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Format: Abstract
Arch Neurol. 2012 Sep;69(9):1141-8. doi: 10.1001/archneurol.2012.590.
Increased cerebral metabolism after 1 year of deep brain stimulation in Alzheimer disease.
1
Division
of Geriatric Psychiatry and Neuropsychiatry, The Johns Hopkins
University School of Medicine, The Johns Hopkins Bayview Medical Center,
5300 Alpha Commons Dr, 4th Floor, Baltimore, MD 21224, USA.
gsmith95@jhmi.edu
Abstract
BACKGROUND:
The
importance of developing unique, neural circuitry-based treatments for
the cognitive and neuropsychiatric symptoms of Alzheimer disease (AD)
was the impetus for a phase I study of deep brain stimulation (DBS) in
patients with AD that targeted the fornix.
OBJECTIVE:
To
test the hypotheses that DBS would increase cerebral glucose metabolism
in cortical and hippocampal circuits and that increased metabolism would
be correlated with better clinical outcomes.
DESIGN:
Open-label trial.
SETTING:
Academic medical center.
PATIENTS:
A total of 5 patients with mild, probable AD (1 woman and 4 men, with a mean [SD] age of 62.6 [4.2] years).
INTERVENTION:
Deep brain stimulation of the fornix.
MAIN OUTCOME MEASURES:
All
patients underwent clinical follow-up and high-resolution positron
emission tomography studies of cerebral glucose metabolism after 1 year
of DBS.
RESULTS:
Functional connectivity analyses
revealed that 1 year of DBS increased cerebral glucose metabolism in 2
orthogonal networks: a frontal-temporal-parietal-striatal-thalamic
network and a frontal-temporal-parietal-occipital-hippocampal network.
In similar cortical regions, higher baseline metabolism prior to DBS and
increased metabolism after 1 year of DBS were correlated with better
outcomes in global cognition, memory, and quality of life.
CONCLUSIONS:
Increased
connectivity after 1 year of DBS is observed, which is in contrast to
the decreased connectivity observed over the course of AD. The
persistent cortical metabolic increases after 1 year of DBS were
associated with better clinical outcomes in this patient sample and are
greater in magnitude and more extensive in the effects on cortical
circuitry compared with the effects reported for pharmacotherapy over 1
year in AD.
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