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 Brown University have identified a subtle brain activity pattern that can forecast Alzheimer's disease in people with mild cognitive impairment up to two and a half years in advance. Using magnetoencephalography and a custom analysis tool, the researchers detected changes in neuronal electrical signals linked to memory processing. This noninvasive approach offers a potential new biomarker for early detection.

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New research reveals that blood from younger mice can protect against Alzheimer's-like brain damage, while older blood accelerates it. Scientists conducted experiments infusing mouse blood over 30 weeks to observe effects on memory and protein buildup. The findings highlight blood's role in brain health and potential new treatments.

Researchers at Brazil’s Federal University of ABC report a simple copper-chelating molecule that reduced beta-amyloid–linked pathology and improved memory in rats. The compound showed no detectable toxicity in preclinical tests and, based on computer modeling, is predicted to cross the blood–brain barrier. The team is seeking industry partners for clinical development.

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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.

Researchers at the University of Vermont have discovered a way to reverse faulty blood flow in the brain linked to dementia by replacing a missing phospholipid. Their study shows that low levels of PIP2 cause overactive Piezo1 proteins in blood vessels, disrupting circulation. Restoring PIP2 normalized flow in preclinical tests, offering hope for new treatments.

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알츠하이머 시험이 암 연구에서 영감을 받은 다중 표적 접근으로 전환 중이며, Novo Nordisk의 세마글루타이드 실패에도 불구하고. Eli Lilly의 Kisunla와 Eisai 및 Biogen의 Leqembi 두 약물만이 진행을 늦추기 위해 널리 승인됨. 이러한 진화는 뇌 퇴화 질환을 복잡한 시스템으로 간주하며, 전 세계적 영향 속에서 이를 멈추는 새로운 방법을 모색함.

 

 

 

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