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对于无糖尿病的受试者,纳曲酮/安非他酮缓释剂所致体重减轻与恶心无关。

Naltrexone/Bupropion extended release-induced weight loss is independent of nausea in subjects without diabetes.

作者信息

Hong K, Herrmann K, Dybala C, Halseth A E, Lam H, Foreyt J P

机构信息

Center for Clinical Nutrition & Applied Health Research, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.

US Medical Affairs Department, Takeda Pharmaceuticals USA Inc., Deerfield, IL, USA.

出版信息

Clin Obes. 2016 Oct;6(5):305-12. doi: 10.1111/cob.12157. Epub 2016 Aug 1.

Abstract

Naltrexone/bupropion extended release (NB) is indicated as an adjunct to a reduced-calorie diet and increased physical activity for chronic weight management in adults with an initial body mass index of ≥30 or ≥27 kg m(-2) and ≥1 weight-related comorbidity (e.g. hypertension, type 2 diabetes and dyslipidaemia). In phase 3 clinical studies, nausea occurred in significantly higher proportions of subjects randomized to NB vs. placebo (PBO). In this pooled analysis of three phase 3, 56-week, PBO-controlled studies, we characterized nausea and weight loss in NB- and PBO-treated subjects without diabetes. Subjects receiving NB (n = 1778) lost significantly more weight than those receiving PBO (n = 1160). Weight change was not significantly different between subjects reporting and not reporting nausea in either treatment arm. Severity of nausea was mild to moderate in ≥95% of all cases. In the NB arm, the highest incidence of nausea onset (9%) was reported during week 1. The median duration of mild, moderate and severe nausea in subjects receiving NB was 14, 9 and 13 days, respectively. Our results demonstrate that nausea associated with NB is rarely severe, primarily occurs early in treatment and is not a contributor to weight loss.

摘要

纳曲酮/安非他酮缓释片(NB)被指定作为低热量饮食和增加体育活动的辅助手段,用于初始体重指数≥30或≥27kg/m²且伴有≥1种与体重相关合并症(如高血压、2型糖尿病和血脂异常)的成年患者的慢性体重管理。在3期临床研究中,随机接受NB治疗的受试者中恶心发生率显著高于接受安慰剂(PBO)的受试者(PBO)。在这项对三项56周的3期PBO对照研究的汇总分析中,我们对未患糖尿病的接受NB和PBO治疗的受试者的恶心和体重减轻情况进行了描述。接受NB治疗的受试者(n = 1778)比接受PBO治疗的受试者(n = 1160)体重减轻显著更多。在两个治疗组中,报告恶心和未报告恶心的受试者之间体重变化无显著差异。在所有病例中,≥95%的恶心严重程度为轻度至中度。在NB组中,第1周报告的恶心发作发生率最高(9%)。接受NB治疗的受试者中,轻度、中度和重度恶心的中位持续时间分别为14天、9天和13天。我们的结果表明,与NB相关联的恶心很少严重,主要发生在治疗早期,且并非体重减轻的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d0d/5129540/829dff60ec2e/COB-6-305-g002.jpg

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