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大剂量羟钴胺可实现迟发性钴胺素C缺乏症成年患者的生化纠正及神经精神缺陷改善。

High-dose hydroxocobalamin achieves biochemical correction and improvement of neuropsychiatric deficits in adults with late onset cobalamin C deficiency.

作者信息

Higashimoto Tomoyasu, Kim Alexander Y, Ogawa Jessica T, Sloan Jennifer L, Almuqbil Mohammed A, Carlson Julia M, Manoli Irini, Venditti Charles P, Gunay-Aygun Meral, Wang Tao

机构信息

Department of Genetic Medicine and Pediatrics Johns Hopkins University Baltimore Maryland.

Medical Genomics and Metabolic Genetics Branch National Institute of Human Genome Research, National Institutes of Health Bethesda Maryland.

出版信息

JIMD Rep. 2019 Dec 13;51(1):17-24. doi: 10.1002/jmd2.12087. eCollection 2020 Jan.

Abstract

Cobalamin C () deficiency is the most common inborn error of intracellular cobalamin metabolism caused by pathogenic variant(s) in and manifests with methylmalonic acidemia, hyperhomocysteinemia, and hypomethioninemia with a variable age of presentation. Individuals with late-onset may be asymptomatic until manifesting neuropsychiatric symptoms, thromboembolic events, and renal disease. Although hydroxocobalamin provides a foundation for therapy, optimal dose regimen for adult patients has not been systematically evaluated. We report three adult siblings with late-onset disease, and their biochemical and clinical responses to high-dose hydroxocobalamin. The 28-year-old proband presented with severe psychosis, progressive neurological deterioration, and deep venous thrombosis complicated by a pulmonary embolism. MRI studies identified lesions in the spinal cord, periventricular white matter, and basal ganglia. Serum homocysteine and methylmalonic acid levels were markedly elevated. Hydroxocobalamin at standard dose (1 mg/day) initially resulted in partial metabolic correction. A regimen of high-dose hydroxocobalamin (25 mg/day) together with betaine and folic acid resulted in rapid and sustainable biochemical correction, resolution of psychosis, improvement of neurological functions, and amelioration of brain and spinal cord lesions. Two siblings who did not manifest neuropsychiatric symptoms or thromboembolism achieved a satisfactory metabolic control with the same high-dose regimen. Hydroxocobalamin injection was then spaced out to 25 mg weekly with good and sustainable metabolic control. All three patients are compound heterozygotes for c.271dupA p.Arg91LysfsX14 and c.389A > G p.Tyr130Cys. This study highlights the importance of evaluating intracellular cobalamin metabolism in adults with neuropsychiatric manifestations and/or thromboembolic events, and demonstrates that high-dose hydroxocobalamin achieves rapid and sustainable metabolic control and improvement in neuropsychiatric outcomes in adults with late-onset disease.

摘要

钴胺素C(cblC)缺乏症是细胞内钴胺素代谢最常见的先天性缺陷,由 中的致病变异引起,表现为甲基丙二酸血症、高同型半胱氨酸血症和低蛋氨酸血症,发病年龄不一。迟发性cblC患者在出现神经精神症状、血栓栓塞事件和肾脏疾病之前可能无症状。尽管羟钴胺素是治疗的基础,但尚未对成年患者的最佳剂量方案进行系统评估。我们报告了三名患有迟发性cblC疾病的成年兄弟姐妹,以及他们对高剂量羟钴胺素的生化和临床反应。28岁的先证者表现为严重精神病、进行性神经功能恶化以及深静脉血栓形成并伴有肺栓塞。MRI研究发现脊髓、脑室周围白质和基底神经节有病变。血清同型半胱氨酸和甲基丙二酸水平显著升高。标准剂量(1毫克/天)的羟钴胺素最初导致部分代谢纠正。高剂量羟钴胺素(25毫克/天)联合甜菜碱和叶酸的方案导致快速且可持续的生化纠正、精神病症状缓解、神经功能改善以及脑和脊髓病变改善。两名未出现神经精神症状或血栓栓塞的兄弟姐妹通过相同的高剂量方案实现了满意的代谢控制。然后将羟钴胺素注射间隔延长至每周25毫克,代谢控制良好且可持续。所有三名患者都是c.271dupA p.Arg91LysfsX14和c.389A>G p.Tyr130Cys的复合杂合子。这项研究强调了评估有神经精神表现和/或血栓栓塞事件的成年人细胞内钴胺素代谢的重要性,并表明高剂量羟钴胺素可实现快速且可持续的代谢控制,并改善迟发性cblC疾病成年患者的神经精神预后。

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