Tseng Laura A, Abdenur Jose E, Andrews Ashley, Aziz Verena G, Bok Levinus A, Boyer Monica, Buhas Daniela, Hartmann Hans, Footitt Emma J, Grønborg Sabine, Janssen Mirian C H, Longo Nicola, Lunsing Roelineke J, MacKenzie Alex E, Wijburg Frits A, Gospe Sidney M, Coughlin Curtis R, van Karnebeek Clara D M
Department of Pediatrics, Emma Children's Hospital, Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, the Netherlands; On behalf of United for Metabolic Diseases, the Netherlands.
Division of Metabolic Disorders, CHOC Children's Hospital, Orange, CA, USA.
Mol Genet Metab. 2022 Apr;135(4):350-356. doi: 10.1016/j.ymgme.2022.02.005. Epub 2022 Feb 17.
Seventy-five percent of patients with pyridoxine-dependent epilepsy due to α-aminoadipic semialdehyde dehydrogenase deficiency (PDE-ALDH7A1) suffer intellectual developmental disability despite pyridoxine treatment. Adjunct lysine reduction therapies (LRT), aimed at lowering putative neurotoxic metabolites, are associated with improved cognitive outcomes. However, possibly due to timing of treatment, not all patients have normal intellectual function.
This retrospective, multi-center cohort study evaluated the effect of timing of pyridoxine monotherapy and pyridoxine with adjunct LRT on neurodevelopmental outcome. Patients with confirmed PDE-ALDH7A1 with at least one sibling with PDE-ALDH7A1 and a difference in age at treatment initiation were eligible and identified via the international PDE registry, resulting in thirty-seven patients of 18 families. Treatment regimen was pyridoxine monotherapy in ten families and pyridoxine with adjunct LRT in the other eight. Primary endpoints were standardized and clinically assessed neurodevelopmental outcomes. Clinical neurodevelopmental status was subjectively assessed over seven domains: overall neurodevelopment, speech/language, cognition, fine and gross motor skills, activities of daily living and behavioral/psychiatric abnormalities.
The majority of early treated siblings on pyridoxine monotherapy performed better than their late treated siblings on the clinically assessed domain of fine motor skills. For siblings on pyridoxine and adjunct LRT, the majority of early treated siblings performed better on clinically assessed overall neurodevelopment, cognition, and behavior/psychiatry. Fourteen percent of the total cohort was assessed as normal on all domains.
Early treatment with pyridoxine and adjunct LRT may be beneficial for neurodevelopmental outcome. When evaluating a more extensive neurodevelopmental assessment, the actual impairment rate may be higher than the 75% reported in literature.
TAKE- HOME MESSAGE: Early initiation of lysine reduction therapies adjunct to pyridoxine treatment in patients with PDE-ALDH7A1 may result in an improved neurodevelopmental outcome.
由于α-氨基己二酸半醛脱氢酶缺乏症(PDE-ALDH7A1)导致的吡哆醇依赖性癫痫患者中,75%的患者尽管接受了吡哆醇治疗,但仍患有智力发育障碍。旨在降低假定神经毒性代谢物的辅助赖氨酸减少疗法(LRT)与改善认知结果相关。然而,可能由于治疗时机的原因,并非所有患者都具有正常的智力功能。
这项回顾性、多中心队列研究评估了吡哆醇单一疗法以及吡哆醇联合辅助LRT的治疗时机对神经发育结局的影响。确诊为PDE-ALDH7A1且至少有一个患有PDE-ALDH7A1的兄弟姐妹且治疗开始时年龄存在差异的患者符合条件,并通过国际PDE登记处进行识别,最终纳入了18个家庭的37名患者。治疗方案为10个家庭采用吡哆醇单一疗法,另外8个家庭采用吡哆醇联合辅助LRT。主要终点是标准化和临床评估的神经发育结局。临床神经发育状况通过七个领域进行主观评估:整体神经发育、言语/语言、认知、精细和粗大运动技能、日常生活活动以及行为/精神异常。
在临床评估的精细运动技能领域,大多数接受吡哆醇单一疗法且治疗较早的兄弟姐妹比治疗较晚的兄弟姐妹表现更好。对于接受吡哆醇联合辅助LRT的兄弟姐妹,大多数治疗较早的兄弟姐妹在临床评估的整体神经发育、认知和行为/精神方面表现更好。整个队列中有14%在所有领域的评估中被判定为正常。
吡哆醇联合辅助LRT早期治疗可能对神经发育结局有益。在评估更广泛的神经发育评估时,实际损伤率可能高于文献报道的75%。
对于PDE-ALDH7A1患者,在吡哆醇治疗的基础上早期开始赖氨酸减少疗法辅助治疗可能会改善神经发育结局。