Journal Article DZNE-2022-01651

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Cholinergic white matter pathways along the Alzheimer's disease continuum.

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2023
Oxford Univ. Press Oxford

Brain 146(5), 2075-2088 () [10.1093/brain/awac385]

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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.

Keyword(s): Humans (MeSH) ; Alzheimer Disease: psychology (MeSH) ; White Matter (MeSH) ; Brain (MeSH) ; Cognitive Dysfunction: psychology (MeSH) ; Cholinergic Agents (MeSH) ; Alzheimer’s disease ; Alzheimer’s disease ; Alzheimer’s disease ; cerebrospinal fluid markers ; cholinergic system ; magnetic resonance imaging ; nucleus basalis of Meynert ; CSF markers ; MRI ; Cholinergic Agents

Classification:

Contributing Institute(s):
  1. Clinical Dementia Research (Rostock /Greifswald) (AG Teipel)
  2. Interventional Trials and Biomarkers in Neurodegenerative Diseases (Biomarker)
  3. Vascular Cognitive Impairment & Post-Stroke Dementia (AG Dichgans)
  4. Linking imaging projects iNET (AG Speck)
  5. Molecular Neurobiology (AG Simons)
  6. Patient Studies Bonn (Patient Studies Bonn)
  7. Clinical Neurophysiology and Memory (AG Düzel)
  8. Cooperation Unit for Applied Prevention Research (KAP) (KAP)
  9. Parkinson Genetics (AG Gasser)
  10. Translational Neuropsychiatry (AG Priller)
  11. Neuropsychology (AG Wagner)
  12. Clinical Research Platform (CRP) (Clinical Research Platform (CRP))
  13. Translational Dementia Research (Bonn) (AG Schneider)
  14. Epigenetics and Systems Medicine in Neurodegenerative Diseases (AG Fischer)
  15. Clinical Alzheimer’s Disease Research (AG Jessen)
  16. Interdisciplinary Dementia Research (AG Endres)
  17. Molecular biomarkers for predictive diagnostics of neurodegenerative diseases (AG Wiltfang)
  18. Delcode (Delcode)
Research Program(s):
  1. 353 - Clinical and Health Care Research (POF4-353) (POF4-353)
  2. 352 - Disease Mechanisms (POF4-352) (POF4-352)
  3. 351 - Brain Function (POF4-351) (POF4-351)
Experiment(s):
  1. Longitudinal Cognitive Impairment and Dementia Study

Appears in the scientific report 2023
Database coverage:
Medline ; Creative Commons Attribution-NonCommercial CC BY-NC 4.0 ; OpenAccess ; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; Current Contents - Clinical Medicine ; Current Contents - Life Sciences ; Ebsco Academic Search ; Essential Science Indicators ; IF >= 10 ; JCR ; NationallizenzNationallizenz ; PubMed Central ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection
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The record appears in these collections:
Institute Collections > BN DZNE > BN DZNE-Clinical Research Platform (CRP)
Institute Collections > MD DZNE > MD DZNE-Applied Prevention Research
Institute Collections > BN DZNE > BN DZNE-Patient Studies (Bonn)
Document types > Articles > Journal Article
Institute Collections > GÖ DZNE > GÖ DZNE-AG Wiltfang
Institute Collections > BN DZNE > BN DZNE-AG Schneider
Institute Collections > GÖ DZNE > GÖ DZNE-AG Fischer
Institute Collections > ROS DZNE > ROS DZNE-AG Teipel
Institute Collections > TÜ DZNE > TÜ DZNE-AG Gasser
Institute Collections > BN DZNE > BN DZNE-AG Jessen
Institute Collections > MD DZNE > MD DZNE-AG Düzel
Institute Collections > BN DZNE > BN DZNE-AG Wagner
Institute Collections > BN DZNE > BN DZNE-Biomarker
Institute Collections > M DZNE > M DZNE-AG Dichgans
Institute Collections > B DZNE > B DZNE-AG Priller
Institute Collections > MD DZNE > MD DZNE-AG Speck
Institute Collections > M DZNE > M DZNE-AG Simons
Institute Collections > B DZNE > B DZNE-AG Endres
Institute Collections > M DZNE > M DZNE-Delcode
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 Record created 2022-11-14, last modified 2024-08-26