Mahapatra Sidharth, Ananth Amitha, Baugh Nancy, Damian Mihaela, Enns Gregory M
Division of Critical Care, Department of Pediatrics, University of Nebraska Medical Center, Omaha, NE, 68198, USA.
Pediatric Neurology, Brain and Spine Institute, Providence Health and Services, Portland, OR, 97225, USA.
JIMD Rep. 2018;39:19-23. doi: 10.1007/8904_2017_36. Epub 2017 Jul 9.
Carnitine-acylcarnitine translocase (CACT) deficiency is a rare long-chain fatty acid oxidation disorder (LC-FAOD) with high mortality due to cardiomyopathy or lethal arrhythmia. Triheptanoin (UX007), an investigational drug composed of synthetic medium odd-chain triglycerides, is a novel therapy in development for LC-FAOD patients. However, cases of its safe and efficacious use to reverse severe heart failure in CACT deficiency are limited. Here, we present a detailed report of an infant with CACT deficiency admitted in metabolic crisis that progressed into severe cardiogenic shock who was successfully treated by triheptanoin. The child was managed, thereafter, on triheptanoin until her death at 3 years of age from a cardiopulmonary arrest in the setting of acute respiratory illness superimposed on chronic hypercarbic respiratory failure.
肉碱-脂酰肉碱转位酶(CACT)缺乏症是一种罕见的长链脂肪酸氧化障碍(LC-FAOD),因心肌病或致死性心律失常导致死亡率很高。三庚酸甘油酯(UX007)是一种由合成中链奇数链甘油三酯组成的研究性药物,是正在为LC-FAOD患者开发的一种新型疗法。然而,关于其安全有效地用于逆转CACT缺乏症所致严重心力衰竭的病例有限。在此,我们详细报告了一名患有CACT缺乏症的婴儿,该婴儿在代谢危机中进展为严重的心源性休克,经三庚酸甘油酯成功治疗。此后,该患儿接受三庚酸甘油酯治疗,直至3岁时在慢性高碳酸血症呼吸衰竭基础上并发急性呼吸道疾病导致心肺骤停死亡。