Evaluation of the effect of liraglutide therapy on body weight and insulin resistance.

Dorota Szydlarska, A. Jakubowska, Jakub Owoc, W. Wierzba
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Abstract

Introduction and Objective. Insulin resistance is a state of reduced tissue sensitivity to insulin action despite normal or elevated serum insulin levels. Liraglutide (a GLP-1 receptor agonist) stimulates insulin secretion from the pancreas while decreasing excessive glucagon release. GLP-1 analogues have a unique beneficial effect on weight loss by stimulating insulin secretion without increasing blood sugar levels excessively. The aim of the study was to investigate the effects of liraglutide on body mass index and insulin resistance in overweight and obese non-diabetic individuals. Materials and Method. The study involved 31 overweight and obese women (BMI of ≥25 kg/m2) who received liraglutide treatment between 2021–2022. Liraglutide 3.0 mg was used as an adjunct to behavioural therapy, which included a low-calorie diet and exercise programme. The study collected BMI, glucose and insulin levels, and HOMA index before and during liraglutide treatment. Body weight and blood tests were examined at baseline (BMI1, HOMA1), as well as at 3 (BMI2, HOMA2), and 6 months (BMI3, HOMA3) of treatment to observe any changes. Results. Average age of participants – 38.32±7.41 years. Changes in BMI from baseline (32.36±4.56 kg/m²) to 6 months (27.46±4.45kg/m²) were associated with a significant reduction in weight (p <0.001). Changes in HOMA index from baseline (4.73±1.48) to 3 (3.59±1.26) and 6 months (2.47±0.91) were statistically significant (p <0.03, p < 0.001). Conclusions. Liraglutide represents a promising option for reducing body weight and obesity in non-diabetic patients as an adjunct to behavioural therapy. Agonists GLP-1 receptor, representing a new class of antidiabetic drug, undoubtedly offer unique benefits for overweight or obesity patients. Liraglutide in 3.0 mg use was associated with a significant weight reduction and lowering of insulin resistance.
评估利拉鲁肽疗法对体重和胰岛素抵抗的影响。
引言和目的。胰岛素抵抗是指在血清胰岛素水平正常或升高的情况下,组织对胰岛素作用的敏感性降低。利拉鲁肽(一种 GLP-1 受体激动剂)可刺激胰腺分泌胰岛素,同时减少胰高血糖素的过度释放。GLP-1 类似物通过刺激胰岛素分泌而不会过度增加血糖水平,对减肥具有独特的益处。本研究旨在探讨利拉鲁肽对超重和肥胖非糖尿病患者体重指数和胰岛素抵抗的影响。材料和方法。研究涉及 31 名超重和肥胖女性(体重指数≥25 kg/m2),她们在 2021-2022 年间接受了利拉鲁肽治疗。利拉鲁肽 3.0 毫克是行为疗法的辅助药物,行为疗法包括低热量饮食和运动计划。研究收集了利拉鲁肽治疗前和治疗期间的体重指数、血糖和胰岛素水平以及HOMA指数。在基线(BMI1、HOMA1)、治疗3个月(BMI2、HOMA2)和6个月(BMI3、HOMA3)时对体重和血液检测进行检查,以观察任何变化。研究结果参与者的平均年龄为(38.32±7.41)岁。体重指数从基线(32.36±4.56 kg/m²)到治疗 6 个月(27.46±4.45 kg/m²)的变化与体重的显著下降有关(p <0.001)。HOMA 指数从基线(4.73±1.48)到 3 个月(3.59±1.26)和 6 个月(2.47±0.91)的变化具有统计学意义(P <0.03,P <0.001)。结论作为行为疗法的辅助疗法,利拉鲁肽是减轻非糖尿病患者体重和肥胖症的一种很有前景的选择。GLP-1 受体激动剂是一种新型抗糖尿病药物,无疑能为超重或肥胖患者带来独特的益处。使用 3.0 毫克的利拉鲁肽可显著减轻体重,降低胰岛素抵抗。
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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