[18F]RO948 Tau PET Imaging in Early and Late‐Onset Alzheimer's Disease: Regional Evolution and Correlations with Plasma Biomarkers

TL;DR

This study uses [18F]RO948 PET imaging to track tau buildup in Alzheimer's patients, finding differences in brain regions affected in early and late-onset disease and correlations with blood biomarkers.

Contribution

The study reveals distinct regional tau deposition patterns in early and late-onset Alzheimer's and shows plasma p-Tau217 correlates strongly with PET imaging findings.

Findings

EOAD and LOAD patients showed higher [18F]RO948 uptake in medial temporal regions compared to controls.

EOAD dementia patients had broader cortical involvement compared to LOAD dementia patients.

Plasma p-Tau217 levels correlated more strongly with PET uptake than other plasma biomarkers.

Abstract

Using [18F]RO948 as a tau PET ligand, we assessed tau deposition in a cohort of memory clinic patients and cognitively unimpaired controls. Regional tau binding was then compared to levels of plasma p‐Tau217, p‐Tau181, p‐Tau231 biomarkers.

Thirty‐seven patients from the Memory Clinic at Karolinska University Hospital Huddinge were evaluated: 27 patients with biomarker confirmed AD (CSF A+) at clinical stage of MCI (n = 14) or dementia (n = 13). Thirteen cases qualified for an early onset disease (EOAD) and fourteen for late onset (LOAD), and 10 cognitively normal (CN) participants. On the same day, participants underwent [18F]RO948 tau PET imaging, magnetic resonance imaging (MRI), and blood sampling for plasma biomarker analysis using the NuLISAseq (Alamarbio) CNS panel.

EOAD and LOAD patients, whether MCI or dementia, showed significantly higher [18F]RO948 uptake in the entorhinal cortex, hippocampus and amygdala compared to the CN participants (Figure A‐C). Only the EOAD dementia patients displayed significantly higher uptake in the parietal cortex compared to CN participants but also compared to the other AD subgroups (p = 0.04) (Figure 1E‐F). Voxel‐wise analyses showed a significantly higher [18F]RO948 uptake confined in medial temporal lobe areas in the patients with EOAD MCI or LOAD MCI compared to the CN. The LOAD dementia patients showed involvement primarily of the temporal neocortex while the EOAD dementia a broader involvement of even parietal and frontal cortices (Figure 1G). p‐Tau217, p‐Tau231, and p‐Tau181 plasma levels were elevated in both MCI and dementia patients, compared to controls (data not shown, all p < 0.05). In the dementia patients (EOAD and LOAD), plasma p‐Tau217 exhibited a stronger correlation with [18F]RO948 uptake across multiple brain regions compared to p‐Tau231 and p‐Tau181 where less broad areas were involved. In the MCI patients (EOAD and LOAD) p‐Tau217 correlated with uptake in the amygdala (Figure 2).

[18F]RO948 PET can capture tau deposition at early stages of AD, particularly in medial temporal regions when plasma p‐Tau217 levels similarly elevated. As the disease progresses to the clinical dementia stage, tau accumulation extends into cortical regions, with distinct regional deposition patterns observed between EOAD and LOAD.

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