developmental psychology - clinical Flashcards

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1
Q

when does schizophrenia develop?

A
  • typical age of onset = early to mid 20s in males and late 20s for females
  • several perinatal and birth complications e.g. premature births are also associated with the development of Sz
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2
Q

what does the dopamine hypothesis suggest about the development of Sz?

A
  • positive symptoms caused by excess dopamine in the mesolimbic pathways and negative symptoms from a deficit of dopamine in mesocortical areas
  • this links to dopamine activity peaking in adolescence and may further set the stage for onset of symptoms
  • PFC also matures at this stage
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3
Q

how does brain structure and neurotransmitters relate to each other on the concept of super-sensitivity?

A
  • there is a pathway rich in glutamate that runs from the PFC to the mesolimbic pathway
  • these areas said to be smaller in volume so it is underdeveloped
  • lower levels of glutamate activity lead to lower basal release of dopamine
  • this causes dopamine receptors to be hypersensitive so they overreact giving positive symptoms
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4
Q

what did wright et al and susser et al find about Sz and development?

A
  • wright = incidence of Sz in children born to mothers who had flu during pregnancy, especially when between 4 and 7 months
  • susser = children conceived during famine had twice the normal risk of developing Sz
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5
Q

how does brain injury link to developmental?

A
  • if the brain damage occurs early and then Sz develops later onwards it could be because the brain injury interacts with normal brain development
  • PFC develops typically in adolescence so damage in the area before birth wouldn’t initially show
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6
Q

how does brain development overall link to Sz?

A
  • as the brain develops, if any environmental or genetic factors were slow to develop then it would impact how the brain is able to deal with neurotransmission which results in Sz
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7
Q

what is a strength of the brain structure explanation ?

A
  • brain scans provide scientific objective data e.g. fMRIs
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8
Q

what is a weakness of the brain structure explanation?

A
  • the focus is only on biological factors so it is a reductionist explanation
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9
Q

what is a strength of the neurotransmitters explanation?

A
  • falkai et al = studied autopsies and found that those with Sz had a larger than usual number of dopamine receptors
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10
Q

what is a weakness of the neurotransmitter explanation?

A
  • newer antipsychotics have been found to actually increase dopamine levels in some parts of the brain which contradicts the dopamine hypothesis
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11
Q

what have family studies found about the rate of Sz?

A
  • risk for the general population = 1%
  • second degree Sz relative = 6%
  • first degree Sz relative = 17%
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12
Q

what are two weaknesses about the findings of family studies?

A
  • family study research has failed to isolate a single dominant or recessive gene that causes the illness
  • tiwari = fewer than 1/3 of people with Sz have a family history of the disorder
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13
Q

what have adoption studies found and what is a supporting study of this?

A
  • Sz spectrum disorders are more frequent in adopted children of Sz mothers than control
  • kety et al = concordance rate of Sz in 33 adopted twin pairs and there was a high concordance rate even amongst adopted twins which showed a clear genetic factor
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14
Q

what is found about NGR1?

A
  • NGR1 is expressed at central nervous system synapses and has a clear role in activation of NT receptors
  • variations of the gene contribute to the pathogenesis of Sz
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15
Q

what is a supporting study of NGR1?

A
  • stefansson found that the NGR1 mutation mice are hyperactive
  • clozapine reduced the hyperactivity
  • further supports that the NGR1 mutation is related to Sz phenotypes
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16
Q

what is a weakness of NGR1?

A
  • potential pathogenic involvements lack reliability as there has been a lack of consistency in findings and there is limited knowledge of genes involved