Bb. Gelman, DIFFUSE MICROGLIOSIS ASSOCIATED WITH CEREBRAL ATROPHY IN THE ACQUIRED-IMMUNODEFICIENCY-SYNDROME, Annals of neurology, 34(1), 1993, pp. 65-70
The cause of cerebral atrophy in patients with acquired immunodeficien
cy syndrome (AIDS) is obscure because human immunodeficiency virus typ
e 1 (HIV-1)-related histopathological changes hardly correlate with ce
rebral atrophy. In this study, brain ventricular expansion was compare
d to the frontal lobe density of mononuclear and astroglial cells at a
utopsy. Twenty-eight male patients with AIDS displaying varying degree
s of atrophy were compared to 17 age-matched male control subjects wit
hout AIDS or atrophy. An index of ventricular expansion was measured i
n uniformly sliced, formalin-fixed brain specimens, and immunochemical
ly marked cells in coronal sections of the left superior frontal gyrus
(Brodmann area 8) were quantified by field counting and planimetry. I
n the cortex, diffuse ferritin-stained microglia and glial fibrillary
acidic protein-positive astrocytes were about twice as numerous in the
patients with AIDS. Sixty-five percent (18/28) of the patients with A
IDS had a microglial cell density greater than 2 standard deviations a
bove the control mean. Microglial cell density was correlated positive
ly with the severity of ventricular expansion (r = 0.71, p < 0.0001),
while hypertrophied astroglial cells were very weakly related. In whit
e matter, Ham-56-positive macrophages and glial fibrillary acidic prot
ein-positive astrocytes were not meaningfully correlated with the inde
x of ventricular expansion. Brain ventricular expansion and diffuse co
rtical microgliosis are highly prevalent anomalies in patients with AI
DS, and their interrelationship may be more important than previously
recognized.