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Table 3 Associations between plasma NTA-tau and disease progression

From: Plasma N-terminal containing tau fragments (NTA-tau): a biomarker of tau deposition in Alzheimer’s Disease

NTA associations with:

n

β[95%CI]

p

R2

BioFINDER-2

 Tau-PET

294

0.06 [0.05, 0.08]

<0.001

0.27

 Cortical thickness

288

-0.1 [-0.13, -0.08]

<0.001

0.18

 MMSE

441

-1.04 [-1.27, -0.81]

<0.001

0.28

 mPACC

380

-0.42 [-0.52, -0.32]

<0.001

0.27

BioFINDER-1

 Cortical thickness

212

-0.13 [-0.16, -0.1]

< 0.001

0.29

 MMSE

324

-1.96 [-2.29, -1.63]

< 0.001

0.37

 mPACC

211

-0.41 [-0.52, -0.31]

< 0.001

0.29

  1. We used linear mixed models with tau-PET, cortical thickness or cognition (mPACC and MMSE) as outcome and the interaction of baseline plasma biomarkers and time as predictor with random intercepts and random time-slopes. Age and sex (and years of education for cognition) were used as covariates. Only Aβ+ within the AD continuum (excluding nonAD+) were included in these analyses, as were those expected to progress
  2. Abbreviations: amyloid-β, AD Alzheimer’s disease, MMSE Mini-Mental State Examination, nonAD+ non-Alzheimer’s type dementia Aβ positive, mPACC modified preclinical Alzheimer’s cognitive composite, SUVR standardized uptake value ratio