Liraglutide in adolescents with simple obesity and gastrointestinal comorbidities: treatment experience

A. Vitebskaya, A. V. Popovich
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Abstract

BACKGROUND: Liraglutide was approved for treatment of obesity in children and adolescents since 12 years. Due to gastrointestinal (GI) side effects not all patients reach maximal dose; this can affect the efficacy of obesity treatment.AIM: To study efficacy and tolerability of liraglutide in adolescents with obesity.MATERIALS AND METHODS: We analyzed medical data of adolescents with simple obesity and GI comorbidities before and in 3 months after start of liraglutide (BMI SDS; obesity complications; liraglutide side effects, and maximal doses), duration of therapy, reasons for discontinuation, and BMI SDS in 3–6 months after discontinuation.RESULTS: Liraglutide was administered for 10 adolescents (7 girls, 3 boys) 15.4 (13.5; 16.2) years with BMI SDS 3.3 (2.9; 3.7). Three months of treatment led to significant (p=0.001) decrease of BMI SDS till 2.8 (2.6; 3.5). Maximal dose of liraglutide was 3.0 mg (6 patients), 2.4 mg (2), 1.8 mg (1), and 1.2 mg (1). No correlation between maximal dose and BMI ΔSDS was detected. While dose titration patients complained of nausea (9), diarrhea (3), obstipation (1), and flatulence (1). In majority of cases complains were not dose-dependent. Only in 1 patient nausea and diarrhea that did not allow to increase liraglutide dose above 1.2 mg; additional investigation after discontinuation of therapy revealed GI infection.Therapy was discontinued in 3 months by 2 patients (1 — side effects, 1 — satisfactory result), in 4–5 months by 3 patients (1 — relapse of excessive weight gain, 2 — financial reasons), in 6 months by 1 patient (satisfactory result); 4 continued therapies. In 3–6 months after discontinuation of therapy BMI SDS increased and did not significantly differ from basal.CONCLUSION: Liraglutide is effective for treatment of obesity in adolescents and well tolerated by majority of patients. In case of pronounced adverse events additional GI investigation is recommended. Patients can discontinue treatment not only due to side effects, but also when they achieve their goal, and due to financial reasons.
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利拉鲁肽治疗青少年单纯性肥胖和胃肠道合并症:治疗经验
背景:利拉鲁肽自12年以来被批准用于治疗儿童和青少年肥胖。由于胃肠道(GI)副作用,并非所有患者都达到最大剂量;这会影响肥胖治疗的疗效。目的:研究利拉鲁肽治疗青少年肥胖症的疗效和耐受性。材料和方法:我们分析了服用利拉鲁肽前后3个月内患有单纯性肥胖和胃肠道合并症的青少年的医疗数据(BMI SDS;肥胖并发症;利拉鲁的副作用和最大剂量)、治疗持续时间、停药原因以及停药后3-6个月的BMI SDS。结果:10名青少年(7名女孩,3名男孩)服用利拉鲁肽15.4(13.5;16.2)岁,BMI SDS 3.3(2.9;3.7)。治疗三个月后,BMI SDS显著(p=0.001)下降至2.8(2.6;3.5)。利拉鲁的最大剂量为3.0 mg(6名患者)、2.4 mg(2)、1.8 mg(1)和1.2 mg(1。未检测到最大剂量与BMIΔSDS之间的相关性。而剂量滴定患者抱怨恶心(9)、腹泻(3)、便秘(1)和胀气(1)。在大多数情况下,投诉不是剂量依赖性的。只有1名患者出现恶心和腹泻,利拉鲁肽的剂量不能增加到1.2 mg以上;停止治疗后的额外调查显示胃肠道感染。2名患者在3个月内停止治疗(1-副作用,1-满意结果),3名患者在4-5个月内(1-体重过度增加复发,2-经济原因),1名患者在6个月内终止治疗(满意结果);4种持续治疗。在停止治疗后的3-6个月内,BMI SDS增加,与基础没有显著差异。结论:利拉鲁肽治疗青少年肥胖有效,大多数患者耐受良好。如果出现明显的不良事件,建议进行额外的胃肠道检查。患者不仅可以因为副作用而停止治疗,还可以在达到目标时以及由于经济原因而停止治疗。
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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Obesity and Metabolism-Milan
Obesity and Metabolism-Milan 医学-内分泌学与代谢
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