The spectrum of pyridoxine dependent epilepsy across the age span: A nationwide retrospective observational study
Related Experiment Video
Updated: Aug 11, 2025

Author Spotlight: Advancing Pediatric Epilepsy Surgery in Children Through Novel Biomarkers and Enhanced Localization
Published on: September 20, 2024
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.
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.
Background:
Pyridoxine-dependent epilepsy (PDE) is a rare seizure disorder usually presenting with neonatal seizures. Most cases are caused by biallelic pathogenic ALDH7A1variants. While anti-seizure medications are ineffective, pyridoxine provides seizure control, and dietary interventions may be of benefit. As the natural history beyond adolescence is insufficiently explored, our study aimed to assess the spectrum of PDE at various ages in Norway.
Methods:
Patients were ascertained by contacting all Norwegian paediatric, neurological, and neurohabilitation departments and relevant professional societies. Medical records were collected and reviewed.
Results:
We identified 15 patients treated for PDE; 13 had ALDH7A1 variants (PDE-ALDH7A1), one had PNPO deficiency, and in one, aetiology remained obscure. Of those with PDE-ALDH7A1, 12 were alive at time of study; five were > 18 years old and six were < 4 years. Median age was 10 years (range 2 months-53 years). Estimated minimum prevalence was 6.3/million among children and 1.2/million among adults. Ten had seizure onset on the first day of life. Perinatal complications and neuroradiological abnormalities suggested additional seizure aetiologies in several patients. Pyridoxine had immediate effect in six, while six had delayed (>1 h) or uncertain effect. Median delay from first seizure to continuous treatment was 11 days (range 0-42). Nine experienced breakthrough seizures with intercurrent disease or due to pyridoxine discontinuation. Cognitive outcomes ranged from normal to severe intellectual disability. The condition appeared to remain stable in adult life.
Significance:
We found a much higher prevalence of PDE-ALDH7A1 in children relative to adults, suggesting previous underdiagnosis and early mortality. Perinatal complications are common and can delay diagnosis and initiation of pyridoxine treatment. Lifelong and continuous treatment with pyridoxine is imperative. Due to better diagnostics and survival, the number of adult patients is expected to rise.
More Related Videos
10:22Interictal High Frequency Oscillations Detected with Simultaneous Magnetoencephalography and Electroencephalography as Biomarker of Pediatric Epilepsy
Published on: December 6, 2016
08:43Long-term Continuous EEG Monitoring in Small Rodent Models of Human Disease Using the Epoch Wireless Transmitter System
Published on: July 21, 2015
Related Concept Videos
Epilepsy and Seizures: Overview
Various factors can trigger epilepsy, including genetic factors, brain damage, metabolic causes, and unknown etiology. Diagnosis of epilepsy involves electroencephalography (EEG), which...
Seizures: Classification
Seizures are typically classified into two main categories: focal and generalized seizures.
Focal Seizures
Focal seizures originate from specific regions of the brain. These seizures are further sub-classified into two types:
Antiepileptic Drugs: Glutamate Antagonists
Antiepileptic Drugs: GABAergic Pathway Potentiators
The key GABA pathway potentiators used in epilepsy management are as follows.
Benzodiazepines are a well-known class of drugs used for...
Antiepileptic Drugs: Potassium Channel Activators
Ezogabine has gained approval as an adjunctive treatment...
Prevalence and Incidence
Prevalence indicates the proportion of individuals in a population who have a specific disease or health...