Lecture Notes: Functional Magnetic Resonance Imaging (fMRI)
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Email: matt.roser@plymouth.ac.uk
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Dr Matt Roser
Lecture 1 Part 2: Functional Magnetic Resonance Imaging (fMRI)
Reading Material:
Baars, B., & Gage, N. M. (2013). Fundamentals of cognitive neuroscience: a beginner's guide. Academic Press. Chapter 3.
Savoy, R. (2001). History and future direction of human brain mapping and functional neuroimaging. Acta Psychologica, 107, 9-42.
Ward, J. The student's guide to cognitive neuroscience. Chapter 4.
Note: Slide 7 contains an image of open brain surgery.
Web Resources
Animation 2.1: Magnetic Resonance Imaging (MRI)
SLMENS
MRI animations with narration
http://sites.sinauer.com/cogneuro2e/animations02.01.html
fMRI for Newbies (from which I've grabbed images)
http://www.fmri4newbies.com/
The Essential Question
What do those blobs represent in fMRI images?
Historical Images of the Brain and Mind
Brain Structure:
Some images are still in use today.
Often interpretive and require labor/skill.
Examples:
Christopher Wren (1664).
Brodmann cytoarchitecture maps.
Brain function: *Phrenology (19thC)
Electrophysiological mapping 1957
Magnetic Resonance Imaging (MRI) Physics
Uses a magnetic field (B_0) and radio energy to produce an image.
A large magnet (50,000 times Earth's magnetic field) aligns nuclei that have a net magnetic moment (from odd number of protons/neutrons), e.g., H_2O.
Nuclei absorb and re-emit radio frequency energy.
How is an Image Acquired?
Nuclei spin around the main magnetic field.
RF pulse (oscillating magnetic field) tips M out of alignment with B_0 and synchronizes the phase of spins.
M gradually returns to alignment, and spins lose phase coherence.
These changes are detected as the ‘MRI signal’.
Spins oriented with or against B_0.
M = net magnetization.
M deflected by RF pulse.
M Applied Magnetic Field (B_0).
Mapping Lesions
A new extension of an older technique for mapping structure to function.
Images make complex patterns of data intelligible.
Imaging the Structure of the Brain.
Mapping Normal Variability in Structure
Map second-order structure, such as sulcal asymmetry.
Colour-coded maps for statistical significance of gyral/sulcal variability.
Large numbers of neurologically-normal participants.
Thompson, P. M. et al. (1998). Cereb. Cortex, 8, 492–509.
Mapping Change Over Time
Examples:
grey matter volume.
commissural myelination.
Myelination by age (mths).
Grey-matter development.
Functional MRI (fMRI)
Brain Mapping Publications: an exponential rise.
References to journals and abstracts related to brain mapping, illustrating the growth in the field.
The Blood Oxygen Level Dependent (BOLD) Response – the basis of fMRI
Relative levels of de/oxyhaemoglobin change from regional cortical activity.
Momentary decrease in blood oxygenation immediately after neural activity increases, known as the “initial dip” in the haemodynamic response function (HRF).
Followed by a period where the blood flow increases to a level which overcompensates for the increased demand.
Regional blood oxygenation actually increases following neural activation.
The blood flow peaks after around 6 seconds and then falls back to baseline, often accompanied by a “post-stimulus undershoot”.
De/oxyhaemoglobin and Magnetic Properties
De/oxyhaemoglobin have different magnetic properties.
Local field strength is affected by relative levels.
This affects the local signal in the image.
Increased signal is obtained from ‘active’ regions.
Take Home Points:
It’s complicated!!!
Change to the image is far removed from neural events.
An fMRI Experiment
Components:
Magnet
Video projector
Video screen
Gradient coil
Radio-frequency coil
Prism glasses
Headphones
Radio-frequency amplifier
Button response box
Amplifiers control magnetic field in three dimensions
Stimulus control computer
Spectrometer control computer
fMRI – Experimental Logic: Cognitive Subtraction
Originated with reaction time experiments (F. C. Donders, a Dutch physiologist).
Measure the time for a process to occur by comparing two reaction times, one which has the same components as the other + the process of interest.
Assumption of pure insertion: Can insert a component process into a task without disrupting the other components.
Task difficulty (a confound) may differ between conditions, resulting in changed attention.
Examples:
T1: Hit a button when you see a light.
T2: Hit a button when the light is green but not red.
T3: Hit the left button when the light is green and the right button when the light is red.
T2 – T1 = time to make discrimination between light color.
T3 – T2 = time to make a decision.
Experimental Design 1: Block Design fMRI
Alternating blocks of task and rest.
Example: 30s Task, 30s Rest.
Experimental Design 2: Event-Related fMRI
Allows (pseudo)random presentation of stimuli.
Allows retrospective coding of events (e.g., memory experiments).
Event-related design with Condition 1 Event and Condition 2 Event.
fMRI Preprocessing and Analysis
Steps:
Build Model
Realignment & motion correction
Smoothing
Normalisation
Image Data
Anatomical Reference
Parameter Estimation
Kernel Data
Design Matrix
Statistical Parametric Mapping
Contrasts
It's complicated!!!
Analysis - Modelling the data fMRI signal (data)
Block model convolved with HRF
We regress our model of our experiment against the signal-change data.
Least-squares best-fit analysis of the data that best estimates the amplitudes of the predictors (minimize residuals).
A T-test tests whether the slope of the function differs from 0 (i.e. flat).
Data Analysis at Every Voxel
This analysis is done independently at every voxel (3D pixel/volume) - i.e. thousands of times!
Contrasts allow one to test for voxels where activation in one condition is greater than another.
Voxels with significant T statistics can then be coloured in according to the size of T.
The essential question – what do those blobs represent?
Interpreting Blobs
Blobs are clusters of significant statistics for either a main effect or a contrast between two sets of regressors at each voxel.
Shows areas where the signal change was significantly predicted by the model (or where the degree of prediction differed between contrasted conditions).
Importantly…! This is the end result after much preprocessing and analysis.
Change in the signal is due to regional hemodynamics.
Thus, activations are distantly related to the underlying neurological events.
What has functional brain imaging told us?
Identified functional areas – e.g. Fusiform face area – stimuli; Anterior Cingulate - attention.
Corroborated findings from other methods (e.g. hippocampal involvement in memory).
Allowed the localization of function from undamaged brains.
Meta-analyses bring some order to the flood of data, but are these maps from multiple different studies any more useful than the 1957 electrophysiology map (slide 10)?
Cabeza & Nyberg. (2001). Journal of Cognitive Neuroscience 12:1, pp. 1–47.
New Directions in fMRI
Functional-connectivity analyses: calculate correlations between activations in different areas.
Dynamic causal modelling: explicit models of distributed networks are tested to see which best fits the observed data.
Both these techniques investigate distributed processing and overcome some of the limitations of lesion studies and earlier fMRI studies.
Functional-connectivity analysis.
Dynamic causal model.