The Behavioral Complications of Pallidal Stimulation: A Case Report

We report a case of recurrent manic episodes associated with chronic deep brain stimulation (DBS) targeting globus pallidus (GP) in the treatment of Parkinson's disease (PD). Cardinal PD symptoms and dyskinesia improved with DBS, and neuropsychological testing found improvements in visuospatial measures associated with left DBS and in verbal memory with right DBS when compared to the patient's preoperative baseline. Under conditions of right, left, and bilateral DBS, the patient experienced bouts of mania and hypomania lasting several days at a time. Positron emission tomography (PET) with (15)O-labeled water was performed after his first manic episode under four conditions: no stimulation, right DBS, left DBS, and bilateral DBS. Although no manic switch occurred during the course of the PET study, all three DBS conditions were associated with decreases in regional flow in the left parahippocampus and hippocampus and right mid-cingulate gyrus. Increases in flow in left inferior frontal area, bilateral insula, dorsolateral prefrontal cortex, and cuneus were common to all DBS conditions. GP stimulation in PD may be associated with behavioral and cognitive effects. Distributed blood flow changes observed with pallidal DBS support a role for the pallidum in cognition and affective regulation.

[1]  P T Fox,et al.  A Highly Accurate Method of Localizing Regions of Neuronal Activation in the Human Brain with Positron Emission Tomography , 1989, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[2]  F. Plum Handbook of Physiology. , 1960 .

[3]  J. A. Obeso,et al.  Restoration of thalamocortical activity after posteroventral pallidotomy in Parkinson's disease , 1994, The Lancet.

[4]  P. Strick,et al.  The temporal lobe is a target of output from the basal ganglia. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[5]  E. London,et al.  Morphine decreases cerebral glucose utilization in limbic and forebrain regions while pain has no effect , 1991, Neuropharmacology.

[6]  D. Calne,et al.  Assessment of Parkinson's Disease , 1984, Clinical neuropharmacology.

[7]  R. C. Oldfield The assessment and analysis of handedness: the Edinburgh inventory. , 1971, Neuropsychologia.

[8]  M. Molinari,et al.  Multiple cortical targets of one thalamic nucleus: The projections of the ventral medial nucleus in the cat studied with retrograde tracers , 1986, The Journal of comparative neurology.

[9]  J. Mazziotta,et al.  MRI‐PET Registration with Automated Algorithm , 1993, Journal of computer assisted tomography.

[10]  Schulz Sc,et al.  Nursing assessment using the BPRS: a structured interview. , 1988 .

[11]  J. Mazziotta,et al.  Rapid Automated Algorithm for Aligning and Reslicing PET Images , 1992, Journal of computer assisted tomography.

[12]  M. Mintun,et al.  A Noninvasive Approach to Quantitative Functional Brain Mapping with H215O and Positron Emission Tomography , 1984, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[13]  M. Raichle,et al.  A Stereotactic Method of Anatomical Localization for Positron Emission Tomography , 1985, Journal of computer assisted tomography.

[14]  T L Babb,et al.  Increased glucose metabolism during long-duration recurrent inhibition of hippocampal pyramidal cells , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[15]  D Burke,et al.  Changes in excitability of human cutaneous afferents following prolonged high-frequency stimulation. , 1989, Brain : a journal of neurology.

[16]  H N Wagner,et al.  Mania after brain injury: Neuroradiological and metabolic findings , 1990, Annals of neurology.

[17]  C. Marsden,et al.  Alterations in cognitive performance and affect-arousal state during fluctuations in motor function in Parkinson's disease. , 1984, Journal of neurology, neurosurgery, and psychiatry.

[18]  A. Parent,et al.  Functional anatomy of the basal ganglia. II. The place of subthalamic nucleus and external pallidium in basal ganglia circuitry , 1995, Brain Research Reviews.

[19]  K Wienhard,et al.  The ECAT EXACT HR: Performance of a New High Resolution Positron Scanner , 1994, Journal of computer assisted tomography.

[20]  B. Horwitz,et al.  Brain activity during transient sadness and happiness in healthy women. , 1995, The American journal of psychiatry.

[21]  G. E. Alexander,et al.  Parallel organization of functionally segregated circuits linking basal ganglia and cortex. , 1986, Annual review of neuroscience.

[22]  M. Delong,et al.  Functional and pathophysiological models of the basal ganglia , 1996, Current Opinion in Neurobiology.

[23]  P. Yakovlev,et al.  Limbic Nuclei of Thalamus and Connections of Limbic Cortex: IV. Thalamocortical Projection of the Ventral Anterior Nucleus in Man , 1961 .

[24]  K. Lyons,et al.  High-frequency stimulation of the globus pallidus for the treatment of Parkinson's disease , 1997, Neurology.

[25]  A. Benabid,et al.  Effect on parkinsonian signs and symptoms of bilateral subthalamic nucleus stimulation , 1995, The Lancet.

[26]  D. Murphy,et al.  Levodopa: Alterations in behavior , 1971, Clinical pharmacology and therapeutics.

[27]  A. Tröster,et al.  Neuropsychological functioning before and after unilateral thalamic stimulating electrode implantation in Parkinson's disease , 1997 .

[28]  Overall Je,et al.  The semistructured BPRS interview and rating guide. , 1988 .

[29]  M S Mega,et al.  Frontal-subcortical circuits and neuropsychiatric disorders. , 1994, The Journal of neuropsychiatry and clinical neurosciences.

[30]  R. Albin,et al.  The pathophysiology of chorea/ballism and Parkinsonism. , 1995, Parkinsonism & related disorders.

[31]  A. Benabid,et al.  Long-term suppression of tremor by chronic stimulation of the ventral intermediate thalamic nucleus , 1991, The Lancet.

[32]  P. Strick,et al.  Multiple output channels in the basal ganglia. , 1993, Science.

[33]  N. Geschwind,et al.  Left-handedness: association with immune disease, migraine, and developmental learning disorder. , 1982, Proceedings of the National Academy of Sciences of the United States of America.

[34]  A. Tröster,et al.  Chronic Electrical Stimulation of the Left Ventrointermediate (Vim) Thalamic Nucleus for the Treatment of Pharmacotherapy-Resistant Parkinson's Disease: A Differential Impact on Access to Semantic and Episodic Memory? , 1998, Brain and Cognition.

[35]  G. Glover,et al.  Characterization of spatial distortion in magnetic resonance imaging and its implications for stereotactic surgery. , 1994, Neurosurgery.

[36]  C. Marsden,et al.  The behavioural and motor consequences of focal lesions of the basal ganglia in man. , 1994, Brain : a journal of neurology.

[37]  V. B. Domesick Thalamic relationships of the medial cortex in the rat. , 1972, Brain, behavior and evolution.

[38]  R. Duvoisin,et al.  Mood changes and “on‐off” phenomena in Parkinson's disease , 1990, Movement disorders : official journal of the Movement Disorder Society.

[39]  R A PATTON,et al.  Limbic nuclei of thalamus and connections of limbic cortex. , 1960, Archives of neurology.

[40]  M. Raichle,et al.  Brain blood flow measured with intravenous H2(15)O. I. Theory and error analysis. , 1983, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[41]  F M Miezin,et al.  Activation of the hippocampus in normal humans: a functional anatomical study of memory. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[42]  W. Nauta,et al.  Efferent connections of the ventral pallidum: Evidence of a dual striato pallidofugal pathway , 1985, The Journal of comparative neurology.