Session Three (Neuro-Imaging) Flashcards

1
Q

What are the two most commonly used forms of neuro-imaging?

A

SMRI (Structural MRI) and FMRI (Functional MRI).

These are the best methods we have for looking at the structure and the function of the brain, respectively.

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2
Q

What is MR Spectroscopy and how is it used?

A
  • Form of neuro-imaging that looks at what chemicals are present in different parts of the brain.
  • Compounds studied are usually metabolites.
  • Normally compare a suspect region (e.g. a tumour) to a control region (healthy brain).
  • The differing levels of compounds, as well as the presence of others, can aid in diagnoses (e.g. of cancer) as well as research.
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3
Q

What is Arterial Spin Labelling?

A

A form of neuro-imaging that provides very accurate details on brain perfusion.

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4
Q

What is Diffusion Tensor Imaging?

A

A form of MRI that looks into how different chemicals, normally water, diffuse across a tissue.

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5
Q

What is Tractography?

A

A form of MRI that allows us to see white matter, more specifically the nerve tracts white matter ranges itself into.

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6
Q

What is the difference between fMRI and sMRI practically?

A
  • Same machine, just used in a different way.
  • Different programmes initiate different pulse sequences, generating the different results.
  • S takes about 3-5 minutes and produces a super high quality image of the brain’s anatomy, from which diagnoses can be made.
  • F is taken very quickly, normally among to produce a different image every second. In this way it can tell us more about what is happening in the brain at a given moment.
  • F sacrifices anatomical accuracy for info on what the brain was doing that second, the reverse is true for S.
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7
Q

Is there a middle ground between sMRI and fMRI? What is it’s purpose?

A
  • Yes, but it is usually only done for a specific area of the brain, e.g. the visual centre in the occipital lobe.
  • This allows pictures to be taken rapidly but with a degree of anatomical accuracy, producing a mixed result.
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8
Q

What are some issues with using MRI as an imaging method?

A
  • Machine is very loud
  • Patient has to be in there for a long time
  • Claustrophobic, deeply unpleasant for the patient
  • Inappropriate for some patients (fat, psychotic, metal implants, claustrophobic, tattoos at the shoulder)
  • Get magnetic distortion at the very front of the brain and also by the ears, producing inaccurate results and possibly missing lesions in these areas.
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9
Q

What is EEG and how does it work?

A
  • Electroencephalography
  • 64/128 leads placed on the outside of the scalp measure changes in electrical activity in the brain and are able to triangulate them to a rough location.
  • Very little anatomical accuracy but non-invasive.
  • Less accurate than fMRI as only measuring effect of activity on outside of the skull, not activity itself.
  • However can provide more accurate time-based data as is constantly recording changes rather than taking pictures at a set rate.
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10
Q

What is MEG and how does it work?

A
  • Magneto-encephalography.
  • EEG measures changes in electrical activity, MEG measures the tiny changes in magnetic fields generated by brain activity.
  • Of little clinical use outside of epilepsy and migraine research.
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11
Q

What are some examples of functional neuro-imaging methods?

A
  • fMRI (most common)
  • EEG
  • MEG
  • PET scans
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12
Q

What are PET scans and how do they work?

A
  • Positron Emission Tomography
  • Uses a compound like Tagged Glucose as a contrast.
  • Scan patient before and after injection, areas that have taken up more glucose appear brighter, this suggests greater metabolic activity, greater activation.
  • Provides a highly accurate picture of what is happening in the brain in terms of activity.
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13
Q

What are some issues with using PET scans?

A
  • Require injection therefore moderately invasive.
  • Radioactive compound, which limits use (no kids, no pregnant women, can’t be done in research, can’t be done more than once)
  • Very expensive.
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14
Q

What is fNIRS and how is it used?

A
  • Functional near-infrared spectroscopy.
  • Non-invasive imaging method that relies on how near-IR light responds to different levels of oxygen in the blood to judge perfusion in one area of the brain and therefore activity in that part of the brain.
  • Machine measures different levels of reflection and refraction of the light beams.
  • Mostly done in babies as non-invasive and works best if you have little hair and a thin skull.
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15
Q

What is the BOLD effect? And how is it used in neuro-imaging?

A
  • Blood Oxygenation Level Dependent.
  • Essentially oxyHb doesn’t disturb local magnetic fields as much as deoxyHb does.
  • This is what an fMRI picks up.
  • Increases in regional oxygen delivery causes an increase in oxyHb and a drop in deoxyHb, magnetic fields become less disturbed, area appears brighter on an fMRI.
  • E.g: Person hears a noise, blood flow increases to the auditory centres of the brain, these areas appear brighter.
  • fNIRS also uses the BOLD effect.
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16
Q

What are the important steps in designing an fMRI experiment?

A
  • Hypothesis generation (should be specific).

- Manipulate the exercise/behaviour/stimulus involved to produce a DETECTABLE functional change.

17
Q

What are the different ways you can manipulate an fMRI experiment to try and produce a change that is detectable?

A
  • Change stimulus TYPE or PROPERTY (e.g. audio or visual, vary intensity of stimulus)
  • Change stimulus TIMING (block or event-related methodology).
  • Change PARTICIPANT INSTRUCTIONS (e.g. implicit or explicit, distractions)
18
Q

Describe Block Design in fMRI studies?

A
  • Multiple repetitions of each experimental condition within a block or ‘epoch’.
  • Test involves alternating between one or more condition blocks and control/baseline blocks.
  • Blocks are typically 20-30 seconds long.
  • Whole test usually lasts between 5 and 10 minutes.
  • Most common form of fMRI study.
19
Q

What are the pros and cons of Block Design fMRI studies?

A

PROS:

  • Adequate for many types of experiments.
  • Allows for some flexibility.
  • Simple to design, carry out and analyse.
  • Most powerful design when it comes to statistical analysis.

CONS:

  • Can be predictable or boring, leading to rapid habitation from the patient, anticipation and reduced response.
  • May be difficult for patients to maintain a specific cognitive state for 30 seconds.
  • Cannot extract the response to one stimulus specifically, only to a block.
  • Assumes the patient isn’t still thinking about the stimulus in the baseline period.
20
Q

Describe Event-Related Design in fMRI studies?

A
  • Each stimulus becomes an individual epoch so we can associate brain processes with more discrete and therefore specific events.
  • Closer to a behavioural study.
  • Algorithms exist to help randomise the delivery of these stimuli.
21
Q

What are the Pros and Cons of Event-Related Design in fMRI studies?

A

PROS:

  • Able to detect signals to individual trial events.
  • More flexible in their design than Block studies.
  • Allows for post-hoc sorting of stimuli (e.g. correct vs incorrect responses, aware vs unaware, remembered vs forgotten , quick vs slow response etc)

CONS:

  • Requires a greater understanding of fMRI because the design and analysis is so much more complicated.
  • Less statistical power than block design except if we have a lot of well separated single events.
22
Q

Is there a mid ground between Block and Event Design.

A

Yes, Mixed design.

Pros: Sustained activity (and therefore focus) throughout task AND allows us to model brain response evoked by each trial.
Can also dissociated transient and sustained events.

Cons: Really difficult, expensive, complicated to design.

23
Q

In what circumstances would a different form of study be better than an fMRI?

A
  • If you don’t need them to be doing a task (Resting State MRI).
  • If you want a more direct measure of cerebral blood flow (ASL)
  • When measuring really fast brain processes (EEG or MEG).
  • If you need the results available in real time (real time fMRI).