Targeting glutamate in OCD: a placebo-controlled, double-blind augmentation trial of the glutamate-modulating agent riluzole in treatment-refractory OCD. Obsessive-compulsive disorder (OCD) affects approximately 2.5% of the population worldwide. About a quarter of patients have symptoms that are resistant to available medications and psychotherapeutic approaches. Many of those described as `responders'to existing treatments suffer substantial residual symptoms and lead constricted lives. New treatment approaches are urgently needed. Several lines of evidence suggest that the ubiquitous amino acid neurotransmitter glutamate may be dysregulated in the brains of patients with OCD. This leads to the hypothesis that medications that target glutamate may represent a novel treatment strategy. The glutamate-modulating medication riluzole, which has been FDA approved for over ten years for use in amyotrophic lateral sclerosis, is one such agent. Preliminary open-label data suggest that a substantial fraction of patients with profoundly treatment-resistant OCD, who suffer severe symptoms and impaired quality of life despite medication and psychological treatment, improve when riluzole is added to their regimen. Importantly, several patients with compulsive hoarding, which is notoriously refractory to current treatments, have responded to pharmacological augmentation with riluzole. These preliminary observations do not provide adequate evidence of the efficacy of riluzole in OCD to justify its general clinical use. A more rigorous, controlled trial is essential. As a step towards this end, and to explore feasibility issues essential to the design of a larger, multi-site trial, this application proposes a pilot placebo-controlled, double-blind trial of riluzole augmentation in OCD. 60 outpatients with treatment-resistant OCD on stable medication regimens will be randomized to receive either riluzole (at the standard dose of 50 mg twice daily) or placebo, following a two-week single-blind placebo lead-in phase. The primary outcome measure will be improvement in Y-BOCS;measures of depression, anxiety, quality of life, and other variables will be analyzed in secondary analyses. In exploratory analyses, we will investigate genetic and clinical variables as potential predictors of response. DNA will be collected from all patients. Exploratory analyses of candidate genes in the serotonin and glutamate systems and of specific dimensions of symptomatology may help identify predictors of treatment response. While this study is not powered to definitively identify the predictors of response to riluzole, it will allow the generation of specific hypotheses to be further explored in a larger future trial. Many patients suffer from treatment-resistant OCD. This trial is a critical step towards exploring the efficacy glutamate modulating agents such as riluzole as a new alternative to alleviate their suffering.

Public Health Relevance

Obsessive-compulsive disorder (OCD) affects approximately 2.5 percent of the world's population and produces enormous suffering and loss of productivity, but available treatments provide little benefit to as many as a quarter of patients. New treatments are urgently needed;and glutamate-modulating drugs, such as the neuroprotective agent riluzole, represent one promising such treatment. If this trial of riluzole augmentation in treatment-resistant OCD is successful it will provide new hope millions of patients and will validate a focus on glutamate dysregulation in the further understanding of the neurobiology of OCD and in the development of other novel treatments in the future.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Planning Grant (R34)
Project #
5R34MH083115-03
Application #
7991339
Study Section
Interventions Committee for Adult Mood and Anxiety Disorders (ITMA)
Program Officer
Hillefors, MI
Project Start
2009-01-15
Project End
2013-05-31
Budget Start
2010-12-01
Budget End
2013-05-31
Support Year
3
Fiscal Year
2011
Total Cost
$210,128
Indirect Cost
Name
Yale University
Department
Psychiatry
Type
Schools of Medicine
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
06520
Pittenger, Christopher; Bloch, Michael H; Wasylink, Suzanne et al. (2015) Riluzole augmentation in treatment-refractory obsessive-compulsive disorder: a pilot randomized placebo-controlled trial. J Clin Psychiatry 76:1075-84
Pittenger, Christopher (2015) Glutamatergic agents for OCD and related disorders. Curr Treat Options Psychiatry 2:271-283
Pittenger, Christopher; Bloch, Michael H (2014) Pharmacological treatment of obsessive-compulsive disorder. Psychiatr Clin North Am 37:375-91
Pittenger, Christopher; Bloch, Michael H; Williams, Kyle (2011) Glutamate abnormalities in obsessive compulsive disorder: neurobiology, pathophysiology, and treatment. Pharmacol Ther 132:314-32
Bloch, M H; McGuire, J; Landeros-Weisenberger, A et al. (2010) Meta-analysis of the dose-response relationship of SSRI in obsessive-compulsive disorder. Mol Psychiatry 15:850-5
Landeros-Weisenberger, Angeli; Bloch, Michael H; Kelmendi, Ben et al. (2010) Dimensional predictors of response to SRI pharmacotherapy in obsessive-compulsive disorder. J Affect Disord 121:175-9
Bloch, Michael H; Pittenger, Christopher (2010) The Genetics of Obsessive-Compulsive Disorder. Curr Psychiatry Rev 6:91-103