Elsevier

Analytical Biochemistry

Volume 529, 15 July 2017, Pages 48-64
Analytical Biochemistry

1D-spectral editing and 2D multispectral in vivo 1H-MRS and 1H-MRSI - Methods and applications

https://doi.org/10.1016/j.ab.2016.12.020Get rights and content
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Highlights

  • Spectral editing achieves separation of overlapping J-coupled resonances.

  • 1D spectral editing, such as J-difference editing, and multiple quantum coherence filtering.

  • 2D NMR spectroscopy, such as correlation spectroscopy and J-resolved NMR.

  • Application to neurotransmitters, antioxidants, onco-markers, metabolic processes.

Abstract

This article reviews the methodological aspects of detecting low-abundant J-coupled metabolites via 1D spectral editing techniques and 2D nuclear magnetic resonance (NMR) methods applied in vivo, in humans, with a focus on the brain. A brief explanation of the basics of J-evolution will be followed by an introduction to 1D spectral editing techniques (e.g., J-difference editing, multiple quantum coherence filtering) and 2D-NMR methods (e.g., correlation spectroscopy, J-resolved spectroscopy). Established and recently developed methods will be discussed and the most commonly edited J-coupled metabolites (e.g., neurotransmitters, antioxidants, onco-markers, and markers for metabolic processes) will be briefly summarized along with their most important applications in neuroscience and clinical diagnosis.

Keywords

Spectral editing
2D NMR spectroscopy
Correlation spectroscopy
J-resolved NMR spectroscopy
J-difference editing
Multiple quantum coherence filtering

Abbreviations

2HG
2-hydroxyglutarate
αKG
α-ketoglutarate
BASING
band selective inversion with gradient dephasing
Cho
choline
COSY
2D correlation spectroscopy
Cr
creatine
CSDE
chemical shift displacement error
CSI
chemical shift imaging
CT-PRESS
constant time PRESS
DQC
double quantum coherence
EPI
echo-planar imaging
FFT
fast Fourier transformation
FOCI
frequency offset corrected inversion
GABA
γ-amino butyric acid
GABA+
γ-amino butyric acid and macromolecules
Glu
glutamate
Gln
glutamine
Glx
Glu + Gln
GOIA
gradient offset independent adiabaticity
GPC
glycerylphosphorylcholine
GSH
glutathione
GSSG
oxidized glutathione
1H-MRS
proton MR spectroscopy
HERMES
Hadamard encoding and reconstruction of MEGA-edited spectroscopy
ISIS
image-selected in vivo spectroscopy
J-PRESS
J-resolved PRESS
Lac
lactate
LASER
localization by adiabatic selective refocusing
MEGA
Mescher-Garwood
MM
macromolecules
MQC
multiple quantum coherence
MQF
multiple quantum filtering
MRSI
MR spectroscopic imaging
mIns
myo-inositol
NAA
N-acetyl-aspartate
NAAG
N-acetyl-aspartyl glutamate
NADPH
nicotinamide adenine dinucleotide phosphate
PC
phosphocholine
PCr
phosphocreatine
PRESS
point-resolved spectroscopy
RF
radio-frequency
SAR
specific absorption rate
Sel-MQF
frequency-selective MQF
SNR
signal-to-noise ratio
SPECIAL
spin echo, full intensity acquired localized spectroscopy
S-PRESS
strong coupling PRESS
SQC
single quantum coherence
SS-Sel-MQF
spectrally selective MQF
STEAM
stimulated echo acquisition mode
SVS
single voxel spectroscopy
tCho
Cho + PC + GPC
tCr
Cr + PCr
TE
echo time
tNAA
NAA + NAAG
TOCSY
total correlation spectroscopy
ZQC
zero quantum coherence

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