Neurobiology of Avoidant/Restrictive Food Intake Disorder

Sophie Scharner
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Abstract

Avoidant/restrictive food intake disorder (ARFID) is a complex, phenotypically heterogenous, and often severe feeding and eating disorder. Genetic studies suggest that ARFID is highly heritable, and that genes involved in taste perception and neurodevelopmental disorders may confer increased risk for the disorder. Neuroimaging studies are limited but point toward greater activation in reward circuitry among individuals with ARFID who are also overweight or obese, compared to those of normal weight. Endocrine studies have identified maladaptively high satiety-promoting (Peptide YY, cholecystokinin, oxytocin) and low hunger-promoting (ghrelin) hormone levels among individuals with ARFID, which may contribute to disease etiology and/or maintenance. Although research is limited, emerging insights into the pathophysiology of this common and impairing disorder may pave the way for the development of novel biological and pharmacological treatments. [ Psychiatr Ann. 2024;54(2):e47–e50.]
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回避型/限制型食物摄入障碍的神经生物学
回避型/限制型食物摄入障碍(ARFID)是一种复杂的、表型异质性的、通常严重的进食和饮食障碍。遗传学研究表明,ARFID 具有高度遗传性,涉及味觉感知和神经发育障碍的基因可能会增加患这种疾病的风险。神经影像学研究有限,但研究表明,与体重正常者相比,超重或肥胖的 ARFID 患者的奖赏回路激活程度更高。内分泌研究发现,ARFID 患者体内促进饱腹感的激素(肽 YY、胆囊收缩素、催产素)水平偏高,而促进饥饿感的激素(胃泌素)水平偏低,这可能是疾病的病因和/或维持因素。尽管研究有限,但对这种常见的损伤性疾病的病理生理学的新认识可能为开发新型生物和药物治疗方法铺平道路。 [ 《精神病学年鉴》,2024;54(2):e47-e50]。
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