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EU-Certified Blood Test Predicts Alzheimer’s Progression in Patients With Mild Cognitive Impairment

Developers say the MAP‑AD assay, based on mitochondrial DNA methylation, is slated for hospital rollout in Catalonia within a year.

Overview

  • The Hospital Universitari de Bellvitge and spin‑off ADmit Therapeutics report MAP‑AD as a prognostic blood biomarker for people with mild cognitive impairment who will progress to Alzheimer’s disease.
  • Peer‑reviewed data in iScience show about 84% accuracy in studied blood samples from patients who later developed Alzheimer’s dementia.
  • The test has obtained CE‑IVDR certification, clearing it for clinical use in the European Union, with Bellvitge coordinating clinical work and IDIBELL as the originating research center.
  • Unlike amyloid or tau assays, MAP‑AD measures mitochondrial DNA methylation patterns, with analysis aided by artificial intelligence to detect predictive changes.
  • Researchers highlight potential uses in earlier counseling, trial recruitment and treatment planning, while noting the need for broader validation and health‑system guidance as Europe’s disease‑modifying antibodies roll out unevenly.