G. Garraux et al., Comparison of impaired subcortico-frontal metabolic networks in normal aging, subcortico-frontal dementia, and cortical frontal demential, NEUROIMAGE, 10(2), 1999, pp. 149-162
Normal aging, progressive supranuclear palsy (PSP), and frontotemporal deme
ntia (PID) are characterized by different degrees of decline in frontal lob
e functions. We used (18)FDG-PET and statistical parametric mapping (SPM96)
to compare relative subcorticofrontal metabolic impairment at rest in 21 h
ealthy elderly subjects (HES), 20 PSP patients, and 6 FTD patients. When HE
S were compared to 22 healthy young subjects, widespread decrease in metabo
lism was observed in bilateral medial prefrontal areas including anterior c
ingulate cortices, in dorsolateral prefrontal areas, in left lateral premot
or area, in Broca's area, and in left insula. In PSP compared to the 43 hea
lthy subjects (HS), we observed subcorticofrontal-metabolic impairment incl
uding both motor and cognitive neural networks. Impairment of functional co
nnections between midbrain tegmentum and cerebellar, temporal and pallidal
regions was demonstrated in PSP as com pared to HS. When comparing FTD to H
S, glucose uptake was primarily reduced in dorsolateral and ventrolateral p
refrontal cortices and in frontopolar and anterior cingulate regions. There
was also bilateral anterior temporal, right inferior parietal, and bilater
al striatal hypometabolism. Finally,FTD showed more severe striatofrontal m
etabolic impairment than PSP, while mesencephalothalamic involvement was on
ly observed in PSP. Our data suggest that subcorticofrontal metabolic impai
rment is distributed in distinct subcorticocortical networks: in normal agi
ng, PSP, and PTD. Subcorticofrontal dementia in PSP is related to hypometab
olism in discrete frontal areas, which are probably disconnected from certa
in subcortical structures. The concept of subcortical dementia is reinforce
d by our data, which show disrupted functional connections between mesencep
halon and cerebellar cortex, inferior and medial temporal regions, and pall
idum. (C) 1999 Academic Press.