The spectrum of pyridoxine dependent epilepsy across the age span: A nationwide retrospective observational study

Ahmed Jamali1, Erle Kristensen2, Trine Tangeraas3

  • 1Department of Neuromedicine and Movement Science, Norwegian University of Science and Technology, Trondheim, Norway; Department of Neurology and Clinical Neurophysiology, St. Olav University Hospital, Trondheim, Norway.

Epilepsy Research
|February 2, 2023
PubMed

Insights

Pyridoxine-dependent epilepsy (PDE) is a rare genetic disorder. Lifelong pyridoxine treatment is crucial for seizure control, and its prevalence is higher in children, indicating underdiagnosis in adults.

Area of Science:

  • Neurology
  • Genetics
  • Pediatrics

Background:

  • Pyridoxine-dependent epilepsy (PDE) is a rare neonatal seizure disorder.
  • Most cases stem from ALDH7A1 gene variants.
  • Pyridoxine is effective, but dietary interventions may also help.

Purpose of the Study:

  • To investigate the age spectrum and prevalence of PDE in Norway.
  • To understand the long-term natural history of PDE beyond adolescence.

Main Methods:

  • Patient ascertainment through Norwegian pediatric, neurological, and neurohabilitation departments.
  • Review of collected medical records for 15 PDE patients.

Main Results:

  • 13 patients had ALDH7A1 variants (PDE-ALDH7A1), one PNPO deficiency, one unknown etiology.
  • Median age was 10 years (range 2 months-53 years); 5 patients were adults (>18 years).
  • Estimated minimum prevalence: 6.3/million children, 1.2/million adults; lifelong pyridoxine essential.

Conclusions:

  • Higher pediatric prevalence suggests underdiagnosis and potential early mortality in adults.
  • Perinatal complications can delay diagnosis and treatment initiation.
  • Continuous pyridoxine treatment is imperative; adult patient numbers are expected to increase.
Abstract

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