Schizophrenia - Pathophysiology Flashcards

1
Q

What is Schizophrenia? Why is Schizophrenia the most important psychotic disorder?

A

is a psychotic disorder
- disorder of thought
= mental state is out of touch, profound alterations in behaviour and abnormal perceptions/ideas/thought

has early onset (aged 18-20) (earlier in men)
is prevalent
is chronically disabling
- responsible for a high percentage of the population morbidity §

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2
Q

What are the classes of schizophrenia?

A

class are grouped into their predominate symptoms

  • positive
  • negative
  • cognitive

must persist for at least 6 months to be classed a schizophrenia

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3
Q

What are the positive symptoms of schizophrenia?

A

hallucinations (perceptions without stimuli)

  • auditory = voices talking to them/about them/echoing thoughts/commentary
  • visual

delusions (fixed/unshakable belief inconsistent with norms)

  • often paranoid or persecutory
  • passivity of thoughts and actions

movement disorders (motor/volitional/behavioural)

  • stereotypies = purposeless, repetitive acts
  • bizarre postures, strange mannerisms
  • altered facial expressions = grimacing
  • catalepsy = waxy flexible (loss of voluntary limbs)

disorganised thought/speech

  • catatonia = motionless, mute, expressionless
  • impulsive behaviour
  • extreme hyperactivity = walk around naked

formal thought disorder
- speech that is difficult to understand and rapidly switches from one subject to another (derailment of speech)

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4
Q

What are the negative symptoms of schizophrenia?

- more prevalent in men

A

social withdrawal
lack of motivation or initiative

formal thought disorder

  • speech is difficult to understand
  • poverty of speech = distorted/illogical
  • loosening of associations (cannot flow train of thought)

emotional flatness
anhedonia

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5
Q

What are the cognitive symptoms of schizophrenia?

A

impaired working memory
impaired attention (selective)
impaired cognition

blunted affect - decreased responsiveness to emotional issues
incongruous effect - mismatch between experienced emotion and its expression

insight - lack of understanding of what is wrong (do not accept anything is wrong)

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6
Q

What are the phases of schizophrenia?

A

The Prodrome
- early onset in late teens/early twenties
= often mistaken for depression or anxiety
- can be triggered by stress

The Active/Acute Phase
- onset of positive symptoms e.g. delusion, hallucinations

Remission
- treatment return to ‘normality’ but schizophrenia is a chronic relapsing disorder (cycle of relapse and remission is common)

Relapse
- schizophreniform = positive symptoms for at least a month, but < 6 months

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7
Q

What is schizophrenia caused by?

A

genetics
- is not directly inherited but can run in families
- mutation of candidate risk genes increases the likely hood of getting it
= COMT, DISC 1, GRM 3

environmental
- pregnancy/birth complications
= early life stress, e.g. low birth weight, asphyxia during birth, viruses
- stress/early bereavement/loss of job/abuse
- drug abuse
= psychotostimulants (amphetamine, LSD), cannabis

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8
Q

What are the potential pathophysiologies of schizophrenia?

A

dopamine hypothesis
- hyper DAergic and hypo DAergic

brain structure abnormalities

hypofrontality
- decreased activity in the frontal cortex

NMDA receptor hypofunction

oxidative stress

neuroinflammation

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9
Q

What is the DA hypothesis?

A

hyperactivity in the mesolimbic DAergic pathway

  • VTA to nucleus acccumbens, amygdala and hippocampus
  • associated with the positive symptoms

hypoactivity in the mesocorticol DAergic pathway
- VTA to frontal cortex
- associated with negative symptoms
= decreased cognition

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10
Q

What is the pharmacological evidence FOR the DA hypothesis?

A

amphetamine (psychotostimulant) enhances DA release in schizophrenia
- is associated with psychotic episodes (induces)

reserpine depletes DA
- controls positive symptoms

stimulation of D2 receptors induces stereotyped behaviours

D2 antagonists is an important mechanism of anti-psychotics

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11
Q

What is the pharmacological evidence AGAINST the DA hypothesis?

A

no clear increase in dopamine levels in cerebrospinal fluid homovanillic acid concentration (CSF HVA)

no change in DA receptors in drug-free patients (but there’s increased D2 receptors in patients taking drug treatment)

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12
Q

What is the evidence for and against brain structure abnormalities?

A

in schizophrenic patients:

  • overall brain size is smaller
  • reductions in gray matter (contain neural cell bodies)
  • enlarged lateral ventricles and smaller hippocampus

not all patients have such profound structural differences

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13
Q

What is the evidence for and against hypofrontality?

A

shown by MRI scans
- schizophrenic patients have reduced activity in the frontal cortex
= decreased cognitive functioning

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14
Q

What is the evidence for and against NMDA receptor hypofunctioning?

A

decreased glutamate and glutamate receptors concentration in the prefrontal cortex of schizophrenic patients

blocking NMDA receptors increases psychotic symptoms
- hallucinations, thought disorder

transgenic mice with reduced NMDA receptor expression have
- stereotyped behaviour, decreased social interaction

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15
Q

What is the evidence for and against 5-HT involvement in schizophrenia?

A

lysergic acid diethylamide (LSD) is a partial 5HT agonist
- causes hallucinations = positive symptom

many antipsychotics block 5-HT receptors

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