4.7 Article

Cortical connectivity of the nucleus basalis of Meynert in Parkinson's disease and Lewy body dementias

期刊

BRAIN
卷 144, 期 3, 页码 781-788

出版社

OXFORD UNIV PRESS
DOI: 10.1093/brain/awaa411

关键词

DBS; MEG; DTI; coherence; oscillations

资金

  1. NIHR Academic Clinical Lectureship
  2. Academy of Medical Sciences Starter Grant
  3. Wellcome [203147/Z/16/Z]
  4. Medical Research Council [MK/K005464/1, MC_UU_12024/5]
  5. NIH/NINDS [2RF1NS023945-28]
  6. NIHR
  7. Michael J Fox Foundation
  8. Cure Parkinson's Trust
  9. Innovate UK
  10. John Black Charitable Foundation
  11. Janet Owens Fellowship
  12. Brain Research Trust [157806]
  13. National Institute for Health Research University College London Hospitals Biomedical Research Centre
  14. Parkinson's Appeal
  15. Sainsbury Monument Trust
  16. Defeat MSA
  17. MRC [MR/K022172/1, MC_UU_12024/1, MC_UU_12024/5] Funding Source: UKRI

向作者/读者索取更多资源

Parkinson's disease dementia (PDD) and dementia with Lewy bodies (DLB) are related to dysfunction of the nucleus basalis of Meynert (NBM), with networks connecting NBM to supplementary motor area, medial temporal lobe structures, and visual areas playing important roles in motor control, memory, and visual function. The findings reveal the significance of NBM functional networks in various cognitive functions and suggest future studies to understand their contributions to disease phenotypes.
Parkinson's disease dementia (PDD) and dementia with Lewy bodies (DLB) are related conditions that are associated with cholinergic system dysfunction. Dysfunction of the nucleus basalis of Meynert (NBM), a basal forebrain structure that provides the dominant source of cortical cholinergic innervation, has been implicated in the pathogenesis of both PDD and DLB. Here we leverage the temporal resolution of magnetoencephalography with the spatial resolution of MRI tractography to explore the intersection of functional and structural connectivity of the NBM in a unique cohort of PDD and DLB patients undergoing deep brain stimulation of this structure. We observe that NBM-cortical structural and functional connectivity correlate within spatially and spectrally segregated networks including: (i) a beta band network to supplementary motor area, where activity in this region was found to drive activity in the NBM; (ii) a delta/theta band network to medial temporal lobe structures encompassing the parahippocampal gyrus; and (iii) a delta/theta band network to visual areas including lingual gyrus. These findings reveal functional networks of the NBM that are likely to subserve important roles in motor control, memory and visual function, respectively. Furthermore, they motivate future studies aimed at disentangling network contribution to disease phenotype.

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