The aim of this study was to evaluate the efficacy of lamotrigine, a glutam
ate antagonist blocking voltage-sensitive sodium channels, in the prophylax
is of migraine aura symptoms, Glutamate is one of the main neurotransmitter
s involved in the development of cortical spreading depression, The study w
as conducted as an open longitudinal trial over 7 months, with a treatment
phase of 4 months and a post-treatment period of 3 months. Thirteen patient
s suffering from migraine with aura and 2 patients with aura but without mi
graine were enrolled and treated with lamotrigine. The dose was gradually i
ncreased in steps of 25 mg up to 100 mg per day, depending on the patient's
aura symptoms. Aura symptoms were reduced from baseline tan average of 1.3
aura episodes per month) to month 4 (0.1, p<0.001). High statistical signi
ficance was also observed with regard to aura duration (23 min at baseline
vs 4 min at 4 months, p<0.001). In all 15 cases, increases in aura frequenc
y ton average sevenfold, p<0.001) and aura duration (minutes; on average mo
re than threefold, p<0.001) were evident following cessation of treatment.
A number of mild to moderate adverse events without any medical consequence
s occurred. The study outcome suggests that lamotrigine is effective in pre
venting migraine aura symptoms and in influencing migraine headache frequen
cy.