Publication Type | Academic Article |
Authors | Mathew S, Price R, Shungu D, Mao X, Smith E, Amiel J, Coplan J |
Journal | J Psychopharmacol |
Volume | 24 |
Issue | 8 |
Pagination | 1175-81 |
Date Published | 02/09/2009 |
ISSN | 1461-7285 |
Keywords | Anxiety Disorders, Aspartic Acid, Hippocampus, Neurons, Paroxetine, Selective Serotonin Reuptake Inhibitors |
Abstract | The neural basis of generalized anxiety disorder (GAD) is poorly characterized. The effect of chronic administration (12 weeks) of paroxetine, a selective serotonin reuptake inhibitor, on N-acetylaspartate (NAA), a marker of neuronal viability, was evaluated in adults with GAD using proton magnetic resonance spectroscopic imaging ((1)H MRSI) at 1.5 T. We hypothesized that, pretreatment abnormalities in hippocampal NAA/creatine (NAA/Cr) would normalize with symptomatic improvement. Nine GAD patients (mean age = 41.7 year; 4 females) received 12 weeks of open-label paroxetine treatment, flexibly dosed up to 60 mg/day. Clinical outcome was assessed with the Hamilton Anxiety Rating Scale (HAM-A). Multislice ( 1)H MRSI scans were performed at unmedicated baseline and following 6 and 12 weeks of treatment. Ten untreated healthy volunteers (HVs) (mean age = 37.1 year; 4 females) received scans at the same intervals. All patients achieved remission (HAM-A |
DOI | 10.1177/0269881108101796 |
PubMed ID | 19204062 |