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The DROP-AD study signals a practical breakthrough in Alzheimer’s detection by validating finger-prick dried blood spot testing for key biomarkers, including p-tau217, GFAP and NfL. By enabling accurate, room-temperature samples that can be self-collected and mailed, the approach could make screening faster, cheaper and widely accessible — supporting earlier identification, earlier treatment pathways and large-scale population monitoring. The test also has potential for other neurodegenerative diseases such as Parkinson’s, ALS and MS.
While the DROP-AD findings are promising, past experience with Alzheimer’s blood tests urges caution. Earlier commercial screeners have shown high false-positive rates, and major groups like the Alzheimer’s Association caution that blood biomarkers cannot yet stand alone for diagnosis. Experts note that accuracy, interpretation, disclosure and real-world implementation — especially in primary care — require further validation before widespread clinical use.