fMRI Flashcards

(111 cards)

1
Q

what does fMRI BOLD signal measure

A

The changes in oxygenated vs deoxygenated blood in response to neuronal activity’s demand for oxygen.

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2
Q

What is spatial resolution?

A

The size of each voxel (e.g., 2×2×2 mm). Smaller voxels → better detail but lower SNR.

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3
Q

Why is fMRI a low-SNR modality?

A

Because BOLD changes are tiny (~1–5%), heavily affected by thermal and physiological noise.

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4
Q

What drives BOLD signal?

A

Neuronal activity increases oxygen demand → triggers vasodilation → more oxygenated blood enters region → changes ratio of oxygenated to deoxygenated hemoglobin, which alters the MR signal.

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5
Q

Describe magnetic properties of oxygenated vs deoxygenated hemoglobin

A

Oxygenated hemoglobin: diamagnetic, meaning it does not disturb local magnetic
fields

Deoxygenated hemoglobin: paramagnetic: distorts local magnetic fields and reduces BOLD signal

Therefore, the presence of deoxy blood is what creates the magnetic field differences;
when oxygen is pumped in, deoxy levels go down, making BOLD signals stronger

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6
Q

Why does oxygenated vs deoxygenated blood matter?

A

Oxygenated hemoglobin is diamagnetic (does not distort the field), while deoxygenated hemoglobin is paramagnetic (distorts field and reduces signal). More oxygenation → stronger BOLD signal.

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7
Q

Why is T2 weighted imaging used in

A

Because T2 is sensitive to magnetic field inhomogeneity caused by deoxyhemoglobin

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8
Q

Describe the HRF and its characteristics

A

It is the characteristic shape of BOLD signal over time, reflecting the physiological mechanism underlying the signal captured by fMRI.

20-30 seconds and is; a rise peaking at
5-6s after stimulus onset and a decay back
to baseline in the remaining 15-25 seconds.

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9
Q

is the HRF constant across individuals

A

has some variance (within and between individuals), but it is robust enough
to serve as the basic building block in fMRI modelling software, usually approximated using gamma functions.

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10
Q

Why do we convolve regressors with the HRF?

A

Because the BOLD response is delayed and smoothed; convolution models how neural events generate predicted BOLD timecourses.

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11
Q

What is T2 weighting?

A

Contrast based on local magnetic field inhomogeneities—critical for measuring BOLD.

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12
Q

What is the difference between T2 and T2*?

A

T2: Loss of phase coherence due to proton–proton interactions

T2* Includes T2 decay + magnetic field inhomogeneities

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13
Q

In fMRI what changes with higher field strength?

A

Higher SNR (signal-to-noise ratio)

Stronger T2* sensitivity → stronger BOLD contrast

More susceptibility artifacts (more distortion near sinuses, orbitofrontal cortex, temporal poles)

Shorter T2* values overall

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14
Q

Why don’t we use T1-weighted sequences for fMRI?

A

T1-weighted imaging is too slow and does not capture rapid changes needed for BOLD.

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15
Q

What is a localiser scan?

A

A localizer scan is a functional scan designed to activate a known brain region so that this region can be identified in each participant for ROI-based analysis.

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16
Q

What is a localizer scan usually?

A

Short (1–3 minutes)

Simple task that strongly drives the target area

High-contrast condition pair (faces vs houses, motion vs static, words vs scrambled)

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17
Q

What is a block design

A

Repeated stimuli of the same condition presented in blocks; produces strong signal-to-noise but cannot separate individual trials.

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18
Q

What is an event-related design

A

Each trial modeled individually; flexible, supports trial-level effects, but lower signal-to-noise.

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19
Q

When would you do a block related design vs an event related design

A

You would use a block design for tasks that are sustained over time when you need high statistical power to detect activity, such as language or motor tasks. In contrast, you would choose an event-related design for tasks where you need to study individual, transient responses, when the order of stimuli needs to be randomized, or when events cannot be blocked

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20
Q

When are short TRs better and why?

A

Short TRs are better when high temporal resolution is needed (event-related designs), but they increase physiological noise.

Long TRs are better for block designs; higher signal-to-noise but more motion sensitivityf

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21
Q

Explain field strength

A

● The strength of the main magnetic field in, measured in Tesla
● A higher field strength corresponds to stronger magnetic resonance signal
○ This leads to a higher signal to noise ratio and thus better spatial resolution
○ Also better sensitivity to small changes in brain activity
○ But it can also lead to greater susceptibility to signal distortions

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22
Q

What does a higher field strength correspond with

A

A higher field strength corresponds to stronger magnetic resonance signal
○ This leads to a higher signal to noise ratio and thus better spatial resolution
○ Also better sensitivity to small changes in brain activity
○ But it can also lead to greater susceptibility to signal distortions

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23
Q

What are RF pulses

A

Pulses of electromagnetic energy that excite hydrogen protons in the body

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24
Q

What does resonance refer to

A

The protons’ response when the pulse is turned

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25
Explain what happens when an RF tuned to a certain frequency is applied
The protons it is applied to spin out of their usual alignment ● When they relax back into their usual alignment they release energy which emits the magnetic resonance (MR) signal ○ How the pulses are applied (in what timing and pattern) determines the type of image that is produced (t1, t2, etc.)
26
Flip angle
angle by which the RF pulse disrupts the spin of the protons measured in degrees or radians and it can be adjusted by changing the RF pulse's strength or duration, to optimize the BOLD signal
27
The two TR definitions
**Physics perspective: **Time between RF pulses applied to the same slice. **fMRI perspective: **Time between the start of one whole-brain volume and the next.time between RF pulses; crucial time interval between each volume acquisition
28
What determines the minimum TR?
The number of slices × the time to acquire each slice. More slices = longer TR unless
29
What is echo time and what does it determine
delay between that RF pulse and MR signal reading. It determins T2* sensitivity.
30
Why is TE important for BOLD?
BOLD is a T2 effect; TE must be set near the T2 of tissue (~30 ms at 3T) to maximize sensitivity to oxygenation changes.
31
What is a volume
A complete 3D picture of the entire brain taken at a single moment, created by stacking up all the individual (horizontal) slices acquired during the specific moment in time, sequentially
32
What are slices and what are the two types
A slice is a 2D cross-section of the brain. -when a fmri scanner takes a ‘picture’ it cannot capture the whole 3D brain at once, instead it takes a series of these flat 2D slides sequentially - two types of slice capturing: in order (ascending or descending) = sequential acquisition, or alternating = interleaved acquisition. The choice between one or the other depends largely on the type of scanner (e.g. Siemens vs Philips)
33
Slices and volumes in short
Slices are the 2D pictures, and a Volume is the complete 3D brain composed of all the slices collected over 1 TR
34
When is eye fixation preferred in resting-state scans?
When maximizing reliability and consistency of most RSNs (attention, auditory, DMN). Eyes-open no-fixation is best for primary visual network.
35
Contrast short TR vs long TR
**Short tr:** have lower signal to noise ratio, and are more suited for event-related designs. Are more susceptible to physiological noise. **Long tr:** More used in block designs; better signal to noise ratio, but more sensitive to motion.
36
contrast short and long echo time
**Short TE:** stronger signal, because the signal is collected before it decays :( less contrast = change in active/inactive regions not as clear yet (BOLD response takes time to develop) **- Long TE:** strong contrast :( weaker signal
37
How is ideal flip angle estimated
Based on field strength (Tesla) and repetition time
38
What is field of view
The specific area of the participant’s body that is captured in the MRI image; it is the “window” captured by the scan, which has to be selected before the scan
39
Describe relationship between field of view and resolution
larger area = larger pixels and lower resolution smaller area = smaller pixels and higher resolution)
40
FOV effect on scan time
having a larger FOV can increase scan time, because there are more voxels of data being sampled
41
why do we want isotropic voxels?
because equal dimensions in x/y/z reduce bias in spatial normalization and smoothing
42
what is partial volume effect
when a voxel contains more than one tissue type, blurring signal interpretation (e.g. gray matter and white matter)
43
The different parts of preprocessing
1. slice timing correction 2. realignment/motion correction 3. coregistration 4. normalization 5. smoothing
44
What is multiband acquisition?
Technique that acquires multiple slices simultaneously to reduce TR and increase temporal resolution.
45
What is the tradeoff of multiband acquisition?
Higher temporal resolution but increased leakage artifacts and potential noise amplification.
46
What problem does interleaved acquisition solve?
It reduces cross-talk between adjacent slices caused by RF excitation overlap.
47
What issue does slice timing correction address
The fact that in a typical fMRI acquisition the 2D slices of a volume are not acquired simultaneously within one TR. Instead, the 3D image made within one TR (eg. 2 seconds) is made of multiple 2D slices, those slices are made at varying times (eg. slice 1 at 0s, slice 5 at 1.5s, slice 10 at 2.0s).
48
What does slice timing correction do
solves the problem presented by interleaved slice acquisition (which is done to control cross-slice excitation), when djacent slices of the brain acquired at non-adjacent time points
49
What is the reason for slice timing correction
- Reason: Help with temporal accuracy. Also depends on experiment type and setup (eg. TR length).
50
why is STC often placed before motion correction?
Because STC assumes that voxel locations are stable across time. Doin motion correction after STC avoids mixing motion artifacts with timing interpolation.
51
What does realignment/motion correction do?
It estimates and corrects for head movements occurring during scanning by rigid-body aligning each volume to a reference volume (typically the first or mean image) using 6 parameters: x/y/z translation and pitch/roll.yaw rotation.
52
why is realignment/motion correction needed?
Because fMRI relies on consistent spatial alignment between voxels across time, even small movements can distort results and introduce false correlations. The whole idea of localizing brain structures in fMRI hinges on the assumption that each voxel is in the same position throughout the whole scan So we have to account for movement in the data (remove movement artifacts)
53
Why does motion severely threaten fMRI validity?
Motion creates spurious changes in voxel intensity that mimic task effects, introduces systematic differences between conditions, and correlates with group membership (children, patients), producing false activations.
54
What are motion regressors?
The 6 estimated motion parameters (plus their derivatives/expanded terms) included in the GLM as nuisance regressors to model residual motion-related signal variation.
55
How does motion correction work
Realigning each brain image (volume) to a reference image - usually the mean, first, or last volume - using a rigid-body transformation. This accounts for three translations (x, y, z) and three rotations (pitch, yaw, roll). By aligning all the functional images together We quantify how much alignment is necessary - so how much each volume deferred from the reference We end up with movement parameters that we can incorporate in our analysis later on to control for movement And we can create a mean functional image to use later on in the coregistration
56
Output of realignment/motion correction
- quantify amount of movement in motion parameters to be used later on - create a mean functional image to use later on in the coregistration
57
What is the purpose of coregistration
Aligning the subject’s mean fMRI image (low resolution, T2) to their high-resolution anatomical T1 image. This ensures functional data overlays correctly on anatomy.
58
Why is coregistration challenging?
Because T1 and T2-weighted images have very different contrast (bright vs dark CSF, inverted tissue intensities), requiring intensity-based algorithms that maximize mutual information.
59
What is the process of spatial normalization
Warping each participant’s brain into a standard space (e.g., MNI) using nonlinear transformations, enabling voxelwise group comparisons.
60
What is the purpose of normalization
To make it possible to compare data across participants by reducing intersubject variability and facilitate reporting in the form of standard (x,y,z) coordinates. This means brain activity or anatomy can be analyzed and averaged at the group level.
61
What happens if normalization fails?
Group maps become anatomically misaligned, producing false positives/negatives because activation is smeared or misplaced across subjects.
62
What is smoothing
Spatial averaging: replaces the signal values of each voxel with a weighted average of the surrounding voxels using a small filter (called a Gaussian kernel)
63
What are the positive consequences of smoothing?
- Reduce random noise in the data, - Increase the signal-to-noise ratio (SNR) - Makes brain activity patterns more similar across participants (since everyone’s brain anatomy differs a bit). - Helps the data meet the statistical assumptions used later in analysis (like the General Linear Model). - Makes activity maps more comparable between participants
64
What is the purpose of smoothing
Increase SNR Increase normality of the data
65
What are the consequences of too much smoothing
This can blur important fine details, so the kernel size must be chosen carefully, usually around 4-10 mm, depending on voxel size and study goals
66
what is the correct order of preprocessing steps?
67
What is the goal of first-level analysis?
To model each voxel’s BOLD time series using the GLM and estimate how strongly each task condition explains the signal for that participant, producing β (beta) maps and contrast maps for group analysis.
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Basic definition of first level analysis
Estimate
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What is the GLM
A statistical model that explains each voxel’s BOLD timecourse as a combination of predicted responses to experimental events (after HRF convolution) plus noise. The GLM estimates a beta value for each predictor, and contrasts of these betas reveal which voxels respond more to one condition than another.
70
What does the GLM do conceptually?
It predicts how much each experimental condition and nuisance factor contributes to the BOLD signal at each timepoint and estimates those contributions for every voxel independently.
71
What is a time series
The sequence of signal intensity values measured from the same voxel (or ROI) across consecutive time points during the scan. It reflects how the BOLD signal in that location changes over time in response to neural activity, noise, motion, and physiological fluctuations.
72
What is the equation of the GLM
Y = Xβ + ε **Y**is the observed BOLD time series **X** is the design matrix (task regressors convolved with the HRF plus nuisance regressors to give predicted BOLD responses) **β** are the estimated parameter weights **ε** is the residual noise.
73
Is 1st level analysis within or between subjects
Within
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How are regressors estimated
By multiplying events/stimuli with HRF to produce predicted "convolved" BOLD signal
75
What does comparing the beta values of the GLM show us
Whether a voxel responds more strongly to one condition than another, revealing which brain regions are engaged by specific task conditions.
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What is model specification
the specific way study conditions are contrasted/analyzed in order to accurately extract BOLD signal information to your variables of interest – model specification is how you analyze the data; which contrasts, baselines and parameters are chosen
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Simple subtraction model
One method of model specification (A-B) Shows the difference in brain activation between a target and control task
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Factorial design
One type of model specification Contrasting multiple factors at different/multiple levels, so the conditions would be contrasts themselves. allows to test both main and interaction effects.
79
Parametric design
One type of model specification Used when a variable changes continuously (ex. increasing task difficulty). Tests whether brain activity increases or decreases linearly with that variable.
80
What is a design matrix
A matrix that encodes the predicted BOLD response for each task and nuisance regressor at every timepoint. It represents the experimental design (after HRF convolution) and forms the X in the GLM equation.ally showing what happened in the experiment and at what time. It is represented as the X in the GLM equation.
81
What is a beta weight?
A value estimating how strongly a regressor explains a voxel’s BOLD time series. Larger β = stronger relationship between that condition and the voxel’s activation.
82
What does comparing beta values tell us?
Whether a voxel responds more to one condition than another (e.g., β_faces > β_houses), revealing condition-specific neural activity.
83
What is a contrast?
A linear combination of beta weights (e.g., [1 –1]) that tests a specific hypothesis such as Condition A > Condition B. Produces a contrast map for each subject.
84
What does a contrast map represent?
Voxelwise values showing the estimated difference between conditions for that participant (e.g., Faces – Houses). These maps are inputs to second-level analysis.
85
what are nuisance regressors
Regressors included to model noise, such as motion parameters, physiological signals, session drifts, and outlier volumes, so they do not confound task-related betas.
86
What is collinearity in the GLM?
When two regressors overlap too much in predicted time courses, making it difficult to distinguish their contributions (unstable β estimates).
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How does the design matrix work?
Each column represents a predictor (regressor), such as a task condition, convolved with the HRF, or a nuisance/control variable (e.g., motion). Each row represents a time point (one TR), corresponding to each acquired brain volume.
88
What do the numbers in a design matrix show
The numbers in each column of the design matrix represent the predicted BOLD response for a condition at each timepoint, showing how much that condition is expected to contribute to the voxel’s signal at that moment.
89
What is a parametric modulator
A regressor added to the GLM that models how the BOLD response varies with a continuous trial-by-trial variable (e.g., intensity, rating, reaction time).
90
What does the beta of a parametric modulator represent?
Whether the voxel’s activation increases, decreases, or remains constant as the parametric value increases across trials.
91
What is serial autocorrelation in fMRI?
Adjacent timepoints are not independent because the BOLD response is slow. Prewhitening or temporal filtering corrects this violation of GLM assumptions.
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What is overspecification?
Including too many regressors (especially correlated ones), limiting the model’s ability to estimate β reliably and increasing noise.
93
What is functional connectivity
The temporal correlation of different BOLD signals within different areas of the brain.
94
What does functional connectivity show in resting-state fMRI
FC shows intrinsic brain networks. E.g. sensory networks, attention.
95
What does functional connectivity show in a task-based fMRI
FCs shows that the relationship between different regions of the brain changes based on the task.
96
What is psychophysiological interaction analysis (PPI)
A method for assessing how functional connectivity between two brain regions changes depending on the psychological context or task condition. Testing whether functional coupling between areas is stronger or weakter depending on different psychological contexts or task blocks.
97
What do significant PPI results indicate
Context-dependent changes in connectivity between the seed region and other regions across the brain.
98
What is dynamic causal modelling
A model-based method that estimates the directed (causal) influences that brain regions exert on each other and how these effective connections are modulated by experimental conditions. ## Footnote DCM is about effective connectivity (directed causal influence), not functional connectivity (correlation).
99
What are resting state networks (RSNs) characterized by
Resting State Networks (RSNs) are characterized by large-scale patterns of functional connectivity that are consistently observed across individuals, sessions, scanners, and analytic approaches when no explicit task is being performed.
100
Describe traditional RSN design
Participants are instructed to keep their eyes closed and not think about anything or fall asleep. Alternatively, participants keep their eyes open and fixate or don’t fixate on objects in the visual field.
101
What is the best RSN design if reliability and consistency are the concerns
Eye fixated condition preferred (exception: when monitoring primary visual network connectivity is more reliable with eyes open without fixation.)
102
What is the best RSN design if the focus is on increasing functional connectivity strength
Eyes open fixated or non fixated condition to be used
103
What is statistical power?
the probability of correctly rejecting the null hypothesis when a true effect exists (i.e., 1 – Type II error).
104
What determines statistical power according to the paper?
Sample size (n) True effect size Statistical threshold / Type I error rate (α)
105
What does second level analysis do
combines the first-level results from all participants to test whether an effect is reliable at the group level.
106
What does first level analysis do
First-level analysis estimates the GLM separately for each participant to determine how each voxel’s BOLD time series relates to the experimental conditions.
107
What is the multiple comparison issue?
fMRI analyzes tens of thousands of voxels simultaneously. If you run a statistical test on each voxel independently, most “significant activations” will be false positives simply due to chance.
108
What is family wise error
A very strict correction for the multiple comparison issue. It is used to ensure the entire brain map has a less than .1% chance of containing false positives (given a p-value of .001). It is often over conservative and may prevent true results from being detected. ## Footnote Voxel-based thresholding
109
What is the Fasle Discovery Rate
A less strict correction for the multiple comparison issue. FDR controls the proportion of false positives among all voxels declared significant, making it a less conservative multiple-comparisons correction than FWE and more sensitive to true effects. ## Footnote Voxel-based thresholding
110
What are the differences between FWE and FDR
On the one hand, FWE is better when looking to have a high confidence in the results. On the other hand, FDR is used more when wanting to explore brain areas and detecting broader patterns. ## Footnote Voxel-based thresholding
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