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

Publication ,  Journal Article
Tseng, LA; Abdenur, JE; Andrews, A; Aziz, VG; Bok, LA; Boyer, M; Buhas, D; Hartmann, H; Footitt, EJ; Grønborg, S; Janssen, MCH; Longo, N ...
Published in: Mol Genet Metab
April 2022

BACKGROUND: 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. 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.

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Published In

Mol Genet Metab

DOI

EISSN

1096-7206

Publication Date

April 2022

Volume

135

Issue

4

Start / End Page

350 / 356

Location

United States

Related Subject Headings

  • Retrospective Studies
  • Pyridoxine
  • Lysine
  • Humans
  • Genetics & Heredity
  • Epilepsy
  • Cohort Studies
  • Activities of Daily Living
  • 3202 Clinical sciences
  • 3105 Genetics
 

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Tseng, L. A., Abdenur, J. E., Andrews, A., Aziz, V. G., Bok, L. A., Boyer, M., … van Karnebeek, C. D. M. (2022). Timing of therapy and neurodevelopmental outcomes in 18 families with pyridoxine-dependent epilepsy. Mol Genet Metab, 135(4), 350–356. https://doi.org/10.1016/j.ymgme.2022.02.005
Tseng, Laura A., Jose E. Abdenur, Ashley Andrews, Verena G. Aziz, Levinus A. Bok, Monica Boyer, Daniela Buhas, et al. “Timing of therapy and neurodevelopmental outcomes in 18 families with pyridoxine-dependent epilepsy.Mol Genet Metab 135, no. 4 (April 2022): 350–56. https://doi.org/10.1016/j.ymgme.2022.02.005.
Tseng LA, Abdenur JE, Andrews A, Aziz VG, Bok LA, Boyer M, et al. Timing of therapy and neurodevelopmental outcomes in 18 families with pyridoxine-dependent epilepsy. Mol Genet Metab. 2022 Apr;135(4):350–6.
Tseng, Laura A., et al. “Timing of therapy and neurodevelopmental outcomes in 18 families with pyridoxine-dependent epilepsy.Mol Genet Metab, vol. 135, no. 4, Apr. 2022, pp. 350–56. Pubmed, doi:10.1016/j.ymgme.2022.02.005.
Tseng LA, Abdenur JE, Andrews A, Aziz VG, Bok LA, Boyer M, Buhas D, Hartmann H, Footitt EJ, Grønborg S, Janssen MCH, Longo N, Lunsing RJ, MacKenzie AE, Wijburg FA, Gospe SM, Coughlin CR, van Karnebeek CDM. Timing of therapy and neurodevelopmental outcomes in 18 families with pyridoxine-dependent epilepsy. Mol Genet Metab. 2022 Apr;135(4):350–356.
Journal cover image

Published In

Mol Genet Metab

DOI

EISSN

1096-7206

Publication Date

April 2022

Volume

135

Issue

4

Start / End Page

350 / 356

Location

United States

Related Subject Headings

  • Retrospective Studies
  • Pyridoxine
  • Lysine
  • Humans
  • Genetics & Heredity
  • Epilepsy
  • Cohort Studies
  • Activities of Daily Living
  • 3202 Clinical sciences
  • 3105 Genetics