Binge-eating disorder: Clinical and therapeutic advances

被引:37
作者
Hutson, Peter H. [1 ]
Balodis, Iris M. [2 ]
Potenza, Marc N. [3 ,4 ,5 ,6 ]
机构
[1] Teva Pharmaceut, CNS Discovery, Dept Neurobiol, W Chester, PA 19380 USA
[2] McMaster Univ, Dept Psychiat & Behav Neurosci, Peter Boris Ctr Addict Res, Hamilton, ON, Canada
[3] Yale Univ, Sch Med, Dept Psychiat, Child Study Ctr, New Haven, CT USA
[4] Yale Univ, Sch Med, Dept Neurosci, New Haven, CT USA
[5] Natl Ctr Addict & Subst Abuse, New York, NY USA
[6] Connecticut Mental Hlth Ctr, New Haven, CT USA
关键词
Binge-eating disorder; Impulsivity; Compulsivity; Reward; Neurobiology; Pharmacotherapy; OPIOID RECEPTOR ANTAGONIST; ACID AMIDE HYDROLASE; CAUDOLATERAL ORBITOFRONTAL CORTEX; SEROTONIN TRANSPORTER BINDING; PLACEBO-CONTROLLED TRIAL; NUCLEUS-ACCUMBENS SHELL; SELF-REGULATORY CONTROL; VENTRAL TEGMENTAL AREA; FOOD-SEEKING BEHAVIOR; DOUBLE-BLIND TRIAL;
D O I
10.1016/j.pharmthera.2017.08.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Binge-eating disorder (BED) is the most prevalent eating disorder with estimates of 2-5% of the general adult population. Nonetheless, its pathophysiology is poorly understood. Furthermore, there exist few therapeutic options for its effective treatment. Here we review the current state of binge-eating neurobiology and pharmacology, drawing from clinical therapeutic, neuroimaging, cognitive, human genetic and animal model studies. These studies, which are still in their infancy, indicate that while there are many gaps in our knowledge, several key neural substrates appear to underpin binge-eating and may be conserved between human and animals. This observation suggests that behavioral intermediate phenotypes or endophenotypes relevant to BED may be modeled in animals, facilitating the identification and testing of novel pharmacological targets. The development of novel, safe and effective pharmacological therapies for the treatment of BED will enhance the ability of clinicians to provide optimal care for people with BED.
引用
收藏
页码:15 / 27
页数:13
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