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. 2019 Mar 11;8(3):341. doi: 10.3390/jcm8030341

Table 6.

ATN classification in regard to the biomarker profile and cognitive stage among participants with cerebrospinal fluid (CSF) AD biomarker results.

ATN Profile Biomarker Category Syndromal Cognitive Stage
CN (n = 29) SCD
(n = 58)
MCI
(n = 29)
ADD
(n = 23)
A−/T−/N− Normal AD biomarkers 20 (69.0%) 13 (22.4%) 2 (6.9%) 0
A+/T−/N− Alzheimer’s pathologic change 1 (3.4%) 1 (1.7%) 3 (10.3%) 0
A+/T+/N− Alzheimer’s disease 0 3 (5.2%) 2 (6.9%) 1 (4.4%)
A+/T+/N+ Alzheimer’s disease 0 6 (10.3%) 7 (24.1%) 17 (73.9%)
A+/T−/N+ Alzheimer’s and SNAP 2 (6.9%) 4 (6.9%) 4 (13.8%) 3 (13.0%)
A−/T+/N− Non-AD pathologic change 2 (6.9%) 0 2 (6.9%) 0
A−/T+/N+ Non-AD pathologic change 0 3 (5.2%) 3 (10.3%) 0
A−/T−/N+ Non-AD pathologic change 4 (13.8%) 28 (48.3%) 6 (20.7%) 2 (8.7%)

Data are shown as number (%). CN, cognitively normal; SCD, subjective cognitive decline; MCI, mild cognitive impairment; ADD, Alzheimer’s disease dementia; ATN, amyloid, tau, and neurodegeneration or neuronal injury; A−, absence of amyloid pathology determined by normal amyloid PET finding or CSF Aβ42 level above cut point; A+, presence of amyloid pathology determined by abnormal amyloid PET finding or CSF Aβ42 level below cut point; T−, normal CSF p-tau level below cut point; T+, abnormal CSF p-tau above cut point; N−, absence of neurodegeneration or neuronal injury determined by cortical thickness or hippocampal volume; N+, presence of neurodegeneration or neuronal injury determined by cortical thickness or hippocampal volume; SNAP, suspected non Alzheimer’s pathologic change.