Schizophrenia Flashcards
who was Emil Kraepelin (1898)
- at this time SZ patients were first systematically described as separate psychiatric category of patients
- first to describe symptoms of SZ patients
- Described symptoms of patients as ‘dementia praecox’:
- dementia = global disruption of perceptual and cognitive processes
- praecox = early adulthood onset
- Main symptoms: impairments in attention, memory and goal-directed behaviour
- Described condition as progressive, no return to premorbid functioning
who was Eugen Bleuler (1911)
- Reformulated dementia praecox
- Coined the term schizophrenia:
- schizo = split
- phrene = mind
- Characterised fragmented thinking
- First to distinguish between positive and negative symptoms
what is Schizophrenia?
- as defined in the Diagnostic and Statistical Manual of Mental Disorders (or DSM), schizophrenia is characterized by a combination of positive and negative symptoms and these can be demonstrated to variable degrees
- one patient could show predominantly positive symptoms, but not as many negative symptoms, while another patient may show mainly negative symptoms.
- has positive and negative symptoms as well as cognitive deficits (70-80% of patients have cognitive deficits)
what are positive (type 1) symptoms?
delusions:
- false belief despite evidence to contrary, distorting reality (e.g. patient beliefs someone is plotting against them)
- thought insertion
- thought withdrawal
- thought broadcasting
- not being in control of own actions
Hallucinations:
- perceptual experience seems real in absence of physical proof; most common: auditory, visual, olfactory (e.g seeing an animal or person that isn’t real)
Disorganised behaviour
- can affect speech, difficulties with routine tasks, inappropriate behaviour
what are negative (type II) symptoms
diminished emotional expression
- affect: blunted affect, mood or emotional state, limited range of emotions
- alogia: poverty of speech, lack of conversation
Avolition
- apathy (lack of motivation)
- social withdrawal
- Anhedonia: inability to feel pleasure
what are cognitive deficits?
- substantial impairment in overall cognitive performance (occurs in most SZ patients)
- can be variable across patients
most common deficits in: - executive functions/cognitive control (incl. verbal frequency and problem solving
- attention (incl. vigilance)
- processing speed
- memory (working memory, episodic memory)
- social cognition
Presence of cognitive deficits associated with poor daily functioning and quality of life
tetsing for cognitive deficits
- Impairments in cognitive functions already detectable in childhood/adolescence neurodevelopmental disorder
- Objective assessment of cognitive impairments and subjectively perceived impairments only weakly correlated
- anosognosia for cognitive deficits (in particular, in individuals with more severe deficits)
Schizophrenia as a neurodevelopmental disorder
- SZ is a neurodevelopmental disorder
- typically develops during late adolescence
- cognitive impairments can often be detected much earlier, i.e. in childhood or early adolescence
- Brain abnormalities slowly emerge during adolescence, therefore it is described as neuro developmental condition.
- Combination of genetics and environment (~80% heritable)
- Prevalence of SZ: 1%
what are the genetic risk factors of developing SZ?
- Children or siblings of affected individuals 10 x more likely to develop SZ
- Polygenic disorder: at least 108 genes implicated
- Genetics only explain small percentage of cognitive variance
what are the environmental risk factors of developing SZ?
- adverse events prenatally or perinatally (adverse events before or during birth) (e.g. poor maternal nutrition, infection, obstetric complications)
- Perinatal hippocampal injuries in rats ➟ development of abnormal dopamine organization in prefrontal cortex
- Contact with certain viruses in early childhood might increase risk
- Growing up in urban environment
- Air pollution
- Drugs: some individuals develop SZ after taking certain drugs, e.g. cannabis
what are the 4 neurotransmitters involved in SZ?
- Dopamine = linked with positive symptoms and attention, WM, cognitive control
- Acetylcholine = linked to attention and memory
- Glutamate (Glu) = main excitatory neurotransmitter
- GABA = main inhibitory neurotransmitter
what is the dopamine hypothesis?
dopamine hypothesis:
- Important role of mesocortical dopaminergic pathway (from tegmentum)
- dopaminergic agonist, i.e. drugs that increase dopamine levels, like cocaine, amphetamine or L-Dopa, can induce psychotic symptoms, which resemble positive symptoms in individuals with schizophrenia
- plausible to assume a crucial role of the DA system in schizophrenia, with high levels of dopamine causing positive symptoms
- Disturbances in this transmitter system could explain various cognitive impairments seen in individuals with schizophrenia
- Typical antipsychotic medication reduces DA levels in the brain
- these reduce positive symptoms
- but not very effective at attenuating the negative symptoms; on the contrary, they sometimes even worsen the negative symptom
dopamine hypothesis: dissociation between cortical and striatal DA
- suggested that there is a dissociation between cortical and striatal DA.
- There might be too little DA in cortical areas, i.e. a hypo-dopaminergic state
- there might be too much DA in the striatum, i.e. a hyper-dopaminergic state in the striatum
- DA levels fluctuate in individuals with SZ over time, cognitive symptoms much more stable -> close link is unlikely
Overall, the DA hypothesis cannot be the whole story. Usually, modulations in one transmitter system can also affect other neurotransmitter systems
Glutamate (Glu)
- glutamate plays a central role in schizophrenia, and that the dysregulation of the dopaminergic system is only secondary to impaired glutamatergic functions
- Glu is the main excitatory neurotransmitter in the brain, and Glu levels can modulate DA release in the Ventral Tegmental Area, so DA and Glu systems are not working independently, but they interact.
- Postmortem brains of schizophrenia patients: loss of Glu neurons in ACC (and other brain areas; Squires et al., 1993)
Moghaddam & Javitt (2012): 2 phases of Glu modulations in SZ patients
- NMDA-mediated interneuron dysfunction ➜ loss of inhibitory control, increased Glu levels
- Glu-induced excitotoxicity ➜ loss of Glu connections; decreased Glu levels