2017-03-15 12:36:42

Prelude

Today's Topics

  • Prevalence of mental illness
  • Schizophrenia

Mental illness lifetime prevalence

Schizophrenia

Simulating the Experience

Overview

  • Lifetime prevalence ~ 1/100
  • ~1/3 chronic & severe
  • Onset post-puberty, early adulthood
  • Pervasive disturbance in mood, thinking, movement, action, memory, perception

Screening (Yale PRIME test)

  1. I think that I have felt that there are odd or unusual things going on that I can’t explain.
  2. I think that I might be able to predict the future.
  3. I may have felt that there could possibly be something interrupting or controlling my thoughts, feelings, or actions.

http://www.schizophrenia.com/sztest/primetest.pdf

Screening (continued)

  1. I get confused at times whether something I experience or perceive may be real or may be just part of my imagination or dreams.
  2. I have thought that it might be possible that other people can read my mind, or that I can read other’s minds.
  3. I wonder if people may be planning to hurt me or even may be about to hurt me.

Historical background

  • Bleuler
    • Introduced “schizophrenia” or “split mind”
    • Not multiple personality disorder
  • Kraeplin
    • Dementia Praecox and Paraphrenia (1919)
    • Emphasized developmental and hereditary origins

"Positive" symptoms

  • “Additions” to behavior
  • Disordered thought
  • Delusions of grandeur, persecution
  • Hallucinations (usually auditory)
  • Bizarre behavior

"Negative" symptoms

  • “Reductions” in behavior
  • Poverty of speech
  • Flat affect
  • Social withdrawal
  • Impaired executive function
  • Anhedonia (loss of pleasure)
  • Catatonia (reduced movement)

Cognitive symptoms

  • Memory
  • Attention
  • Planning, decision-making
  • Social cognition
  • Movement

Biological bases

  • Genetic disposition
  • Brain abnormalities
  • Developmental origins

Genetic disposition

Ventricles larger, esp in males

Hip and amygdala smaller

  • Related to ventricular enlargement?
  • Early disturbance in brain development?

(Jiao et al. 2017)

  • Dentate gyrus (DG) in hippocampus critical for spatial coding, learning and memory, and emotion processing.
  • DG dysfunction implicated in schizophrenia.
  • Gene linked to schizophrenia, Transmembrane protein 108 (Tmem108) enriched in DG granule neurons
  • Tmem108 expression increased during postnatal period critical for DG development.

(Jiao et al. 2017)

  • Tmem108-deficient neurons form fewer and smaller spines.
  • Tmem108-deficient mice display schizophrenia-relevant behavioral deficits.

Rapid gray matter loss in adolescents?

Dopamine hypothesis

Evidence for DA hypothesis

  • DA (D2 receptor) antagonists (e.g. chlorpromazine)
    • improve positive symptoms
  • Typical antipsychotics are DA D2 antagonists
  • DA agonists
    • amphetamine, cocaine, L-DOPA
    • mimic or exacerbate symptoms

Tardive Dyskinesia a side effect of DA antagonists

Evidence against…

  • New, atypical antipsychotics
    • (e.g. Clozapine) INCREASE DA in frontal cortex, affect 5-HT
  • Mixed evidence for high DA metabolite levels in CSF

Glutamate hypothesis

  • Psychomimetic drugs induce schizophrenia-like states
    • Phencyclidine (PCP), ketamine
    • NMDA receptor antagonists
  • Schizophrenia == underactivation of NMDA receptors?
    • NMDA receptor role in learning, plasticity
    • DG neurons in (Jiao et al. 2017) were glutamate-releasing.

Schizophrenia summed up

  • Wide-ranging disturbance of mood, thought, action, perception
  • Broad changes in brain structure, function, chemistry, development
  • Genetic risk + environmental factors

Early life stress increases risk

  • Urban vs. rural living
  • Exposure to infection in utero, other birth complications

(Levine et al. 2016)

  • Children (N=51,233) of parents who born during Nazi era (1922-1945)
  • Emigrated before (indirect exposure) or after (direct exposure) to Nazi era
  • Children exposed to direct stress of Nazi era in utero or postnatally
    • Did not differ in rates of schizophrenia, but
    • Had higher rehospitalization rates

(Debost et al. 2015)

  • Danish cohort (n=1,141,447)
  • Exposure to early life stress
    • in utero did not increase risk of schizophrenia, but
    • during 0-2 years increased risk
  • Increased risk associated with an allele of a cortisol-related gene

Next time…

  • Bipolar disorder

References

Debost, Jean-Christophe, Liselotte Petersen, Jakob Grove, Anne Hedemand, Ali Khashan, Tine Henriksen, Ole Mors, et al. 2015. “Investigating Interactions Between Early Life Stress and Two Single Nucleotide Polymorphisms in HSD11B2 on the Risk of Schizophrenia.” Psychoneuroendocrinology 60 (October): 18–27. doi:10.1016/j.psyneuen.2015.05.013.

Jiao, Hui-Feng, Xiang-Dong Sun, Ryan Bates, Lei Xiong, Lei Zhang, Fang Liu, Lei Li, et al. 2017. “Transmembrane Protein 108 Is Required for Glutamatergic Transmission in Dentate Gyrus.” Proceedings of the National Academy of Sciences 114 (5): 1177–82. doi:10.1073/pnas.1618213114.

Levine, Stephen Z., Itzhak Levav, Inna Pugachova, Rinat Yoffe, and Yifat Becher. 2016. “Transgenerational Effects of Genocide Exposure on the Risk and Course of Schizophrenia: A Population-Based Study.” Schizophrenia Research 176 (2): 540–45. doi:10.1016/j.schres.2016.06.019.

Thompson, Paul M., Christine Vidal, Jay N. Giedd, Peter Gochman, Jonathan Blumenthal, Robert Nicolson, Arthur W. Toga, and Judith L. Rapoport. 2001. “Mapping Adolescent Brain Change Reveals Dynamic Wave of Accelerated Gray Matter Loss in Very Early-Onset Schizophrenia.” Proceedings of the National Academy of Sciences 98 (20): 11650–5. doi:10.1073/pnas.201243998.