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病例报告:用司美格鲁肽治疗黑素皮质素 4 受体基因突变相关肥胖症儿童的神经纤维再生。

Case report: Nerve fiber regeneration in children with melanocortin 4 receptor gene mutation related obesity treated with semaglutide.

机构信息

Research Department, Weill Cornell Medicine-Qatar, Doha, Qatar.

Endocrinology Department, Sidra Medicine, Doha, Qatar.

出版信息

Front Endocrinol (Lausanne). 2024 Jun 21;15:1385463. doi: 10.3389/fendo.2024.1385463. eCollection 2024.

Abstract

Melanocortin 4 receptor () mutations are the commonest cause of monogenic obesity through dysregulation of neuronal pathways in the hypothalamus and prefrontal cortex that regulate hunger and satiety. also regulates neuropathic pain pathways via JNK signaling after nerve injury. We show evidence of corneal small fiber degeneration in 2 siblings carrying a heterozygous missense variant c.508A>G, p.Ille170Val in the gene. Both children were treated with once weekly semaglutide for 6 months with no change in weight, and only a minor improvement in HbA1c and lipid profile. However, there was evidence of nerve regeneration with an increase in corneal nerve fiber density (CNFD) [child A (13.9%), child B (14.7%)], corneal nerve branch density (CNBD) [child A (110.2%), child B (58.7%)] and corneal nerve fiber length (CNFL) [child A (21.5%), child B (44.0%)].

摘要

黑素皮质素 4 受体 (MC4R) 突变是通过调节下丘脑和前额叶皮层中调节饥饿和饱腹感的神经元通路,导致单基因肥胖的最常见原因。MC4R 还通过神经损伤后的 JNK 信号通路调节神经性疼痛通路。我们在携带杂合错义变异 c.508A>G,p.Ile170Val 的 2 个兄弟姐妹中发现了角膜小纤维变性的证据。这两个孩子都接受了每周一次的 semaglutide 治疗 6 个月,但体重没有变化,HbA1c 和血脂谱只有轻微改善。然而,有证据表明神经再生,角膜神经纤维密度 (CNFD) [孩子 A (13.9%),孩子 B (14.7%)]、角膜神经分支密度 (CNBD) [孩子 A (110.2%),孩子 B (58.7%)] 和角膜神经纤维长度 (CNFL) [孩子 A (21.5%),孩子 B (44.0%)] 增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f701/11227249/e431d87da1da/fendo-15-1385463-g001.jpg

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