Genetic Causes (biological) Flashcards

1
Q

What did Ripke et al (2014) suggest?

A
  • schizophrenia might be polygenic

- a number of candidate genes might be responsible for the illness

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2
Q

What study did Ripke et al (2014) conduct and what was found?

A
  • investigated candidate genes
  • meta-analysis of studies
  • 37,000 patients, 11,000 control
  • 108 separate genetic variations = increased risk
  • high levels of dopamine
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3
Q

Evaluate Ripke et al (2014).

A

(+) High level of research support. Evidence is robust and hard to ignore as a cause for sz

(+) supported by dopamine hypothesis - D1/D2 receptors cause sz.

(-) other approaches need to be considered - behavioural develops sz

(-) diathesis stress model - more likely to get sz if gene is present but environmental factor triggers it

(-) mutation in parental DNA that causes offspring to get sz. Positive correlation between age of father and risk of sz. age <25, 0.7%. age >50 , 2%

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4
Q

What study did Gottesman and Shields conduct?

A
  • investigated 224 sets of twins (106 monozygotic, 118 dizygotic)
  • 120M, 104F
  • avg age 46 years, range of ethnic backgrounds
  • conducted in London hospital
  • longitudinal study over 25 years (1948 - 1993)
  • one twin already had sz, measured concordance rates - likelihood of healthy twin developing sz
  • in-depth interview, case notes, DSM used to diagnose sz
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5
Q

What were the results from Gottesman and Shields’ study?

A
  • 48% of MZ twins were concordant for sz at the end of the study
  • 17% of DZ twins were concordant for sz at the end of the study
  • sz has a genetic basis to some extent, esp MZ
  • genetics less prominent of a cause for DZ
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6
Q

Evaluate Gottesman and Shields.

A

(+) it was longitudinal, so development could be monitored

(+) results show concordance rates that support the biological argument

(+) both valid and reliable. Uses qualitative methods for diagnosis. 3 methods mean inter-rater reliability and high validity

(-) ignores behavioural approach. twins copy and model behavioural.

(-) relies on interviews - sz have difficulty with speech and communication. Negative effect on diagnosis and classification.

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7
Q

What study did Kety et al (1994) conduct?

A

The Copenhagen High-Risk Study:

  • prospective longitudinal study in 1972 (follow-up study 1974 - 1989)
  • 207 adopted children, biological mothers had sz (high-risk)
  • matched control group of 104 adopted children, healthy biological mothers (low-risk)
  • ages of 10-18 at start of the study, matched in terms of age, gender, parental social-economic status
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8
Q

What were the results from Kety et al (1994)?

A
  • strong genetic basis for mental disorders
  • 16.2% high risk, 1.9% low risk diagnosed with sz
  • 18.8% high risk, 5% low risk diagnosed with schizotypal personality disorder
  • overall: 35% high, 6.9% low for mental disorders
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9
Q

Evaluate Kety et al (1994).

A

(+) ‘New York High-Risk Project’, longitudinal study for 25 yrs. Found similar results to Kety.

(+) Prospective study looks before symptoms develop. Doesn’t rely on self-reports (retrospective) - unreliable

(+) Fair, controlled, valid bc eliminates confounding variables - matched pairs

(-) cannot separate genes from environment. Children share environment with sz mother. Needs to be considered when interpreting results

(-) Mothers were diagnosed without DSM - may not have sz. Reliability of diagnosis is problematic

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