Pd. Mozley et al., EFFECTS OF AGING ON THE CEREBRAL DISTRIBUTION OF TC-99M HEXAMETHYLPROPYLENE AMINE OXIME IN HEALTHY HUMANS, European journal of nuclear medicine, 24(7), 1997, pp. 754-761
Some brain functions decline at a linear rate throughout adulthood. Ot
hers remain relatively stable until very late in the life cycle. This
study characterized the effects of aging on the regional cerebral dist
ribution of hexamethylpropylene amine oxime (HMPAO) in healthy human v
olunteers. The sample consisted of 26 men and 18 women with a mean age
of 41.6+/-14.9 years (range: 19-73). Their past medical histories, ph
ysical examinations, and laboratory screening tests were normal. Singl
e-photon emission tomography (SPET) scans of the brain were performed
with a standardized acquisition and processing protocol on a triple-he
aded camera equipped with fan beam collimators. A 3-D restorative filt
er and a correction for uniform attenuation were applied before the im
ages were reinterpolated in planes parallel to the line connecting the
frontal and occipital poles. Mean counts per pixel were measured in m
ultiple regions of interest (ROIs) within each hemisphere by custom fi
tting a set of templates to the images. The mean activity in each ROI
was compared with the mean activity per pixel in the whole brain. Regr
ession analyses were used to relate the activity ratios to age with bo
th linear and nonlinear models. The relative concentration of radioact
ivity decreased significantly with age in most, but not all, gray matt
er structures. It increased in the white matter regions. The nonlinear
model of aging fit the data significantly better than a straight line
did. Most of the changes with age occurred during young adulthood. No
further changes were detectable after the onset of middle age. The me
dian breakpoint age at which the rate of change became negligible was
36.6 years. Aging significantly affects the relative uptake of HMPAO i
n healthy humans. It decreases in many gray matter regions and increas
es in most white matter regions. However, the changes do not appear to
be linear. Most seem to occur during young adulthood before people re
ach their late thirties, The distribution then appears to remain relat
ively stable throughout middle age.