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Volume 63, Issue 9, Pages 891-898 (1 May 2008)


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Hippocampal N-Acetylaspartate Concentration and Response to Riluzole in Generalized Anxiety Disorder

Sanjay J. MathewaCorresponding Author Informationemail address, Rebecca B. Pricea, Xiangling Maob, Eric L.P. Smithc, Jeremy D. Coplanc, Dennis S. Charneya, Dikoma C. Shungub

Received 25 April 2007; received in revised form 31 July 2007; accepted 18 September 2007. published online 29 October 2007.

Background

Previous research has suggested the therapeutic potential of glutamate-modulating agents for severe mood and anxiety disorders, potentially resulting from enhancement of neuroplasticity. We used proton magnetic resonance spectroscopic imaging (1H MRSI) to examine the acute and chronic effects of the glutamate-release inhibitor riluzole on hippocampal N-acetylaspartate (NAA), a neuronal marker, in patients with generalized anxiety disorder (GAD) and examined the relationship between changes in NAA and clinical outcome.

Methods

Fourteen medication-free GAD patients were administered open-label riluzole and then evaluated by 1H MRSI before drug administration, and 24 hours and 8 weeks following treatment. Patients were identified as responders (n = 9) or nonresponders (n = 5). Seven untreated, medically healthy volunteers, comparable in age, sex, IQ, and body mass index to the patients, received scans at the same time intervals. Molar NAA concentrations in bilateral hippocampus, and change in anxiety ratings were the primary outcome measures.

Results

A group-by-time interaction was found, with riluzole responders showing mean increases in hippocampal NAA across the three time points, whereas nonresponders had decreases over time. In GAD patients at Week 8, hippocampal NAA concentration and proportional increase in NAA from baseline both were positively associated with improvements in worry and clinician-rated anxiety.

Conclusions

These preliminary data support a specific association between hippocampal NAA and symptom alleviation following riluzole treatment in GAD. Placebo-controlled investigations that examine hippocampal NAA as a viable surrogate endpoint for clinical trials of neuroprotective and plasticity-enhancing agents are warranted.

a Department of Psychiatry, Mount Sinai School of Medicine, New York, New York

b Department of Radiology, Weill Medical College of Cornell University, New York, New York

c Department of Psychiatry, Downstate Medical Center, Brooklyn, New York.

Corresponding Author InformationAddress reprint requests to Sanjay J. Mathew, M.D., Department of Psychiatry, Mount Sinai School of Medicine, One Gustave L. Levy Place, Box 1217, New York, NY 10029

PII: S0006-3223(07)00887-6

doi:10.1016/j.biopsych.2007.09.012


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