UBC researchers launch first-in-Canada testing program for Alzheimer’s disease
For the first time, Canadians can access a new test to diagnose Alzheimer’s disease, thanks to a study being led by researchers at UBC’s faculty of medicine.
For the first time, Canadians can access a new test to diagnose Alzheimer’s disease, thanks to a study being led by researchers at UBC’s faculty of medicine.
The test—which measures proteins known as biomarkers in the cerebrospinal fluid surrounding the brain and spinal cord—could assist with earlier and more accurate diagnosis of the disease, giving patients and their families much needed answers and assistance with planning.
Over half a million Canadians are currently living with Alzheimer’s disease or a related form of dementia. With a rapidly aging population, that number is projected to double by 2031.
“This is an urgent and rapidly growing health care issue,” says principal investigator Dr. Mari DeMarco (she/hers), a clinical associate professor at UBC’s department of pathology and laboratory medicine and clinical chemist at Providence Health Care. “The Alzheimer’s disease biomarker test, which we have now made available to all Canadians, can help doctors accurately diagnose the disease even when only mild symptoms are present.”
Through the study, called IMPACT-AD, Dr. DeMarco and her team developed a key component of the biomarker test and worked with individuals with lived experience with dementia, along with health care providers and other partners, to implement a comprehensive diagnostic testing strategy.
The team recently achieved one of their major goals by making the test available for people across Canada. The test must be ordered by doctors specializing in dementia care, who may recommend it for individuals experiencing mild to moderate symptoms that they suspect are caused by Alzheimer’s disease.
Early and accurate diagnosis of Alzheimer’s disease is critical as it can provide patients with more timely access to health care and community services, which have the potential to lead to more effective treatment and improve quality of life. While current approaches for diagnosis rely on imaging tests and observation of the signs and symptoms of the disease, the researchers say the new test can provide added benefits.
“This is an important addition to the toolkit we use to diagnose Alzheimer’s disease,” said Dr. DeMarco. “Adding the measure of biomarkers has been shown to help correctly identify the disease and predict those with mild symptoms that are likely to progress to dementia.”
In Alzheimer’s disease, the proteins amyloid-beta and tau clump together in the brain to form amyloid plaques and tau tangles, respectively. As it is not possible to see these clumps using regular imaging techniques, the new test measures protein levels in the cerebrospinal fluid, using them as biomarkers that help determine if a person’s declining brain health is likely due to Alzheimer’s disease.
As part of the study, patients are also able to provide their perspective on how the test results impacted their lives. With additional input from patients’ families and their doctors, DeMarco and her colleagues hope to address barriers to uptake and use in the Canadian healthcare system.
“Our aim is to gain a better understanding of how this testing impacts personal and medical decision making, and health care costs. We want to inform positive change in the Canadian health care system and improve care and support for individuals living with Alzheimer’s disease and their families,” said Dr. DeMarco.
This project was made possible with the support of Health Canada, Brain Canada, Michael Smith Health Research BC, UBC’s Faculty of Medicine and Djavad Mowafaghian Centre for Brain Health, Women’s Brain Health Initiative, St. Paul’s Foundation, and in collaboration with the Alzheimer Society of Canada and the Canadian Consortium on Neurodegeneration in Aging. For more information, view the original news release from Brain Canada.
Interview language(s): English