Mr. Estilaei et al., Effects of chronic alcohol consumption on the broad phospholipid signal inhuman brain: An in vivo P-31 MRS study, ALC CLIN EX, 25(1), 2001, pp. 89-97
Background: Phosphorus magnetic resonance spectroscopy (P-31 MRS) allows fo
r the measurement of phospholipids and their breakdown products in the huma
n brain. Fairly mobile membrane phospholipids give rise to a broad signal t
hat co-resonates with metabolic phosphodiesters. Chronic alcohol exposure i
ncreases the rigidity of isolated brain membranes and, thus, may affect the
amount and transverse relaxation times (T-2) of MRS-detectable phospholipi
ds. We tested the hypothesis that subjects who were heavy drinkers have sti
ffer membranes than controls who were light drinkers, as reflected in a sma
ller broad signal component and a shorter T-2 of the broad signal in P-31 M
R spectra of the brain.
Methods: Thirteen alcohol-dependent heavy drinkers (mean age 44 years) were
studied by localized P-31 MRS in the centrum semiovale and compared with 1
7 nondependent light drinkers of similar age. The broad component signal wa
s separated from the metabolite signal by convolution difference, which is
based on the large difference in line widths of these two signals. Longitud
inal and T-2 relaxation times were measured using standard methods.
Results: The broad component integral was 13% lower in the brain of heavy d
rinkers compared with light drinkers (p < 0.001) and remained significantly
smaller after corrections for both longitudinal and transverse relaxations
(p < 0.01). The T-2 distribution of the broad component consistently showe
d two resolvable components in both groups. The fast relaxing component had
the same T-2 in both groups (T-2 = 1.9 msec). The slower relaxing componen
t T-2 was 0.6 msec shorter in heavy drinkers compared with light drinkers (
p = 0.08).
Conclusions: These results, observed in the absence of white matter volume
loss, are consistent with biochemical alterations and higher rigidity of wh
ite matter phospholipids associated with long-term chronic alcohol abuse. T
he observed smaller broad signal component in these relatively young heavy
drinkers is a sensitive measure of white matter phospholipid damage.