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Updated: Jan 8, 2026

Hybrid PET/MRI Imaging of Alzheimer's Disease Based on 18F-AV-1451
Published on: April 18, 2025
Alzheimer's Imaging Consortium
Rayan Mroué1, Pamela C L Ferreira1, Guilherme Povala1
1University of Pittsburgh, Pittsburgh, PA, USA.
Background:
Quantifying tau aggregates in the human brain can be achieved using Positron Emission Tomography (PET) techniques, which can potentially be affected by binding competition due to medication use. Patients with dementia often have high rates of comorbidities and polypharmacy. Therefore, this study aims to investigate the potential influence of multiple medications on the uptake of the tau tracers MK6240 (MK) and Flortaucipir (FTP).
Method:
Five classes of medications were evaluated: Anti-Hypertensives, Statins, Anti-Diabetics, Psychoactive drugs, and NSAIDs (Table 1). We included 292 individuals [170 cognitively unimpaired (CU) Aβ-negative and 122 cognitively impaired (CI) Aβ-positive] from the HEAD study (Table 2). We compared MK and FTP SUVR in the Medial Temporal Lobe (MTL) and Neotemporal Cortex (NTC) in individuals on and off medications. The linear regressions that tested associations were corrected for confounding factors, including age, sex, education, and MoCA score. Correction for multiple comparisons was applied using the Bonferroni method (adjusted p-value at 0.00125).
Result:
Among CI Aβ-positive individuals, Anti-Diabetics were associated with lower SUVR in the NTC for both FTP and MK. However, these associations did not remain significant after correction for multiple comparisons. (Table 3).
Conclusion:
Our findings indicate that there are no significant associations between the use of the medications studied and MK or FTP uptake when accounting for covariates and applying multiple comparison corrections.
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