Tau in Atypical Parkinsonisms: A Meta‐Analysis of in Vivo PET Imaging Findings

Author:

Mena Anastassia M.12ORCID,Chen Robert234,Graff‐Guerrero Ariel12,Martin Sarah L.1,Uribe Carme1,Strafella Antonio P.1234

Affiliation:

1. Brain Health Imaging Centre, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health University of Toronto Toronto Ontario Canada

2. Institute of Medical Science University of Toronto Toronto Ontario Canada

3. Division of Brain, Imaging and Behaviour–Systems Neuroscience, Krembil Brain Institute, UHN University of Toronto Toronto Ontario Canada

4. Edmond J. Safra Parkinson Disease Program & Morton and Gloria Shulman Movement Disorder Unit, Neurology Division, Department of Medicine, Toronto Western Hospital, UHN University of Toronto Toronto Ontario Canada

Abstract

AbstractBackgroundProgressive supranuclear palsy (PSP) and corticobasal degeneration (CBD) are atypical parkinsonisms (APs) that are classified as tauopathies. Patients with these APs may present with similar early clinical manifestations to Parkinson's disease (PD), but they prove unresponsive to anti‐parkinsonian medications.ObjectiveThe main objective of this meta‐analysis was to compare first‐ and second‐generation tau PET tracer efficacy in patients with the APs to identify potential diagnostic biomarkers.MethodsPubMed and Web of Science were searched between January 1, 1999 and December 31, 2022. We included case–control studies that were published in English and report tau PET tracer binding as mean ± SD in at least one region of interest (ROI). Differences in tau PET binding values were meta‐analyzed using random‐effects meta‐analytic models and subgroup analyses based on ROIs in the statistical programming language R (version 4.2.1).ResultsOverall, 29 studies with 665 patients were included in the final review. [18F]PI‐2620 outperformed first‐generation tracers when comparing PSP‐HC (g = −1.68, 95% CI: −2.05 to −1.30) and CBD‐HC (g = −1.37, 95% CI: −2.25 to −0.49). When comparing PSP‐PD, the first‐generation tracer, [18F]AV‐1451, presented with higher binding to PSP patients (g = −0.80, 95% CI: −1.24 to −0.35).ConclusionsOur results demonstrate the efficacy of [18F]PI‐2620 PET in imaging AP‐tau. These findings contribute towards identifying a diagnostic imaging biomarker for patients with APs. The main limitation of this study was the heterogeneity of the results. Future studies should conduct AP‐PD comparisons with second‐generation tracers to confirm the preliminary results found here.

Funder

Canadian Institutes of Health Research

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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