Genetic/Biological Explanation for Anorexia TEST ON EVAL MONDAY Flashcards
Genetic Explanation for Anorexia
4
EPHX2 Gene
ITPR3 Gene
Strober (2000)
Gorwood (2003)
EPHX2 Gene
Codes for an enzyme that regulates cholesterol metabolism.
Van Zeeland found EPHX2 is linked with AN
ITPR3 Gene
Encodes an enzyme involved in detecting taste.
Strober (2000)
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
Gorwood (2003)
Estimated heritability of AN was 70%
Dopamine & AN
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)
Serotonin & AN
5-HTR2A gene mutations affect seratonin binding to receptors. Kaye (2005). Appetite-related neural info is thus not processed correctly
Eval. of Bio/Genetic explanation for AN
1 Strength, 2 Weaknesses
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