TASK 3 - EEG Flashcards

1
Q

EEG

A

= measure electrical signals outside of the brain

  • signal of electrode is the difference between reference electrode and the active/measuring electrode
  • -> electrodes (= small electrodes) are either glued to skin or included in a stretchable cap
  • recording from each electrode reflects the electrical activity of the underlying brain region
  • yields a continuous recording of the overall brain activity
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2
Q

neural source

A
  • EEG not sensitive to action potentials (too fast, too small)
  • EEG sensitive to post-synaptic potentials: slower, (= dipoles)
  • for large groups of neurones to be measured the neurones need to have a) same input (excitatory or inhibitory) and b) same orientation (parallel)
  • -> synchronised activity: activity of neurones add up
  • -> de-synchronised activity: the activity of neurones cancel each other out (differing input or perpendicular)
    a) electrodes detect the sum of positive and negative charges in the area
    b) pyramidal cells (organised along cortical columns) are arranged in parallel + perpendicular to the cortex (in the gyri)
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3
Q

neural source

- dipole

A

= one end of neurone more positive and one end more negative

a) source = region of positive charge
b) sink = region of negative charge
- produce positive and negative deflection at different regions of the scalp
1. radial dipole: oriented perpendicular to the surface; directly measured in gyri
2. tangential dipole: oriented parallel to the scalp; sulci

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4
Q

within brain

- volume conduction

A

= ions of the same charge repel another –> repel other ions of the same charge –> wave of charge that travel

  • -> principal: opposite attract and similar repel
  • responsible for the propagation of the EEG signal within the brain
  • signal from a large dipole may travel much further than signal from a small dipole (process continues further)
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5
Q

from brain to electrode

- capacitive conduction

A

= electrical signal must travel from the brain through the dura layers –> skull layers –> scalp –> to the electrode

  • volume conduction can only happen within the brain
  • -> relates to low spatial resolution: cannot differentiate where exactly the signal originated
  • one electrode collects data from several locations –> can only infer about the locations (different reactions inside can lead to same information outside)
  • spatial smearing = unclear borders of the locations
  • -> inverse problem
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6
Q

capacitative conduction

- capacitor

A

= 2 pools of charges separated by an insulating layer (without layer charges would freely mix = neutral pool)

  • within capacitors there are ions: volume conduction within capacitors –> goes until the insulating layer
  • charge difference builds up across insulating layer (neg. ions push against one side, pos. ions accumulate on the other)
  • how much charge builds up depends on properties of layer, size of charged pool, distance between pool of charge and layer
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7
Q

measurement of EEG

- design

A

head –> electrode –> amplifier + filter –> analog-digital (AD) converter –> computer –> disk + monitor
- presented on a scale with time on X and microvolts (amplitude) on Y

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8
Q

measurement of EEG

- output

A
  • yields a continuous recording of the overall brain activity
  • -> linear superposition: measured voltage is the weighted sum of electrical activity of multiple regions in brain (largest effect by regions near electrode)
  • weights depend on distance from electrode, conductivity, source orientation
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9
Q

measurement of EEG

- topography

A

= colour plot = colour indicates the voltage that was measured at some location on the scalp across time

  • -> get picture of distribution voltage across scalp
  • map changes rapidly: every single image presents single moment in time)
  • sensitive to dipole location, orientation and strength
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10
Q

noise (artifacts)

A

= artifacts = signals recorded in EEG that are not produced by the brain
a) physiological artifacts: ocular, muscle, cardiac activity (produce electricity
b) technical artifacts: cable movement, incorrect reference placement, body movements
- measured by signal-to-noise ratio (SNR) (signal/noise)
- pre-stimulus baseline period: needed to compare the amount of noise in both groups
–> if different, the observed effect post-stimulus may not be valid
TO AVOID NOISE
- signal must be large enough to be measurable (orientation not a problem)
- need electrode gel: for ions to pass through skull
- remove very slow + very fast voltage changes, as they are likely to be due to noise
- amplifier is needed: if amplified before introduction of external noise, this noise will have a smaller impact on the measurement (larger SNR)

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11
Q

inverse problem (localisation)

A

= inverse problem = only know final voltage pattern and must work back to determine which sources within brain produced this pattern

  • cannot really determine location by looking at scalp distribution
    a) single dipole: use scalp distribution to estimate location + orientation (unless deep in the brain or data is noisy)
    b) multiple dipoles active: they sum together –> precision is lost but still works when the dipoles are far apart (capacitive conduction)
  • difficult to localise two dipoles of similar orientation and location
  • -> the more dipoles are added, the more difficult it is
  • need converging evidence
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12
Q

electrode placement

A
  • 10-20 system = standardisation of locations
    1. measure total distance between landmark points on the head (front-back and left-right dimension)
    2. total distance is divided in number of segments of 10% and 20% of total
  • each electrode is then referred to by there neighbouring brain regions (F = frontal), whether it is left or right from midline (left (odd), right (even)) and distance from midline (close (1), far (7-8))
  • needed to replicate EEG results
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13
Q

electrode placement

- reference electrode

A
  • any output voltage is defined as coltage-difference between two locations between head-electrode and reference electrode
  • should be placed close to the head but be silent
  • -> as little brain activity as possible
  • mastoid bone often used: skull is really thick right behind the ear
  • right placement needed to reduce noise and correct recordings
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14
Q

state effects

A

the more excited the brain, the smaller and the faster the waves

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15
Q

oscillations

A

= recurring waveforms in the data pattern; have 3 features

1) frequency: amount of a full waveform in some period (1s)
- measured in Hertz: 1 Hz = 1 full waveform in 1s
2) amplitude: amount of volt from 0 to peak; describes the height of the peak
- measured in microvolts
3) phase: shift of the waveform on the time axis (where in the waveform the signal begins)
- measured in radians or degrees

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16
Q

oscillations

- feature analysis (Fourier)

A

= analyse amplitude and phase for many frequencies

  • decomposes any irregular signal into its underlying simple sine waves
  • outcome = frequency, amplitude and phase of the signal
  • frequency/power spectrum: bar graph with frequency on X and amplitude on Y –> shows the underlying frequencies of the signal
17
Q

research fields

1. without stimuli

A

= look at resting oscillations, interested in ongoing EEG
- state of subject: sleep analysis
state of cortical area (activated)
- neurometrics
- neurofeedback: inform individuals about their ongoing EEG to improve in some way

18
Q

research fields

2. with stimuli

A

= repeatedly present stimulus that participant needs to respond to –> waveform is going to present are that is responsible for the action

  • extract by averaging EEG –> ERPs
  • excellent time resolution moment-by-moment tracking of processing
  • see difference between different stimuli/tasks
  • -> track activation of individual processing stages
  • attention research
19
Q

ERPs

A

= event-related potentials = tiny signal embdded in the ongoing EEG that was triggered by stimulus

  • focus on components of ERPs that are sensitive to stimulus and action of the participant related to stimulus
  • -> how brain is activated in response to task
20
Q

ERPs

- extracting signal

A

1) EEG traces are recorded from series of trials
2) average together EEG traces by aligning them relative to stimulus onset
- epochs: start shortly before stimulus onset, end ≈ 1ms after
- alignment eliminates variations in the electrical activity that are unrelated to event of interest

21
Q

ERP components

- naming

A
  1. polarity (N = negative, P = positive)
    a) latency: time in ms after stimulus onset
    b) order: first, second major peak of signal
    c) topography: location related to neighbouring brain areas
    d) function: readiness potential (RP)
22
Q

ERP components

A. exogenous

A

= obligatorily triggered by the presence of a stimulus (always there if there was a stimulus)

  • come relatively early, short latency (≈ 150ms)
  • don’t depend on task instructions (attend to stimulus or not)
  • depend on physical properties of stimulus (more intensity = more amplitude)
  • depend on modality (auditory, written presentation)
  • -> P1, N1
23
Q

exogenous components

- P1

A

= first positive peak

  • generated in extrastriate areas of visual cortex
  • influenced by sensory factors, attention + arousal
24
Q

exogenous components

- N1

A

= several distinct subcomponents (several areas produce N-wave in same approximate time range)

  • N170 component = face processing (larger when stimulus is face as compared to non-face object)
  • difference begins roughly 150ms after stimulus onset = distinguish between faces and other objects after 150ms
  • suggested location in visual cortex (right occipito-termporal regions, FEF)
  • modulated by attention under some conditions
  • same process used for complex stimuli in expertise area
25
Q

ERP components

B. endogenous

A

= task-dependent activation

  • come later, typically >150ms
  • depend on task instructions
  • less dependent on physical properties
  • less dependent on modality
  • -> P2, P300, N400
  • N2: conflict monitoring; connected to the function of dorsal ACC
  • N400: sensitive to semantic processes, stereotyping
26
Q

endogenous components

- P300

A
  • larger for infrequently occurring stimuli, large for stimuli that require a response
  • correlated with RT
  • sensitive to selective attention
    a) P3a = sensitive to highly distinctive improbable stimuli, even when task doesn’t require discrimination of these stimuli
    b) P3b = sensitive to task-defined probability
  • larger only when task requires sorting the stimuli in a way that makes a given category more improbably
  • e.g. 0-9 appear in equal likelihood but we only want 4’s it ends up having a 0.1 probability
27
Q

ERP components

C. motor

A

= accompany motor response

  • usually generated by motor cortex
  • response-related components = averaged ERPs time-locked to motor response rather than stimulus onset
  • -> RD
28
Q

motor components

- readiness potential

A

= large negative voltage over motor cortex that build up gradually over several hundred milliseconds
- lateralised (LRP): present just before the button press; dynamic measure of motor cortex activation associated with preparation and initiation of behavioural responses

29
Q

ERPs components

- ERN

A

= error-related negativity = detection and handling of errors when responding

  • response-locked component: fronto-central negativity that develops with onset of behavioural response
  • peaking around 50-80 ms
30
Q

ERP components

- MSN

A

= mismatch negativity = sensitive to automatic sensory memory

31
Q

ERP research

- attention

A
  • endogenous cueing = attention is internally controlled, voluntarily focus + purposely select info to process (cocktail party effect)
  • -> spatial attention has the earliest effect on stimulus processing –> supports early selection models (= stimulus can be tossed out before perceptual analysis)
  • exogenous cueing = attention doesn’t shift by choice but automatically by salience of stimuli in our environment
  • -> reflexive + voluntary shifts in spatial attention induce similar physiological modulations in early visual processing
32
Q

EEG

- advantages

A
  • measure continously during processing: high temporal resolution
  • studied in all trials (independent of isntructions to respond or not)
33
Q

EEG

- disadvantages

A
  • inverse problem/low spatial resolution

- -> due to capacitative conduction (due to thickness of skull)

34
Q

ERPs

- advantages

A
  • address time course of cognition rather than localising brain areas
  • -> precise timing of responses/mental activity
  • measure psychological process independently from behavioural response
  • -> “covertly” monitor mental activity in the absence of behavioural response (e.g. infants)
  • lower costs relative to neuroimaging methods
  • less impactful data collection environment
  • sit upright during data acquisition
35
Q

ERPs

- limitations

A
  • can’t be used if mental process isn’t reasonably well time-locked to a discrete, observable event (e.g. spontaneous emotional responses)
  • need many trials to average, which some paradigms do not permit
  • most sensitive to short processes < 2sec –> slower processes are difficult to see in ERPs
  • ERPs must have same latency variability, otherwise wrong conclusion that conditions differ in magnitude of response although it’s actually the timing
  • -> measure mean voltage, rather than peak voltage over specific period (monophasic only)
  • using peak as magnitude doesn’t represent magnitude properly
  • -> sensitive to noise, latency variability and overlapping ERP components
36
Q

ECOG

A

= electrodes are placed directly on the surface of the brain

  • only for people who are undergoing neurosurgical treatment
  • useful clinical information: monitor brain activity to identify the location and frequency of abnormal brain activity
  • -> excellent spatial and temporal resolution: far less signal distortion than EEG
  • used to stimulate the brain + localise cortical and subcortical neurological functions