Background: Because a GABAergic hypofunction has been implied in the pathop
hysiology of mania, we have tested the antimanic properties of the GABA tra
nsporter 1 inhibitor tiagabine.
Method: An open trial was conducted in 8 acutely manic inpatients with DSM-
IV bipolar I disorder, 2 of them with tiagabine monotherapy and 6 with tiag
abine as an add-on to previously insufficient mood-stabilizing medication.
The study duration was 14 days. Changes in psychopathology were assessed by
the Bech-Rafaelsen Mania Rating Scale.
Results: None of the patients showed clear-cut relief from manic symptoms d
uring the 2-week observation period. In 2 patients, we saw pronounced side
effects (nausea and vomiting in one and a generalized tonic-clonic seizure
in the other).
Conclusion: The results from this open trial suggest that tiagabine seems t
o have no pronounced antimanic efficacy compared with standard treatments s
uch as valproate, lithium, or neuroleptics. It also appears that rapid dosa
ge increases for antimanic treatment can cause potentially severe side effe
cts.