Table 2.
Amyloid (A) | Tau (T) | Neurodegeneration (N) | Comment | Trial Population |
---|---|---|---|---|
Negative | Negative | Negative | Normal | Primary prevention trials; before amyloid is present |
Positive | Negative | Negative | Alzheimer pathology; this defines preclinical AD before any changes associated with amyloid have begun | Secondary prevention trials; amyloid is present, tau is not; delay of tau spread as a potential outcome |
Positive | Positive | Negative | AD; amyloid and tau changes are present; no effect on neurodegeneration | Secondary prevention trials; amyloid and tau are present, neurodegeneration is not; delay in tau spread or development of neurodegeneration are potential outcomes |
Positive | Positive | Positive | AD; amyloid, tau, and neurodegeneration | Treatment trials; all 3 basic biomarkers are present; slowing of progression or delay to milestone are appropriate designs |
This category will also include mixed dementia where AD co-exists with other brain disorders such as cerebrovascular disease. Comorbid conditions contribute to the neurodegeneration component. | Combination treatment trials could include this population; for example, trials including AD and CVD | |||
Positive | Negative | Positive | Alzheimer pathology plus some other cause of neurodegeneration | Combination treatment trials of anti-amyloid agent and drugs addressing concomitant pathology may be warranted |
Negative | Negative | Positive | Not AD; neurodegeneration only | Non-AD trials such as VaD, FTD, PSP, CBD |
Negative | Positive | Negative | Not AD; elevated tau without neurodegeneration | Non-AD trials of CVD, prion disease, or early tauopathies |
Negative | Positive | Positive | Not AD; elevated tau and neurodegeneration | Non-AD trials of VaD or prion disease |
CBD – corticobasal degeneration; CVD – cerebrovascular disease; FTD – frontotemporal dementia; PSP – progressive supranuclear palsy; VaD – vascular dementia