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. 2020 Jun 2;75(3):751–765. doi: 10.3233/JAD-200175

Table 3.

AT(N) profile by diagnostic group

AT(N) profile AD MCI FTD LBD and PD VaD and stroke Indeterminate No diagnosis Total
A-T-(N)- 6 8 8 6 4 21 10 63
A+T-(N)- 11 2 6 1 4 9 2 35
A+T+(N)- 4 1 1 1 0 0 1 8
A+T+(N)+ 22 0 2 2 0 4 0 30
A+T-(N)+ 5 0 1 0 0 1 0 7
A-T+(N)- 0 0 0 0 0 3 2 5
A-T-(N)+ 1 0 0 0 0 1 1 0
A-T+(N)+ 5 1 1 0 1 2 0 10
Total 54 12 19 10 9 41 16 161

There was a statistically significant difference between all groups (χ2 = 71.22, p = 0.003). AD, Alzheimer’s disease or Alzheimer’s disease atypical variant; MCI, mild cognitive impairment; FTD, frontotemporal dementia; LBD and PD, Lewy’s body dementia and Parkinson’s disease combined; VaD and stroke, vascular dementia and stroke combined; Indeterminate, indeterminate condition; No diagnosis, no neurodegenerative disease; A, biomarker of Aβ plaques (labeled “A”) is low CSF Aβ42; T, biomarker of fibrillary tau (labeled “T”) is elevated CSF phosphorylated tau (P-tau); [N], biomarker of neurodegeneration or neuronal injury [labeled (“N”)] is CSF T-tau.