# Cortical freewater increases in areas of tau tangle aggregation, independent of cortical thinning

## TL;DR

The study finds that tau tangle accumulation in Alzheimer's disease is linked to increased freewater in specific brain regions, independent of other factors like cortical thinning.

## Contribution

The study identifies a novel link between tauopathy and microstructural changes in the brain, independent of amyloid and cortical thinning.

## Key findings

- Tau PET correlates with freewater in gray matter of temporal and occipital regions.
- p-tau217 correlates with freewater in periventricular white matter in tau-positive individuals.
- Astrogliosis may contribute to microstructural changes linked to tau tangles.

## Abstract

It is unclear how cortical microstructure changes across biological stages of Alzheimer's disease (AD), and how this occurs in response to amyloid plaques, tauopathy, and inflammation. We hypothesize that tauopathy is chiefly responsible. To test this, we investigated how different measures of tauopathy, including plasma and PET, influence the microstructure in the whole brain, temporal meta‐ROI, and hippocampus.

We sampled 301 participants (59% female, age 67±10) from the TRIAD cohort with T1 MRI, diffusion‐weighted MRI, amyloid PET (F18‐NAV4694), tau PET (F18‐MK6240), and plasma biomarkers. We used the NODDI‐flow pipeline to estimate the diffusion characters of the TRIAD cohort (Dparallel, Dorthogonal,Disotropic) and run the NODDI‐Bingham algorithm to calculate whole‐brain isotropic volume fraction images (“freewater”). FreeSurfer 7 was used to derive hippocampal and temporal meta‐ROI masks (entorhinal, fusiform, interior temporal, and middle temporal gyri). The Standard Uptake Value Ratio (SUVR) method produced amyloid and tau PET images. Plasma biomarkers were measured by Simoa assay. For group comparison, we stratified participants by amyloid SUVR positivity, plasma ptau 217 positivity (T1), and tau SUVR positivity (T2). We performed voxel‐wise correlations between freewater and tauopathy markers via VoxelStats MATLAB toolbox. Mediation analyses were performed in R 4.4.1. Models covaried for amyloid SUVR, age, sex, APOE4 genotype status, and meta‐ROI cortical thickness. Multiple comparisons correction performed by random field theory method.

Tau PET positively correlated with freewater in gray matter within temporal and occipital regions, whereas p‐tau217 did so in periventricular white matter (Figure 1A, Figure 2A). The effect of p‐tau217 is only present in participants positive for tau tangles (Figure 2C). Freewater increased only in the A+T2+ group in the meta‐ROI and hippocampus (Figure 1B,C). Tau SUVR in meta‐ROI mediated the correlations between both GFAP and ‐tau217 with freewater in the A+T+ group (Figure 3).

In regions of AD‐relevant gray matter, increased freewater correlates with tau tangle accumulation independent of cortical thinning and amyloidopathy. Additionally, the positive correlation of p‐tau217 with freewater in the periventricular white matter suggests involvement with ventricular remodeling or local CSF/ISF dynamics. Astrogliosis may be involved with microstructural changes secondary to neurofibrillary tangles.