在初级保健中适当使用纳曲酮和安非他酮的固定剂量缓释联合治疗肥胖症

Ethan Lazarus
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引用次数: 0

摘要

背景:肥胖被认为是一种慢性疾病,受生物、环境和行为因素的影响,这些因素可促进其发展。虽然生活方式的改变对于治疗肥胖和保持健康的体重是不可或缺的,但仅仅通过行为干预来减轻体重往往是不够的,因为神经生理因素可能会对生活方式和行为的改变起作用。研究表明,食物渴望和肥胖的潜在机制与大脑中的多巴胺能信号和成瘾途径重叠。因此,受食物渴望不同影响的患者可能会有更好的结果,针对涉及稳态和享乐性食物消费或成瘾行为的神经系统进行治疗。方法通过对纳曲酮与安非他酮固定剂量缓释联合用药(NB-ER)与单一治疗成分(纳曲酮和安非他酮)的安全性和有效性进行比较,探讨NB-ER在肥胖患者治疗中的合理应用。结果:snb - er被批准用于治疗肥胖患者,研究表明,与安慰剂相比,当治疗与低热量饮食和增加体育活动相结合时,患者可以实现显着的体重减轻。在NB-ER 3期试验中,对治疗有反应的患者在56周时平均体重减轻11.7%。值得注意的是,在NB-ER中,纳曲酮(阿片受体拮抗剂)和安非他酮(去甲肾上腺素-多巴胺再摄取抑制剂)的独特组合可能共同作用于POMC细胞,以防止内源性负反馈,从而降低食欲并改善体重相关结果。结论NB-ER联合其组份药物联合单药治疗肥胖是一种较理想的治疗方法。NB-ER的适当使用应考虑个体的具体特征和肥胖相关并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Appropriate use of the fixed-dose, extended-release combination of naltrexone and bupropion as treatment for obesity in primary care

Appropriate use of the fixed-dose, extended-release combination of naltrexone and bupropion as treatment for obesity in primary care

Background

Obesity is considered a chronic disease and is influenced by biological, environmental, and behavioral factors that can contribute to its progression. Although lifestyle changes are integral to treating obesity and maintaining a healthful weight, weight reduction from behavioral intervention alone is often insufficient because neurophysiologic factors may work against such changes in lifestyle and behavior. Research suggests that the mechanisms underlying food cravings and obesity overlap with dopaminergic signaling in the brain and pathways involved in addiction. As a result, patients who are differentially impacted by food cravings may have better outcomes with treatments targeting neural systems implicated in both homeostatic and hedonic food consumption or addictive behaviors.

Methods

In this clinical review, we describe the safety and efficacy data for the fixed-dose, extended-release combination of naltrexone and bupropion (NB-ER) compared with its monotherapy constituents (naltrexone and bupropion), as well as discuss the appropriate use of NB-ER to treat patients with obesity.

Results

NB-ER is approved for the treatment of patients with obesity, with studies showing that patients can achieve significant weight reduction compared with placebo when treatment is combined with a reduced-calorie diet and increased physical activity. Across NB-ER phase 3 trials, responders to treatment had a mean body weight reduction of 11.7 % at 56 weeks. Of note, the unique combination of naltrexone, an opioid receptor antagonist, and bupropion, a norepinephrine-dopamine reuptake inhibitor associated with stimulating pro-opiomelanocortin cells (POMC), in NB-ER may work together to target POMC cells to prevent endogenous negative feedback, thereby decreasing appetite and improving weight-related outcomes.

Conclusions

Unlike monotherapy with its component drugs, NB-ER is optimized for the treatment of obesity. The appropriate use of NB-ER should consider the specific characteristics and adiposity-related complications of an individual.
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