赛特美拉肽治疗青春期前儿童的有效性和安全性的现实经验。

IF 5.3 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Ahmet Kahveci, Ilknur Kurt, Serap Turan, Tulay Guran, Abdullah Bereket, Belma Haliloglu
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引用次数: 0

摘要

单基因肥胖的特点是由于单基因缺陷导致的严重的早发性肥胖,通常抵制传统的体重管理策略。本报告介绍了4例LEPR和POMC缺乏的青春期前儿童(3-9岁)使用MC4R激动剂setmelanotide的有效性和安全性的实际经验。研究结果表明,对于POMC缺乏症患者(0.3-0.5 mg/天),setmelanotide比LEPR缺乏症患者(2.5 mg/天)更低剂量有效。治疗通常耐受性良好,注射部位反应和色素沉着是常见的副作用。作为新发现,在2例患者中观察到与促性腺激素相关的影响,如下丘脑-垂体-性腺轴激活和睾丸下降。2例儿童出现生长减速,1例POMC缺乏症患者出现中枢性甲状腺功能减退。总的来说,setmelanotide似乎对单基因肥胖的幼儿有效且耐受性良好。然而,需要进一步的研究来评估早期干预对生长和青春期发育的长期影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Real-life experience on efficacy and safety of setmelanotide treatment in prepubertal children.

Monogenic obesity, characterized by severe, early-onset obesity due to single-gene defects, often resists traditional weight management strategies. This report presents real-life experiences on the efficacy and safety of setmelanotide, an MC4R agonist, in 4 prepubertal children (ages 3-9) with LEPR and POMC deficiencies. Findings indicate that setmelanotide is effective at lower doses in our patients with POMC deficiency (0.3-0.5 mg/day) than the patients with LEPR deficiency (2.5 mg/day). Treatment was generally well-tolerated, with injection site reactions and hyperpigmentation as common side effects. As novel findings, gonadotropin-related effects such as hypothalamo-pituitary-gonadal axis activation and testicular descent were observed in 2 patients. Growth deceleration was noted in 2 children, and recovery from central hypothyroidism in 1 patient with POMC deficiency. Overall, setmelanotide appears to be effective and well-tolerated in young children with monogenic obesity. However, further studies are necessary to evaluate the long-term effects of early intervention on growth and pubertal development.

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来源期刊
European Journal of Endocrinology
European Journal of Endocrinology 医学-内分泌学与代谢
CiteScore
9.80
自引率
3.40%
发文量
354
审稿时长
1 months
期刊介绍: European Journal of Endocrinology is the official journal of the European Society of Endocrinology. Its predecessor journal is Acta Endocrinologica. The journal publishes high-quality original clinical and translational research papers and reviews in paediatric and adult endocrinology, as well as clinical practice guidelines, position statements and debates. Case reports will only be considered if they represent exceptional insights or advances in clinical endocrinology. Topics covered include, but are not limited to, Adrenal and Steroid, Bone and Mineral Metabolism, Hormones and Cancer, Pituitary and Hypothalamus, Thyroid and Reproduction. In the field of Diabetes, Obesity and Metabolism we welcome manuscripts addressing endocrine mechanisms of disease and its complications, management of obesity/diabetes in the context of other endocrine conditions, or aspects of complex disease management. Reports may encompass natural history studies, mechanistic studies, or clinical trials. Equal consideration is given to all manuscripts in English from any country.
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