneration and that older people may develop symptoms at lower levels of Alzheimer's pathology. For example, if a person had elevated p-tau217 in their plasma at age 60, they developed symptoms 20 years later. If p-tau217 wasn't elevated until age 80, they developed symptoms only 11 years later.
"Our work shows the feasibility of using blood tests, which are substantially cheaper and more accessible than brain imaging scans or spinal fluid tests, for predicting the onset of Alzheimer's symptoms," said senior author Suzanne E. Schindler, an associate professor in the WashU Medicine Department of Neurology. The current ways of searching for tau as a result of neurofibrillary tangles requires a significant amount of equipment; the idea of analyzing a blood sample is much less resource-dependent.
This method could have implications both for clinical trials developing preventive Alzheimer's treatments and for eventually identifying individuals likely to benefit from these treatments. "In the near term, these models will accelerate our research and clinical trials," Schindler said. "Eventually, the goal is to be able to tell individual patients when they are likely to develop symptoms, which will help them and their doctors to develop a plan to prevent or slow symptoms."
More than seven million Americans live with Alzheimer's disease, with health and long-term care costs for Alzheimer's and other forms of dementia projected to reach nearly $400 billion in 2025, according to the Alzheimer's Association. This massive public health burden currently has no cure, but predictive models could help efforts to develop treatments that prevent or slow the onset of Alzheimer's symptoms.
Levels of p-tau217 in the plasma can currently be used to help doctors diagnose Alzheimer's in patients with cognitive impairment. These tests are not currently recommended in cognitively unimpaired individuals outside of clinical trials or research. The authors note that the margin of error of three to four years may "limit its utility for individual decision-making, but it could still be useful for group-level studies."