Babiker Amir, Alfaraidi Haifa, Aljarallah Gadah, Albaraki Joud, Alharbi Reem, Alsomali Nouf, Alkhalaf Abeer, Yenugadhati Nagarajkumar, Al Juraibah Fahad, Al Alwan Ibrahim
College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
King Abdullah Specialized Children's Hospital, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.
Front Endocrinol (Lausanne). 2025 Apr 15;16:1573109. doi: 10.3389/fendo.2025.1573109. eCollection 2025.
Obesity has increased in adolescents with a rising incidence of metabolic consequences, including type 2 diabetes, necessitating new pharmacotherapeutic approaches. Liraglutide is the first FDA-approved therapy for obesity in adolescents in less than a decade. We assessed its efficacy combined with lifestyle interventions in our patients.
A retrospective cohort study was conducted at a specialized children hospital in Riyadh (2019-2022). All patients had simple, non-syndromic obesity and received intensive education on lifestyle modification. Data was collected from patients in two groups: Lifestyle modification (LifeSG) Vs Lifestyle and Liraglutide (LiraglG). Comparisons of two repeated measures obtained at T1 (baseline) and T2 (6-9 months) or T3 (9-12 months), including changes in body mass index (BMI), glycated hemoglobin (HbA1c) and other metabolic markers, were performed in the two matched groups using paired t-tests. Regression analysis using linear mixed models (SAS 9.4) were used to assess the effect of treatment status over time (P-value ≤ 0.05).
Data collected from 138 patients (n=69 in each group) with mean BMI and HbA1c of 35.78 kg/m and 5.85%, respectively. Notably, BMI declined by 0.48 kg/m over time in the LiraglG (p=0.003). An interaction effect (p=0.027) suggested a treatment impact until the first follow-up, which was not sustained thereafter. LifeSG exhibited no significant changes in biomarkers throughout T1-T3 period. In contrast, significant reductions were observed in BMI between T1-T2 (p=0.0057) and T1-T3 (p=0.010), total cholesterol (T1-T2) (p=0.023), alkaline phosphatase (T1-T3) (p<0.05) and low-density lipoprotein mean levels (T1-T3) (p=0.05) in the LiraglG group. A decline of 0.13% in A1c was observed in LiraglG; which may not clinically meaningful except in patients with pre-diabetes range of A1c (≥ 5.8%).
Liraglutide combined with lifestyle intervention is effective in treating obese Saudi adolescents, especially in the first 6-9 months. Continuous lifestyle intervention plays a key role in sustainability.
青少年肥胖率有所上升,包括2型糖尿病在内的代谢后果发生率也在增加,因此需要新的药物治疗方法。利拉鲁肽是近十年来首个获得美国食品药品监督管理局(FDA)批准用于治疗青少年肥胖的药物。我们评估了其与生活方式干预相结合对我们患者的疗效。
在利雅得的一家专科医院进行了一项回顾性队列研究(2019 - 2022年)。所有患者均为单纯性、非综合征性肥胖,并接受了强化的生活方式改变教育。数据收集自两组患者:生活方式改变组(LifeSG)和生活方式加用利拉鲁肽组(LiraglG)。使用配对t检验对在T1(基线)和T2(6 - 9个月)或T3(9 - 12个月)获得的两项重复测量指标进行比较,包括体重指数(BMI)、糖化血红蛋白(HbA1c)和其他代谢标志物的变化。使用线性混合模型(SAS 9.4)进行回归分析,以评估治疗状态随时间的影响(P值≤0.05)。
收集了138例患者的数据(每组n = 69),平均BMI和HbA1c分别为35.78 kg/m²和5.85%。值得注意的是,LiraglG组的BMI随时间下降了0.48 kg/m²(p = 0.003)。交互作用效应(p = 0.027)表明在首次随访前有治疗影响,但此后未持续。LifeSG组在整个T1 - T3期间生物标志物无显著变化。相比之下,LiraglG组在T1 - T2(p = 0.0057)和T1 - T3(p = 0.010)期间BMI显著降低,总胆固醇在T1 - T2期间(p = 0.023)、碱性磷酸酶在T1 - T3期间(p < 0.05)以及低密度脂蛋白平均水平在T1 - T3期间(p = 0.05)均显著降低。LiraglG组的A1c下降了0.13%;除了A1c处于糖尿病前期范围(≥5.8%)的患者外,这在临床上可能无意义。
利拉鲁肽与生活方式干预相结合对治疗肥胖的沙特青少年有效,尤其是在最初的6 - 9个月。持续的生活方式干预在维持疗效方面起关键作用。