Cortical Amyloid Burden Relates to Basal Forebrain Volume in Subjective Cognitive Decline

Author:

Daamen Marcel1,Scheef Lukas123,Li Shumei1,Grothe Michel J.4,Gaertner Florian C.5,Buchert Ralph67,Buerger Katharina89,Dobisch Laura10,Drzezga Alexander11112,Essler Markus5,Ewers Michael13,Fliessbach Klaus114,Herrera Melendez Ana Lucia15,Hetzer Stefan16,Janowitz Daniel9,Kilimann Ingo1718,Krause Bernd Joachim19,Lange Catharina6,Laske Christoph2021,Munk Matthias H.2022,Peters Oliver1523,Priller Josef23242526,Ramirez Alfredo114272829,Reimold Matthias30,Rominger Axel3132,Rostamzadeh Ayda33,Roeske Sandra1,Roy Nina1,Scheffler Klaus34,Schneider Anja114,Spottke Annika135,Spruth Eike Jakob2324,Teipel Stefan J.1718,Wagner Michael114,Düzel Emrah1036,Jessen Frank12733,Boecker Henning12,

Affiliation:

1. German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany

2. Department for Diagnostic and Interventional Radiology, University Hospital Bonn, Bonn, Germany

3. RheinAhrCampus, University of Applied Sciences Koblenz, Remagen, Germany

4. Unidad de Trastornos del Movimiento, Servicio de Neurología y Neurofisiología Clínica, Instituto de Biomedicina de Sevilla, Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Seville, Spain

5. Department of Nuclear Medicine, University Hospital Bonn, Bonn, Germany

6. Department of Nuclear Medicine, Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany

7. Department of Diagnostic and Interventional Radiology and Nuclear Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany

8. German Center for Neurodegenerative Diseases (DZNE), Munich, Germany

9. Institute for Stroke and Dementia Research (ISD), University Hospital, Ludwig-Maximilian University Munich, Munich, Germany

10. German Center for Neurodegenerative Diseases (DZNE), Magdeburg, Germany

11. Department of Nuclear Medicine, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany

12. Institute of Neuroscience and Medicine (INM-2), Molecular Organization of the Brain, Forschungszentrum Jülich, Jülich, Germany

13. Institute for Clinical Radiology, Ludwig-Maximilians-University Munich, Munich, Germany

14. Department of Neurodegenerative Disease and Geriatric Psychiatry, University Hospital Bonn, Bonn, Germany

15. Institute of Psychiatry and Psychotherapy, Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany

16. Berlin Center of Advanced Neuroimaging, Charité –Universitätsmedizin Berlin, Berlin, Germany

17. German Center for Neurodegenerative Diseases (DZNE), Rostock/Greifswald, Germany

18. Department of Psychosomatic Medicine, Rostock University Medical Center, Rostock, Germany

19. Department of Nuclear Medicine, Rostock University Medical Centre, Rostock, Germany

20. German Center for Neurodegenerative Diseases (DZNE), Tuebingen, Germany

21. Section for Dementia Research, Hertie Institute for Clinical Brain Research and Department of Psychiatry and Psychotherapy, University of Tübingen, Tübingen, Germany

22. Department of Psychiatry and Psychotherapy, University of Tübingen, Tübingen, Germany

23. German Center for Neurodegenerative Diseases (DZNE), Berlin, Germany

24. Department of Psychiatry and Psychotherapy, Charité Universitätsmedizin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany

25. Department of Psychiatry and Psychotherapy, School of Medicine, Technical University of Munich, Munich, Germany

26. University of Edinburgh and UK Dementia Research Institute, Edinburgh, UK

27. Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Cologne, Germany

28. Department of Psychiatry and Psychotherapy, Division of Neurogenetics and Molecular Psychiatry, Faculty of Medicine and University Hospital Cologne, University of Cologne, Medical Faculty, Cologne, Germany

29. Department of Psychiatry & Glenn Biggs Institute for Alzheimer’s and Neurodegenerative Diseases, San Antonio, TX, USA

30. Department of Nuclear Medicine and Clinical Molecular Imaging, Eberhard-Karls-University, Tübingen, Germany

31. Department of Nuclear Medicine, Ludwig-Maximilian-University Munich, Munich, Germany

32. Department of Nuclear Medicine, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland

33. Department of Psychiatry and Psychotherapy, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany

34. Department for Biomedical Magnetic Resonance, University of Tübingen, Tübingen, Germany

35. Department of Neurology, University Hospital Bonn, Bonn, Germany

36. Institute of Cognitive Neurology and Dementia Research (IKND), Otto-von-Guericke University, Magdeburg, Germany

Abstract

Background: Atrophy of cholinergic basal forebrain (BF) nuclei is a frequent finding in magnetic resonance imaging (MRI) volumetry studies that examined patients with prodromal or clinical Alzheimer’s disease (AD), but less clear for individuals in earlier stages of the clinical AD continuum. Objective: To examine BF volume reductions in subjective cognitive decline (SCD) participants with AD pathologic changes. Methods: The present study compared MRI-based BF volume measurements in age- and sex-matched samples of N = 24 amyloid-positive and N = 24 amyloid-negative SCD individuals, based on binary visual ratings of Florbetaben positron emission tomography (PET) measurements. Additionally, we assessed associations of BF volume with cortical amyloid burden, based on semiquantitative Centiloid (CL) analyses. Results: Group differences approached significance for BF total volume (p = 0.061) and the Ch4 subregion (p = 0.059) only, showing the expected relative volume reductions for the amyloid-positive subgroup. There were also significant inverse correlations between BF volumes and CL values, which again were most robust for BF total volume and the Ch4 subregion. Conclusions: The results are consistent with the hypothesis that amyloid-positive SCD individuals, which are considered to represent a transitional stage on the clinical AD continuum, already show incipient alterations of BF integrity. The negative association with a continuous measure of cortical amyloid burden also suggests that this may reflect an incremental process. Yet, further research is needed to evaluate whether BF changes already emerge at “grey zone” levels of amyloid accumulation, before amyloidosis is reliably detected by PET visual readings.

Publisher

IOS Press

Subject

Psychiatry and Mental health,Geriatrics and Gerontology,Clinical Psychology,General Medicine,General Neuroscience

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