A. Pfefferbaum et al., FRONTAL-LOBE VOLUME LOSS OBSERVED WITH MAGNETIC-RESONANCE-IMAGING IN OLDER CHRONIC-ALCOHOLICS, Alcoholism, clinical and experimental research, 21(3), 1997, pp. 521-529
This study used magnetic resonance imaging to quantify the extent and
pattern of tissue volume deficit and cerebrospinal fluid volume enlarg
ement in younger versus older chronic alcoholics relative to normal co
ntrols. In the present analysis, we divided our previously reported gr
oup of 62 alcoholic men into a younger group (n = 33, age mean = 37.5
+/- 4.5, and range = 26 to 44 years) and an older group (n = 29, age m
ean = 52.7 +/- 6.0, and range = 45 to 63 years) to examine whether, in
addition to extent, the two age groups differed in pattern of tissue
type and regional brain volume abnormalities quantified with magnetic
resonance imaging, Brain volumes were adjusted for normal variation in
head size and age established from a group of healthy controls and we
re expressed as Z-scores. The younger group had significant cortical g
ray, but not white, matter volume deficits and sulcal and ventricular
enlargement relative to age-matched controls. The older group had volu
me deficits in both cortical gray and white matter and sulcal and vent
ricular enlargement that significantly exceeded the younger alcoholic
group. An analysis of six cortical regions revealed that, although bot
h age groups had gray matter volume deficits throughout the cortex, th
e older alcoholic group had a selectively more severe deficit in prefr
ontal gray matter relative to the younger alcoholic group. Similarly,
the cortical white matter volume deficit in the older alcoholics was e
specially severe in the prefrontal and frontal regions. The difference
s in brain dysmorphology between the two alcoholic groups cannot easil
y be attributed to potential alcohol history differences typically rel
ated to age because the two groups had similar disease durations and a
mounts of lifetime alcohol consumption. These results provide in vivo
evidence that the frontal lobes are especially vulnerable to chronic a
lcoholism in older men.