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奥利司他和利拉鲁肽在真实世界环境中肥胖患者中的疗效和耐受性:XENSOR 研究。

Effectiveness and tolerability of orlistat and liraglutide in patients with obesity in a real-world setting: The XENSOR Study.

机构信息

Unit of Endocrinology and Nutrition, Hospital Universitario Fundación Alcorcón, Madrid, Spain.

出版信息

Int J Clin Pract. 2019 Nov;73(11):e13399. doi: 10.1111/ijcp.13399. Epub 2019 Aug 19.

Abstract

AIMS

To evaluate in a real-world setting the effectiveness of two drugs, orlistat and liraglutide, in patients with overweight or obesity and insufficient weight loss (WL) after a lifestyle modification programme.

METHODS

Retrospective, observational cohort study comparing clinical outcomes of orlistat 120 mg three times a day and liraglutide (up to 3 mg daily) in adult patients with BMI ≥30 kg/m or ≥27 kg/m with at least a weight-related comorbidity who had failed to lose at least 5% of their weight after 6 months of lifestyle modification. The co-primary end-points, assessed at 3-6 months and at the end of the follow-up, were weight change from baseline, proportion of patients who lost at least 5% of their baseline weight and adjusted differences in WL between both drugs.

RESULTS

Five hundred patients, 400 in the group of orlistat (age 47.0, weight 107.8 kg) and 100 in the group of liraglutide (age 51.9 years, weight 105.1 kg), were included. Treatment with both drugs significantly reduced weight, fasting plasma glucose, systolic BP, low-density lipoprotein-cholesterol and alanine transaminase over a median follow-up period of 7 months. WL with liraglutide (-7.7 kg) was significantly greater than that observed with orlistat (-3.3 kg), and more individuals lost at least 5% of their baseline weight with liraglutide (64.7%) than with orlistat (27.4%). Rates of prediabetes significantly decreased with liraglutide in comparison to orlistat.

CONCLUSIONS

In this real-world study, liraglutide showed a greater effectiveness in WL compared with orlistat and improved several obesity-associated metabolic and cardiovascular risk factors.

摘要

目的

在真实环境中评估两种药物,奥利司他和利拉鲁肽,在生活方式改变方案后超重或肥胖且减重不足(WL)的患者中的疗效。

方法

回顾性观察性队列研究比较了奥利司他 120mg 每日三次和利拉鲁肽(最高 3mg 每日)在 BMI≥30kg/m 或≥27kg/m 且至少有与体重相关的合并症的成年患者中的临床结局,这些患者在生活方式改变 6 个月后体重至少减轻 5%。主要终点为从基线的体重变化、至少减轻基线体重 5%的患者比例以及两种药物之间 WL 调整差异,评估时间为 3-6 个月和随访结束时。

结果

共纳入 500 例患者,其中 400 例患者接受奥利司他治疗(年龄 47.0 岁,体重 107.8kg),100 例患者接受利拉鲁肽治疗(年龄 51.9 岁,体重 105.1kg)。两种药物治疗均显著降低体重、空腹血糖、收缩压、低密度脂蛋白胆固醇和丙氨酸转氨酶,中位随访时间为 7 个月。利拉鲁肽的 WL(-7.7kg)明显大于奥利司他(-3.3kg),并且更多的患者至少减轻了 5%的基线体重(64.7%),而奥利司他(27.4%)。与奥利司他相比,利拉鲁肽使糖尿病前期的发生率显著降低。

结论

在这项真实世界研究中,利拉鲁肽在 WL 方面比奥利司他更有效,并改善了几种与肥胖相关的代谢和心血管危险因素。

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