Topiramate enhances gamma-amino-butyric acid effects, has antiglutaminergic effects, and is a state-dependent sodium channel blocker.1 It is registered as an adjunctive treatment for epilepsy but is not registered for psychiatric indications. Nevertheless, it may be useful beyond its initial indication, considering the promising literature on which I report below. However, much more research evidence is needed to establish sufficient scientific justification for prescribing it routinely for psychiatric purposes.
Eating disordersThree randomised, double-blind, placebo-controlled studies on the use of topiramate for bulimia nervosa have been undertaken.
2-4All reported promising reductions in binging and purging behaviour, as well as body mass. One study specifically reported an improvement in body image, eating attitudes, anxiety and selfesteem. 3 Treatment was phased in at 25 mg per day, and increased where necessary to up to 400 mg per day. Topiramate appears to have been well tolerated but was discontinued in a small minority of subjects owing to side-effects. These studies were of relatively short duration (10 weeks) on relatively small numbers of subjects (60 -70). Barbee reported 5 cases of severe bulimia nervosa with co-morbid mood and/or anxiety disorders. were less convincing regarding depression, and the investigators were concerned about central nervous system (CNS) side-effects.A case was reported of a woman suffering from anorexia nervosa and epilepsy, whose epilepsy was treated with topiramate. After topiramate was started, the anorexia nervosa flared up again.The authors concluded that it might have been precipitated by topiramate. Although the literature clearly indicates that weight loss can occur on topiramate, it is not registered for that purpose; neither did I find any practice guidelines in this regard.Weight loss on topiramate has also been described in children suffering from bipolar disorder who gained weight due to psychotropic treatment. The study was small (10 subjects), relatively brief (11 weeks) and had an open-label design.14 Of note are the findings of Canitano. 15 This paper describes children and adolescents with autistic spectrum disorders who gained weight substantially after having received neuroleptics for behavioural control. The study was also small (10 subjects) with an open-label design. Topiramate was slowly titrated up to 1 -3