Related Experiment Video
Updated: Jul 15, 2026

Non-restraining EEG Radiotelemetry: Epidural and Deep Intracerebral Stereotaxic EEG Electrode Placement
Published on: June 25, 2016
Pyridoxine induces non-specific EEG alterations in infants with therapy resistant seizures
L K Teune1, J H vd Hoeven, N M Maurits
1Department of Neurology, University Medical Center Groningen, University of Groningen, The Netherlands.
Insights
Pyridoxine-IV administration in infants with therapy-resistant seizures (TRS-infants) causes non-specific EEG changes. These alterations do not reliably identify pyridoxine-dependency (PD) or pyridoxine-responsiveness (PR).
Area of Science:
- Pediatric Neurology
- Clinical Neurophysiology
Background:
- Infants with therapy-resistant seizures (TRS-infants) may have pyridoxine-dependency (PD) or pyridoxine-responsiveness (PR).
- Diagnosis often involves empirical intravenous (IV) pyridoxine administration during EEG monitoring.
- The specificity of EEG changes following pyridoxine-IV in undiagnosed TRS-infants is not well understood.
Purpose of the Study:
- To investigate whether EEG alterations induced by pyridoxine-IV in TRS-infants are specific to PD/PR or represent non-specific responses.
- To determine if pyridoxine-IV can be used to reliably identify PD/PR in infants.
Main Methods:
- Studied 10 infants under 1 year of age with TRS-infants.
- Administered intravenous pyridoxine (pyridoxine-IV) during EEG recordings.
- Analyzed EEG amplitude and total power changes post-administration.
Main Results:
- Pyridoxine-IV administration led to a significant decline (10-15%) in EEG amplitudes.
- Total EEG power across frequency bands also decreased significantly at multiple electrode sites.
- These EEG changes were observed in all infants, irrespective of PD/PR status.
Conclusions:
- Pyridoxine-IV administration induces non-specific changes in EEG amplitude and total power in TRS-infants.
- These non-specific EEG alterations do not reliably identify pyridoxine-dependency or pyridoxine-responsiveness.
- Further research is needed to establish specific biomarkers for PD/PR in infants.
Purpose:
In infants with frequent therapy resistant seizures (TRS-infants), clinical detection of pyridoxine-dependency (PD) or -responsiveness (PR) occurs by empirical intravenous (IV) pyridoxine administration during recording of the EEG. However, in undiagnosed TRS-infants it is still unclear to what extent EEG alterations by pyridoxine-IV are attributable to PD/PR or to non-specific responses. Before EEG alterations by pyridoxine-IV can be ascribed to PD/PR, these non-specific responses should be excluded first.
Methods:
In 10 TRS-infants under 1 year of age, we determined the EEG effect by pyridoxine-IV on the EEG-recording.
Results:
After pyridoxine-IV administration, our data indicate declined (10-15%; p<0.05) EEG-amplitudes and total power (magnitude/frequency-band) at frontal, central and centro-temporal electrodes.
Conclusion:
In TRS-infants, pyridoxine-IV affects EEG-amplitude and -total power in a non-specific way, which does not identify PD/PR.
Related Concept Videos
Antiepileptic Drugs: Potassium Channel Activators
Ezogabine has gained approval as an adjunctive treatment...
Antiepileptic Drugs: Modulators of Neurotransmitter Release Mediated by SV2A Protein
SV2A is a transmembrane glycoprotein located predominantly in the brain, modulating the release of neurotransmitters for neuronal communication. Both levetiracetam and brivaracetam exhibit a high affinity for...
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 their...
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...
Pharmacokinetics in Pediatric Patients: Drug Metabolism
Antiepileptic Drugs: Glutamate Antagonists

