We explored factors that may predispose patients to adverse mood effec
ts during treatment with vigabatrin (gamma-vinyl GABA; VGB): mood diso
rders before VGB treatment, type of epilepsy, seizure type and seizure
frequency, type and number of comedication, and VGB dose. The clinica
l relevance of such a study is that it may help identify circumstances
in which VGB should be administered with caution. Seventy-three patie
nts (40 males, 33 females), all with refractory epilepsies, who receiv
ed VGB as add-on therapy, were assessed by the Amsterdamse Stemmingsly
st (ASL), a mood-rating scale, before the start of treatment, and demo
graphic and clinical data were recorded. The patients were followed fo
r 6 months after the start of VGB treatment. Treatment with VGB had to
be discontinued in 38 patients (52% of the total sample). Mood proble
ms were the main reason for discontinuation in 9 (12.3% of the total s
ample). In 6 other patients, mood problems were mentioned as the reaso
n for discontinuing treatment, in combination with lack of drug effica
cy. Development of adverse mood effects could not be predicted by a sp
ecific mood profile on the ASL. Before treatment, the ''mood problems
discontinuation group'' did not show extreme scores for any assessed a
reas of mood and no significant differences from other patients were n
oted on the mood scales. Neither did clinical or demographic data show
statistically confirmed specific characteristics for the mood problem
s discontinuation group, though the patients tended to use more antiep
ileptic drugs (AEDs) as cotherapy, to have a slightly lower daily dose
of VGB, to be slightly older, and were mostly female. Especially the
trend toward a relation with AED as comedication deserves further stud
y.