lecture 7- introduction to neuropsychology Flashcards

1
Q

neuropsychology

A
  • studying the link between brain and behaviour
  • fundamentally about studying impairments in individuals who have suffered brain damage, using this to understand how brains normally function
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2
Q

causes of brain damage

A
  • Traumatic injury (car accidents, falls, projectile)
  • Stroke (leading cause on non-traumatic injury)
  • Lack of oxygen (hypoxia)
  • Tumors
  • Brain infections or inflammation (e.g., encephalitis, hydrocephalus)
  • Nutritional deficiencies
  • Chronic alcohol abuse (e.g., Korsakoff’s syndrome)
  • Surgery (e.g., intractable epilepsy)
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3
Q

what are the two kinds of neuropsychology?

A
  • clinical neuropsychology (clinical neuropsychologists are interested in understanding the impairment)
  • cognitive neuropsychology (cognitive neuropsychologists are interested in learning about normal functions from studying impairment

both concern impairments in normal functions in the brain

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4
Q

clinical neuropsychology

A
  • focuses on understanding the condition
  • trying diagnose and access and understand the cause of the disorder
    -focus on assessment (diagnosis and prognosis), management and rehabilitation for patients
  • define pathological conditions/characterise deficits considering cognitive, behavioural, emotional and social aspects
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5
Q

cognitive neuropsychology

A
  • understand how the brain normally works, rather than trying to characterise the disorder itself just by understanding the disorder and what its like for the patient
  • understand normal functions in the brain by studying patterns of impairment after brain damage
  • map functions to brain regions
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6
Q

what are the two types of cognitive neuropsychology?

A
  • strong: use patient data to infer/ construct theory (starting out with no theory, study a bunch of patients and from that study of the patients you build a new theory, fundamentally construct
  • weak: use patient data to constrain/ refine theory
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7
Q

assumptions in cognitive neuropsychology

A
  • universality
  • modularity
  • fractionation
  • transparency
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8
Q

universality

A
  • idea here fundamentally the way our brains are organised are roughly the same
  • cognitive processes are the same in all individuals
  • still some scope for individual differences but the average of a group of individuals should be a good reflection of any individual in the wider population
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9
Q

modularity

A
  • idea here is if you look at any cognitive process in the brain, you can break it down into a series of steps
  • complex cognitive processes can be broken down into simpler processing units
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10
Q

fractionation

A
  • brain damage can result in the selective impairment of a particular cognitive process
  • whole level destruction or destruction to a particular component
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11
Q

transparency (aka subtractivity)

A
  • idea here is when you have selective impairment that it shouldn’t impair any other functions in the brain
  • the cognitive system of a brain-damaged patient is fundamentally the same as that of a normal subject except for a ‘local’ modification of the system = all other processes are intact
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12
Q

are these assumptions justified?

A
  • fractionation
  • modularity
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13
Q

assumptions of universality

A
  • structure wise all the lines of folds in the brain are similar to each other
  • active locations are in different parts of the brain for different ppl
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14
Q

assumptions of transparency

A
  • everything else is functioning normally and we’ve just got a selective impairment
  • behaviourally compensated for the damage in his brain in order to then be able to do the task a different way.
  • neural re-organisation
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15
Q

assumptions of transparency cont

A
  • sometimes the damage that occurs in the brain as a result of surgery
  • pre-surgery brain function
  • other surgical damage
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16
Q

methods in cognitive neuropsychology

A
  • Studies of individuals (and groups of individuals) with localised brain damage
  • Studies of individuals who have been surgically operated on
  • Behavioural studies of healthy individuals
  • Imaging studies of both healthy and brain-damaged individuals
  • Inducing temporary ‘lesions’ in healthy brains
17
Q

how are the two ways we can study brain damaged individuals?

A
  • patient-group studies
  • single-patient studies
18
Q

group study approach

A

test a bunch of people and look for the common deficits or the common abilities that these individuals have, and then from that whole group data, you try to make inferences about the overall processes that are going on

  • Data aggregated across subjects (i.e. averaging)
  • Inferences drawn from between-group comparisons: patient group vs. control group
  • Looking for ‘syndromes’: collection of symptoms which often co-occur in individuals
  • Thus looking for associations of common deficits
  • Can also look for common sites of damage
19
Q

group study problems

A
  • Averaging across patients - the assumption of universality
  • Similar behavioural symptoms may arise from very different underlying patterns of damage
  • Prosopagnosia from damage to right (Marotta, Genovese & Behrmann, 2001) and left (Mattson, Levin & Grafman, 2000) hemispheres
  • Similar sites of damage may be associated with very different symptoms
  • Damage to right fusiform gyrus found in patients with prosopagnosia (Marotta, Genovese & Behrmann, 2001) and alexia (Leśniak, Soluch, Stępień, Czepiel & Seniów, 2014)
  • Specific behavioural impairments within a syndrome may vary considerably
  • e.g., different types of prosopagnosia
  • Time consuming to find patients
  • Risk of over-interpreting associations: the deficits may depend on functionally distinct processes that are anatomically related
  • e.g., lesions to the ventral occipital lobe can produce severe deficits in colour vision (achromatopsia) and face recognition (prosopagnosia)
20
Q

case study approach

A
  • look for specific single deficits in a patient
  • mainly concerns dissociations between behaviours patients can and cant do
  • single and double dissociations
21
Q

single dissociation

A
  • we have an individual who has a particular problem, they cant do one task, but they can do something else
22
Q

double dissociation

A
  • one patient can do A but not B, another patient can do B but not A
23
Q

are double dissociations really the ‘gold standard’

A
  • the need for pure cases
  • hard to find patients with damage purely to one cognitive process (and depending on the cause of the damage, damage may be to several brain regions)
  • the impossibility of precise replication
24
Q

linking (impaired) functions to structures in the brain

A
  • what can we conclude about localisation of function in the brain from studying a brain damaged patient?
  • post mortem
  • confirm / associate deficits with anatomy after death
  • imaging techniques
  • ways of imaging the brain
25
Q

structural imaging

A
  • computed tomography (x-rays)
    =damage shows up as lighter, as brain tissue has died
  • # magnetic resonance imaging (MRI) (radio waves/ magnetic field)
26
Q

linking (impaired) functions to structures in the brain cont

A
  • can functional imaging resolve these issues?
  • can compare function in brain damaged and healthy brains
27
Q

is there a way to get around it by looking at functions in the brain?

A
  • yes, fMRI
  • method that is commonly used to try understand activity in the brain

some problems
- doesn’t actually measure activity in the brain, it measures changes in the oxygenation level in the blood supply to the brain
- the reason that this is assumed to be connected is that essentially active tissue, muscles or neural tissue requires oxygen to be active to generate that energy. so when you are doing something active with your brain, you increase the blood flow in that area and lots of the oxygen is leaving the blood, the blood at the location and being used to drive the activity

28
Q

other types of functional imaging

A
  • PET
  • MEG
  • EEG
29
Q

take a healthy brain and temporality disrupts activity in a localised region

A
  • TMS (transcranial magnetic stimulation)
  • magnetic pulse over region of cortex
  • ‘transient lesion’
  • rTMS