New test detects Alzheimer's with a finger prick

European scientists have developed a preliminary method to identify Alzheimer's using a drop of dried blood from a finger, achieving 86% accuracy in detecting amyloid pathology. The study, validated in 337 patients from several countries, is published in Nature Medicine and aims to simplify early diagnosis of this disease affecting over 50 million people worldwide.

A team of scientists from Europe and North America has refined a test that detects Alzheimer's from dried capillary blood obtained via a simple finger prick. Validated in 337 patients with and without dementia symptoms at centers in Barcelona, Sweden, the UK, and Italy, it quantifies proteins such as p-tau217, GFAP, and NfL. The test identifies amyloid pathology, a key indicator of the disease, with 86% accuracy.

Unlike current methods requiring invasive lumbar punctures or costly PET scans, this approach uses just a drop of blood dried on filter paper, needing no refrigeration or complex equipment. Existing blood tests detect p-tau217 with over 90% accuracy, but this system eases collection in remote areas or even at home.

Xavier Morató, neuroscientist at the Alzheimer's Center Ace in Barcelona and co-author of the study, states: “This method could accelerate the identification of people at risk of Alzheimer's, streamlining their referral to specialized memory units.” He emphasizes the goal of “democratizing access to early diagnosis.”

Alzheimer's, incurable and progressing silently for decades, affects over 50 million people worldwide. Spain's Neurological Society estimates over 50% of mild cases go undiagnosed, with a two-to-three-year delay between symptoms and confirmation. New drugs delay progression by about 18 months if applied early.

Independent experts provide balanced views. Raquel Sánchez Valle from Barcelona's Hospital Clínic sees it as simplifying large-scale research but advises against current clinical use or population screening without medical oversight, warning of risks from direct-to-consumer commercialization. David Pérez, neurologist at Madrid's Hospital 12 de Octubre, calls it “interesting” for quickly ruling out healthy individuals, though he notes its lower sensitivity compared to venous blood and the need for technical refinements before widespread clinical application.

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NAU scientists in a lab analyzing a non-invasive blood sample for early Alzheimer’s detection via brain glucose microvesicles.
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NAU researchers test non-invasive blood method for early Alzheimer’s detection

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Scientists at Northern Arizona University are developing a non-invasive blood test that could help detect Alzheimer’s disease before symptoms appear by examining how the brain uses glucose through tiny blood-borne microvesicles. Led by assistant professor Travis Gibbons and supported in part by the Arizona Alzheimer’s Association, the project aims to enable earlier diagnosis and intervention, similar to how doctors manage cardiovascular disease.

Scientists at Washington University School of Medicine in St. Louis have developed a blood test that estimates when Alzheimer's symptoms may begin, using levels of the protein p-tau217. The model predicts onset within about three to four years, potentially aiding clinical trials and early interventions. This advance relies on data from 603 older adults in ongoing studies.

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Researchers at Scripps Research have developed a blood test that detects Alzheimer's disease by analyzing structural changes in blood proteins. The method identifies differences in three specific proteins, allowing accurate distinction between healthy individuals, those with mild cognitive impairment, and Alzheimer's patients. Published in Nature Aging on February 27, 2026, the findings could enable earlier diagnosis and treatment.

Researchers have developed a blood test that detects pancreatic ductal adenocarcinoma with over 90% accuracy by combining four biomarkers, including two newly identified proteins. The test performs well even in early stages, potentially improving survival rates for this deadly cancer. The findings appear in Clinical Cancer Research.

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Rice University scientists say they have created the first complete, label-free molecular atlas of an Alzheimer’s brain in an animal model, combining hyperspectral Raman imaging with machine learning to map chemical changes that appear unevenly across brain regions and extend beyond amyloid plaques.

Scientists in the U.K. and Canada report the first direct visualization and measurement of alpha‑synuclein oligomers—the small protein clusters long suspected of triggering Parkinson’s—in human brain tissue. Using an ultra‑sensitive imaging method, the team found these clusters were larger and more numerous in Parkinson’s than in age‑matched controls, a result published in Nature Biomedical Engineering that may help guide earlier diagnosis and targeted therapies.

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Researchers have identified the gene ADAMTS2 as significantly more active in brain tissue from African Americans with Alzheimer's disease, marking a potential shared biological pathway across racial groups. This finding emerges from the largest study of its kind using brain samples from over 200 African American donors. The gene's prominence also appeared in a separate analysis of White individuals, suggesting broader implications for treatment.

 

 

 

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