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Comparison of Locus Coeruleus Pathology with Nigral and Forebrain Pathology in Parkinson's Disease

Huynh, Benjamin ; Fu, Yuhong ; Kirik, Deniz LU ; Shine, James M. and Halliday, Glenda M (2021) In Movement Disorders 36(9). p.2085-2093
Abstract

Background: Pathology in the noradrenergic A6 locus coeruleus has not been compared with more rostral dopaminergic A9 substantia nigra and A10 ventral tegmental area, and cholinergic Ch4 basal nucleus and Ch1/2 septal regions in the same cases of Parkinson's disease (PD). Objective: To determine whether there is a gradient of caudal to rostral cell loss in PD. Methods: Postmortem brains were collected from longitudinally followed donors with PD (n = 14) and aged-matched healthy donors (n = 13), six with restricted brainstem Lewy pathology (RLP), fixed in formalin and serial tissue slabs processed for cell and pathological quantitation. Noradrenergic A6 neurons were assessed and compared with previously published midbrain and basal... (More)

Background: Pathology in the noradrenergic A6 locus coeruleus has not been compared with more rostral dopaminergic A9 substantia nigra and A10 ventral tegmental area, and cholinergic Ch4 basal nucleus and Ch1/2 septal regions in the same cases of Parkinson's disease (PD). Objective: To determine whether there is a gradient of caudal to rostral cell loss in PD. Methods: Postmortem brains were collected from longitudinally followed donors with PD (n = 14) and aged-matched healthy donors (n = 13), six with restricted brainstem Lewy pathology (RLP), fixed in formalin and serial tissue slabs processed for cell and pathological quantitation. Noradrenergic A6 neurons were assessed and compared with previously published midbrain and basal forebrain data. From these data, regression estimates of pathological onset and progression were determined. Results: Restricted Lewy pathology (RLP) cases had high pathological variability but no significant reduction in neurons. Pathology containing A6 neuron loss started at PD diagnosis and progressed faster (2.4% p.a) than the loss of dopaminergic A9 neurons (2% loss p.a.). Cases with dementia had significantly more pathology in noradrenergic and cholinergic neurons, had greater noradrenergic A6 neuron loss (29% more, progressing at 3.2% p.a.), and a selective loss of lateral A10 nonmelanized dopamine-producing neurons (starting a decade following diagnosis). Conclusions: These findings show that in the same Parkinson's disease cases cell loss in these neurotransmitter systems does not follow a strict caudal to rostral trajectory and suggests symptom onset may relate to substantial pathology in the noradrenergic A6 locus coeruleus neurons in people with reduced dopamine-producing A9 substantia nigra neurons.

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author
; ; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
dementia, locus coeruleus, noradrenaline, Parkinson's disease, pathology
in
Movement Disorders
volume
36
issue
9
pages
2085 - 2093
publisher
John Wiley & Sons Inc.
external identifiers
  • scopus:85104832577
  • pmid:33899954
ISSN
0885-3185
DOI
10.1002/mds.28615
language
English
LU publication?
yes
id
c3a147b1-fd00-45a3-9dd8-773db0d263c2
date added to LUP
2021-05-10 14:50:25
date last changed
2024-06-15 10:58:01
@article{c3a147b1-fd00-45a3-9dd8-773db0d263c2,
  abstract     = {{<p>Background: Pathology in the noradrenergic A6 locus coeruleus has not been compared with more rostral dopaminergic A9 substantia nigra and A10 ventral tegmental area, and cholinergic Ch4 basal nucleus and Ch1/2 septal regions in the same cases of Parkinson's disease (PD). Objective: To determine whether there is a gradient of caudal to rostral cell loss in PD. Methods: Postmortem brains were collected from longitudinally followed donors with PD (n = 14) and aged-matched healthy donors (n = 13), six with restricted brainstem Lewy pathology (RLP), fixed in formalin and serial tissue slabs processed for cell and pathological quantitation. Noradrenergic A6 neurons were assessed and compared with previously published midbrain and basal forebrain data. From these data, regression estimates of pathological onset and progression were determined. Results: Restricted Lewy pathology (RLP) cases had high pathological variability but no significant reduction in neurons. Pathology containing A6 neuron loss started at PD diagnosis and progressed faster (2.4% p.a) than the loss of dopaminergic A9 neurons (2% loss p.a.). Cases with dementia had significantly more pathology in noradrenergic and cholinergic neurons, had greater noradrenergic A6 neuron loss (29% more, progressing at 3.2% p.a.), and a selective loss of lateral A10 nonmelanized dopamine-producing neurons (starting a decade following diagnosis). Conclusions: These findings show that in the same Parkinson's disease cases cell loss in these neurotransmitter systems does not follow a strict caudal to rostral trajectory and suggests symptom onset may relate to substantial pathology in the noradrenergic A6 locus coeruleus neurons in people with reduced dopamine-producing A9 substantia nigra neurons.</p>}},
  author       = {{Huynh, Benjamin and Fu, Yuhong and Kirik, Deniz and Shine, James M. and Halliday, Glenda M}},
  issn         = {{0885-3185}},
  keywords     = {{dementia; locus coeruleus; noradrenaline; Parkinson's disease; pathology}},
  language     = {{eng}},
  number       = {{9}},
  pages        = {{2085--2093}},
  publisher    = {{John Wiley & Sons Inc.}},
  series       = {{Movement Disorders}},
  title        = {{Comparison of Locus Coeruleus Pathology with Nigral and Forebrain Pathology in Parkinson's Disease}},
  url          = {{http://dx.doi.org/10.1002/mds.28615}},
  doi          = {{10.1002/mds.28615}},
  volume       = {{36}},
  year         = {{2021}},
}