Diagnostic value of amyloid-PET and tau-PET: a head-to-head comparison.


Journal

European journal of nuclear medicine and molecular imaging
ISSN: 1619-7089
Titre abrégé: Eur J Nucl Med Mol Imaging
Pays: Germany
ID NLM: 101140988

Informations de publication

Date de publication:
07 2021
Historique:
received: 28 10 2020
accepted: 07 02 2021
pubmed: 28 2 2021
medline: 29 6 2021
entrez: 27 2 2021
Statut: ppublish

Résumé

Assess the individual and combined diagnostic value of amyloid-PET and tau-PET in a memory clinic population. Clinical reports of 136 patients were randomly assigned to two diagnostic pathways: AMY-TAU, amyloid-PET is presented before tau-PET; and TAU-AMY, tau-PET is presented before amyloid-PET. Two neurologists independently assessed all reports with a balanced randomized design, and expressed etiological diagnosis and diagnostic confidence (50-100%) three times: (i) at baseline based on the routine diagnostic workup, (ii) after the first exam (amyloid-PET for the AMY-TAU pathway, and tau-PET for the TAU-AMY pathway), and (iii) after the remaining exam. The main outcomes were changes in diagnosis (from AD to non-AD or vice versa) and in diagnostic confidence. Amyloid-PET and tau-PET, when presented as the first exam, resulted in a change of etiological diagnosis in 28% (p = 0.006) and 28% (p < 0.001) of cases, and diagnostic confidence increased by 18% (p < 0.001) and 19% (p < 0.001) respectively, with no differences between exams (p > 0.05). We observed a stronger impact of a negative amyloid-PET versus a negative tau-PET (p = 0.014). When added as the second exam, amyloid-PET and tau-PET resulted in a further change in etiological diagnosis in 6% (p = 0.077) and 9% (p = 0.149) of cases, and diagnostic confidence increased by 4% (p < 0.001) and 5% (p < 0.001) respectively, with no differences between exams (p > 0.05). Amyloid-PET and tau-PET significantly impacted diagnosis and diagnostic confidence in a similar way, although a negative amyloid-PET has a stronger impact on diagnosis than a negative tau-PET. Adding either of the two as second exam further improved diagnostic confidence. PB 2016-01346.

Identifiants

pubmed: 33638661
doi: 10.1007/s00259-021-05246-x
pii: 10.1007/s00259-021-05246-x
pmc: PMC8175315
doi:

Substances chimiques

Amyloid 0
Amyloid beta-Peptides 0
tau Proteins 0

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2200-2211

Subventions

Organisme : EU-EFPIA Innovative Medicines Initiatives 2 Joint Undertaking (IMI 2 JU)
ID : 115952
Organisme : Swiss National Science Foundation
ID : 320030_169876
Pays : Switzerland
Organisme : Swiss National Science Foundation
ID : 320030_185028
Pays : Switzerland

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Auteurs

Daniele Altomare (D)

Laboratory of Neuroimaging of Aging (LANVIE), University of Geneva, Geneva, Switzerland. Daniele.Altomare@unige.ch.
Memory Clinic, Geneva University Hospitals, Geneva, Switzerland. Daniele.Altomare@unige.ch.

Camilla Caprioglio (C)

Laboratory of Neuroimaging of Aging (LANVIE), University of Geneva, Geneva, Switzerland.
Memory Clinic, Geneva University Hospitals, Geneva, Switzerland.

Frédéric Assal (F)

Division of Neurology, Department of Clinical Neurosciences, Geneva University Hospitals, Geneva, Switzerland.
Faculty of Medicine, University of Geneva, Geneva, Switzerland.

Gilles Allali (G)

Division of Neurology, Department of Clinical Neurosciences, Geneva University Hospitals, Geneva, Switzerland.
Department of Neurology, Division of Cognitive & Motor Aging, Albert Einstein College of Medicine, Yeshiva University, Bronx, NY, USA.

Aline Mendes (A)

Division of Geriatrics, Department of Rehabilitation and Geriatrics, Geneva University Hospitals, Geneva, Switzerland.

Federica Ribaldi (F)

Laboratory of Neuroimaging of Aging (LANVIE), University of Geneva, Geneva, Switzerland.
Laboratory of Alzheimer's Neuroimaging and Epidemiology (LANE), Saint John of God Clinical Research Centre, Brescia, Italy.
Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.

Kelly Ceyzeriat (K)

Laboratory of Neuroimaging and Innovative Molecular Tracers (NIMTlab), Geneva University Neurocenter and Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Division of Adult Psychiatry, Department of Psychiatry, Geneva University Hospitals, Geneva, Switzerland.

Marta Martins (M)

Laboratory of Neuroimaging of Aging (LANVIE), University of Geneva, Geneva, Switzerland.
Memory Clinic, Geneva University Hospitals, Geneva, Switzerland.

Szymon Tomczyk (S)

Laboratory of Neuroimaging of Aging (LANVIE), University of Geneva, Geneva, Switzerland.
Memory Clinic, Geneva University Hospitals, Geneva, Switzerland.

Sara Stampacchia (S)

Laboratory of Neuroimaging and Innovative Molecular Tracers (NIMTlab), Geneva University Neurocenter and Faculty of Medicine, University of Geneva, Geneva, Switzerland.

Alessandra Dodich (A)

Center for Mind/Brain Sciences (CIMeC), University of Trento, Rovereto, Italy.

Marina Boccardi (M)

Late Translational Dementia Research Group, German Center for Neurodegenerative Diseases (DZNE), Rostock-Greifswald site, Rostock, Germany.

Christian Chicherio (C)

Memory Clinic, Geneva University Hospitals, Geneva, Switzerland.

Giovanni B Frisoni (GB)

Laboratory of Neuroimaging of Aging (LANVIE), University of Geneva, Geneva, Switzerland.
Memory Clinic, Geneva University Hospitals, Geneva, Switzerland.

Valentina Garibotto (V)

Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Division of Nuclear Medicine and Molecular Imaging, Geneva University Hospitals, Geneva, Switzerland.

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