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Deep Brain Stimulation of Frontal Lobe Networks to Treat Alzheimer's Disease.
Scharre, Douglas W; Weichart, Emily; Nielson, Dylan; Zhang, Jun; Agrawal, Punit; Sederberg, Per B; Knopp, Michael V; Rezai, Ali R.
Affiliation
  • Scharre DW; Department of Neurology, Cognitive Neurology Division, The Ohio State University Wexner Medical Center, OH, USA.
  • Weichart E; Department of Psychology, The Ohio State University, Columbus, OH, USA.
  • Nielson D; Department of Neurosurgery, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
  • Zhang J; Department of Radiology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
  • Agrawal P; Department of Neurology, Movement Disorder Division, The Ohio State University Wexner Medical Center, OH, USA.
  • Sederberg PB; Department of Psychology, The Ohio State University, Columbus, OH, USA.
  • Knopp MV; Department of Radiology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
  • Rezai AR; Department of Neurosurgery, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
J Alzheimers Dis ; 62(2): 621-633, 2018.
Article in En | MEDLINE | ID: mdl-29400666
ABSTRACT
The study objective was to evaluate the safety and efficacy of deep brain stimulation (DBS) at the ventral capsule/ventral striatum (VC/VS) region to specifically modulate frontal lobe behavioral and cognitive networks as a novel treatment approach for Alzheimer's disease (AD) patients. This is a non-randomized phase I prospective open label interventional trial of three subjects with matched comparison groups. AD participants given DBS for at least 18 months at the VC/VS target were compared on the Clinical Dementia Rating-Sum of Boxes (CDR-SB), our primary outcome clinical measure, to matched groups without DBS from the AD Neuroimaging Initiative (ADNI) cohort. Serial 2-Deoxy-2-[18F]fluoro-D-glucose (FDG) positron emission tomography (PET) images of AD participants were also compared longitudinally over time. Three AD DBS participants were matched to subjects from the ADNI cohort. All participants tolerated DBS well without significant adverse events. All three AD DBS participants had less performance decline and two of them meaningfully less decline over time on our primary outcome measure, CDR-SB, relative to matched comparison groups from the ADNI using score trajectory slopes. Minimal changes or increased metabolism on FDG-PET were seen in frontal cortical regions after chronic DBS at the VC/VS target. The first use of DBS in AD at a frontal lobe behavior regulation target (VC/VS) was well-tolerated and revealed less performance decline in CDR-SB. Frontal network modulation to improve executive and behavioral deficits should be furthered studied in AD.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Deep Brain Stimulation / Alzheimer Disease / Frontal Lobe Type of study: Clinical_trials / Observational_studies Limits: Aged / Female / Humans / Male / Middle aged Country/Region as subject: America do norte Language: En Journal: J Alzheimers Dis Journal subject: GERIATRIA / NEUROLOGIA Year: 2018 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Deep Brain Stimulation / Alzheimer Disease / Frontal Lobe Type of study: Clinical_trials / Observational_studies Limits: Aged / Female / Humans / Male / Middle aged Country/Region as subject: America do norte Language: En Journal: J Alzheimers Dis Journal subject: GERIATRIA / NEUROLOGIA Year: 2018 Document type: Article Affiliation country: United States
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