GABA quantification in human anterior cingulate cortex

PLoS One. 2021 Jan 15;16(1):e0240641. doi: 10.1371/journal.pone.0240641. eCollection 2021.

Abstract

γ-Aminobutyric acid (GABA) is a primary inhibitory neurotransmitter in the human brain. It has been shown that altered GABA concentration plays an important role in a variety of psychiatric and neurological disorders. The main purpose of this study was to propose a combination of PRESS and MEGA-PRESS acquisitions for absolute GABA quantification and to compare GABA estimations obtained using total choline (tCho), total creatine (tCr), and total N-acetyl aspartate (tNAA) as the internal concentration references with water referenced quantification. The second aim was to demonstrate the fitting approach of MEGA-PRESS spectra with QuasarX algorithm using a basis set of GABA, glutamate, glutamine, and NAA in vitro spectra. Thirteen volunteers were scanned with the MEGA-PRESS sequence at 3T. Interleaved water referencing was used for quantification, B0 drift correction and to update the carrier frequency of RF pulses in real time. Reference metabolite concentrations were acquired using a PRESS sequence with short TE (30 ms) and long TR (5000 ms). Absolute concentration were corrected for cerebrospinal fluid, gray and white matter water fractions and relaxation effects. Water referenced GABA estimations were significantly higher compared to the values obtained by metabolite references. We conclude that QuasarX algorithm together with the basis set of in vitro spectra improves reliability of GABA+ fitting. The proposed GABA quantification method with PRESS and MEGA-PRESS acquisitions enables the utilization of tCho, tCr, and tNAA as internal concentration references. The use of different concentration references have a good potential to improve the reliability of GABA estimation.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Algorithms*
  • Female
  • Gyrus Cinguli* / diagnostic imaging
  • Gyrus Cinguli* / metabolism
  • Humans
  • Magnetic Resonance Spectroscopy*
  • Male
  • Middle Aged
  • gamma-Aminobutyric Acid / metabolism*

Substances

  • gamma-Aminobutyric Acid

Grants and funding

J.P. and A. F. were supported by the Swedish Research Council, the Swedish Brain Foundation, and the Swedish Foundation for Humanities and Social Sciences (Riksbankens jubileumsfond). A.F. was supported by The Kjell and Märta Beijer Foundation and J.P. was supported by a postdoctoral grant from the Swedish Brain Foundation. The funders provided support in the form of salaries for authors [J.P., A.F.], but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of these authors are articulated in the ‘author contributions’ section.