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Visual cortex excitability in migraine before and after valproate prophylaxis: a pilot study using TMS
W M Mulleners1, E P Chronicle, J W Vredeveld
1Department of Neurology, Atrium Medical Center, Heerlen, The Netherlands. w.mulleners@freeler.nl
European Journal of Neurology
|January 11, 2002
Summary
Sodium valproate improved migraine symptoms and increased occipital cortical excitability thresholds in some patients. This suggests that gamma-aminobutyric acid (GABA)-ergic interventions may reduce cortical excitability for migraine prophylaxis.
Area of Science:
- Neuroscience
- Neurology
- Pharmacology
Background:
- Migraine is a common neurological disorder characterized by recurrent headaches.
- Cortical excitability changes are implicated in migraine pathophysiology.
- Sodium valproate is a standard migraine prophylaxis treatment.
Purpose of the Study:
- To investigate the effect of sodium valproate on occipital cortical excitability in migraine patients.
- To determine if reduced clinical migraine parameters correlate with changes in cortical excitability.
Main Methods:
- 31 migraine patients underwent transcranial magnetic stimulation (TMS) assessments before and after 1 month of sodium valproate prophylaxis.
- Occipital cortical excitability was measured using phosphene threshold determination with circular and figure-of-eight coils.
- Headache parameters were recorded by patients throughout the study.
Main Results:
- Sodium valproate significantly improved headache indexes.
- Phosphene thresholds, indicating cortical excitability, were significantly higher post-treatment in migraine with aura (MA) patients assessed with a figure-of-eight coil.
- No significant changes in phosphene thresholds were observed in migraine without aura (MO) patients or MA patients assessed with a circular coil.
- A modest correlation was found between increased phosphene threshold and decreased headache index in MA patients.
Conclusions:
- Sodium valproate therapy is effective in improving migraine symptoms.
- The findings suggest that sodium valproate may reduce cortical excitability, particularly in MA patients, supporting the role of gamma-aminobutyric acid (GABA)-ergic mechanisms in migraine prophylaxis.
- Further research is warranted to explore the effects of sodium valproate and similar agents on cortical excitability in migraine.