Reduced expression of fMRI subsequent memory effects with increasing severity across the Alzheimer’s disease risk spectrum

Author:

Soch Joram123,Richter Anni456,Kizilirmak Jasmin M.17,Schütze Hartmut89,Altenstein Slawek1011,Dechent Peter12,Fliessbach Klaus1314,Glanz Wenzel8,Herrera Ana Lucia11,Hetzer Stefan15,Incesoy Enise I.8916,Kilimann Ingo1718,Kimmich Okka13,Lammerding Dominik11,Laske Christoph1920,Lohse Andrea11,Lüsebrink Falk8,Munk Matthias H.1921,Peters Oliver1011,Preis Lukas11,Priller Josef10112223,Rostamzadeh Ayda24,Roy-Kluth Nina13,Scheffler Klaus25,Schneider Anja1314,Spottke Annika1326,Spruth Eike Jakob1011,Teipel Stefan1718,Wiltfang Jens12728,Jessen Frank132429,Düzel Emrah89,Schott Björn H.142730

Affiliation:

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

2. Bernstein Center for Computational Neuroscience (BCCN), Berlin, Germany

3. Max Planck Institute for Human Cognitive and Brain Sciences (MPI CBS), Leipzig, Germany

4. Leibniz Institute for Neurobiology (LIN), Magdeburg, Germany

5. German Center for Mental Health (DZPG), site Jena-Magdeburg-Halle, Germany

6. Center for Intervention and Research on Adaptive and Maladaptive Brain Circuits Underlying Mental Health (C-I-R-C), Jena-Magdeburg-Halle, Germany

7. German Center for Higher Education Research and Science Studies (DZHW), Hannover, Germany

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

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

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

11. Department of Psychiatry and Psychotherapy, Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany

12. MR-Research in Neurosciences, Department of Cognitive Neurology, Georg August University Göttingen, Göttingen, Germany

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

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

15. Berlin Center for Advanced Neuroimaging, Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany

16. Department for Psychiatry and Psychotherapy, University Clinic Magdeburg, Magdeburg, Germany

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

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

19. German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany

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

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

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

23. University of Edinburgh and UK DRI, Edinburgh, United Kingdom

24. Department of Psychiatry, University of Cologne, Medical Faculty, Cologne, Germany

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

26. Department of Neurology, University of Bonn, Bonn, Germany

27. Department of Psychiatry and Psychotherapy, University Medical Center, Göttingen, Germany

28. Neurosciences and Signaling Group, Institute of Biomedicine (iBiMED), Department of Medical Sciences, University of Aveiro, Aveiro, Portugal

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

30. Center for Behavioral Brain Sciences (CBBS), Magdeburg, Germany

Abstract

Abstract In functional magnetic resonance imaging (fMRI) studies, episodic memory is commonly investigated with the subsequent memory paradigm in which brain activity is recorded during encoding and analyzed as a function of subsequent remembering and forgetting. Impaired episodic memory is common in individuals with or at risk for Alzheimer’s disease (AD), but only few studies have reported subsequent memory effects in AD or its risk states like mild cognitive impairment (MCI). One reason for this might be that subsequent memory responses may be blunted in AD or MCI and thus less likely to manifest in fMRI signal differences. Here, we used Bayesian model selection of single-subject fMRI general linear models (GLMs) for a visual novelty and memory encoding experiment to compare the model performance of categorical and parametric subsequent memory models as well as memory-invariant models in a clinical cohort (N = 468) comprising healthy controls (HC) as well as individuals with subjective cognitive decline (SCD), MCI, and AD, plus healthy relatives of AD patients (AD-rel). We could replicate the previously reported superiority of parametric subsequent memory models over categorical models (Soch, Richter, Schütze, Kizilirmak, Assmann, Knopf, et al., 2021) in the HC and also in the SCD and AD-rel groups. However, memory-invariant models outperformed any model assuming subsequent memory effects in the MCI and AD groups. In the AD group, we additionally found substantially lower model preference for models assuming novelty compared to models not differentiating between novel and familiar stimuli. Our results suggest that voxel-wise memory-related fMRI activity patterns in AD and also MCI should be interpreted with caution and point to the need for additional or alternative approaches to investigate memory function.

Publisher

MIT Press

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