ORCID: https://orcid.org/0000-0001-6157-0363; Franzmeier, Nicolai
ORCID: https://orcid.org/0000-0001-9736-2283; Palleis, Carla
ORCID: https://orcid.org/0000-0002-4331-8145; Wagemann, Olivia
ORCID: https://orcid.org/0000-0003-3211-9105; Weidinger, Endy; Katzdobler, Sabrina
ORCID: https://orcid.org/0000-0002-3512-5984; Wlasich, Elisabeth
ORCID: https://orcid.org/0009-0002-2733-7511; Sandkühler, Katja
ORCID: https://orcid.org/0009-0000-7117-2270; Böning, Guido
ORCID: https://orcid.org/0000-0003-0986-2929; Gnörich, Johannes
ORCID: https://orcid.org/0000-0003-1554-7765; Scheifele, Maximilian; Eckenweber, Florian; Janowitz, Daniel
ORCID: https://orcid.org/0009-0003-4090-547X; Kurz, Carolin
ORCID: https://orcid.org/0000-0003-4299-6240; Perneczky, Robert
ORCID: https://orcid.org/0000-0003-1981-7435; Bürger, Katharina; Danek, Adrian
ORCID: https://orcid.org/0000-0001-8857-5383; Höglinger, Günter
ORCID: https://orcid.org/0000-0001-7587-6187; Levin, Johannes
ORCID: https://orcid.org/0000-0001-5092-4306; Brendel, Matthias
ORCID: https://orcid.org/0000-0002-9247-2843 und Schönecker, Sonja
ORCID: https://orcid.org/0000-0003-4499-7861
(2026):
Additive value of early-phase β-Amyloid-PET for the differential diagnosis of non-Alzheimer’s disease dementia.
In: NeuroImage: Clinical, Vol. 49, 103963
[PDF, 6MB]
Abstract
Purpose: Recent studies demonstrated strong agreement between early-phase β-amyloid-PET perfusion imaging and glucose hypometabolism assessed by [18F]FDG-PET, indicating the potential of early-phase β-amyloid-PET as a surrogate biomarker of neuronal injury. We therefore aimed to investigate the additive value of early-phase β-amyloid-PET for the differential diagnosis of non-Alzheimer’s disease dementia syndromes in clinical routine.
Materials and methods: [18F]florbetaben- and [18F]flutemetamol-PET scans (n = 379) performed between July 2013 and July 2021 were analyzed for their amyloid status and the presence of a neurodegenerative hypoperfusion pattern using visual assessment and z-score maps. In patients visually rated as amyloid-negative/neurodegeneration-positive (A-N+), the most likely diagnosis based on perfusion patterns was compared to the final clinical diagnosis, i.e. frontotemporal dementia or psychiatric disorders, suspected 4R-tauopathy, and suspected non-Alzheimer pathophysiology. Logistic regression models based on a data-driven selection of cerebral regions of hypoperfusion by principal component analysis were used to predict neurodegenerative disease and clinical diagnoses. Diagnostic accuracy was compared between visual assessment and the regression models.
Results: Neurodegeneration status was correctly identified in 78.8% (119/151) of amyloid-negative patients through visual rating, compared to 67.5% (102/151) using logistic regression. Visual assessment assigned 75.3% (67/89) of A-N+ patients to the correct diagnostic category. In contrast, the regression model classified 69.7% (62/89) of patients.
Conclusions: The current study demonstrates an additive value of early-phase β-amyloid-PET for the differential diagnosis of dementia syndromes. While visual assessment of early-phase β-amyloid-PET already provides substantial diagnostic accuracy, a data-driven analysis approach could aid in cases of uncertainty.
| Item Type: | Journal article |
|---|---|
| Faculties: | Medicine > Munich Cluster for Systems Neurology (SyNergy) Medicine > Medical Center of the University of Munich > Neurological Clinic and Polyclinic with Friedrich Baur Institute Medicine > Medical Center of the University of Munich > Clinic and Polyclinic for Nuclear Medicine Medicine > Medical Center of the University of Munich > Clinic and Polyclinic for Psychiatry and Psychotherapy |
| Subjects: | 600 Technology > 610 Medicine and health |
| URN: | urn:nbn:de:bvb:19-epub-133101-4 |
| ISSN: | 22131582 |
| Language: | English |
| Item ID: | 133101 |
| Date Deposited: | 12. Mar 2026 15:24 |
| Last Modified: | 12. Mar 2026 15:24 |
| DFG: | Gefördert durch die Deutsche Forschungsgemeinschaft (DFG) - 390857198 |
