4.7 Article

Cholinergic white matter pathways in dementia with Lewy bodies and Alzheimer's disease

期刊

BRAIN
卷 145, 期 5, 页码 1773-1784

出版社

OXFORD UNIV PRESS
DOI: 10.1093/brain/awab372

关键词

nucleus basalis of Meynert; basal forebrain; mild cognitive impairment; diffusion-weighted imaging; probabilistic tractography

资金

  1. Alzheimer's Research UK [ARUKPG2015-13]
  2. Wellcome Trust Intermediate Clinical Fellowship [WT088441MA]
  3. NIHR Newcastle Biomedical Research Centre [BH120812, BH120878]
  4. Northumberland Tyne and Wear NHS Foundation Trust

向作者/读者索取更多资源

Patients with dementia with Lewy bodies and Alzheimer's disease exhibited early degeneration of the cholinergic nucleus basalis of Meynert. However, it remains unknown how white matter projections between the nucleus basalis of Meynert and the cortex are affected in neurodegenerative diseases. This study utilized diffusion-weighted imaging to investigate the white matter pathways originating from the nucleus basalis of Meynert in patients with different cognitive conditions. The results demonstrated that the integrity of these pathways is associated with cognition and attention, and might serve as an early indicator for the risk of dementia conversion in individuals with mild cognitive impairment.
Patients who have dementia with Lewy bodies and Alzheimer's disease show early degeneration of the cholinergic nucleus basalis of Meynert. However, how white matter projections between the nucleus basalis of Meynert and the cortex are altered in neurodegenerative disease is unknown. Tractography of white matter pathways originating from the nucleus basalis of Meynert was performed using diffusion-weighted imaging in 46 patients with Alzheimer's disease dementia, 48 with dementia with Lewy bodies, 35 with mild cognitive impairment with Alzheimer's disease, 38 with mild cognitive impairment with Lewy bodies and 71 control participants. Mean diffusivity of the resulting pathways was compared between groups and related to cognition, attention, functional EEG changes and dementia conversion in the mild cognitive impairment groups. We successfully tracked a medial and a lateral pathway from the nucleus basalis of Meynert. Mean diffusivity of the lateral pathway was higher in both dementia and mild cognitive impairment groups than controls (all P < 0.03). In the patient groups, increased mean diffusivity of this pathway was related to more impaired global cognition (beta = -0.22, P = 0.06) and worse performance on an attention task (beta = 0.30, P = 0.03). In patients with mild cognitive impairment, loss of integrity of both nucleus basalis of Meynert pathways was associated with increased risk of dementia progression [hazard ratio (95% confidence interval), medial pathway: 2.51 (1.24-5.09); lateral pathway: 2.54 (1.24-5.19)]. Nucleus basalis of Meynert volume was reduced in all clinical groups compared to controls (all P < 0.001), but contributed less strongly to cognitive impairment and was not associated with attention or dementia conversion. EEG slowing in the patient groups as assessed by a decrease in dominant frequency was associated with smaller nucleus basalis of Meynert volumes (beta = 0.22, P = 0.02) and increased mean diffusivity of the lateral pathway (beta = -0.47, P = 0.003). We show that degeneration of the cholinergic nucleus basalis of Meynert in Alzheimer's disease and dementia with Lewy bodies is accompanied by an early reduction in integrity of white matter projections that originate from this structure. This is more strongly associated with cognition and attention than the volume of the nucleus basalis of Meynert itself and might be an early indicator of increased risk of dementia conversion in people with mild cognitive impairment.

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