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7T 1 H-MRS in major depressive disorder: a Ketamine Treatment Study.

Authors :
Evans JW
Lally N
An L
Li N
Nugent AC
Banerjee D
Snider SL
Shen J
Roiser JP
Zarate CA Jr
Source :
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology [Neuropsychopharmacology] 2018 Aug; Vol. 43 (9), pp. 1908-1914. Date of Electronic Publication: 2018 Apr 05.
Publication Year :
2018

Abstract

The glutamatergic modulator ketamine has striking and rapid antidepressant effects in major depressive disorder (MDD), but its mechanism of action remains unknown. Proton magnetic resonance spectroscopy (1H-MRS) is the only non-invasive method able to directly measure glutamate levels in vivo; in particular, glutamate and glutamine metabolite concentrations are separable by 1H-MRS at 7T. This double-blind, placebo-controlled, crossover study that included <superscript>1</superscript> H-MRS scans at baseline and at 24 h post ketamine and post-placebo infusions sought to determine glutamate levels in the pregenual anterior cingulate (pgACC) of 20 medication-free MDD subjects and 17 healthy volunteers (HVs) 24 h post ketamine administration, and to evaluate any other measured metabolite changes, correlates, or predictors of antidepressant response. Metabolite levels were compared at three scan times (baseline, post-ketamine, and post-placebo) in HVs and MDD subjects at 7T using a <superscript>1</superscript> H-MRS sequence specifically optimized for glutamate. No significant between-group differences in <superscript>1</superscript> H-MRS-measured metabolites were observed at baseline. Antidepressant response was not predicted by baseline glutamate levels. Our results suggest that any infusion-induced increases in glutamate at the 24-h post ketamine time point were below the sensitivity of the current technique; that these increases may occur in different brain regions than the pgACC; or that subgroups of MDD subjects may exist that have a differential glutamate response to ketamine.

Details

Language :
English
ISSN :
1740-634X
Volume :
43
Issue :
9
Database :
MEDLINE
Journal :
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology
Publication Type :
Academic Journal
Accession number :
29748628
Full Text :
https://doi.org/10.1038/s41386-018-0057-1