Assessment of glutamate in striatal subregions in obsessive-compulsive disorder with proton magnetic resonance spectroscopy.

TitleAssessment of glutamate in striatal subregions in obsessive-compulsive disorder with proton magnetic resonance spectroscopy.
Publication TypeJournal Article
Year of Publication2015
AuthorsSimpson HBlair, Kegeles LS, Hunter L, Mao X, Van Meter P, Xu X, Kimeldorf MB, Pearlstein SL, Slifstein M, Shungu DC
JournalPsychiatry Res
Volume232
Issue1
Pagination65-70
Date Published2015 Apr 30
ISSN1872-7123
KeywordsAdolescent, Adult, Corpus Striatum, Female, gamma-Aminobutyric Acid, Glutamic Acid, Glutamine, Humans, Male, Middle Aged, Obsessive-Compulsive Disorder, Proton Magnetic Resonance Spectroscopy, Young Adult
Abstract

Glutamatergic signaling abnormalities in cortico-striatal circuits are hypothesized to lead to the repetitive thoughts and behaviors of obsessive-compulsive disorder (OCD). To test this hypothesis, studies have used proton magnetic resonance spectroscopy (1H MRS) to measure glutamatergic compounds in the striatum of individuals with OCD. However, no studies have used methods that could measure glutamate minimally contaminated by glutamine and γ-aminobutyric acid (GABA) in striatal subregions. Therefore, in this study, a proton MRS imaging (1H MRSI) technique with relatively high spatial resolution at 3.0 T was used to measure minimally contaminated glutamate levels in three striatal subregions (i.e., dorsal caudate, dorsal putamen, and ventral striatum) in 15 unmedicated adults with OCD and 16 matched healthy control subjects. No significant group differences in glutamate levels were found in any of the three striatal subregions. In contrast, a study in unmedicated pediatric OCD patients that measured glutamatergic compounds in the dorsal caudate by MRS at 1.5 T found significant elevations. Further studies are warranted to assess whether these discrepant MRS findings are due to differences in subject age or MRS methodology, or potentially are associated with glutamatergic gene variants implicated in OCD.

DOI10.1016/j.pscychresns.2015.01.009
Alternate JournalPsychiatry Res
PubMed ID25715904
PubMed Central IDPMC4404189
Grant ListK24 MH091555 / MH / NIMH NIH HHS / United States
K24MH091555 / MH / NIMH NIH HHS / United States
Related Institute: 
MRI Research Institute (MRIRI)

Weill Cornell Medicine
Department of Radiology
525 East 68th Street New York, NY 10065