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全羧化酶合成酶缺乏症急性失代偿伴高血糖和酮症酸中毒时的胰岛素治疗

Insulin therapy in acute decompensation of holocarboxylase synthetase deficiency with hyperglycemia and ketoacidosis.

作者信息

Demaret Tanguy, Joyal Jean-Sébastien, Karalis Aspasia, Parente Fabienne, Delrue Marie-Ange, Mitchell Grant A

机构信息

Service de Génétique médicale, Department of Pediatrics, CHU Sainte-Justine and U Montréal, Montréal, Québec, Canada.

Centre de Génétique Humaine, Institut de Pathologie et Génétique, Gosselies, Belgium.

出版信息

Mol Genet Metab Rep. 2024 Mar 21;39:101073. doi: 10.1016/j.ymgmr.2024.101073. eCollection 2024 Jun.

Abstract

An 11-month-old girl with severe acidosis, lethargy and vomiting, was diagnosed with holocarboxylase synthetase deficiency. She received biotin and was stable until age 8 years when vomiting, severe acidosis, hypoglycemia, and hyperammonemia developed. Management with intravenous glucose aiming to stimulate anabolism led to hyperglycemic ketoacidosis. Insulin therapy rapidly corrected biochemical parameters, and clinical status improved. We propose that secondary Krebs cycle disturbances affecting pancreatic beta cells impaired glucose-stimulated insulin secretion, resulting in insulinopenia.

摘要

一名11个月大的女童,伴有严重酸中毒、嗜睡和呕吐,被诊断为全羧化酶合成酶缺乏症。她接受了生物素治疗,病情稳定至8岁,此时出现呕吐、严重酸中毒、低血糖和高氨血症。旨在刺激合成代谢的静脉葡萄糖治疗导致了高血糖酮症酸中毒。胰岛素治疗迅速纠正了生化指标,临床状况得到改善。我们认为,影响胰腺β细胞的继发性三羧酸循环紊乱损害了葡萄糖刺激的胰岛素分泌,导致胰岛素缺乏。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d024/10973194/f3f576a92edd/ga1.jpg

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