تست خون کشف آلزایمر با دقت ۸۶ درصد
تست خون کشف آلزایمر با دقت ۸۶ درصد
محققان دانشگاه واشنگتن از ابداع یک آزمایش خون جدید خبر داده اند که با دقت ۸۶ درصد قادر به شناسایی پروتئین های سمی عامل ابتلای افراد به بیماری آلزایمر است.
آلزایمر بیماری است که مغز انسان را بی سروصدا و به طور نامحسوس تخریب می کند و حافظه و قدرت شناخت انسان را از بین می برد. شناسایی این بیماری که نشانه های آن بسیار دیر ظاهر می شوند کار ساده نیست و حالا یک آزمایش خون به کمک حل این مشکل آمده است.
تا به حال از روش های مختلفی برای شناسایی سریع بیماری آلزایمر استفاده شده است. یکی از روش های جدید این کار ردگیری پروتئینی موسوم به آمیلوئید بتا است که تجمع زود هنگام آن در مغز بیماران آلزایمری شناسایی این بیماری را تسهیل می کند. پروتئین مذکور در قالب پلاکت های سمی بخش های زیادی از مغز را آلوده می کند.
پروتئین سمی دیگری که در اثر ابتلا به آلزایمر در بدن تولید می شود پی تائو ۱۸۱ نام دارد که در مایع مغزی مبتلایان به این بیماری در قالب پلاک آمیلوئید قابل شناسایی است. نمونه برداری از این مایع کار پرهزینه ای است، اما یک روش آزمایش خون جدید می تواند جایگزین این روش شود.
برخی پروتئین های سمی موجود در این مایع به خون منتقل شده و از این طریق قابل شناسایی هستند. تجمع این پروتئین در خون افراد مبتلا به آلزایمر ۳.۵ برابر افراد عادی است و فعلا دقت این روش برای شناسایی اشخاص مبتلا به آلزایمر ۸۶ درصد است.
CHICAGO, JULY 28, 2020 — A simple blood test for Alzheimer’s would be a great advance for individuals with — and at risk for — the disease, families, doctors and researchers.
At the Alzheimer’s Association International Conference® (AAIC®) ۲۰۲۰, scientists reported results of multiple studies on advances in blood “tests” for abnormal versions of the tau protein, one of which may be able to detect changes in the brain 20 years before dementia symptoms occur. In particular, the reports focus on a specific form of tau known as p-tau217, which seems to be the most specific to Alzheimer’s and the earliest to show measurable changes.
Changes in brain proteins amyloid and tau, and their formation into clumps known as plaques and tangles, respectively, are defining physical features of Alzheimer’s disease in the brain. Buildup of tau tangles is thought to correlate closely with cognitive decline. In these newly reported results, blood/plasma levels of p-tau 217, one of the forms of tau found in tangles, also seem to correlate closely with buildup of amyloid.
Currently, the brain changes that occur before Alzheimer’s dementia symptoms appear can only be reliably assessed by positron-emission tomography (PET) scans, and from measuring amyloid and tau proteins in spinal fluid (CSF). These methods are expensive and invasive. And, too often, they are unavailable because they are not covered by insurance or difficult to access, or both.
“There is an urgent need for simple, inexpensive, non-invasive and easily available diagnostic tools for Alzheimer’s. New testing technologies could also support drug development in many ways. For example, by helping identify the right people for clinical trials, and by tracking the impact of therapies being tested,” said Maria C. Carrillo, Ph.D., Alzheimer’s Association chief science officer. “The possibility of early detection and being able to intervene with a treatment before significant damage to the brain from Alzheimer’s disease would be game changing for individuals, families and our healthcare system.”
A blood test, for example, will enable interpretation and understanding of Alzheimer’s progression in much larger, more diverse and more robust populations.
“While these new reports are encouraging, these are early results, and we do not yet know how long it will be until these tests are available for clinical use. They need to be tested in long-term, large-scale studies, such as Alzheimer’s clinical trials,” Carrillo added. “In addition, we need to continue research to refine and verify the tests that are the current state-of-the-art — including cerebrospinal fluid and PET imaging biomarkers.”
Blood P-tau217 Detects Alzheimer’s Disease (i.e., Both Plaques and Tangles) with High Accuracy
As reported at AAIC 2020, an international team of researchers have identified a highly accurate, blood-based biomarker for the detection of Alzheimer’s disease by measuring levels of p-tau217 in blood, and validated the finding in multiple, diverse populations. The scientists found that, “the diagnostic precision of blood p-tau217 was as high as established diagnostic methods, including positron emission tomography (PET) imaging and cerebrospinal fluid biomarkers, which are invasive, costly and less available.”
The research team was led by Oskar Hansson, M.D., Ph.D., from Lund University, Sweden in coordination with Sebastian Palmqvist, M.D., Ph.D., and Shorena Janelidze, Ph.D. from Lund, Eric Reiman, M.D., from Banner Alzheimer’s Institute, USA, Jeffrey Dage, Ph.D., from Eli Lilly, USA, and other research colleagues. The Lund University researchers presented the results at AAIC, and they were also published online.
They studied three different cohorts comprising more than 1,400 cases, including a large clinic-based study from Sweden (the BioFINDER-2 study), a cohort with neuropathological confirmation of Alzheimer’s (the Arizona Study of Aging and Neurodegenerative Disorders), and a large kindred with genetically-caused Alzheimer’s (Colombian autosomal-dominant Alzheimer’s registry).They analyzed other current experimental biomarkers (p-tau217, p-tau181, Aβ۴۲/۴۰ and neurofilament light chain) in both blood and cerebrospinal fluid, as well as performed PET imaging for tau and amyloid pathology.
The main finding of the study was that blood p-tau217 could distinguish Alzheimer’s from other neurodegenerative disorders with diagnostic accuracy between 89 and 98 percent. In this study, the p-tau217 assessment was more accurate for Alzheimer’s than blood-based tests for p-tau181, neurofilament light or amyloid beta 42/40 ratio, as well as magnetic resonance imaging (MRI). In fact, according to the researchers, performance was similar to significantly more costly methods, such as PET imaging and cerebrospinal fluid biomarkers.
The researchers also found that p-tau217 analyzed in blood collected during life could detect tau brain changes measured in brain tissue analyzed after death. These tau brain changes are thought to be related to amyloid plaque accumulation. P-tau217 distinguished persons who had plaques and tangles from those without Alzheimer’s pathology with 89% accuracy, those with plaques and more extensive tangles with 98% accuracy, and the outcome of tau PET imaging with 93% accuracy.
The p-tau217 levels were increased about seven-fold in Alzheimer’s, and, in individuals with a gene causing Alzheimer’s, the levels started to increase already 20 years before onset of cognitive impairment. “This test, once verified and confirmed, opens the possibility of early diagnosis of Alzheimer’s before the dementia stage, which is very important for clinical trials evaluating novel therapies that might stop or slow down the disease process,” Hansson said.
Blood Amyloid and P-tau are Precise Markers of Brain Amyloidosis, Tauopathy
To advance research on a blood test for Alzheimer’s disease, Suzanne Schindler, M.D., Ph.D., of Washington University School of Medicine in St. Louis and colleagues evaluated the performance of a variety of amyloid and tau measures in blood.
Using mass spectrometry, the scientists mapped the blood plasma tau protein and compared the results to CSF and PET imaging measures. Compared to the better-known tau form p-tau181, they found that p-tau217 was more closely linked to build up of amyloid plaques in the brain as measured by a PET scan.
Additionally, their findings suggest that measuring levels of several different forms of p-tau in blood over time may enable clinicians and researchers to track the stages of Alzheimer’s progression in people living with the disease.
According to the researchers, a blood test for Alzheimer’s disease that incorporates both amyloid and tau measures may allow earlier and more accurate dementia diagnoses not only in research participants but also in clinic patients.
The scientists launched the Study to Evaluate Amyloid in Blood and Imaging Related to Dementia (SEABIRD) to develop and validate Alzheimer’s blood biomarkers in a cohort that is more diverse and representative of the greater St. Louis region. SEABIRD will enroll more than 1,100 individuals including diversity in race, socioeconomic status, medical history and cognitive status.
Plasma P-tau217 is Comparable to P-tau181 for Distinguishing Between Alzheimer’s and Frontotemporal Lobar Degeneration
Recent studies have shown that p-tau181 is more than three times as high in people with Alzheimer’s compared to healthy elderly people or people with a neurodegenerative disease known as frontotemporal lobar degeneration (FTLD). At AAIC 2020, Elisabeth Thijssen, M.Sc., and Adam L. Boxer, M.D., Ph.D., of the UCSF Memory and Aging Center and colleagues reported a comparison of p-tau181 to a related form of tau called p-tau217 to determine which form can best identify people with Alzheimer’s.
The retrospective study included 617 participants: 119 healthy controls, 74 Alzheimer’s cases (biomarker-confirmed) and 294 FTLD. In this study group, plasma p-tau181 was increased three-fold in people with Alzheimer’s compared to controls and FTLD. Increase in plasma p-tau217 was even higher; five-fold in Alzheimer’s compared to healthy controls and four-fold relative to FTLD. The plasma comparison results mirrored the findings of tau PET imaging in the brain. P-tau181 had a 91% accuracy and p-tau217 had 96% accuracy in predicting whether a person had a tau positive brain scan.
According to the researchers, the study shows that both p-tau217 and p-tau181 measured in blood are elevated in Alzheimer’s, and that measurements closely correspond to “gold standard” PET scan results. These blood tests are likely to be useful for diagnosing Alzheimer’s and as monitoring tools in clinical trials to measure treatment effects of new Alzheimer’s therapies.
About the Alzheimer’s Association International Conference® (AAIC®)
The Alzheimer’s Association International Conference (AAIC) is the world’s largest gathering of researchers from around the world focused on Alzheimer’s and other dementias. As a part of the Alzheimer’s Association’s research program, AAIC serves as a catalyst for generating new knowledge about dementia and fostering a vital, collegial research community.
AAIC 2020 home page: www.alz.org/aaic
AAIC 2020 newsroom: www.alz.org/aaic/pressroom.asp
About the Alzheimer’s Association®
The Alzheimer’s Association is the leading voluntary health organization in Alzheimer’s care, support and research. Our mission is to lead the way to end Alzheimer’s and all other dementia — by accelerating global research, driving risk reduction and early detection, and maximizing quality care and support. Visit alz.org or call +1 800.272.3900.
- Oskar Hansson, PhD, et al. Phospho-tau217 and phospho-tau181 in plasma and CSF as biomarkers for Alzheimer’s disease. (Funder(s): Swedish Research Council, the Knut and Alice Wallenberg Foundation, and the Swedish Alzheimer Foundation)
- Shorena Janelidze, PhD, et al. Plasma phospho-tau217 is a potential early diagnostic and prognostic biomarker of Alzheimer’s disease. (Funder(s): Swedish Research Council, the Knut and Alice Wallenberg Foundation, and the Swedish Alzheimer Foundation)
- Suzanne Schindler, MD, PhD, et al. Mass spectrometry measures of plasma Aβ, tau and p-tau isoforms relationship to amyloid PET, tau PET, and clinical stage of Alzheimer’s disease. (Funder(s): U.S. National Institute on Aging)
- Elisabeth Thijssen, MSc, et al. Comparative diagnostic performance of plasma P-tau217 and P-tau181 in Alzheimer’s Disease and Frontotemporal Lobar Degeneration and correlations with [18F]Flortaucipir-PET uptake. (Funder(s): U.S. National Institute on Aging, National Center for Advancing Translational Sciences, Tau Research Consortium)
*** AAIC 2020 news releases may contain updated data that does not match what is reported in the abstracts.