Exploratory Tau PET/CT with [11C]PBB3 in Patients with Suspected Alzheimer’s Disease and Frontotemporal Lobar Degeneration: A Pilot Study on Correlation with PET Imaging and Cerebrospinal Fluid Biomarkers

Author:

Strobel Joachim1ORCID,Yousefzadeh-Nowshahr Elham1ORCID,Deininger Katharina1,Bohn Karl Peter1,von Arnim Christine A. F.2,Otto Markus3,Solbach Christoph1,Anderl-Straub Sarah4,Polivka Dörte4,Fissler Patrick5ORCID,Glatting Gerhard1ORCID,Riepe Matthias W.6,Higuchi Makoto7,Beer Ambros J.1ORCID,Ludolph Albert4,Winter Gordon1ORCID

Affiliation:

1. Department of Nuclear Medicine, Ulm University Medical Center, 89081 Ulm, Germany

2. Department of Geriatrics, University Medical Center Göttingen, 37073 Göttingen, Germany

3. Department of Neurology, Halle University, 06120 Halle, Germany

4. Department of Neurology, Ulm University Medical Center, 89081 Ulm, Germany

5. Psychiatric Services Thurgau (Academic Teaching Hospital of the University of Konstanz), 8596 Münsterlingen, Switzerland

6. Department of Psychiatry and Psychotherapy II, Ulm University, 89075 Ulm, Germany

7. National Institute of Radiological Sciences, Chiba 263-8555, Japan

Abstract

Accurately diagnosing Alzheimer’s disease (AD) and frontotemporal lobar degeneration (FTLD) is challenging due to overlapping symptoms and limitations of current imaging methods. This study investigates the use of [11C]PBB3 PET/CT imaging to visualize tau pathology and improve diagnostic accuracy. Given diagnostic challenges with symptoms and conventional imaging, [11C]PBB3 PET/CT’s potential to enhance accuracy was investigated by correlating tau pathology with cerebrospinal fluid (CSF) biomarkers, positron emission tomography (PET), computed tomography (CT), amyloid-beta, and Mini-Mental State Examination (MMSE). We conducted [11C]PBB3 PET/CT imaging on 24 patients with suspected AD or FTLD, alongside [11C]PiB PET/CT (13 patients) and [18F]FDG PET/CT (15 patients). Visual and quantitative assessments of [11C]PBB3 uptake using standardized uptake value ratios (SUV-Rs) and correlation analyses with clinical assessments were performed. The scans revealed distinct tau accumulation patterns; 13 patients had no or faint uptake (PBB3-negative) and 11 had moderate to pronounced uptake (PBB3-positive). Significant inverse correlations were found between [11C]PBB3 SUV-Rs and MMSE scores, but not with CSF-tau or CSF-amyloid-beta levels. Here, we show that [11C]PBB3 PET/CT imaging can reveal distinct tau accumulation patterns and correlate these with cognitive impairment in neurodegenerative diseases. Our study demonstrates the potential of [11C]PBB3-PET imaging for visualizing tau pathology and assessing disease severity, offering a promising tool for enhancing diagnostic accuracy in AD and FTLD. Further research is essential to validate these findings and refine the use of tau-specific PET imaging in clinical practice, ultimately improving patient care and treatment outcomes.

Publisher

MDPI AG

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