6.2 fMRI 2 Flashcards

(35 cards)

1
Q

What is an important step after fitting a model to your fMRI data?
(after convolving + adding linear ramp)

A

creating a statistic which tells you how well the model fits the data (model fit goodness)

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2
Q

What is the amplitude parameter called in a fMRI model of the fMRI data?
What sort of parameter should it be?
How is it calculated? what model is it in?

A

-Beta = amplitude parameter
-free parameter so you can adjust it based on the data
-Beta estimates by a computer algorithm (usually a GLM)

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3
Q

What is the residual noise?

A

residual noise is the calculated error between the model function and the acquired data (at each data point)

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4
Q

What is the equation for the GLM model? What does each variable mean?
What does the GLM show?

A

y = XBeta + e
y=voxel time series data
X=design matrix (red line)
Beta = regression parameter (eg amplitude)
e = Gaussisan noise/residual noise

shows the pattern that the fMRI data follows

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5
Q

What does the t statistic tell?
How do you calculate it?

A

-the RATIO of the fitted amplitude to the residual noise
- t stat = Beta/residual noise (e)

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6
Q

What does it tell you about model fit when the t stat is low or high?

What values give a high t stat?

A

low = bad model fit
high = good model fit

higher the t stat, the better the model fit

high amplitude, low residual error => high t stat, good model fit

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7
Q

What is the H0 null hypothesis for an fMRI experiment?

A

H0 = there is no activation

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8
Q

What is the t stat formally defined as in an fMRI experiment?
What are each term in the definition mean? 3 terms

A

the ratio of the departure of the estimated value of a parameter from its hypothesised value to its standard error

hypothesised value = no activation

departure = Beta

standard error = residual noise

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9
Q

Is fMRI data qualitative of quantitative?
What does fMRI data/images rely on to give it meaning

A

fMRI is qualitative! arbitrary signal changes
the signal contrast generated between different states eg at rest, task, different tasks

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10
Q

What is a block design?

Is the same trial type used in each block? WHY?

What is block design in layman’s terms?

A

-alternates between rest and task intervals of time called blocks. Task block consists of many closely spaced successive trials (over a short interval of time).

-utilises blocks of identical trial types to establish a task-specific condition.

you have a task block and a rest block with each a length of 20s

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11
Q

What experiment was block fMRI derived from?

A

PET trial

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12
Q

What is the advantage of using block design for fMRI?

A

-best design for detecting BOLD signal amplitude differences between states
-fairly robust when there is uncertainty to the timing/shape of haemodynamic response because block duration is usually longer than the haemodynamic response
-most efficient for acquiring more trials in less time than other designs because you don’t have to worry about spacing the individual trials apart to get an estimate of each individual event
you can put a lot of trials into each block eg you dont have to worry about the spacing between each finger tap in a block

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13
Q

Why must you repeat tasks many times in the task block for block design fMRI experiments? eg tap finger repeatedly for 20s

A

lots of baseline noise and the BOLD effect is only a small percentage change in signal maybe 3% -> repeated action to get a significant result

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14
Q

For fMRI terminology what is a trial?

A

stimulus presentation followed by a response.

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15
Q

What are the disadvantages of using block design for fMRI?

A

-stimuli are highly predictable and may affect patient’s response strategy/ no surprise element
-inflexible for more complex tasks: can’t use oddball stimuli within a block as you can’t distinguish between trial types in a block
-does not account for transient responses at the start/end of the task: takes subject a second to process the task
-block trials can also change the psychological process you are interested in
-determining appropriate baseline condition can be challenging - what is the best way to design experiment to show significance?

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16
Q

What are the main types of fMRI experimental design?

A

block
slow event related
fast event related
mixed design

17
Q

What is slow event related (ER) design?

A

a short stimuli separated by an inter-stimulus interval (ISI) which allows allows enough time for the haemodynamic response to fall back to baseline before the next trial
usually about 10-20s

18
Q

What are the advantages and disadvantages of slow event related design?

A

-can isolate individual BOLD responses to a single trial because of the long ISI
-more exploratory - good if you dont know what the haemodynamic response will be for your experiment -> you can estimate it from slow event

-it makes experiments longer -> so only used when necessary

19
Q

What is unique about the shape of the GLM model which fits slow event related data?

A

once the model is convolved with the haemodynamic response function (HRF) -> the signal always return back to baseline after a stimulus because of the long ISI

20
Q

What is fast event related design?
What is the advantage of this design?
What are the disadvantages?

A

-short stimuli presented in a random order separated by short and jittered ISI

-you can put odd ball stimuli, events can be trully randomised
-faster than slow ER

-less sensitive to signal change = 1% whereas block design is 3%
-issues with truly randomising the order of the trials
-more complicated model fit and statistics

21
Q

What does the GLM model look like for a fast event related study?

A

some peaks merge together, a mix of ISI so not all peaks go back to baseline, (not usually colour coded as its difficult to clearly separate stimuli in a convolved model

22
Q

What is the most commonly used experimental design for complicated tasks?

A

fast event related design

23
Q

What is mixed design?

A

builds on block design but with different stimuli within same blocks

24
Q

What are some examples of good practice in fMRI?

A

-use appropriate stimulus
-collect as much fMRI data as possible and data from as many participants
-if you can do a block design -> do it to maximise BOLD signal
-get a measure of the subject’s bahaviour in the scanner: are they actually doing the task?

25
Which design is the best choice?
try block first if you cant do that then do fast ER, then slow ER
26
What is the number of Beta values and design matrices changed by in an fMRI experiment? How does this change from block to ER designs?
-one Beta/design matrix per stimulus TYPE (eg 2 for places and faces) -block usually has lower number of Betas/design matrices than ER designs as block is chosen for simpler experiments
27
What are COPEs? What is the purpose of COPEs? Give an example of a COPE combination?
Contrast Of Parameter Estimates: its a statistical comparison which evaluates linear combinations of Beta weights which associated with different experimental conditions/stimuli. show where voxels activate in experiments with more than one stimuli/Betas/regressors eg Beta1 is a picture of faces and Beta2 is a picture of places. Beta1 -Beta2 = voxels where Faces activate more than Places
28
Is the GLM fitted in every voxel? Why?
yes it is to show a map of Beta values or residual noise e values
28
How do you decide the threshold to show which voxels show statistical significance?
29
What was the issue with fMRI data in the early days?
there was a slider to for the t statistic threshold for each voxel and most researchers just determined the threshold values based on what 'looked right'
30
What is the value under t value distribution curve? Why is this important?
area under curve = pvalue when pvalue is 0.05 or less -> t value threshold -> significant, active voxel
31
Why is it important for fMRI data analysis to transform t values to z values? How is this achieved?
- the pvalues (from T-stat) vary depending on the number of DOF even if the tvalues stays the same. converting t to z values STANDARDISES INTERPRETATION-> makes consistent thresholds across studies so they can be compared/ no false positives use a probability preserving transform
32
What issue in fMRI credibility did the dead salmon study raise?
you test every voxel 100s or 1000s and if you don’t correct for multiple comparisons -> some voxels will appear “active” just by chance -> false positives this is because fMRI studies were not pcorrected tvalues depenedent on DOFs
33
What are some potential multiple comparison corrections used in fMRI? what are the positives and negatives of each test?
-Bonferroni: strong control over false positives but the least sensitive to signal change as it assumes all voxels are independent of each other (too harsh) -Gaussian Random Fields: strong control over false positives but somewhat conservative -False Discovery Rate: admits false positives but is more lenient than the others -Cluster Enhancement
34
The larger the Z stat, what happens to the likelihood that the voxel is active or has significant activation?
as z stat increases, likelihood of significance increases