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Analysis of Gene Expression Changes in the Rat Hippocampus After Deep Brain Stimulation of the Anterior Thalamic Nucleus
Published on: March 8, 2015
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Memory and mood outcomes after anterior thalamic stimulation for refractory partial epilepsy
Alexander I Tröster1, Kimford J Meador2, Christopher P Irwin3
1Department of Clinical Neuropsychology and Center for Neuromodulation, Barrow Neurological Institute, Phoenix, AZ, USA.
Seizure
|January 7, 2017
Summary
Bilateral deep brain stimulation (DBS) of the anterior nucleus of the thalamus (ANT) for epilepsy is safe, with subjective memory and depression issues not linked to long-term neurobehavioral decline. Monitoring is recommended.
Area of Science:
- Neuroscience
- Neurosurgery
- Neurology
Background:
- Bilateral deep brain stimulation (DBS) of the anterior nucleus of the thalamus (ANT) is an established epilepsy treatment.
- While generally safe and effective in reducing seizures, ANT-DBS may be associated with adverse events (AEs) such as memory problems and depression.
Purpose of the Study:
- To investigate the incidence of memory and depression AEs during the blinded phase of the SANTE study.
- To examine the relationship between these AEs and objective neurobehavioral measures, baseline characteristics, quality of life, and long-term outcomes.
Main Methods:
- Analysis of neurobehavioral AEs and neuropsychological data from the SANTE prospective randomized trial.
- Calculation of reliable change indices (RCIs) for memory and mood measures.
- Examination of associations between AEs, RCIs, demographic and seizure variables, and long-term neurobehavioral outcomes.
Main Results:
- No significant cognitive decline or worsening depression scores were observed during the blinded phase or at 7-year follow-up.
- Executive functions and attention scores improved at 7 years.
- Memory and depression AEs were not linked to objective neurobehavioral changes, long-term outcomes, or quality of life.
Conclusions:
- Subjective memory and depression AEs in a minority of patients receiving ANT-DBS were not associated with objective neurobehavioral worsening.
- Neuropsychological monitoring for memory and depression is recommended due to higher AE incidence in the active stimulation group.

