Background
Hunger enhances sensitivity to reward, yet individuals with anorexia nervosa (AN) are not motivated to eat when starved. This study examined whether diminished response to reward could underlie food restriction in AN by investigating brain response to rewards during hunger and satiated states.
Methods
Using a delay discounting monetary decision task known to discriminate brain regions contributing to processing of immediate rewards and cognitive control important for decision making regarding future rewards, we compared 23 adults remitted from AN (to reduce the confounding effects of starvation [RAN]) to 17 healthy women (CW). Monetary rewards were used because the rewarding value of food may be confounded by anxiety in AN.
Results
Interactions of group (RAN, CW) × visit (hunger, satiety) revealed that, for CW, hunger significantly increased activation in reward salience circuitry (ventral striatum, dorsal caudate, anterior cingulate cortex) during processing of immediate reward, whereas satiety increased activation in cognitive control circuitry (ventrolateral prefrontal cortex, insula) during decision-making. In contrast, brain response in reward and cognitive neurocircuitry did not differ during hunger and satiety in RAN. A main effect of group revealed elevated response in the middle frontal gyrus for RAN.
Conclusions
RAN failed to increase activation of reward valuation circuitry when hungry and showed elevated response in cognitive control circuitry independent of metabolic state. Decreased sensitivity to hunger’s motivational drive may explain AN individuals’ ability to restrict food when emaciated. Moreover, difficulties in valuating emotional salience may contribute to inabilities to appreciate the risks inherent in this deadly disorder.