Cholinergic white matter pathways along the Alzheimer's disease continuum

Author:

Nemy Milan123ORCID,Dyrba Martin4ORCID,Brosseron Frederic5,Buerger Katharina67,Dechent Peter8,Dobisch Laura9,Ewers Michael67ORCID,Fliessbach Klaus510,Glanz Wenzel9,Goerss Doreen411ORCID,Heneka Michael T510,Hetzer Stefan12,Incesoy Enise I913,Janowitz Daniel7,Kilimann Ingo411ORCID,Laske Christoph1415,Maier Franziska16,Munk Matthias H1415,Perneczky Robert617181920,Peters Oliver2122,Preis Lukas22,Priller Josef21232425,Rauchmann Boris-Stephan17,Röske Sandra5,Roy Nina5,Scheffler Klaus26,Schneider Anja510,Schott Björn H272829ORCID,Spottke Annika530,Spruth Eike J2123,Wagner Michael510,Wiltfang Jens272831,Yakupov Renat9ORCID,Eriksdotter Maria332ORCID,Westman Eric333ORCID,Stepankova Olga2ORCID,Vyslouzilova Lenka2ORCID,Düzel Emrah913ORCID,Jessen Frank51634ORCID,Teipel Stefan J411ORCID,Ferreira Daniel3ORCID

Affiliation:

1. Department of Cybernetics, Faculty of Electrical Engineering, Czech Technical University in Prague , Prague , Czech Republic

2. Department of Biomedical Engineering and Assistive Technology, Czech Institute of Informatics, Robotics and Cybernetics, Czech Technical University in Prague , Prague , Czech Republic

3. Division of Clinical Geriatrics, Center for Alzheimer Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institute , Stockholm , Sweden

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

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

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

7. Institute for Stroke and Dementia Research (ISD), University Hospital, LMU Munich , Munich , Germany

8. MR-Research in Neurosciences, Department of Cognitive Neurology, Georg-August-University Goettingen , Goettingen , Germany

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

10. Department for Neurodegenerative Diseases and Geriatric Psychiatry, University Hospital Bonn , Bonn , Germany

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

12. Berlin Center for Advanced Neuroimaging, Charité—Universitätsmedizin Berlin , Berlin , Germany

13. Institute of Cognitive Neurology and Dementia Research, Otto-von-Guericke University , Magdeburg , Germany

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

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

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

17. Department of Psychiatry and Psychotherapy, University Hospital, LMU Munich , Munich , Germany

18. Munich Cluster for Systems Neurology (SyNergy) , Munich , Germany

19. Ageing Epidemiology Research Unit (AGE), School of Public Health, Imperial College London , London , UK

20. Sheffield Institute for Translational Neurosciences (SITraN), University of Sheffield , Sheffield , UK

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

22. Department of Psychiatry, Charité-Universitätsmedizin Berlin, Campus Benjamin Franklin , Berlin , Germany

23. Department of Psychiatry and Psychotherapy, Charité , Berlin , Germany

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

25. Centre for Clinical Brain Sciences, University of Edinburgh and UK DRI , Edinburgh , UK

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

27. German Center for Neurodegenerative Diseases (DZNE) , Goettingen , Germany

28. Department of Psychiatry and Psychotherapy, University Medical Center Goettingen, University of Goettingen , Goettingen , Germany

29. Leibniz Institute for Neurobiology , Magdeburg , Germany

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

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

32. Theme Inflammation and Aging, Karolinska University Hospital , Stockholm , Sweden

33. Department of Neuroimaging, Centre for Neuroimaging Science, Institute of Psychiatry, Psychology, and Neuroscience, King’s College London , London , UK

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

Abstract

Abstract Previous studies have shown that the cholinergic nucleus basalis of Meynert and its white matter projections are affected in Alzheimer’s disease dementia and mild cognitive impairment. However, it is still unknown whether these alterations can be found in individuals with subjective cognitive decline, and whether they are more pronounced than changes found in conventional brain volumetric measurements. To address these questions, we investigated microstructural alterations of two major cholinergic pathways in individuals along the Alzheimer’s disease continuum using an in vivo model of the human cholinergic system based on neuroimaging. We included 402 participants (52 Alzheimer’s disease, 66 mild cognitive impairment, 172 subjective cognitive decline and 112 healthy controls) from the Deutsches Zentrum für Neurodegenerative Erkrankungen Longitudinal Cognitive Impairment and Dementia Study. We modelled the cholinergic white matter pathways with an enhanced diffusion neuroimaging pipeline that included probabilistic fibre-tracking methods and prior anatomical knowledge. The integrity of the cholinergic white matter pathways was compared between stages of the Alzheimer’s disease continuum, in the whole cohort and in a CSF amyloid-beta stratified subsample. The discriminative power of the integrity of the pathways was compared to the conventional volumetric measures of hippocampus and nucleus basalis of Meynert, using a receiver operating characteristics analysis. A multivariate model was used to investigate the role of these pathways in relation to cognitive performance. We found that the integrity of the cholinergic white matter pathways was significantly reduced in all stages of the Alzheimer’s disease continuum, including individuals with subjective cognitive decline. The differences involved posterior cholinergic white matter in the subjective cognitive decline stage and extended to anterior frontal white matter in mild cognitive impairment and Alzheimer’s disease dementia stages. Both cholinergic pathways and conventional volumetric measures showed higher predictive power in the more advanced stages of the disease, i.e. mild cognitive impairment and Alzheimer’s disease dementia. In contrast, the integrity of cholinergic pathways was more informative in distinguishing subjective cognitive decline from healthy controls, as compared with the volumetric measures. The multivariate model revealed a moderate contribution of the cholinergic white matter pathways but not of volumetric measures towards memory tests in the subjective cognitive decline and mild cognitive impairment stages. In conclusion, we demonstrated that cholinergic white matter pathways are altered already in subjective cognitive decline individuals, preceding the more widespread alterations found in mild cognitive impairment and Alzheimer’s disease. The integrity of the cholinergic pathways identified the early stages of Alzheimer’s disease better than conventional volumetric measures such as hippocampal volume or volume of cholinergic nucleus basalis of Meynert.

Funder

Swedish Research Council

Stockholm County Council

Karolinska Institutet

Center for Innovative Medicine

Swedish Alzheimer Foundation

Swedish Brain Foundation

Neuro Fonden

Czech Alzheimer Foundation

Demensfonden

Czech Technical University in Prague

Federal Ministry of Research

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

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