Factors that accelerate rates of 'normal' age-related cerebral atrophi
c and degenerative changes are important because they may predispose t
o cognitive declines. To determine characteristic patterns of normal a
ging, risk factors were correlated with serial neurological-neuropsych
ological examinations, CT measures of progressive cerebral atrophy, lo
cal tissue hypodensities, or perfusional declines. Both cross-sectiona
l and longitudinal designs were utilized. Ninety-four cognitively and
neurologically normal aging volunteers, 15 with a history of transient
ischemic attacks (TIAs), were followed for mean intervals of 3.0+/-2.
1 years. Results indicated that: (1) after age 60, cerebral atrophy, p
olio-and leuko-araiosis doubled and cerebral perfusion decreased, with
marked individual variations; (2) risk factors independently accelera
ting cerebral atrophy and cortico-subcortical perfusional declines inc
luded TIAs, hypertension, smoking, hyperlipidemia, excessive alcohol c
onsumption and male gender; (3) progressive leuko-araiosis correlated
directly with cortical atrophy and cortical perfusional declines. We p
osit that: (1) cerebral atrophy and degenerative changes result from n
euronal shrinkage and/or loss, which are accelerated by TIAs, hyperten
sion, smoking, hyperlipidemia, excessive alcohol consumption and male
gender; (2) accelerated cerebral atrophic and degenerative changes ide
ntified by neuroimaging should be considered as markers for depleted n
euronal synaptic reserves, which predispose to cognitive declines. Int
erventions available for controlling some of these risk factors includ
e control of TIAs, hypertension, and hyperlipidemia, as well as tobacc
o and alcohol withdrawal. (C) 1997 Elsevier Science B.V.