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A new study adds to a growing sense of optimism that doctors could soon have a faster, simpler and more affordable way to tell if a patient’s symptoms of memory loss and confusion are caused by Alzheimer’s disease, the most common form of dementia that affects nearly 7 million older Americans.
A team of researchers based in Sweden found that a blood test was about 90 percent accurate in diagnosing Alzheimer’s disease in people experiencing thinking and memory problems. In the research study, primary care physicians were 63 percent accurate in an Alzheimer’s diagnosis when not using the blood test; specialists were 73 percent accurate when not using the test, which identifies a specific protein in the blood that serves as an indicator for the buildup of amyloid plaques and tau tangles, two defining characteristics of Alzheimer’s disease.
The study was presented at the 2024 Alzheimer’s Association International Conference and published in the medical journal JAMA.
This blood test and others like it are not widely available to patients outside of research studies, but they could be soon, and that would be a “revolutionary change,” says Paul Newhouse, M.D., director of the Center for Cognitive Medicine at Vanderbilt University Medical Center and clinical core director for the Vanderbilt Alzheimer’s Disease Research Center.
What doctors rely on now when making an Alzheimer’s diagnosis is a patchwork of physical and cognitive tests and pricey brain scans or invasive spinal taps. With more studies like this latest one, blood tests could “serve as the first line of defense in diagnosing the disease,” Howard Fillit, M.D., cofounder and chief science officer of the Alzheimer’s Drug Discovery Foundation, said in a statement.
A study published earlier this year in JAMA Neurology examined the accuracy of a blood test that identifies the same protein in the blood, called p-tau217. The research team found that the blood test was more than 90 percent accurate and was on par with the gold-standard diagnostic tools — positron emission tomography (PET) imaging and cerebrospinal fluid collected from a lumbar puncture — in detecting the brain changes associated with Alzheimer’s disease.
Previous studies have produced promising results, too, so evidence continues to build for the use of blood tests in clinical settings, says Ronald Petersen, M.D., director of the Mayo Clinic Alzheimer’s Disease Research Center and the Mayo Clinic Study of Aging.
“I think this is a step forward; this is important. This is something that the field has been waiting for,” Petersen told AARP.
What are the benefits of a blood test?
For starters, a highly predictive blood test could save a lot of time and money when it comes to making an Alzheimer’s diagnosis, Newhouse says. PET scans and spinal taps can cost thousands of dollars and are performed only in hospitals or specialty clinics.
A faster diagnosis could impact access to new Alzheimer’s treatments that are approved for patients in the early to mild stages of the disease. Research presented at the Alzheimer’s Association’s 2024 conference suggests that the wait time for these treatments could be slashed by several years with an accurate and reliable blood test.
“Currently, eligible patients are falling outside of the treatment window because it takes so long to receive a diagnosis. An easy-to-use blood test could help address that problem,” researcher Soeren Mattke, M.D., director of the Brain Health Observatory at the University of Southern California, Los Angeles, said in a news release issued by the conference.
Another potential implication: Screening individuals for Alzheimer’s disease, even if they don’t have symptoms. Research shows that Alzheimer’s changes in the brain can start years, sometimes decades, before symptoms begin. Enrolling people in clinical trials who are in the earliest stages of Alzheimer’s could help identify treatments that get to work before life-changing symptoms take hold.
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