Dulaglutide use to improve binge eating behaviors in a person with type 2 diabetes and obesity.

IF 2.1 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Britnee Innocent, Amre A Elmaoued, Kevin Cowart, Raechel T White
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Abstract

Disclaimer: In an effort to expedite the publication of articles, AJHP is posting manuscripts online as soon as possible after acceptance. Accepted manuscripts have been peer-reviewed and copyedited, but are posted online before technical formatting and author proofing. These manuscripts are not the final version of record and will be replaced with the final article (formatted per AJHP style and proofed by the authors) at a later time.

Purpose: Binge eating disorder (BED) is a psychological disorder that poses several functional consequences for those affected. Management of BED centers around psychological and pharmacological treatment modalities, which have been associated with variable efficacy and the potential for severe adverse effects. Glucagon-like peptide-1 receptor agonists (GLP-1 RAs), approved by the Food and Drug Administration for conditions such as diabetes and weight management, are an emerging therapy of interest in BED.

Summary: In this case report, we describe use of dulaglutide for treatment of a patient with BED, obesity, and type 2 diabetes mellitus. The patient's baseline binge eating scale (BES) score, glycated hemoglobin level, body mass index (BMI), and weight were obtained. Following these baseline assessments, dulaglutide 0.75 mg once weekly was initiated to optimize management of the patient's type 2 diabetes. Follow-up measurements were obtained 6 weeks after initiation, at which time reductions in the patient's BES score, BMI, weight, and BED symptoms were observed. Moreover, dulaglutide was well tolerated without adverse drug events.

Conclusion: This case report describes the use of dulaglutide in the management of mild BED in the setting of comorbid type 2 diabetes and obesity. Further research is necessary to evaluate the long-term effectiveness of GLP-1 RAs in the management of BED and to determine the optimal duration and dose.

杜拉鲁肽用于改善2型糖尿病和肥胖症患者的暴食行为。
免责声明:为了加快文章的发表,AJHP在接受稿件后将尽快在网上发布。被接受的稿件已经过同行评审和编辑,但在技术格式化和作者校对之前会在网上发布。这些手稿不是记录的最终版本,稍后将被最终文章(按照AJHP风格格式化并由作者校对)所取代。目的:暴食症(BED)是一种心理障碍,对受影响的人造成几种功能上的后果。BED的管理以心理和药物治疗方式为中心,这与不同的疗效和潜在的严重不良反应有关。胰高血糖素样肽-1受体激动剂(GLP-1 RAs)已被美国食品和药物管理局批准用于糖尿病和体重管理等疾病,是一种对BED感兴趣的新兴疗法。摘要:在这个病例报告中,我们描述了使用杜拉鲁肽治疗BED,肥胖和2型糖尿病患者。获得患者的基线暴食量表(BES)评分、糖化血红蛋白水平、体重指数(BMI)和体重。根据这些基线评估,开始使用杜拉鲁肽0.75 mg,每周一次,以优化患者2型糖尿病的管理。开始治疗6周后进行随访测量,观察患者的BES评分、BMI、体重和BED症状的下降。此外,dulaglutide耐受性良好,无药物不良事件。结论:本病例报告描述了在合并2型糖尿病和肥胖的情况下使用杜拉鲁肽治疗轻度BED。进一步研究GLP-1 RAs治疗BED的远期疗效,确定最佳用药时间和剂量是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.90
自引率
18.50%
发文量
341
审稿时长
3-8 weeks
期刊介绍: The American Journal of Health-System Pharmacy (AJHP) is the official publication of the American Society of Health-System Pharmacists (ASHP). It publishes peer-reviewed scientific papers on contemporary drug therapy and pharmacy practice innovations in hospitals and health systems. With a circulation of more than 43,000, AJHP is the most widely recognized and respected clinical pharmacy journal in the world.
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