In vivo H-1 nuclear magnetic resonance (NMR) spectroscopy is an important t
ool in characterizing the metabolic status of brain tissue. Changes in abso
lute concentrations of individual metabolites, like lactate and gamma -amin
obutyric acid (GABA), are important markers associated with specific brain
diseases. The absolute quantification of metabolites by in vivo H-1 NMR is
not a straightforward task, because a large number of metabolites are reson
ating in a small spectral region leading to severe spectral overlap. Furthe
rmore, in vivo H-1 NMR is complicated by the need for complete three-dimens
ional spatial localization and excellent water suppression. The response of
scalar-coupled spin systems to typically employed in vivo H-1 NMR sequence
s can be especially complicated. This article will review the complications
of detecting and quantifying scalar-coupled spin-systems by in vivo H-1 NM
R. The characteristics and consequences of scalar coupling will be describe
d. The scalar coupling can be intelligently used to discriminate scalar-cou
pled resonances from overlapping (uncoupled) resonances by spectral editing
. However, in many cases, the scalar coupling introduces complications aris
ing from spatial localization and water suppression. The effect of typical
in vivo H-1 NMR sequences on scaler-coupled resonances will be analyzed in
detail. Finally, examples of spectral editing of GABA, lactate, and glucose
will be given to describe some of the practical considerations involved wi
th in vivo H-1 NMR. (C) 2001 John Wiley & Sons, Inc.