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.

Alzheimer’s disease Mini-Mental State Examination (MMSE) [11C]PBB3 amyloid-beta cerebrospinal fluid (CSF) biomarkers computed tomography (CT) frontotemporal lobar degeneration neuroimaging positron emission tomography (PET) tauopathies

Journal

Biomedicines
ISSN: 2227-9059
Titre abrégé: Biomedicines
Pays: Switzerland
ID NLM: 101691304

Informations de publication

Date de publication:
01 Jul 2024
Historique:
received: 08 05 2024
revised: 13 06 2024
accepted: 25 06 2024
medline: 27 7 2024
pubmed: 27 7 2024
entrez: 27 7 2024
Statut: epublish

Résumé

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.

Identifiants

pubmed: 39062033
pii: biomedicines12071460
doi: 10.3390/biomedicines12071460
pii:
doi:

Types de publication

Journal Article

Langues

eng

Auteurs

Joachim Strobel (J)

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

Elham Yousefzadeh-Nowshahr (E)

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

Katharina Deininger (K)

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

Karl Peter Bohn (KP)

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

Christine A F von Arnim (CAF)

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

Markus Otto (M)

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

Christoph Solbach (C)

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

Sarah Anderl-Straub (S)

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

Dörte Polivka (D)

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

Patrick Fissler (P)

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

Gerhard Glatting (G)

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

Matthias W Riepe (MW)

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

Makoto Higuchi (M)

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

Ambros J Beer (AJ)

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

Albert Ludolph (A)

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

Gordon Winter (G)

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

Classifications MeSH