Genetic/Biological Explanation for Anorexia TEST ON EVAL MONDAY Flashcards

1
Q

Genetic Explanation for Anorexia

4

A

EPHX2 Gene

ITPR3 Gene

Strober (2000)

Gorwood (2003)

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2
Q

EPHX2 Gene

A

Codes for an enzyme that regulates cholesterol metabolism.

Van Zeeland found EPHX2 is linked with AN

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3
Q

ITPR3 Gene

A

Encodes an enzyme involved in detecting taste.

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4
Q

Strober (2000)

A

Found that AN was rare in relatives of those who had never had an eating disorder. It was 11.3x more prevalent in those who had

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5
Q

Gorwood (2003)

A

Estimated heritability of AN was 70%

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6
Q

Dopamine & AN

A

Mutation in the DAT1 gene disrupts dopamine levels, leaving v high levels of dopamine. This desensitized reward systems, thus the normal rewarding function of eating is limited (Avena & Bocarsly 2012)

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7
Q

Serotonin & AN

A

5-HTR2A gene mutations affect seratonin binding to receptors. Kaye (2005). Appetite-related neural info is thus not processed correctly

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8
Q

Eval. of Bio/Genetic explanation for AN

1 Strength, 2 Weaknesses

A

Strength
- Holland et al. (1988) studied 45 female twins,
found concordance rates of 56% MZ and 5% DZ. Replicated by Holland & Treasure (1995) and similar results found
- Strober (2000) found AN 11.3x more prevalent in those w family members w history of eating disorders
- Gorwood (2003) estimated AN heritability at 70%

Weaknesses

  • Depend on Equal environments assumption. Joseph (2002) argues MZ twins are treated more similarly than DZ.
  • Wide variety of AN symptoms can’t be explained by one gene as there are so many physical, cognitive & behavioural symptoms. AN is polygenic. Oversimplified and reductionist
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