Skip to main content
Erschienen in:

15.01.2024 | Review

Clinical Correlates of the PET-based Braak Staging Framework in Alzheimer’s Disease

verfasst von: A. C. Macedo, D. F. P. A. Durço, C. Tissot, J. Therriault, A. O. Vilela de Faria, É. Aumont, S. Servaes, N. Rahmouni, J. Fernandez-Arias, Y.-T. Wang, F. Z. Lussier, A. Bieger, E. R. Zimmer, T. A. Pascoal, S. Gauthier, Pedro Rosa-Neto

Erschienen in: The Journal of Prevention of Alzheimer's Disease | Ausgabe 2/2024

Einloggen, um Zugang zu erhalten

Abstract

In vivo Alzheimer’s disease diagnosis and staging is traditionally based on clinical features. However, the agreement between clinical and pathological Alzheimer’s disease diagnosis, whose diagnosis assessment includes amyloid and Braak histopathological tau staging, is not completely convergent. The development of positron emission tomography (PET) tracers targeting neurofibrillary tangles offers prospects for advancing the staging of Alzheimer’s disease from both biological and clinical perspectives. Recent advances in radiochemistry made it possible to apply the postmortem Braak staging framework to tau-PET images obtained in vivo. Here, our aim is to provide a narrative review of the current literature on the relationship between Alzheimer’s disease clinical features and the PET-based Braak staging framework. Overall, the available studies support the stepwise increase in disease severity following the advance of PET-based Braak stages, with later stages being associated with worse cognitive and clinical symptoms. In line with this, there is a trend for unimpaired cognition, mild cognitive impairment, and Alzheimer’s disease dementia to be compatible with early, intermediate, and late patterns of tau deposition based on PET-based Braak stages. Moreover, neuropsychiatric symptom severity seems to be linked to the extent of tau-PET signal across Braak areas. In sum, this framework seems to correspond well with the clinical progression of Alzheimer’s disease, which is an indication of its potential utility in research and clinical practice, especially for detecting preclinical tau levels in individuals without symptoms. However, further research is needed to improve the generalizability of these findings and to better understand the applications of this staging framework.
Anhänge
Nur mit Berechtigung zugänglich
Literatur
1.
Zurück zum Zitat McKhann, G.; Drachman, D.; Folstein, M.; Katzman, R.; Price, D.; Stadlan, E.M. Clinical Diagnosis of Alzheimer’s Disease: Report of the NINCDS-ADRDA Work Group* under the Auspices of Department of Health and Human Services Task Force on Alzheimer’s Disease. Neurology 1984, 34, 939–939, doi:https://doi.org/10.1212/WNL.34.7.939.PubMedCrossRef McKhann, G.; Drachman, D.; Folstein, M.; Katzman, R.; Price, D.; Stadlan, E.M. Clinical Diagnosis of Alzheimer’s Disease: Report of the NINCDS-ADRDA Work Group* under the Auspices of Department of Health and Human Services Task Force on Alzheimer’s Disease. Neurology 1984, 34, 939–939, doi:https://​doi.​org/​10.​1212/​WNL.​34.​7.​939.PubMedCrossRef
13.
Zurück zum Zitat Kemper TL. Senile Dementia: A Focal Disease in the Temporal Lobe. In; Nandy E, Ed.Senile Dementia: A Biomedical Approach. Elsevier; 1978:105–113. Kemper TL. Senile Dementia: A Focal Disease in the Temporal Lobe. In; Nandy E, Ed.Senile Dementia: A Biomedical Approach. Elsevier; 1978:105–113.
16.
Zurück zum Zitat Marquié, M.; Normandin, M.D.; Vanderburg, C.R.; Costantino, I.M.; Bien, E.A.; Rycyna, L.G.; Klunk, W.E.; Mathis, C.A.; Ikonomovic, M.D.; Debnath, M.L.; et al. Validating Novel Tau Positron Emission Tomography Tracer [F-18]-AV-1451 (T807) on Postmortem Brain Tissue: Validation of PET Tracer. Ann. Neurol. 2015, 78, 787–800, doi:https://doi.org/10.1002/ana.24517.PubMedPubMedCentralCrossRef Marquié, M.; Normandin, M.D.; Vanderburg, C.R.; Costantino, I.M.; Bien, E.A.; Rycyna, L.G.; Klunk, W.E.; Mathis, C.A.; Ikonomovic, M.D.; Debnath, M.L.; et al. Validating Novel Tau Positron Emission Tomography Tracer [F-18]-AV-1451 (T807) on Postmortem Brain Tissue: Validation of PET Tracer. Ann. Neurol. 2015, 78, 787–800, doi:https://​doi.​org/​10.​1002/​ana.​24517.PubMedPubMedCentralCrossRef
17.
Zurück zum Zitat Sander, K.; Lashley, T.; Gami, P.; Gendron, T.; Lythgoe, M.F.; Rohrer, J.D.; Schott, J.M.; Revesz, T.; Fox, N.C.; Årstad, E. Characterization of Tau Positron Emission Tomography Tracer [18 F]AV-1451 Binding to Postmortem Tissue in Alzheimer’s Disease, Primary Tauopathies, and Other Dementias. Alzheimers Dement. 2016, 12, 1116–1124, doi:https://doi.org/10.1016/j.jalz.2016.01.003.PubMedCrossRef Sander, K.; Lashley, T.; Gami, P.; Gendron, T.; Lythgoe, M.F.; Rohrer, J.D.; Schott, J.M.; Revesz, T.; Fox, N.C.; Årstad, E. Characterization of Tau Positron Emission Tomography Tracer [18 F]AV-1451 Binding to Postmortem Tissue in Alzheimer’s Disease, Primary Tauopathies, and Other Dementias. Alzheimers Dement. 2016, 12, 1116–1124, doi:https://​doi.​org/​10.​1016/​j.​jalz.​2016.​01.​003.PubMedCrossRef
23.
Zurück zum Zitat Hostetler, E.D.; Walji, A.M.; Zeng, Z.; Miller, P.; Bennacef, I.; Salinas, C.; Connolly, B.; Gantert, L.; Haley, H.; Holahan, M.; et al. Preclinical Characterization of 18 F-MK-6240, a Promising PET Tracer for In Vivo Quantification of Human Neurofibrillary Tangles. J. Nucl. Med. 2016, 57, 1599–1606, doi:https://doi.org/10.2967/jnumed.115.171678.PubMedCrossRef Hostetler, E.D.; Walji, A.M.; Zeng, Z.; Miller, P.; Bennacef, I.; Salinas, C.; Connolly, B.; Gantert, L.; Haley, H.; Holahan, M.; et al. Preclinical Characterization of 18 F-MK-6240, a Promising PET Tracer for In Vivo Quantification of Human Neurofibrillary Tangles. J. Nucl. Med. 2016, 57, 1599–1606, doi:https://​doi.​org/​10.​2967/​jnumed.​115.​171678.PubMedCrossRef
26.
Zurück zum Zitat Schwarz, A.J.; Yu, P.; Miller, B.B.; Shcherbinin, S.; Dickson, J.; Navitsky, M.; Joshi, A.D.; Devous, M.D.; Mintun, M.S. Regional Profiles of the Candidate Tau PET Ligand 18 F-AV-1451 Recapitulate Key Features of Braak Histopathological Stages. Brain 2016, 139, 1539–1550, doi:https://doi.org/10.1093/brain/aww023.PubMedCrossRef Schwarz, A.J.; Yu, P.; Miller, B.B.; Shcherbinin, S.; Dickson, J.; Navitsky, M.; Joshi, A.D.; Devous, M.D.; Mintun, M.S. Regional Profiles of the Candidate Tau PET Ligand 18 F-AV-1451 Recapitulate Key Features of Braak Histopathological Stages. Brain 2016, 139, 1539–1550, doi:https://​doi.​org/​10.​1093/​brain/​aww023.PubMedCrossRef
30.
Zurück zum Zitat Okamura, N.; Furumoto, S.; Harada, R.; Tago, T.; Yoshikawa, T.; Fodero-Tavoletti, M.; Mulligan, R.S.; Villemagne, V.L.; Akatsu, H.; Yamamoto, T.; et al. Novel 18 F-Labeled Arylquinoline Derivatives for Noninvasive Imaging of Tau Pathology in Alzheimer Disease. J. Nucl. Med. 2013, 54, 1420–1427, doi:https://doi.org/10.2967/jnumed.112.117341.PubMedCrossRef Okamura, N.; Furumoto, S.; Harada, R.; Tago, T.; Yoshikawa, T.; Fodero-Tavoletti, M.; Mulligan, R.S.; Villemagne, V.L.; Akatsu, H.; Yamamoto, T.; et al. Novel 18 F-Labeled Arylquinoline Derivatives for Noninvasive Imaging of Tau Pathology in Alzheimer Disease. J. Nucl. Med. 2013, 54, 1420–1427, doi:https://​doi.​org/​10.​2967/​jnumed.​112.​117341.PubMedCrossRef
37.
Zurück zum Zitat Arias, J. F.; Therriault J.; Thomas E.; et al. Verbal Memory Formation across PET-Based Braak Stages of Tau Accumulation in Alzheimer’s Disease. Brain Commun 2023 5, fcad146.CrossRef Arias, J. F.; Therriault J.; Thomas E.; et al. Verbal Memory Formation across PET-Based Braak Stages of Tau Accumulation in Alzheimer’s Disease. Brain Commun 2023 5, fcad146.CrossRef
41.
Zurück zum Zitat Yasuno, F.; Minami, H.; Hattori, H.; for the Alzheimer’s Disease Neuroimaging Initiative Relationship between Neuropsychiatric Symptoms and Alzheimer’s Disease Pathology: An in Vivo Positron Emission Tomography Study. Int. J. Geriatr. Psychiatry 2021, 36, 598–605, doi:https://doi.org/10.1002/gps.5459.PubMedCrossRef Yasuno, F.; Minami, H.; Hattori, H.; for the Alzheimer’s Disease Neuroimaging Initiative Relationship between Neuropsychiatric Symptoms and Alzheimer’s Disease Pathology: An in Vivo Positron Emission Tomography Study. Int. J. Geriatr. Psychiatry 2021, 36, 598–605, doi:https://​doi.​org/​10.​1002/​gps.​5459.PubMedCrossRef
43.
Zurück zum Zitat Tissot, C.; Therriault, J.; Pascoal, T.A.; et al. Association between Regional Tau Pathology and Neuropsychiatric Symptoms in Aging and Dementia Due to Alzheimer’s Disease. Alzheimers Dement. Transl. Res. Clin. Interv. 2021, 7, doi:https://doi.org/10.1002/trc2.12154. Tissot, C.; Therriault, J.; Pascoal, T.A.; et al. Association between Regional Tau Pathology and Neuropsychiatric Symptoms in Aging and Dementia Due to Alzheimer’s Disease. Alzheimers Dement. Transl. Res. Clin. Interv. 2021, 7, doi:https://​doi.​org/​10.​1002/​trc2.​12154.
44.
Zurück zum Zitat Lyketsos, C.G.; Steinberg, M.; Tschanz, J.T.; Norton, M.C.; Steffens, D.C.; Breitner, J.C.S. Mental and Behavioral Disturbances in Dementia: Findings From the Cache County Study on Memory in Aging. Am J Psychiatry 2000. Lyketsos, C.G.; Steinberg, M.; Tschanz, J.T.; Norton, M.C.; Steffens, D.C.; Breitner, J.C.S. Mental and Behavioral Disturbances in Dementia: Findings From the Cache County Study on Memory in Aging. Am J Psychiatry 2000.
45.
Zurück zum Zitat Mega, M.S.; Cummings, J.L.; Fiorello, T.; Gornbein, J. The Spectrum of Behavioral Changes in Alzheimer’s. Mega, M.S.; Cummings, J.L.; Fiorello, T.; Gornbein, J. The Spectrum of Behavioral Changes in Alzheimer’s.
47.
Zurück zum Zitat Intrinsic Connectivity of the Human Brain Provides Scaffold for Tau Aggregation in Clinical Variants of Alzheimer’s Disease. Sci. Transl. Med. 2022. Intrinsic Connectivity of the Human Brain Provides Scaffold for Tau Aggregation in Clinical Variants of Alzheimer’s Disease. Sci. Transl. Med. 2022.
Metadaten
Titel
Clinical Correlates of the PET-based Braak Staging Framework in Alzheimer’s Disease
verfasst von
A. C. Macedo
D. F. P. A. Durço
C. Tissot
J. Therriault
A. O. Vilela de Faria
É. Aumont
S. Servaes
N. Rahmouni
J. Fernandez-Arias
Y.-T. Wang
F. Z. Lussier
A. Bieger
E. R. Zimmer
T. A. Pascoal
S. Gauthier
Pedro Rosa-Neto
Publikationsdatum
15.01.2024
Verlag
Springer International Publishing
Erschienen in
The Journal of Prevention of Alzheimer's Disease / Ausgabe 2/2024
Elektronische ISSN: 2426-0266
DOI
https://doi.org/10.14283/jpad.2024.15

Kompaktes Leitlinien-Wissen Neurologie (Link öffnet in neuem Fenster)

Mit medbee Pocketcards schnell und sicher entscheiden.
Leitlinien-Wissen kostenlos und immer griffbereit auf ihrem Desktop, Handy oder Tablet.

Neu im Fachgebiet Neurologie

Kaum Vorteile durch intraarterielle Lyse während Thrombektomie

Nach der Thrombektomie kleinere Fragmente über eine intraarterielle Lyse auflösen – dies könnte die Schlaganfalltherapie verbessern. Zwei aktuelle Studien ergeben für die periprozedurale Lyse jedoch keine großen Vorteile. Die Frage, wie viel sie nützt, bleibt weiter offen.

Nasenstimulation lindert chronische Migräne

Wird die Naseninnenseite durch Vibrationen stimuliert, kann dies offenbar die Zahl der Migränetage von Menschen mit chronischer Migräne deutlich senken. Darauf deuten die Resultate einer randomisiert-kontrollierten deutsch-finnischen Untersuchung.

Stumme Schlaganfälle − ein häufiger Nebenbefund im Kopf-CT?

In 4% der in der Notfallambulanz initiierten zerebralen Bildgebung sind „alte“ Schlaganfälle zu erkennen. Gar nicht so selten handelt es sich laut einer aktuellen Studie dabei um unbemerkte Insulte. Bietet sich hier womöglich die Chance auf ein effektives opportunistisches Screening?

Die elektronische Patientenakte kommt: Das sollten Sie jetzt wissen

Am 15. Januar geht die „ePA für alle“ zunächst in den Modellregionen an den Start. Doch schon bald soll sie in allen Praxen zum Einsatz kommen. Was ist jetzt zu tun? Was müssen Sie wissen? Wir geben in einem FAQ Antworten auf 21 Fragen.

Update Neurologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.