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Improvements in both psychosis and motor signs in Parkinson's disease, and changes in regional cerebral blood flow after electroconvulsive therapy

Psychotic symptoms in Parkinson's disease (PD) are relatively common and, in addition to creating a disturbance in patients' daily lives, have consistently been shown to be associated with poor outcome. The use of anti-PD medications has been the most widely identified risk factor for PD p...

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Published in:Progress in neuro-psychopharmacology & biological psychiatry 2011-08, Vol.35 (7), p.1704-1708
Main Authors: Usui, Chie, Hatta, Kotaro, Doi, Nagafumi, Kubo, Shinichiro, Kamigaichi, Rie, Nakanishi, Atsushi, Nakamura, Hiroyuki, Hattori, Nobutaka, Arai, Heii
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cited_by cdi_FETCH-LOGICAL-c486t-dc375d39dd3dd6ddbdf1978e0841f6fb726db1dcc04e89c8529fd28df88b552c3
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container_title Progress in neuro-psychopharmacology & biological psychiatry
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creator Usui, Chie
Hatta, Kotaro
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Kubo, Shinichiro
Kamigaichi, Rie
Nakanishi, Atsushi
Nakamura, Hiroyuki
Hattori, Nobutaka
Arai, Heii
description Psychotic symptoms in Parkinson's disease (PD) are relatively common and, in addition to creating a disturbance in patients' daily lives, have consistently been shown to be associated with poor outcome. The use of anti-PD medications has been the most widely identified risk factor for PD psychosis (PDP). However, the pathophysiology of PDP remains unclear. Although the efficacy of electroconvulsive therapy (ECT) for PD had been pointed out, only one study has demonstrated the effectiveness of ECT on both psychotic symptoms and motor symptoms. The aim of this study was to examine the acute effectiveness of ECT on PD and to identify the brain areas associated with PDP. The study was conducted at Juntendo University Hospital in Tokyo. Eight patients with L-DOPA- or dopamine (DA) agonist-induced PDP, who were resistant to quetiapine treatment, were enrolled. Severity of PD was evaluated using the Hoehn and Yahr stage. Psychotic symptoms were evaluated using multiple measures from the Scale for the Assessment of Positive Symptoms (SAPS). Technetium-99m ethyl cysteinate dimer single photon emission computed tomography (99mTc ECD SPECT) was used to assess regional cerebral blood flow (rCBF) before and after a course of ECT. A voxel-by-voxel group analysis was performed using Statistical Parametric Mapping (SPM5). Our study clearly demonstrated that PDP was significantly less severe after ECT than before ECT, as indicated by change in mean SAPS total domain score (t=7.2, P=0.0002). Furthermore, the patients showed significant improvement in Hoehn and Yahr stage after ECT (t=11.7, P
doi_str_mv 10.1016/j.pnpbp.2011.05.003
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The use of anti-PD medications has been the most widely identified risk factor for PD psychosis (PDP). However, the pathophysiology of PDP remains unclear. Although the efficacy of electroconvulsive therapy (ECT) for PD had been pointed out, only one study has demonstrated the effectiveness of ECT on both psychotic symptoms and motor symptoms. The aim of this study was to examine the acute effectiveness of ECT on PD and to identify the brain areas associated with PDP. The study was conducted at Juntendo University Hospital in Tokyo. Eight patients with L-DOPA- or dopamine (DA) agonist-induced PDP, who were resistant to quetiapine treatment, were enrolled. Severity of PD was evaluated using the Hoehn and Yahr stage. Psychotic symptoms were evaluated using multiple measures from the Scale for the Assessment of Positive Symptoms (SAPS). Technetium-99m ethyl cysteinate dimer single photon emission computed tomography (99mTc ECD SPECT) was used to assess regional cerebral blood flow (rCBF) before and after a course of ECT. A voxel-by-voxel group analysis was performed using Statistical Parametric Mapping (SPM5). Our study clearly demonstrated that PDP was significantly less severe after ECT than before ECT, as indicated by change in mean SAPS total domain score (t=7.2, P=0.0002). Furthermore, the patients showed significant improvement in Hoehn and Yahr stage after ECT (t=11.7, P&lt;0.0001). A further notable observation was significant increase in rCBF in the right middle frontal gyrus after ECT. We conclude that a course of ECT produced notable improvements not only in PDP but also in the severity of PD. 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Leukodystrophies. Prion diseases ; Dibenzothiazepines - therapeutic use ; Disease Progression ; ECT ; Electroconvulsive therapy ; Electroconvulsive Therapy - methods ; Electroencephalography ; Female ; Humans ; Inpatients ; Levodopa - adverse effects ; Levodopa - pharmacology ; Levodopa - therapeutic use ; Male ; Medical sciences ; Middle Aged ; Neurology ; Neuropharmacology ; Organic mental disorders. Neuropsychology ; Parkinson Disease - complications ; Parkinson Disease - drug therapy ; Parkinson Disease - therapy ; Parkinson's disease ; Parkinson's disease psychosis ; Pharmacology. Drug treatments ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Psychotic Disorders - complications ; Psychotic Disorders - drug therapy ; Psychotic Disorders - therapy ; Quetiapine Fumarate ; Regional Blood Flow - drug effects ; Regional Blood Flow - physiology ; Risk Factors ; SPECT ; Time Factors ; Tokyo ; Tomography, Emission-Computed, Single-Photon ; Treatments</subject><ispartof>Progress in neuro-psychopharmacology &amp; biological psychiatry, 2011-08, Vol.35 (7), p.1704-1708</ispartof><rights>2011 Elsevier Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 Elsevier Inc. 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Technetium-99m ethyl cysteinate dimer single photon emission computed tomography (99mTc ECD SPECT) was used to assess regional cerebral blood flow (rCBF) before and after a course of ECT. A voxel-by-voxel group analysis was performed using Statistical Parametric Mapping (SPM5). Our study clearly demonstrated that PDP was significantly less severe after ECT than before ECT, as indicated by change in mean SAPS total domain score (t=7.2, P=0.0002). Furthermore, the patients showed significant improvement in Hoehn and Yahr stage after ECT (t=11.7, P&lt;0.0001). A further notable observation was significant increase in rCBF in the right middle frontal gyrus after ECT. We conclude that a course of ECT produced notable improvements not only in PDP but also in the severity of PD. 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The use of anti-PD medications has been the most widely identified risk factor for PD psychosis (PDP). However, the pathophysiology of PDP remains unclear. Although the efficacy of electroconvulsive therapy (ECT) for PD had been pointed out, only one study has demonstrated the effectiveness of ECT on both psychotic symptoms and motor symptoms. The aim of this study was to examine the acute effectiveness of ECT on PD and to identify the brain areas associated with PDP. The study was conducted at Juntendo University Hospital in Tokyo. Eight patients with L-DOPA- or dopamine (DA) agonist-induced PDP, who were resistant to quetiapine treatment, were enrolled. Severity of PD was evaluated using the Hoehn and Yahr stage. Psychotic symptoms were evaluated using multiple measures from the Scale for the Assessment of Positive Symptoms (SAPS). Technetium-99m ethyl cysteinate dimer single photon emission computed tomography (99mTc ECD SPECT) was used to assess regional cerebral blood flow (rCBF) before and after a course of ECT. A voxel-by-voxel group analysis was performed using Statistical Parametric Mapping (SPM5). Our study clearly demonstrated that PDP was significantly less severe after ECT than before ECT, as indicated by change in mean SAPS total domain score (t=7.2, P=0.0002). Furthermore, the patients showed significant improvement in Hoehn and Yahr stage after ECT (t=11.7, P&lt;0.0001). A further notable observation was significant increase in rCBF in the right middle frontal gyrus after ECT. We conclude that a course of ECT produced notable improvements not only in PDP but also in the severity of PD. The findings of change in rCBF suggest implications for dysfunction in the middle frontal region for patients with PDP. ► We examined the acute effectiveness of ECT on PD and identified the brain areas associated with PDP. ► ECT improved the PDP and increased in rCBF in the middle frontal gyrus. ► The change in rCBF suggest implications for dysfunction in the middle frontal region for patients with PDP.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>21605615</pmid><doi>10.1016/j.pnpbp.2011.05.003</doi><tpages>5</tpages></addata></record>
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subjects Adult and adolescent clinical studies
Aged
Antiparkinson Agents - adverse effects
Antiparkinson Agents - pharmacology
Antiparkinson Agents - therapeutic use
Antipsychotic Agents - pharmacology
Antipsychotic Agents - therapeutic use
Biological and medical sciences
Clinical Trials, Phase I as Topic
Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
Dibenzothiazepines - therapeutic use
Disease Progression
ECT
Electroconvulsive therapy
Electroconvulsive Therapy - methods
Electroencephalography
Female
Humans
Inpatients
Levodopa - adverse effects
Levodopa - pharmacology
Levodopa - therapeutic use
Male
Medical sciences
Middle Aged
Neurology
Neuropharmacology
Organic mental disorders. Neuropsychology
Parkinson Disease - complications
Parkinson Disease - drug therapy
Parkinson Disease - therapy
Parkinson's disease
Parkinson's disease psychosis
Pharmacology. Drug treatments
Psychology. Psychoanalysis. Psychiatry
Psychopathology. Psychiatry
Psychotic Disorders - complications
Psychotic Disorders - drug therapy
Psychotic Disorders - therapy
Quetiapine Fumarate
Regional Blood Flow - drug effects
Regional Blood Flow - physiology
Risk Factors
SPECT
Time Factors
Tokyo
Tomography, Emission-Computed, Single-Photon
Treatments
title Improvements in both psychosis and motor signs in Parkinson's disease, and changes in regional cerebral blood flow after electroconvulsive therapy
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