In 2024, The National Institute on Aging and the Alzheimer’s Association revised the diagnostic
criteria of Alzheimer’s Disease to require a biological confirmation of the disease process
through various biomarkers.
Early Core 1 biomarkers include amyloid positron emission tomography (PET scan),
cerebrospinal fluid (CSF) biomarkers (amyloid Beta 42/40, p-tau 181/ amyloid B42, total
tau/amyloid B42) and serum biomarkers (p-tau 217), and are used to establish the diagnosis of
the Alzheimer’s Disease process. These markers can be present even before the onset of
symptoms.
These tests may or may not be readily available in your region. Presently, CNO uses
cerebrospinal fluid (CSF) biomarkers to confirm the presence of Alzheimer’s Disease.
Core 2 biomarkers include CSF or plasma, MTBR-tau243, p-tau 205 and tau-PET. As well as
serum or CSF, NFL, GFAP and cerebral MRI. These biomarkers are used for staging, prognosis, and evaluating the treatment effect.