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Cited by 494

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Increased Occipital Cortex GABA Concentrations in Depressed Patients After Therapy With Selective Serotonin Reuptake Inhibitors

Sanacora, Gerard, Mason, Graeme F., Rothman, Douglas L., Krystal, John H.·2002·American Journal of Psychiatry

Abstract

OBJECTIVE: Studies have demonstrated low concentrations of gamma-aminobutyric acid (GABA) in the plasma and CSF of individuals with major depression, and low GABA concentrations have also been found in the occipital cortex of depressed subjects. The goal of this study was to determine whether these occipital cortex GABA concentrations are altered after administration of selective serotonin reuptake inhibitors (SSRIs) in the treatment of depression. METHOD: By means of proton magnetic resonance spectroscopy, occipital cortex GABA concentrations were measured in 11 medication-free depressed patients before initiation of treatment with SSRI medications and after an average of 2 months of treatment. RESULTS: A significant increase in occipital cortex GABA concentrations was seen after SSRI treatment. CONCLUSIONS: SSRI treatment of major depression is associated with increased occipital cortex GABA concentrations. This appears to result in a normalization of low pretreatment GABA concentrations, an effect that may contribute to a common mechanism of antidepressant action.

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Crossref · 10.1176/appi.ajp.159.4.663

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Metadata

Authors
Sanacora, G., Mason, G. F., Rothman, D. L., & Krystal, J. H.
Venue
American Journal of Psychiatry
Published
2002-04-01
Volume
159
Issue
4
Pages
663-665
ISSN
  • 0002-953X (ISSN-L)
  • 1535-7228
OpenAlex
W2162933869
Cited by
494
References
1
FWCI
6.90
Type
journal article
Language
en
Open access
closed

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.