Suppr超能文献

高胰岛素血症性低血糖概述:一种复杂的临床病症。

Hyperinsulinaemic hypoglycaemia-an overview of a complex clinical condition.

机构信息

Research Laboratory of the Division of Paediatric Endocrinology and Diabetes, Department of Paediatrics, School of Medicine, University of Patras, 26500, Patras, Greece.

Endocrinology Department, Great Ormond Street Hospital for Children, NHS Foundation Trust, London, UK.

出版信息

Eur J Pediatr. 2019 Aug;178(8):1151-1160. doi: 10.1007/s00431-019-03414-8. Epub 2019 Jun 26.

Abstract

Hyperinsulinaemic hypoglycaemia (HH) is a major cause of hypoglycaemia in the neonatal period, infancy and childhood. It is caused by unsuppressed insulin secretion in the setting of hypoglycaemia and carries a high risk of significant neurological sequelae, such as cognitive impairment. Genetic mutations have been implicated in the pathogenesis of the condition. Other causes include intra-uterine growth retardation, perinatal asphyxia, maternal diabetes mellitus and syndromes, such as Beckwith-Wiedemann. Based on the aetiology, the clinical presentation can range from absence of symptoms to the typical adrenergic symptoms and coma and even death. The diagnosis is based on biochemical findings and the gold-standard imaging technique is 18F-DOPA PET/CT scanning. Treatment options involve medications, such as diazoxide, nifedipine, glucagon and octreotide, as well as surgery. Novel treatment, such as long-acting octreotide, lanreotide and sirolimus, may be used as an alternative to pancreatectomy. Potential future medical treatments include exendin, a GLP-1 receptor antagonist, and glucagon infusion via a pump.Conclusion: Advances in the fields of genetic testing, imaging techniques and medical treatment are beginning to provide novel insights into earlier detection, less invasive treatment approaches and fewer complications associated with the complex entity of hyperinsulinaemic hypoglycaemia. What is Known: • HH is caused by dysregulated insulin release from the β cell due to genetic mutations and carries a risk for complications, such as neurocognitive impairment. 18F-DOPA PET/CT scanning is presented as the gold-standard imaging technique currently in children with hyperinsulinaemic hypoglycaemia. • Clinical presentation is heterogeneous and treatment options include medical therapy and pancreatectomy. What is New: • 18F-DOPA PET/CT is indicated in suspected focal CHI due to paternal transmitted mutations in ABCC8 or KCNJ11. • Novel treatment options have been introduced, such as long-acting octreotide, lanreotide, sirolimus and selective nonpeptide somatostatin receptor subtype 5 (SSTR5) agonists. Future medical treatments include exendin, a GLP-1 antagonist, and glucagon infusion via a pump. However, all these options are off-label at present.

摘要

高胰岛素血症性低血糖症(HH)是新生儿期、婴儿期和儿童期低血糖症的主要原因。它是由低血糖情况下未被抑制的胰岛素分泌引起的,并伴有严重神经后遗症的高风险,如认知障碍。遗传突变与该疾病的发病机制有关。其他原因包括宫内生长迟缓、围产期窒息、母体糖尿病和贝克威思-威德曼综合征等综合征。根据病因,临床表现范围从无症状到典型的肾上腺素能症状和昏迷,甚至死亡。诊断基于生化发现,金标准成像技术是 18F-DOPA PET/CT 扫描。治疗选择包括药物治疗,如二氮嗪、硝苯地平、胰高血糖素和奥曲肽,以及手术。新型治疗方法,如长效奥曲肽、兰瑞肽和西罗莫司,可作为胰腺切除术的替代方法。潜在的未来医学治疗方法包括 exendin,一种 GLP-1 受体拮抗剂,以及通过泵输注胰高血糖素。结论:遗传检测、成像技术和医学治疗领域的进展开始为高胰岛素血症性低血糖症这一复杂实体的早期检测、微创治疗方法和减少与并发症相关的治疗方法提供新的见解。已知:•HH 是由于遗传突变导致β细胞胰岛素释放失调引起的,并伴有神经认知障碍等并发症的风险。18F-DOPA PET/CT 扫描目前被认为是儿童高胰岛素血症性低血糖症的金标准成像技术。•临床表现呈异质性,治疗选择包括药物治疗和胰腺切除术。新内容:•18F-DOPA PET/CT 适用于因 ABCC8 或 KCNJ11 父系传递突变导致的局灶性 CHI 疑似病例。•已经引入了新的治疗选择,如长效奥曲肽、兰瑞肽、西罗莫司和选择性非肽类生长抑素受体亚型 5(SSTR5)激动剂。未来的医学治疗方法包括 exendin,一种 GLP-1 拮抗剂,以及通过泵输注胰高血糖素。然而,目前所有这些选择都是超适应证的。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验