An increased daily alcohol consumption results in neurological symptoms and
morphological central nervous system changes, e.g. shrinkage of the fronta
l lobes and the cerebellar vermis. Brain shrinkage can be due to neuronal l
oss, gliosis, or alterations of (cell) membrane constitutes/myelin. Neurona
l, glial, and metabolic changes can be measured in vivo with proton magneti
c resonance spectroscopy. A total of 11 alcoholics and 10 age-matched volun
teers were examined by magnetic resonance imaging and localized magnetic re
sonance spectroscopy at an echo time of 135 and 5 msec. Peak integral value
s were calculated for N-acetylaspartate(NAA), choline (Cho), myo-inositol (
ml), glutamate/glutamine (Glx), and normalized to phosphocreatine/creatine
(Cr). Patients had a significant shrinkage of the cerebellar vermis. NAA/Cr
and Cho/Cr ratios were reduced in both sequences, but the NAA/Cr reduction
was only significant in long echo time, although the Cho/Cr reduction was
significant in short echo time. The ml/Cr and Glx/Cr ratios did not show an
y significant difference between volunteers and patients. The decrease of N
AA/Cr in alcohol dependent patients is consistent with neuronal loss. The C
ho/Cr decrease and an unchanged ml/Cr may reflect cell membrane modificatio
n or myelin alterations in alcohol-dependent patients. These changes lead t
o brain shrinkage, although hydration effects and gliosis are less likely.