Lecture 4: Neuroimaging Flashcards

1
Q

What is an MRI scanner?

A

originally developed for structural imaging, more recently also used for functional brain imaging (functional Magnetic Resonance Imaging – fMRI)

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2
Q

What are the benefits of MRI scanners?

A
  • Non-invasive
  • High spatial resolution
  • Reasonably affordable
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3
Q

What are the magnetic details of an MRI?

A
  • Very strong magnet: usually 1.5 – 7 tesla
  • 1.5 tesla = 15,000 gauss
  • Earth’s magnetic field strength = 0.5 gauss
  • Exeter MRI scanner = 30,000 X earth’s magnetic field strength
  • NO METAL IN THE SCANNER!!!
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4
Q

What is a Blood Oxygen level Dependent (BOLD) signal?

A
  • When neurons become active, blood flows to the part of the brain to provide oxygen to fuel the cells.
  • Hemoglobin (the iron-containing oxygen transporting protein present in blood) differs in how it responds to magnetic fields, depending on whether it has a bound oxygen molecule
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5
Q

What does an MRI scanner detect?

A

Small changes in the magnetic field

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6
Q

What does an fMRI do?

A

Measure blood flow
- the magnetic properties of oxygenated vs deoxygenated blood

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7
Q

What are the steps from raw data to functional brain activation maps?

A
  1. Design a task to be used in the scanner
  2. Collect some data
  3. Preprocess the data
  4. Data analysis
  5. Interpret your results
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8
Q

What is an experimental design of an fMRI?

A
  • BOLD signal is arbitrary: It has no stable baseline.
  • Therefore, the most important aspect of any fMRI experiment is that we have to provide both a) an experimental condition and b) a baseline condition.
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9
Q

What is a good baseline condition for an fMRI?

A
  • One that differs from the experimental condition only by the process of interest
    • E.g. Face processing.
    • Baseline = scrambled faces
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10
Q

What are block vs event-related designs?

A
  • BOLD signal is slow – peaks 4-5 seconds after stimulus onset and takes around 16 seconds to return to baseline
  • All fMRI experiments originally employed block designs – long periods of alternating task/baseline performance
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11
Q

What are the disadvantages of block designs?

A
  • Block designs often group together lots of trials
  • Limitations (Psychological)
    • Highly predictable occurrence of stimuli: subjects know what is coming and may alter strategies accordingly (not always a pro)
    • Inflexible for more complex tasks: impact of oddball stimuli? or stimuli or events that occur uncontrollably?
    • Ecological validity. Does blocking trials change the psychological process you are interested in?
  • Can’t separate trials by performance – e.g. to look at activation associated with correct vs incorrect response
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12
Q

What is an alternative to a block design?

A

Event related design

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13
Q

What is an event related design?

A

Trials of different conditions are randomly intermixed and occur close together in time

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14
Q

What are the advantages of event -related designs?

A

In freeing us from the necessity of block designs, event-related fMRI enables us to design more complex and novel experiments.

  1. Flexibility and randomisation
    • eliminate predictability of block designs
    • avoid practice effects
  2. Post hoc sorting
    • (e.g., correct vs. incorrect, aware vs. unaware, remembered vs. forgotten items, fast vs. slow RTs)
  3. Can look at novelty and priming - rare or unpredictable events can be measured
    • e.g., P300
  4. Can look at temporal dynamics of response
    • Dissociation of motion artifacts from activation
    • Dissociate components of delay tasks
    • Mental chronometry
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15
Q

How is best to collect data in an fMRI?

A

To reference each point in the brain in 3D space we divide image into cubes or ‘voxels’

  • Typical voxel size = 3x3x3 mm
  • Refer to each voxel with coordinates (x,y,z)
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16
Q

How to preprocess the data in an fMRI?

A

Correcting for non-task-related variability in experimental data

  • Getting rid of the ‘noise’
17
Q

What are the steps of preprocessing the data of an fMRI?

A
  1. High pass filtering
    • Remove low frequency oscillations such as scanner drift that introduce noise into your data
    • Standard low pass filter is approx 120 secs
  2. Motion correction
    • Keep track of how the head moves through relaxation versus stress
  3. Slice time correction
    • Temporal difference between slices collected so need to shift back into alingment
  4. Coregistration
    • align functional data with structural data
  5. Normalisation
    - Standardised Space
    • Montreal Neurological Institute (MNI) space
      • Combination of 352 MRI scans on normal controls
    • Why normalize? So that we can compare activation across subjects and do group analyses.
  6. Spatial smoothing
    • Application of Gaussian kernel
    • Why smooth?
      • Because neurons do not fire in isolation.
      • If a neuron fires, neurons close to it will tend to fire as well.
      • Smoothing attempts to model the data according to this property of neurons.
18
Q

How best to analyse data in an fMRI?

A
  • Multiple regression is used to determine the effect of a number of independent variables (our conditions) on a single dependent variable (brain activation)
  • For each voxel, we use multiple regression to estimate how closely the BOLD signal correlates with the timecourse of each condition – resulting beta values tell us how close this correlation is.
  • Finally perform a contrast – simply a t-test comparing beta condition 1 beta values to condition 2 beta values
  • Calculating the t-statistic for each of the 130,000 voxels in the brain is equivalent to asking “in which regions is activation greater in condition 2 than in condition 1?”
  • Raw t-map indicates the magnitude of the t-statistic using a colour scale - Yellow = bigger t values
  • The threshold we apply defines what we accept as a significant difference in activation between our 2 conditions
  • Essentially arbitrary (as it is in any statistical procedure)
19
Q

What are the effects of difference thresholds on brain activation maps?

A
  • Where do we ‘draw the line’?
    • Standard alpha level in psychological research is p < 0.05, i.e. we accept a 5% rate of false positives
20
Q

What is the correlation for multiple comparisons?

A
  • Brain images divided into up to 130,000 voxels= 130,000 individual t-tests
  • Chance of a type 1 error (false positive) increases with every test performed
    • With an alpha level of p < 0.05 (standard used in psychological research) with one t-test we have a 5% chance of type 1 error.
    • With 100 independent t-tests, we have a 99.4 % chance of type 1 error
    • In other words, with 130,000 t-tests and an alpha level of 0.05 we are guaranteed to find some significant voxels simply by chance.
    • Very important to correct for multiple comparisons – adjust alpha level (p-value)
21
Q

What are the two difference approaches to data analysis?

A
  1. Whole brain analysis - as we have just seen, examine effects on a voxel by voxel basis across the whole brian
  2. Region of interest (ROI) analysis - restrict out anaylsis to a particular brain region
22
Q

What are the advantages of a whole brain analysis?

A
  • Requires no prior hypotheses about areas involved
  • Includes entire brain
23
Q

What are the disadvantages of a while brain analysis?

A
  • Can lose spatial resolution with inter-subject averaging
  • Can produce meaningless “laundry lists of areas” that are difficult to interpret
  • Depends highly on statistics and threshold selected
  • Multiple comparisons problem
24
Q

What are the advantages of a region of interest analysis?

A
  • Hypothesis driven – avoids meaningless ‘laundry lists’ of activated regions.
  • Avoids multiple comparisons problem – data summarised in a single number per subject reflecting mean activation across voxels in ROI.
  • Simple – data can be exported and treated as any other type of data, requiring no special software for further analysis
  • Generalisable – data can easily be compared across studies, e.g. for meta analysis.
25
Q

What are the disadvantages of a region of interest analysis?

A
  • Easy to miss things going on elsewhere in the brain.
  • Not always simple how to define ROIs.
26
Q

How do you interpret the results from an fMRI?

A

From raw data to functional brain ‘activation’ maps

27
Q

What are the limitations of an fMRI?

A
  • fMRI data is correlative, therefore we can’t say that a region activated during a task/function is essential for that task/function.
    • Need converging evidence from TMS/neuropsychology to make stronger inferences about causation.
  • Temporal resolution of fMRI is low
    • Need converging evidence from EEG/TMS to provide finer grained temporal information.