Manigault Kendra R, Thurston Maria Miller
Consult Pharm. 2016 Dec 1;31(12):685-697. doi: 10.4140/TCP.n.2016.685.
To review the efficacy and safety of liraglutide 3.0 mg for weight loss.
A literature search was performed using PubMed and MEDLINE from 2000 to 2016. The following key terms were used alone or in combination: glucagon-like peptide-1 agonist, liraglutide, obesity, overweight, and weight loss. Additional supporting literature was identified utilizing the reference lists of the preceding articles.
Analyzed studies were published in English and investigated use of liraglutide and its impact on weight loss.
Clinical studies with a primary focus of liraglutide use in weight loss were included in this review. Author consensus determined final study inclusion.
Management of obesity centers on behavior modification that includes diet and exercise; however, pharmacologic therapy may be used. Several studies have indicated that GLP-1 receptor agonists promote weight loss in patients with type 2 diabetes mellitus (T2DM). The efficacy of liraglutide 3.0 mg as a weight-loss agent in patients with and without T2DM was established in three SCALE™ clinical trials. Liraglutide 3.0 mg was generally well tolerated during clinical trials. Common adverse events were typically related to the gastrointestinal system (i.e., nausea, vomiting).
Based on available evidence, liraglutide 3.0 mg appears to be a safe and effective addition to the pharmacologic armamentarium available for chronic weight management in the general population. However, there are limited data within the geriatric population. Clinicians should consider liraglutide's cost, route of administration, and concomitant drug therapy when deciding which patients are appropriate candidates for liraglutide therapy.
AE = Adverse events, AHA/ACC/TOS = American Heart Association/American College of Cardiology/ The Obesity Society, BMI = Body mass index, CV = Cardiovascular, FDA = Food and Drug Administration, GI = Gastrointestinal, GLP-1 = Glucagon-like peptide-1, HbA1c = Hemoglobin A1c, Kcal = Kilocalorie, LCD = Low-calorie diet, MTC = Medullary thyroid carcinoma, NHLBI = National Heart Lung and Blood Institute, NNH = Number needed to harm, PYE = Patient years of exposure, REMS = Risk Evaluation and Mitigation Strategy, SCALE™ = Satiety and Clinical Adiposity - Liraglutide Evidence in Non-diabetic and Diabetic individuals, T2DM = Type 2 diabetes mellitus.
回顾利拉鲁肽3.0毫克用于减肥的疗效和安全性。
使用PubMed和MEDLINE对2000年至2016年的文献进行检索。单独或组合使用以下关键词:胰高血糖素样肽-1激动剂、利拉鲁肽、肥胖、超重和减肥。利用前文的参考文献列表确定了其他支持性文献。
分析的研究以英文发表,并调查了利拉鲁肽的使用及其对减肥的影响。
本综述纳入了主要关注利拉鲁肽用于减肥的临床研究。由作者达成共识确定最终纳入的研究。
肥胖管理以行为改变为中心,包括饮食和运动;然而,也可使用药物治疗。多项研究表明,胰高血糖素样肽-1受体激动剂可促进2型糖尿病(T2DM)患者减肥。三项SCALE™临床试验确定了利拉鲁肽3.0毫克作为减肥药物在有或无T2DM患者中的疗效。利拉鲁肽3.0毫克在临床试验中总体耐受性良好。常见不良事件通常与胃肠道系统有关(即恶心、呕吐)。
根据现有证据,利拉鲁肽3.0毫克似乎是一般人群慢性体重管理可用药物中的一种安全有效的补充药物。然而,老年人群中的数据有限。临床医生在决定哪些患者适合使用利拉鲁肽治疗时,应考虑利拉鲁肽的成本、给药途径和联合药物治疗。
AE = 不良事件,AHA/ACC/TOS = 美国心脏协会/美国心脏病学会/肥胖协会,BMI = 体重指数,CV = 心血管,FDA = 美国食品药品监督管理局,GI = 胃肠道,GLP-1 = 胰高血糖素样肽-1,HbA1c = 糖化血红蛋白,Kcal = 千卡,LCD = 低热量饮食,MTC = 甲状腺髓样癌,NHLBI = 美国国立心肺血液研究所,NNH = 伤害所需人数,PYE = 患者暴露年数,REMS = 风险评估与缓解策略,SCALE™ = 饱腹感与临床肥胖——利拉鲁肽在非糖尿病和糖尿病个体中的证据,T2DM = 2型糖尿病