Obsessive-Compulsive Disorder Clinical Trial
Official title:
Differential Efficacy of Memantine for Obsessive-compulsive Disorder vs. Generalized Anxiety Disorder: an Open-label Trial
The objective of this study was to obtain preliminary open-label data on the efficacy and tolerability of memantine, an anti-glutamatergic medication with a unique pharmacodynamic profile, in individuals with OCD and individuals with GAD. Because glutamatergic hyperactivity in frontal and frontal-subcortical circuits may play a role in the symptomatic expression of OCD, and possibly GAD, agents that reduce glutamatergic neurotransmission should provide unique anti-stress and anti-obsessional benefits. Memantine is a specific, uncompetitive antagonist at the NMDA receptor that blocks sustained activation of the NMDA receptor by high concentrations of glutamate under pathological conditions but rapidly leaves the NMDA channel upon transient physiological activation by low concentrations of glutamate.
Several case reports and an open-label trial have reported efficacy of anti-glutamatergic
medications for the treatment of OCD. In an open-label trial of riluzole, a glutamate release
inhibitor, seven of 13 adult patients with OCD improved, and five were categorized as
treatment responders. Another open trial found riluzole to be effective for four of six
children with treatment-refractory OCD. N-acetylcysteine, an agent that likely attenuates
glutamate neurotransmission, was effective as an augmentation in one patient with OCD. Two
case reports described memantine treatment of OCD. Poyurovsky et al. reported improvement
with memantine augmentation in one patient with treatment resistant OCD, while Pasquini and
Biondi noted improvement in one OCD patient with checking compulsions but not in one with
contamination obsessions. There have been no controlled or open-label trials of memantine in
OCD reported thus far.
Few studies have examined the efficacy of anti-glutamatergic agents in GAD. In an open-label
trial of riluzole treatment in 18 patients with GAD, twelve patients responded and eight
achieved remission. A double-blind, controlled study found that LY354740, a metabotropic
glutamate receptor 2/3 (mGlu2/3) agonist, was significantly more effective than placebo for
GAD. No studies of memantine in GAD have been reported thus far. We hypothesized that
treatment with memantine would result in significant symptom reduction in both OCD and GAD.
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