The white matter in Alzheimer’s - ncl.ac.uk · White and grey matter White matter Grey...
Transcript of The white matter in Alzheimer’s - ncl.ac.uk · White and grey matter White matter Grey...
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The white matter in Alzheimer’s
disease
Dr Kirsty E. McAleese ARUK public meeting, June 13th 2017
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Overview
• What is the white matter?
• White matter damage
• Diagnostic relevance?
• Newcastle University study into cause of white matter
damage in Alzheimer's disease and normal ageing
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White and grey matter
White matter
Grey
matter/cortex
Human brain
MRI
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White and grey matter
Grey matter/cortex White matter
Cell bodies
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White and grey matter: Brain cell
Cortex
White
matter
Cell body
Axon
Dendrites
Terminal synapse
Myelin
Oligodendrocyte
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White and grey matter: tissue
Cortex
White
matter Other brain areas,
spinal cord etc…
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White matter damage
• Loss of the myelin with/without axonal loss
• Visualised under microscope or on an MRI scan
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White matter damage
Normal white matter
Damaged white matter
Tissue section MRI scan
White matter damage
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White matter damage
• Loss of the myelin with/without axonal loss
• Visualised under microscope or on an MRI scan
• Assumed to represent a vessel disease called small vessel disease
(SVD)
• WM damage on MRI scan indicates SVD
• Diagnosis of vascular cognitive impairment/dementia
Atherosclerosis Arteriolosclerosis
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• Studies have shown that WM damage in Alzheimer’s disease (AD) may be
caused by a different mechanism
Alzheimer’s disease - Recap
• Most common neurodegenerative disease that causes dementia
• Symptoms include memory impairment, language and executive function
deficits
• 2 protein depositions seen under the microscope: Amyloid-β and tau
pathology
White matter damage in AD
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Amyloid-β pathology
Tau
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Hyperphosphorylated tau pathology
Hippocampus
Cortex
WM
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• Studies have shown that WM damage in Alzheimer’s disease (AD) may be
caused by a different mechanism
Alzheimer’s disease
• Most common neurodegenerative disease that causes dementia
• Symptoms include memory impairment, language and executive function
deficits
• 2 protein depositions seen under the microscope: Amyloid-β and tau
pathology
• Death of brain cells – leading to shrinkage of the brain
White matter damage in AD
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White matter damage in AD
Non-demented Alzheimer’s disease
To scale
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• Studies have shown that WM damage in Alzheimer’s disease (AD) may be
caused by a different mechanism
• Degenerative myelin and axonal loss caused by the deposition of tau and
amyloid-β.
• Neuronal loss
White matter damage in AD
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Neuronal loss
White matter damage in AD
A
B
E
D
Healthy neuron and axon
Neuronaldysfunc onleadstofailureofaxonaltransportresul nginblockagesat
axonaljunc ons
Amyloid-beta
and tau protein
C Swellingsoftransportmaterial
CompleteblockofaxonaltransporttriggersWLD
Fragmenta onofaxonfromdistalend
Completelossoftheaxon
Proximal Distal
Neuron and axon
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Neuronal loss
White matter damage in AD
A
B
E
D
Healthy neuron and axon
Neuronaldysfunc onleadstofailureofaxonaltransportresul nginblockagesat
axonaljunc ons
Amyloid-beta
and tau protein
C Swellingsoftransportmaterial
CompleteblockofaxonaltransporttriggersWLD
Fragmenta onofaxonfromdistalend
Completelossoftheaxon
Proximal Distal
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Neuronal loss
White matter damage in AD
A
B
E
D
Healthy neuron and axon
Neuronaldysfunc onleadstofailureofaxonaltransportresul nginblockagesat
axonaljunc ons
Amyloid-beta
and tau protein
C Swellingsoftransportmaterial
CompleteblockofaxonaltransporttriggersWLD
Fragmenta onofaxonfromdistalend
Completelossoftheaxon
Proximal Distal
A
B
E
D
Healthy neuron and axon
Neuronaldysfunc onleadstofailureofaxonaltransportresul nginblockagesat
axonaljunc ons
Amyloid-beta
and tau protein
C Swellingsoftransportmaterial
CompleteblockofaxonaltransporttriggersWLD
Fragmenta onofaxonfromdistalend
Completelossoftheaxon
Proximal Distal
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• Studies have shown that WM damage in Alzheimer’s disease (AD) may be
caused by a different mechanism
• Degenerative myelin and axonal loss caused by the deposition of tau and
amyloid-β.
• Neuronal loss
• Wallerian degeneration
White matter damage in AD
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Wallerian degeneration
White matter damage in AD
• ‘Self-destruction’ of the axon (and myelin)
• Triggered by blockage of transport up and down the axon
A
B
E
D
Healthy neuron and axon
Neuronaldysfunc onleadstofailureofaxonaltransportresul nginblockagesat
axonaljunc ons
Amyloid-beta
and tau protein
C Swellingsoftransportmaterial
CompleteblockofaxonaltransporttriggersWLD
Fragmenta onofaxonfromdistalend
Completelossoftheaxon
Proximal Distal
Axonal transport dysfunction
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Wallerian degeneration
White matter damage in AD
A
B
E
D
Healthy neuron and axon
Neuronaldysfunc onleadstofailureofaxonaltransportresul nginblockagesat
axonaljunc ons
Amyloid-beta
and tau protein
C Swellingsoftransportmaterial
CompleteblockofaxonaltransporttriggersWLD
Fragmenta onofaxonfromdistalend
Completelossoftheaxon
Proximal Distal
A
B
E
D
Healthy neuron and axon
Neuronaldysfunc onleadstofailureofaxonaltransportresul nginblockagesat
axonaljunc ons
Amyloid-beta
and tau protein
C Swellingsoftransportmaterial
CompleteblockofaxonaltransporttriggersWLD
Fragmenta onofaxonfromdistalend
Completelossoftheaxon
Proximal Distal
Axonal transport dysfunction
Axonal swellings
• ‘Self-destruction’ of the axon (and myelin)
• Triggered by blockage of transport up and down the axon
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Wallerian degeneration
White matter damage in AD
A
B
E
D
Healthy neuron and axon
Neuronaldysfunc onleadstofailureofaxonaltransportresul nginblockagesat
axonaljunc ons
Amyloid-beta
and tau protein
C Swellingsoftransportmaterial
CompleteblockofaxonaltransporttriggersWLD
Fragmenta onofaxonfromdistalend
Completelossoftheaxon
Proximal Distal
A
B
E
D
Healthy neuron and axon
Neuronaldysfunc onleadstofailureofaxonaltransportresul nginblockagesat
axonaljunc ons
Amyloid-beta
and tau protein
C Swellingsoftransportmaterial
CompleteblockofaxonaltransporttriggersWLD
Fragmenta onofaxonfromdistalend
Completelossoftheaxon
Proximal Distal
A
B
E
D
Healthy neuron and axon
Neuronaldysfunc onleadstofailureofaxonaltransportresul nginblockagesat
axonaljunc ons
Amyloid-beta
and tau protein
C Swellingsoftransportmaterial
CompleteblockofaxonaltransporttriggersWLD
Fragmenta onofaxonfromdistalend
Completelossoftheaxon
Proximal Distal
Axonal transport dysfunction
Axonal swellings
Axonal transport blockage:
release of calpain protease
• ‘Self-destruction’ of the axon (and myelin)
• Triggered by blockage of transport up and down the axon
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Wallerian degeneration
White matter damage in AD
A
B
E
D
Healthy neuron and axon
Neuronaldysfunc onleadstofailureofaxonaltransportresul nginblockagesat
axonaljunc ons
Amyloid-beta
and tau protein
C Swellingsoftransportmaterial
CompleteblockofaxonaltransporttriggersWLD
Fragmenta onofaxonfromdistalend
Completelossoftheaxon
Proximal Distal
A
B
E
D
Healthy neuron and axon
Neuronaldysfunc onleadstofailureofaxonaltransportresul nginblockagesat
axonaljunc ons
Amyloid-beta
and tau protein
C Swellingsoftransportmaterial
CompleteblockofaxonaltransporttriggersWLD
Fragmenta onofaxonfromdistalend
Completelossoftheaxon
Proximal Distal
A
B
E
D
Healthy neuron and axon
Neuronaldysfunc onleadstofailureofaxonaltransportresul nginblockagesat
axonaljunc ons
Amyloid-beta
and tau protein
C Swellingsoftransportmaterial
CompleteblockofaxonaltransporttriggersWLD
Fragmenta onofaxonfromdistalend
Completelossoftheaxon
Proximal Distal
A
B
E
D
Healthy neuron and axon
Neuronaldysfunc onleadstofailureofaxonaltransportresul nginblockagesat
axonaljunc ons
Amyloid-beta
and tau protein
C Swellingsoftransportmaterial
CompleteblockofaxonaltransporttriggersWLD
Fragmenta onofaxonfromdistalend
Completelossoftheaxon
Proximal Distal
Axonal transport dysfunction
Axonal swellings
Axonal transport blockage:
release of calpain protease
Destruction of the axon and
attached myelin
• ‘Self-destruction’ of the axon (and myelin)
• Triggered by blockage of transport up and down the axon
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• Diffusion Tensor Imaging (DTI) studies shown specific WM changes patterns in
patient who have AD
• WM changes in areas connected to the medial temporal lobe (MTL)
White matter damage in AD
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• Tau pathology
• Development of tau in AD starts in the MTL
• Autopsy studies in cases with no SVD shown WM damage more severe
in areas of high amounts of tau pathology
• Tau fundamental component of skeleton of the axon – changes to tau
from AD may lead to axonal transport dysfunction
White matter damage in AD
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Why is it important to understand what causes white
matter damage?
• Overlapping of symptoms between AD and vascular dementia
• MRI evidence of WM damage assumed to represent SVD
• SVD may not be the only causes WM damage – AD?
• Patients may be misdiagnosed as vascular dementia when they may
potentially have AD
• Clinical vs. autopsy diagnosis
• Affect treatment options
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Study conducted at Newcastle University
• It is not clear whether the composition and the cause of WM damage differ
between AD and normal ageing
Aim
Using post-mortem donated brain tissue from the Newcastle Brain Tissue
Resource (NBTR)
1. Identify the differences in the composition of WM lesions
2. Establish the cause of WM lesions
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What we did
• 55 human post-mortem brains : 27 AD, 28 controls
Histological procedures
• Tissue sections cut parietal blocks
• Histological staining
• Immunohistochemistry
• Extensive microscopic assessment
LFB Biel H&E
TauAmyloid-β
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Tissue assessment
1. WM lesion area
2. Myelin loss
3. Axonal loss
4. Tau and amyloid-β
5. Small vessel disease
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OverviewProtein measures in frozen tissue
Right hemisphere fixed:
neuropathology
WML tissue
• Corresponding frozen coronal slices of parietal tissue: left hemisphere
• Wallerian degeneration - Calpain2
• Hypoperfusion - Myelin-associated glycoprotein (MAG) and proteolipid protein (PLP)
• MAG:PLP
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Ai
Ci
Bi
Cii
Aii
Bii
WM
L-B
iA (
%)
NA
WM
-BiA
(%
)
WM
L-L
FB
-IO
D
NA
WM
-LF
B-I
OD
WM
L-B
iA (
%)
NA
WM
-BiA
(%
)
WMLA (%) WMLA (%)
WMLA(%) WMLA(%)
WML LFB-IOD NAWM LFB-IOD
Figure 4
ρ = 0·755**
ρ = 0·413*
Axonal density
AD: More severe WM damage linked to axonal loss
Controls: No axonal loss
Ai
Ci
Bi
Cii
Aii
Bii
WM
L-B
iA (
%)
NA
WM
-BiA
(%
)
WM
L-L
FB
-IO
D
NA
WM
-LF
B-I
OD
WM
L-B
iA (
%)
NA
WM
-BiA
(%
)
WMLA (%) WMLA (%)
WMLA(%) WMLA(%)
WML LFB-IOD NAWM LFB-IOD
Figure 4
Axonal and myelin loss in WM damage
ρ = -0·648** Axo
na
l lo
ss %
Myelin
lo
ss
White matter damage (%) White matter damage (%)
Myelin loss
AD and controls: More severe WM damage
linked to myelin loss
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What has caused the WM damage?
Tau, amyloid-β pathology and small vessel disease
WM damage
severity
Higher
amount of
myelin loss
Tau
No link with
amyloid-β or SVD
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Protein measures
*
A
Figure 5
CB ***
Wallerian degeneration – calpain2
• Calpain2 protein was higher in
damaged WM in AD
• Calpain2 was linked to both tau
and amyloid-β
Calp
ain
2
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Results: biochemical markers of Wallerian degeneration
and ischemia in WM lesion tissue
Hypoperfusion – MAG:PLP
• MAG:PLP reduced in controls
indicates hypoperfusion
MA
G:P
LP
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What does this all mean?
• WM damage in AD is different
• Axon and myelin loss
• Non-demented – myelin loss
• Cause of WM damage is different between AD and normal ageing
• AD - Wallerian degeneration mechanism
• Linked to tau and amyloid-β
• Non-demented – hypoperfusion likely linked to vessel disease
• Clinically important – WM damage on MRI indicates SVD
• SVD is not the only cause and may indeed be indicative of AD
• Accurate diagnosis
• No disputing SVD/vascular influence in AD – not primary cause posterior WM
changes
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Summary
• The white matter contains axons and myelin that connects all brain cells and
different regions of the brain
• WM can become damaged; thought to be caused by small vessels disease -
may lead to a diagnosis of vascular dementia
• New studies show that WM damage is different in AD and the AD process
itself can lead to WM damage
• Important implications for accurate diagnosis of patients with cognitive
impairment or dementia
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Thank youNewcastle University
Prof Johannes Attems
Dr Lauren Walker
Miss Sophie Graham
Miss Elisa Moya
Mr Daniel Erskine
Dr Sean Colloby
Miss Madurhima Dey
Mrs Mary Johnson
Dr Carmen Martin-Ruiz
Dr John-Paul Taylor
Prof Alan Thomas
Prof Ian McKeith
Mrs Debbie Lett
Mrs Lynne Ramsay
Mrs Ros Hall
Dr Ahmad Khundakar
NBTR staff, brain donor
and their families
UC Davis
Prof Charles DeCarli
University of Bristol
Dr Scott Miners