Dira Loredana-Maria, Marin Loredana-Maria, Popa Simona-Georgiana, Singer Cristina-Elena, Cosoveanu Carmen-Simona, Donoiu Ionut, Golli Andreea-Loredana
Department of Pediatrics, University of Medicine and Pharmacy, 200349 Craiova, Romania.
Department of Pharmaceutical Physics, Faculty of Pharmacy, "Carol Davila" University of Medicine and Pharmacy, 020956 Bucharest, Romania.
Int J Mol Sci. 2025 Jun 26;26(13):6143. doi: 10.3390/ijms26136143.
A growing global trend of adult obesity and the increasing prevalence of overweight/obesity in children indicate a higher risk in the future of adult diseases related to obesity. Current anti-obesity medications regulate appetite and metabolism by acting either in peripheral tissues or in the central nervous system. On the other hand, subsequent weight regain is a typical response to weight loss methods, and there is little evidence that current anti-obesity medications can help maintain long-term weight loss without causing a range of undesirable side effects. The combination of anti-obesity drugs targets multiple molecular pathways and structures in the central nervous system that are involved in weight regulation. This systematic review involves trials performed in pediatric populations, published up to 2025 and systematically searched on the ClinicalTrials.gov database, using "Glucagon like peptide-1 analog, Glucagon like peptide-1 receptor agonists" as the criterion for the "Intervention/treatment" category. We evaluated the entero-insular axis in pediatric patients with obesity, along with the mechanisms of action and therapeutic potential of the Glucagon like peptide-1receptor agonists. We analyzed incretin hormones and summarized the drugs approved by the Food and Drug Administration. Our objective is to identify new treatment strategies as we improve our understanding of the pathophysiology of obesity and the incretin axis.
全球成人肥胖趋势不断加剧,儿童超重/肥胖患病率不断上升,这表明未来与肥胖相关的成人疾病风险更高。目前的抗肥胖药物通过作用于外周组织或中枢神经系统来调节食欲和新陈代谢。另一方面,体重反弹是减肥方法的典型反应,几乎没有证据表明目前的抗肥胖药物能够在不引起一系列不良副作用的情况下帮助维持长期体重减轻。抗肥胖药物的组合针对中枢神经系统中参与体重调节的多种分子途径和结构。本系统评价涉及截至2025年发表的、在儿科人群中进行的试验,并在ClinicalTrials.gov数据库中进行系统检索,使用“胰高血糖素样肽-1类似物、胰高血糖素样肽-1受体激动剂”作为“干预/治疗”类别的标准。我们评估了肥胖儿科患者的肠胰岛轴,以及胰高血糖素样肽-1受体激动剂的作用机制和治疗潜力。我们分析了肠促胰岛素激素,并总结了美国食品药品监督管理局批准的药物。我们的目标是在增进对肥胖病理生理学和肠促胰岛素轴理解的同时,确定新的治疗策略。