Advanced Methods - PowerPoint PPT Presentation

1 / 21
About This Presentation
Title:

Advanced Methods

Description:

Effective and Functional Connectivity Analysis. Alternative measures of activation ... Photic dots vs fixation. Motion moving vs static. Attenton detect changes ... – PowerPoint PPT presentation

Number of Views:91
Avg rating:3.0/5.0
Slides: 22
Provided by: chrisr6
Category:

less

Transcript and Presenter's Notes

Title: Advanced Methods


1
Advanced Methods
  • Chris Rorden
  • Advanced fMRI designs
  • Adaptation fMRI
  • Sparse fMRI
  • Resting State fMRI
  • Advanced fMRI analysis
  • ICA
  • Effective and Functional Connectivity Analysis
  • Alternative measures of activation
  • Perfusion
  • msMRI
  • Comparing SPM to FSL

2
Adaptation Designs (from Kanwisher)
  • Show two stimuli in rapid succession.
  • See if a brain region can discriminate if these
    stimuli are the same or different.
  • Classically, regions show adaptation less time
    to process same information twice in a row.

3
Adaptation Designs
  • FFA activates strongly to faces
  • Does it discriminate yes we see adaptation
    response.
  • Similar adaptation is not seen for chairs, so
    suggests special role in face processing.

4
Sparse fMRI
  • Standard fMRI acquires data continuously.
  • Loud noises can make it difficult to examine
    auditory stimuli.
  • Sparse imaging includes a delay between each fMRI
    volume, so stimuli can be presented while scanner
    is silent.

Continuous
Time (sec)
0
10
Sparse
Time (sec)
0
10
5
Sparse fMRI
  • Typically, sparse design like a block design
    each acquisition measures effect of single
    stimuli.
  • Stimuli must be presented 5sec prior to
    acquisition.
  • Sparse designs have less power than continuous
    designs, and it is difficult to estimate latency
    of BOLD response.
  • Due to T1 effects, Sparse designs can still have
    good power.

Sparse
Time (sec)
0
10
6
Resting State fMRI
  • Resting state fMRI allows us to estimate natural
    connectivity between regions which regions cycle
    together.
  • Essentially, have individual lie in scanner
    resting while you collect a lot of fMRI data.
  • Must covary out low frequency scanner drift as
    well as high frequency physiological noise.

7
Independent Component Analysis
  • In conventional analysis, we see if a HRF
    predicts our behavioral design.
  • FSL includes MELODIC for ICA, includes nice
    description
  • www.fmrib.ox.ac.uk/analysis/research/melodic/
  • In ICA, we decompose fMRI data into different
    spatial and temporal components.
  • estimate the BOLD response.
  • estimate artifacts in the data, then run
    conventional analysis on denoised data.
  • find areas of activation which respond in a
    non-standard way.
  • analyse data for which no model of the BOLD
    response is available (e.g. resting state fMRI).

8
ICA vs Conventional Analysis
  • Conventional analysis is confirmatory does my
    model predict data.
  • Results depend on model
  • ICA is exploratory Is there anything interesting
    in the data?
  • Can give unexpected results.
  • What is the potential of ICA?
  • FSL includes melodic, so you can examine our
    data.
  • Many use melodic to remove artifacts.

9
Connectivity
  • Classic fMRI detects all regions involved with
    task
  • Motor task would elicit motor cortex, cerebellum
    and supplementary motor area.
  • It would be much more insightful if we could see
    the direction of connections
  • Examples include Dynamic Causal Modelling

10
Psycho-physiological Interaction (from Henson)
  • Parametric, factorial design, in which one factor
    is psychological (eg attention)
  • ...and other is physiological (viz. activity
    extracted from a brain region of interest)

V1 activity
time
Attention
attention
V5 activity
no attention
Attentional modulation of V1 - V5 contribution
V1 activity
11
Effective vs Functional Connectivity (Henson)
  • No connection between B and C,
  • yet B and C correlated because of common input
    from A, eg
  • A V1 fMRI time-series
  • B 0.5 A e1
  • C 0.3 A e2

Correlations A B C A 1 B 0.49 1 C
0.30 0.12 1
0.49
-0.02
?20.5, ns.
0.31
12
SPM2 Dynamic Causal Modelling (Henson)
Attention
Photic
.52 (98)
.37 (90)
.42 (100)
.56 (99)
.69 (100)
.47 (100)
Büchel Friston (1997)
.82 (100)
Motion
.65 (100)
Friston et al. (2003)
13
Functional Connectivity
  • Observe which regions activity correlates.
  • Can be done while resting in scanner
  • Hampson et al., Hum. Brain. Map., 2002

14
Perfusion imaging
  • Use Gd or blood as contrast agent.
  • Allows us to measure perfusion
  • Static images can detect stenosis and aneurysms
    (MRA)
  • Dynamic images can measure perfusion (PWI)
  • Measure latency acute latency appears to be
    strong predictor of functional deficits.
  • Measure volume
  • Can also measure task-related changes in blood
    flow (ASL), similar to fMRI.

15
Arterial Spin Labeling
  • Tag inflowing arterial blood
  • Acquire Tagged image
  • Repeat scan without tag
  • Acquire Control image
  • Subtract Control image Tagged image

2
1
The difference in magnetization between tagged
and control images is proportional to regional
cerebral blood flow http//www.umich.edu/fmri/
asl.html
4
3
16
ASL
  • MR signal is based proportion of atoms aligned
    with the magnet than without.
  • Slightly lower energy state aligned, so atoms
    preferentially align.
  • More alignment in higher fields
  • However, 180 pulse will reduce this signal.

3T Net Magnetization
  • ?


3T NM after 180 pulse
?

17
Data from MCBI
  • We collect 16 slices 3.5x3.5x6mm
  • TR 2.2sec (4.4sec for tagcontrol pair).
  • TE12ms (very little BOLD artifact).
  • Not wise to collect ASL faster than 2sec
    (otherwise, not enough transit time between
    volumes. Wise to use slower TR for individuals
    with impaired perfusion (stroke).
  • Control
  • Tagged
  • Difference

18
Theory Signal in ASL
  • Tagged image Inflowing inverted spins within the
    blood reducing tissue magnetization more flow
    darker
  • Control Inflowing blood has increased
    magnetization than saturated tissue more flow
    brighter

Control Tagged
Acquisition
Perfusion Signal
Control Tagged
Observation
Mumford et al. (2006)
19
Analysis
  • Easy to analyze ASL data with FSL
  • Select perfusion check box
  • FSL simply subtract tagged image from neighboring
    control
  • FSL is not optimal
  • Control and tagged image are not acquired
    simultaneously
  • Therefore, they sample different points of HRF.
  • There are alternatives
  • Sinc interpolate to estimate simultaneous signals
    (interp_asl)
  • Intertrial subtraction compare control image
    with tagged image that was collected at same
    delay after event (Yang et al, 2000).
  • Add both tagged and control images in a single
    model (Mumford et al, 2006).
  • In general, FSL approach only good for block
    designs.

20
Arterial Spin Labelling
  • Benefits
  • Direct measure of blood flow
  • Less drift Better for assessment of very slow
    (gt1min) changes.
  • Data whiter (less dominated by low frequency
    noise)
  • Signal more from tissue than veins.
  • Less spatial distortion than BOLD (BOLD requires
    long TE without spin-echo)
  • Perhaps better statistical power for group
    analysis (calibrated measure has less
    variability).
  • Disadvantages
  • Requires two images tagged and subtraction,
    therefore TR is twice as long.
  • Less statistical power for individual (fewer
    samples)
  • Can not collect many slices can only see portion
    of brain, normalization difficult (hurts group
    statistics)

21
Magnetic Source MRI
  • fMRI BOLD is very indirect measure.
  • Can we directly measure brain activity?
  • Neural firing influences magnetic field (e.g.
    MEG).
  • Potential of msMRI
  • Stroke patients where blood flow is abnormal
  • Is this effect big enough to measure?
  • How would you design a msMRI study?

Image
Phasemap
Write a Comment
User Comments (0)
About PowerShow.com