Timing of therapy and neurodevelopmental outcomes in 18 families with pyridoxine-dependent epilepsy

被引:12
|
作者
Tseng, Laura A. [1 ,2 ]
Abdenur, Jose E. [3 ]
Andrews, Ashley [4 ]
Aziz, Verena G. [5 ]
Bok, Levinus A. [6 ]
Boyer, Monica [3 ]
Buhas, Daniela [7 ]
Hartmann, Hans [8 ]
Footitt, Emma J. [9 ]
Gronborg, Sabine [10 ,11 ]
Janssen, Mirian C. H. [12 ]
Longo, Nicola [4 ]
Lunsing, Roelineke J. [13 ]
MacKenzie, Alex E. [14 ,15 ]
Wijburg, Frits A. [1 ]
Gospe, Sidney M., Jr. [5 ,16 ,17 ,18 ]
Coughlin, Curtis R., II [19 ]
van Karnebeek, Clara D. M. [1 ,2 ,20 ]
机构
[1] Univ Amsterdam, Amsterdam Univ Med Ctr, Amsterdam Gastroenterol Endocrinol Metab, Dept Pediat,Emma Childrens Hosp, Amsterdam, Netherlands
[2] United Metab Dis, Amsterdam, Netherlands
[3] CHOC Childrens Hosp, Div Metab Disorders, Orange, CA USA
[4] Univ Utah, Dept Pediat, Div Med Genet, Salt Lake City, UT USA
[5] Seattle Childrens Res Inst, Seattle, WA USA
[6] Maxima Med Ctr, Dept Pediat & Neonatol, Veldhoven, Netherlands
[7] McGill Univ, Hlth Ctr, Dept Specialized Med, Div Med Genet, Montreal, PQ, Canada
[8] Hannover Med Sch, Clin Pediat Kidney Liver & Metab Dis, Hannover, Germany
[9] Great Ormond St Hosp Sick Children, Dept Metab Paediat, London, England
[10] Copenhagen Univ Hosp, Rigshosp, Dept Paediat & Adolescent Med, Ctr Inherited Metab Dis, Copenhagen, Denmark
[11] Copenhagen Univ Hosp, Rigshosp, Dept Clin Genet, Copenhagen, Denmark
[12] Radhoud Univ, Med Ctr, Radhoud Ctr Mitochondria & Metab Med, Dept Internal Med, Nijmegen, Gelderland, Netherlands
[13] Univ Groningen, Univ Med Ctr Groningen, Dept Paediat Neurol, Groningen, Netherlands
[14] Childrens Hosp Eastern Ontario Res Inst, Ottawa, ON, Canada
[15] Childrens Hosp Eastern Ontario, Dept Pediat, Ottawa, ON, Canada
[16] Univ Washington, Dept Neurol, Seattle, WA 98195 USA
[17] Univ Washington, Dept Pediat, Seattle, WA 98195 USA
[18] Duke Univ, Dept Pediat, Durham, NC 27706 USA
[19] Univ Colorado, Dept Pediat, Sect Clin Genet & Metab, Anschutz Med Campus,RC1 North, Aurora, CO 80045 USA
[20] Univ Amsterdam, Amsterdam Univ Med Ctr, Dept Human Genet Amsterdam Reprod & Dev, Amsterdam, Netherlands
关键词
Pyridoxine-dependent epilepsy; PDE-ALDH7A1; Lysine reduction therapies; Lysine-restricted diet; Arginine supplementation; Sibling study; Neurodevelopmental outcome; ARGININE SUPPLEMENTATION; ANTIQUITIN DEFICIENCY; FEATURES; DIAGNOSIS; CHILDREN; SIBLINGS; SEIZURES; SPECTRUM; DIET;
D O I
10.1016/j.ymgme.2022.02.005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Seventy-five percent of patients with pyridoxine-dependent epilepsy due to a-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. Methods: 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. Results: 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. Conclusion: 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. (C) 2022 Published by Elsevier Inc.
引用
收藏
页码:350 / 356
页数:7
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