Section of Clinical Genetics and Metabolism, Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Department of Pediatrics Emma Children's Hospital, Amsterdam University Medical Centre, Amsterdam, The Netherlands.
J Inherit Metab Dis. 2021 Jan;44(1):178-192. doi: 10.1002/jimd.12332. Epub 2020 Dec 1.
Pyridoxine-dependent epilepsy (PDE-ALDH7A1) is an autosomal recessive condition due to a deficiency of α-aminoadipic semialdehyde dehydrogenase, which is a key enzyme in lysine oxidation. PDE-ALDH7A1 is a developmental and epileptic encephalopathy that was historically and empirically treated with pharmacologic doses of pyridoxine. Despite adequate seizure control, most patients with PDE-ALDH7A1 were reported to have developmental delay and intellectual disability. To improve outcome, a lysine-restricted diet and competitive inhibition of lysine transport through the use of pharmacologic doses of arginine have been recommended as an adjunct therapy. These lysine-reduction therapies have resulted in improved biochemical parameters and cognitive development in many but not all patients. The goal of these consensus guidelines is to re-evaluate and update the two previously published recommendations for diagnosis, treatment, and follow-up of patients with PDE-ALDH7A1. Members of the International PDE Consortium initiated evidence and consensus-based process to review previous recommendations, new research findings, and relevant clinical aspects of PDE-ALDH7A1. The guideline development group included pediatric neurologists, biochemical geneticists, clinical geneticists, laboratory scientists, and metabolic dieticians representing 29 institutions from 16 countries. Consensus guidelines for the diagnosis and management of patients with PDE-ALDH7A1 are provided.
吡哆醇依赖性癫痫(PDE-ALDH7A1)是一种常染色体隐性疾病,由α-氨基己二酸半醛脱氢酶缺乏引起,该酶是赖氨酸氧化的关键酶。PDE-ALDH7A1 是一种发育性和癫痫性脑病,历史上和经验上都用大剂量吡哆醇治疗。尽管癫痫得到了很好的控制,但大多数 PDE-ALDH7A1 患者报告存在发育迟缓及智力残疾。为了改善预后,推荐限制赖氨酸饮食和通过使用大剂量精氨酸竞争抑制赖氨酸转运作为辅助治疗。这些赖氨酸减少疗法已使许多但不是所有患者的生化参数和认知发育得到改善。这些共识指南的目标是重新评估和更新之前发表的关于 PDE-ALDH7A1 患者的诊断、治疗和随访的两项建议。国际 PDE 联合会的成员启动了循证和共识的流程,以审查之前的建议、新的研究发现以及 PDE-ALDH7A1 的相关临床方面。指南制定小组包括来自 16 个国家的 29 个机构的儿科神经病学家、生化遗传学家、临床遗传学家、实验室科学家和代谢营养师。提供了用于 PDE-ALDH7A1 患者诊断和管理的共识指南。