Elsevier

Biological Psychiatry

Volume 58, Issue 12, 15 December 2005, Pages 969-973
Biological Psychiatry

Original article
Normal Prefrontal Gamma-Aminobutyric Acid Levels in Remitted Depressed Subjects Determined by Proton Magnetic Resonance Spectroscopy

https://doi.org/10.1016/j.biopsych.2005.05.017Get rights and content

Background

There is growing evidence that the brain gamma-aminobutyric acid (GABA) system is involved in depression. Lowered plasma GABA levels were identified as a traitlike abnormality found in patients with remitted unipolar depression and in healthy first-degree relatives of patients with unipolar depression. Major depressive disorder has been associated with neuroimaging and neuropathological abnormalities in the prefrontal cortex by various types of evidence. As a result, the current study investigates whether GABA levels in the prefrontal cortex differ between unmedicated subjects with remitted major depressive disorder (rMDD) and healthy control subjects.

Methods

Sixteen rMDD subjects and 15 healthy control subjects underwent magnetic resonance spectroscopy. We used a 3 Tesla GE whole body scanner with a homogeneous resonator coil providing a homogenous radiofrequency field and capability of obtaining measurement from the prefrontal cortex. Gamma-aminobutyric acid levels were measured in the ventromedial prefrontal cortex and dorsolateral/anterior medial prefrontal cortex.

Results

There was no difference in GABA concentrations between rMDD subjects and healthy control subjects in the ventromedial prefrontal cortex and dorsolateral/anterior medial prefrontal cortex. Secondary analyses provided preliminary evidence for a negative relationship between the glutamate/glutamine (Glx)/GABA ratio and age of onset of major depression in the ventromedial prefrontal cortex.

Conclusions

This result suggests that GABA levels in the prefrontal cortex, if found to be reduced in symptomatic depression, do not represent a persistent characteristic of major depression. Further research is needed to determine brain GABA levels in different brain regions, in different stages of depressive illness, and in different depressive subtypes.

Section snippets

Methods and Materials

Sixteen unmedicated subjects with major depression in full remission according to DSM-IV criteria who had either recurrent depressive episodes or a single episode and a family history of major depression (12 female subjects; ages 41.0 ± 11.6, range: 19 to 58; Hamilton Depression Rating Scale [HDRS] total score 1.3 ± 2.4, range 1 to 8; age at onset 27.7 ± 8.8, range 17 to 52; previous episodes 2.8 ± 2.3, range: 1 to 10) and 15 healthy control subjects (12 female subjects; ages 41.7 ± 12.4, range

Results

A typical set of GABA editing spectra are shown in Figure 1. The upper trace is the intact subspectrum at echo time (TE) = 68 milliseconds. The editing pulse is placed at the resonance frequency of GABA-3 at 1.9 ppm. The effects of the GABA editing pulse can be appreciated in the subspectrum shown in the middle trace. The lower trace shows the edited spectrum. The large NAA signal at 2.0 ppm was inverted due to the action of the editing pulse. The Glx-2 signal at 3.8 ppm and the Glx-4 signal at

Discussion

We have measured, for the first time, GABA concentrations in two different anatomical regions of the prefrontal cortex at 3 Tesla. We showed that subjects with major depression in remission and healthy control subjects did not differ in prefrontal GABA levels. In subjects with remitted depression, we found preliminary evidence for a negative relationship between the Glx/GABA ratio and age of onset of major depression in the ventromedial prefrontal cortex.

Mood state independence is a relevant

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