Abstract

Anorexia nervosa (AN) is an eating disorder often occurring in adolescence. AN has one of the highest mortality rates amongst psychiatric illnesses and is associated with medical complications and high risk for psychiatric comorbidities, persisting after treatment. Remission rates range from 23% to 33%. Moreover, weight recovery does not necessarily reflect cognitive recovery. This issue is of particular interest in adolescence, characterized by progressive changes in brain structure and functional circuitries, and fast cognitive development. We reviewed existing literature on fMRI studies in adolescents diagnosed with AN, following PRISMA guidelines. Eligible studies had to: (1) be written in English; (2) include only adolescent participants; and (3) use block-design fMRI. We propose a pathogenic model based on normal and AN-related neural and cognitive maturation during adolescence. We propose that underweight and delayed puberty—caused by genetic, environmental, and neurobehavioral factors—can affect brain and cognitive development and lead to impaired cognitive flexibility, which in turn sustains the perpetuation of aberrant behaviors in a vicious cycle. Moreover, greater punishment sensitivity causes a shift toward punishment-based learning, leading to greater anxiety and ultimately to excessive reappraisal over emotions. Treatments combining physiological and neurobehavioral rationales must be adopted to improve outcomes and prevent relapses.

Highlights

  • The lifetime prevalence of Anorexia nervosa (AN) in females ranges from 0.5 to 2.2% [1,2], while is tenfold lower in males [3]

  • Adolescent-onset AN seems to be associated with better remission rates [2]

  • We reviewed 12 fMRI studies investigating different cognitive domains in adolescent patients with AN compared with controls

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Summary

Introduction

The lifetime prevalence of AN in females ranges from 0.5 to 2.2% [1,2], while is tenfold lower in males [3]. Adolescent-onset AN seems to be associated with better remission rates [2]. Recovery can take several years [2], and the risk for relapse is high during the first 16 months after treatment and increases with time [3,4,5]. AN is associated with a trait-dependent high prevalence of comorbid psychiatric disorders, persisting after treatment and recovery [2]. The most common comorbidities are mood disorders, personality disorders, anxiety disorders, obsessive-compulsive disorders, and developmental disorders (e.g., autistic spectrum, attention-deficit hyperactivity disorder) [6]. These comorbidities can complicate treatment and need to be addressed in order to achieve a better outcome [6]. AN is associated with several short-and long-term systemic consequences for the reproductive, Nutrients 2019, 11, 1907; doi:10.3390/nu11081907 www.mdpi.com/journal/nutrients

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