# Abnormal Social Reward Responses in Anorexia Nervosa: An fMRI Study

**Authors:** Esther Via, Carles Soriano-Mas, Isabel Sánchez, Laura Forcano, Ben J. Harrison, Christopher G. Davey, Jesús Pujol, Ignacio Martínez-Zalacaín, José M. Menchón, Fernando Fernández-Aranda, Narcís Cardoner

PMC · DOI: 10.1371/journal.pone.0133539 · PLoS ONE · 2015-07-21

## TL;DR

This fMRI study finds abnormal brain responses to social rewards in anorexia nervosa patients, linking these changes to clinical severity and personality traits.

## Contribution

The study is the first to show altered neural responses to social acceptance and rejection in anorexia nervosa using fMRI.

## Key findings

- Patients with anorexia nervosa showed hypoactivation in the dorsomedial prefrontal cortex during social acceptance.
- Hyperactivation of visual areas during social rejection was observed in anorexia nervosa patients.
- Ventral striatum activation during rejection correlated with clinical severity in anorexia nervosa patients.

## Abstract

Patients with anorexia nervosa (AN) display impaired social interactions, implicated in the development and prognosis of the disorder. Importantly, social behavior is modulated by reward-based processes, and dysfunctional at-brain-level reward responses have been involved in AN neurobiological models. However, no prior evidence exists of whether these neural alterations would be equally present in social contexts. In this study, we conducted a cross-sectional social-judgment functional magnetic resonance imaging (fMRI) study of 20 restrictive-subtype AN patients and 20 matched healthy controls. Brain activity during acceptance and rejection was investigated and correlated with severity measures (Eating Disorder Inventory -EDI-2) and with personality traits of interest known to modulate social behavior (The Sensitivity to Punishment and Sensitivity to Reward Questionnaire). Patients showed hypoactivation of the dorsomedial prefrontal cortex (DMPFC) during social acceptance and hyperactivation of visual areas during social rejection. Ventral striatum activation during rejection was positively correlated in patients with clinical severity scores. During acceptance, activation of the frontal opercula-anterior insula and dorsomedial/dorsolateral prefrontal cortices was differentially associated with reward sensitivity between groups. These results suggest an abnormal motivational drive for social stimuli, and involve overlapping social cognition and reward systems leading to a disruption of adaptive responses in the processing of social reward. The specific association of reward-related regions with clinical and psychometric measures suggests the putative involvement of reward structures in the maintenance of pathological behaviors in AN.

## Linked entities

- **Diseases:** anorexia nervosa (MONDO:0005351)

## Full-text entities

- **Genes:** OXT (oxytocin/neurophysin I prepropeptide) [NCBI Gene 5020] {aka OT, OT-NPI, OXT-NPI}
- **Diseases:** psychiatric (MESH:D001523), DSM-IV TR (MESH:D006011), functional impairment (MESH:D003072), DSM-IV Axis I Disorders (MESH:C566610), -2 (MESH:D020803), Depression (MESH:D003866), Anxiety (MESH:D001007), neurological condition (MESH:D019636), social difficulties (MESH:D051346), Social Anxiety (MESH:D000072861), pain (MESH:D010146), AN (MESH:D000856), anorexia (MESH:D000855), Eating Disorder (MESH:D001068), ABA (MESH:D013217), malnutrition (MESH:D044342), analgesia (MESH:D000699), functional and social impairment (OMIM:300082), Disorders (MESH:D009358)
- **Chemicals:** nicotine (MESH:D009538), 3 -       Tricyclic antidepressant (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC4510264/full.md

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC4510264/full.md

## References

91 references — full list in the complete paper: https://tomesphere.com/paper/PMC4510264/full.md

---
Source: https://tomesphere.com/paper/PMC4510264