Hubertus Himmerich, Jessica Bentley, Susan L. McElroy
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引用次数: 0
摘要
暴饮暴食症(BED)是最常见的特殊饮食失调症(ED)。它经常与注意力缺陷多动障碍(ADHD)、抑郁症、双相情感障碍(BD)、焦虑症、酒精和尼古丁使用障碍以及肥胖症相关联。本综述旨在总结 BED 及其合并症的药物治疗证据。我们推荐多动症药物利司他敏(LDX)和抗癫痫及抗偏头痛药物托吡酯用于 BED 的药物治疗。不过,在一些国家,只有 LDX 被批准用于治疗 BED。治疗 BED 常见合并症的药物包括:治疗多动症的阿托西汀和 LDX;治疗焦虑症和抑郁症的西酞普兰、氟西汀、舍曲林、度洛西汀和文拉法辛;治疗 BD 躁狂发作的阿立哌唑;治疗 BD 抑郁发作的拉莫三嗪、利拉西酮和卢马替丙酮;治疗酒精使用障碍的纳曲酮;治疗尼古丁使用障碍的安非他酮;以及治疗肥胖症的利拉鲁肽、赛马鲁肽和安非他酮与纳曲酮的复方制剂。由于肥胖是 BED 常见的健康后果,应尽可能避免使用导致体重增加的药物,如非典型抗精神病药物奥氮平或氯氮平、新型抗抑郁药物米氮平和三环类抗抑郁药物,以及情绪稳定剂丙戊酸钠。目前还不清楚新型和前景看好的胰高血糖素、葡萄糖依赖性促胰岛素多肽(GIP)和胰高血糖素样肽 1(GLP-1)受体激动剂(如替泽帕肽和雷他曲肽)是否有助于治疗 BED 及其合并症。不过,有报道称这些化合物可减少肥胖或超重患者的暴饮暴食。
Pharmacological Treatment of Binge Eating Disorder and Frequent Comorbid Diseases
Binge eating disorder (BED) is the most common specific eating disorder (ED). It is frequently associated with attention deficit hyperactivity disorder (ADHD), depression, bipolar disorder (BD), anxiety disorders, alcohol and nicotine use disorder, and obesity. The aim of this narrative review was to summarize the evidence for the pharmacological treatment of BED and its comorbid disorders. We recommend the ADHD medication lisdexamfetamine (LDX) and the antiepileptic and antimigraine drug topiramate for the pharmacological treatment of BED. However, only LDX is approved for the treatment of BED in some countries. Medications to treat diseases frequently comorbid with BED include atomoxetine and LDX for ADHD; citalopram, fluoxetine, sertraline, duloxetine, and venlafaxine for anxiety disorders and depression; aripiprazole for manic episodes of BD; lamotrigine, lirasidone and lumateperone for depressive episodes of BD; naltrexone for alcohol use disorder; bupropion for nicotine use disorder; and liraglutide, semaglutide, and the combination of bupropion and naltrexone for obesity. As obesity is a frequent health consequence of BED, weight gain-inducing medications, such as the atypical antipsychotics olanzapine or clozapine, the novel antidepressant mirtazapine and tricyclic antidepressants, and the mood stabilizer valproate should be avoided where possible. It is currently unclear whether the novel and promising glucagon, glucose-dependent insulinotropic polypeptide (GIP), and glucagon-like peptide 1 (GLP-1) receptor agonists like tirzepatide and retatrutide help with BED and its comorbidities. However, these compounds have been reported to reduce binge eating in individuals with obesity or overweight.
期刊介绍:
CNS Drugs promotes rational pharmacotherapy within the disciplines of clinical psychiatry and neurology. The Journal includes:
- Overviews of contentious or emerging issues.
- Comprehensive narrative reviews that provide an authoritative source of information on pharmacological approaches to managing neurological and psychiatric illnesses.
- Systematic reviews that collate empirical evidence to answer a specific research question, using explicit, systematic methods as outlined by the PRISMA statement.
- Adis Drug Reviews of the properties and place in therapy of both newer and established drugs in neurology and psychiatry.
- Original research articles reporting the results of well-designed studies with a strong link to clinical practice, such as clinical pharmacodynamic and pharmacokinetic studies, clinical trials, meta-analyses, outcomes research, and pharmacoeconomic and pharmacoepidemiological studies.
Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in CNS Drugs may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances.