European Psychiatry (Jun 2022)

Nucleus accumbens functional connectivity and circulating endocannabinoids levels in anorexia nervosa

  • R. Miranda-Olivos,
  • I. Baenas,
  • A. Pastor,
  • A. Del Pino,
  • E. Codina,
  • I. Sánchez,
  • A. Juaneda-Segui,
  • S. Jimenez-Murcia,
  • R. De La Torre,
  • C. Soriano-Mas,
  • F. Fernandez-Aranda

DOI
https://doi.org/10.1192/j.eurpsy.2022.269
Journal volume & issue
Vol. 65
pp. S90 – S91

Abstract

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Introduction Neuroimaging findings have reported aberrant functional connectivity in brain regions involved reward system in individuals with anorexia nervosa (AN) altering hedonic processing over food. Likewise, endocannabinoids such as Anandamide (AEA) and 2-Arachidonoylglycerol (2-AG) have been involved in rewarding aspects of food intake. Objectives To identify nucleus accumbens (NAcc) functional connectivity with whole-brain comparing between individuals with AN and controls. Furthermore, in a sub-study, to explore the interaction between NAcc functional connectivity and peripheral AEA and 2-AG levels. Methods A total of 60 adult women (18 to 56 years of age) took part in the present study. Twenty-six individuals belonged to the AN group (BMI<18) and 34 to the HC group (BMI=18-24.99). All participants underwent functional magnetic resonance in resting-state, and blood samples were obtained in fasting. Results Negative functional connectivity was observed in the AN group compared with the control group between the NAcc and the cerebellum (pFWE<.001), between the NAcc and the insula (pFWE<.001), between the NAcc and the supramarginal gyrus (pFWE=.019), and between the NAcc and the postcentral gyrus (pFWE=.010). Analyses exploring the association between NAcc functional connectivity and peripheral endocannabinoids levels displayed altered NAcc-cerebellum functional connectivity was negatively associated with peripheral 2-AG levels in the AN group (r= -.553; p=.011). Conclusions Understanding the interaction between the reward system and peripheral endocannabinoids in patients with AN could contribute to better elucidate the pathophysiology of this disorder. Future studies will need to further investigate the clinical and therapeutic implications of these findings in patients with AN. Disclosure No significant relationships.

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