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New Techniques in Brain Imaging in Alzheimers Disease

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Title: New Techniques in Brain Imaging in Alzheimers Disease


1
New Techniques in Brain Imaging in Alzheimers
Disease
  • Susan Bookheimer Ph.D.
  • Center for Cognitive Neurosciences
  • UCLA School of Medicine

2
Brain Imaging Approaches
  • Structural MRI
  • New measures
  • New analysis techniques
  • Functional MRI
  • Early changes in function
  • Prediction of outcome
  • Positron Emission Tomography
  • New radioisotopes

3
MRI in AD
  • Acquisition better scanners
  • Analysis better ways of looking at the data
  • Dynamic measures (vs. static)
  • New types of measurements (location, thickness
    vs. size)

4
Structural MRI
Comfort, claustrophobia
5
New MRI ScannersHigher field strength, speed,
resolution
High Field 3 Tesla
Standard 1.5 Tesla
6
Measuring Structures the Region-of-interest
Approach
7
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8
Location of Atrophy in Hippocampus
9
Measuring Change in Size
10
Hippocampal Circuitry
Known by tracer studies in monkeys, rats, and the
cat.
Sub
CA 1
PRC
ERC
PHG
DG
CA 3
fornix
Anterior
Posterior
11
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12
Normal Volunteer Anterior hippocampus
Normal E-4 Anterior hippocampus
Burggren et al
13
APOE e3/e3
APOE e3/e4
14
Cortical Thickness
15
Hippocampal Circuitry
Known by tracer studies in monkeys, rats, and the
cat.
Sub
CA 1
PRC
ERC
PHG
DG
CA 3
fornix
Anterior
Posterior
16
AD vs. Normal Aging Change Over Time
17
MRI grey matter loss/time
18
Functional MRI
19
Face-Name Association Zeineh et al, Science, 2003
Distractor
Learn Face-Name Pair
Covert Name Recall
Learn
Recall
Learn
Recall
Learn
Recall
Learn
Recall
D
D
D
D
Rest
Rest
Time
7 minutes
20
fMRI in normal subjects with genetic risk for
ADBookheimer, Small, et al, NEJM 2000
  • Purpose use fMRI to identify changes in brain
    function prior to significant cognitive decline
    predict outcome
  • APOE-3 vs E-4 extremely healthy older volunteers
    (X63.5 N30)
  • Memory stress-test in cognitively normal
    elderly
  • Memorize unrelated word pairs justice-club
  • Memorize new faces and names

21
Correct
22
Group Analysis Effect of Genotype
23
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24
What if the test is easier?
25
What if the test is hard, with no memory
643
26
Do fMRI abnormalities in APOE-4 predict outcome?
  • 2-year Neuropsychological outcome
  • Diagnosis of AD
  • fMRI Follow-up

27
2-year outcome conversion to AD
  • Seven subjects lost to illness
  • 4 developed AD
  • 3 other illnesses (cancer)
  • All those converting to AD had APOE-4
  • All others did not

28
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29
Relationship between memory decline and fMRI
change

N3
30
fMRI in APOE e4 at Follow-up Maintainers gt
Decliners
Z - 6
Z - 4
Z 2
L
R
31
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32
Young Normal Volunteer
MCI
33
Does treatment affect brain activity?
  • Donepezil (Aricept) treatment
  • 6 weeks on drug
  • Memory fMRI before and after

34
Donepezil Treatment- Mild AD
Pre-Treatment
Post-Treatment
Related Paired-Associate Learning vs. Rest
35
PET Scanning
New Isotopes -direct measures of
amyloid -measures of neurotransmitters
36
PET Positron Emission Tomography
  • Uses radioactive materials to track specific
    aspects of brain function
  • Add a radioisotope to something the brain uses
    glucose (18FDG) water (H2 15O)
  • Neurotransmitter or precursor (dopamine,
    serotonin, etc)
  • Attach to amyloid plaques

37
PET Scanner
38
CMRgI Abnormalities in Probable Alzheimers
Dementia
39
Correlations Between APOE ?4 Gene Dose and
Reductions in Regional CMRgl (36 HM, 44 HT, 78 NC)
PF
PF
TP
TP
PC
PC
P lt 0.005
40
Positron Emission Tomography (PET) Glucose
Metabolism
41
PET AND GENETIC RISK FOR AD
NORMAL MEMORY
DEMENTIA
PET Imaging
-22
-20
-12
-18
Genetic Risk
? Lower inferior parietal metabolism in
non-demented persons with a single copy of APOE-4
Small et al, PNAS 2000 976037-6042
42
Imaging Amyloid Plaques and Tangles with PET
FDDNP J. Barrio G. Small
  • DDNP 1,1-dicyano-2-6-(dimethylamino)-2-naphthal
    enylpropene
  • Lipophilic small molecule probe
  • Fluorinated analogue (18F-DDNP) provides
    visualizations of plaques, tangles and diffuse
    amyloid

43
Plaques and Tangles
44
FDDNP Autoradiography
Control brain
AD brain
45
FDDNP PET in AD, FTD and normal aging
46
Hippocampal distribution in AD
47
FDDNP in AD, MCI and NC
48
DDNP and MMSE Score
10.0
7.5
Residence Time (min.)
5.0
2.5
r -0.66
0.0
0
10
25
5
15
20
35
30
MMSE
49
DDNP and APOE-4 Genotype
50
Relationship to cognition
51
Pittsburgh Compound B PIB
From Klunk et al 2004 Annals of Neurology
52
PIB and FDG Distribution
From Klunk et al 2004 Annals of Neurology
53
Serotonin 1-a Receptor Mapping 18F-MPPF
18F MPPF Integration with Structural MRI
54
Serotonin 1-a receptor density in AD
55
18F-MPPF in AD relationship to memory
56
Why is imaging important?
  • Potential to detect the preclinical stage
  • Treatments will more likely slow or halt, rather
    than reverse, the disease
  • Identify an earlier time to intervene
  • Help determine when and with whom to intervene
  • Useful as a marker of change/intervention effects
  • Imaging outcome measures vs. disease outcome

57
Result of Treatment
Treatment
Onset
Cognitive Function
Presymptomatic stages
AD
Time
58
Predicted Result of Early Treatment
Early Treatment
Onset
Cognitive Function
Presymptomatic stages
AD
Time
59
Possible Result of Earlier Treatment
Improvement
Onset
Cognitive Function
Presymptomatic stages
AD
Time
60
Diagnosis and Prevention in the Future
Brain Stress (MRI)
Neuron Function (PET)
Brain Aging Index
Brain Amyloid (PET)
Shrinkage (MRI)
Genetic Risk (Blood test)
Memory Scores
61
Thanks!
Dr. Gary Small Dr. Jorge Barrios Dr. Vladimir
Kepe Dr. Linda Ercoli Dr. Karen Miller
Dr. Alison Burggren Meredith Braskie Dr. Paul
Thompson Kiralee Hyashi
UCLA Brain Mapping Center UCLA Center on Aging
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