MovDisordV3, PascalFrancis, Curation, bibRecord, 001449

Hypoperfusion of the visual pathway in parkinsonian patients with visual hallucinations

Identifieur interne : 001449 ( PascalFrancis/Curation ); précédent : 001448; suivant : 001450

Hypoperfusion of the visual pathway in parkinsonian patients with visual hallucinations

Auteurs : Hideaki Matsui [Japon] ; Kazuto Nishinaka [Japon] ; Masaya Oda [Japon] ; Narihiro Hara [Japon] ; Kenichi Komatsu [Japon] ; Tamotsu Kubori [Japon] ; Fukashi Udaka [Japon]

Source :

Movement disorders [ 0885-3185 ] ; 2006.

RBID : Pascal:07-0090867

Descripteurs français

Pascal (Inist)
- Système nerveux pathologie, Parkinson maladie, Hallucination visuelle, Voie visuelle, Homme, Tomoscintigraphie émission monophotonique.
Wicri :
- topic : Homme.

English descriptors

KwdEn :
- Human, Nervous system diseases, Parkinson disease, Single photon emission tomography, Visual hallucination, Visual pathway.

Abstract

Little is known about the developing mechanisms of visual hallucinations in Parkinson's disease. This study aimed to investigate perfusion changes in parkinsonian patients with visual hallucinations using n-isopropyl-p-[¹²³I]iodoamphetamine ([¹²³I]IMP) single photon emission computed tomography imaging. A total of 70 consecutive patients, including 31 patients with visual hallucinations, and 39 patients without hallucinations, participated in this study. Patients with severe cognitive impairment (Mini-Mental State Examination score < 20), nonvisual hallucinations, or confusion were excluded. We compared brain perfusion changes between the two groups. We found that hallucinatory patients had significant perfusion reductions in the bilateral inferior parietal lobule, inferior temporal gyrus, precuneus gyrus, and occipital cortex compared to nonhallucinatory patients. These results suggested that hypoperfusion of the visual pathway was closely related to visual hallucinations in Parkinson's disease.

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A08	`01`	`1`	`ENG`	`@1 Hypoperfusion of the visual pathway in parkinsonian patients with visual hallucinations`
A11	`01`	`1`		`@1 MATSUI (Hideaki)`
A11	`02`	`1`		`@1 NISHINAKA (Kazuto)`
A11	`03`	`1`		`@1 ODA (Masaya)`
A11	`04`	`1`		`@1 HARA (Narihiro)`
A11	`05`	`1`		`@1 KOMATSU (Kenichi)`
A11	`06`	`1`		`@1 KUBORI (Tamotsu)`
A11	`07`	`1`		`@1 UDAKA (Fukashi)`
A14	`01`			`@1 Department of Neurology, Sumitomo Hospital @2 Kita-ku, Osaka @3 JPN @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 5 aut. @Z 6 aut. @Z 7 aut.`
A14	`02`			`@1 Department of Radiology, Sumitomo Hospital @2 Kita-ku, Osaka @3 JPN @Z 4 aut.`
A20				`@1 2140-2144`
A21				`@1 2006`
A23	`01`			`@0 ENG`
A43	`01`			`@1 INIST @2 20953 @5 354000145356790170`
A44				`@0 0000 @1 © 2007 INIST-CNRS. All rights reserved.`
A45				`@0 27 ref.`
A47	`01`	`1`		`@0 07-0090867`
A60				`@1 P`
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A64	`01`	`1`		`@0 Movement disorders`
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C01	`01`		`ENG`	@0 Little is known about the developing mechanisms of visual hallucinations in Parkinson's disease. This study aimed to investigate perfusion changes in parkinsonian patients with visual hallucinations using n-isopropyl-p-[¹²³I]iodoamphetamine ([¹²³I]IMP) single photon emission computed tomography imaging. A total of 70 consecutive patients, including 31 patients with visual hallucinations, and 39 patients without hallucinations, participated in this study. Patients with severe cognitive impairment (Mini-Mental State Examination score < 20), nonvisual hallucinations, or confusion were excluded. We compared brain perfusion changes between the two groups. We found that hallucinatory patients had significant perfusion reductions in the bilateral inferior parietal lobule, inferior temporal gyrus, precuneus gyrus, and occipital cortex compared to nonhallucinatory patients. These results suggested that hypoperfusion of the visual pathway was closely related to visual hallucinations in Parkinson's disease.
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C02	`02`	`X`		`@0 002B17F`
C02	`03`	`X`		`@0 002B16B`
C03	`01`	`X`	`FRE`	`@0 Système nerveux pathologie @5 01`
C03	`01`	`X`	`ENG`	`@0 Nervous system diseases @5 01`
C03	`01`	`X`	`SPA`	`@0 Sistema nervioso patología @5 01`
C03	`02`	`X`	`FRE`	`@0 Parkinson maladie @5 02`
C03	`02`	`X`	`ENG`	`@0 Parkinson disease @5 02`
C03	`02`	`X`	`SPA`	`@0 Parkinson enfermedad @5 02`
C03	`03`	`X`	`FRE`	`@0 Hallucination visuelle @2 NM @5 03`
C03	`03`	`X`	`ENG`	`@0 Visual hallucination @2 NM @5 03`
C03	`03`	`X`	`SPA`	`@0 Alucinación visual @2 NM @5 03`
C03	`04`	`X`	`FRE`	`@0 Voie visuelle @5 09`
C03	`04`	`X`	`ENG`	`@0 Visual pathway @5 09`
C03	`04`	`X`	`SPA`	`@0 Vía visual @5 09`
C03	`05`	`X`	`FRE`	`@0 Homme @5 10`
C03	`05`	`X`	`ENG`	`@0 Human @5 10`
C03	`05`	`X`	`SPA`	`@0 Hombre @5 10`
C03	`06`	`X`	`FRE`	`@0 Tomoscintigraphie émission monophotonique @5 11`
C03	`06`	`X`	`ENG`	`@0 Single photon emission tomography @5 11`
C03	`06`	`X`	`SPA`	`@0 Tomografía emisión fotón único @5 11`
C07	`01`	`X`	`FRE`	`@0 Encéphale pathologie @5 37`
C07	`01`	`X`	`ENG`	`@0 Cerebral disorder @5 37`
C07	`01`	`X`	`SPA`	`@0 Encéfalo patología @5 37`
C07	`02`	`X`	`FRE`	`@0 Extrapyramidal syndrome @5 38`
C07	`02`	`X`	`ENG`	`@0 Extrapyramidal syndrome @5 38`
C07	`02`	`X`	`SPA`	`@0 Extrapiramidal síndrome @5 38`
C07	`03`	`X`	`FRE`	`@0 Maladie dégénérative @5 39`
C07	`03`	`X`	`ENG`	`@0 Degenerative disease @5 39`
C07	`03`	`X`	`SPA`	`@0 Enfermedad degenerativa @5 39`
C07	`04`	`X`	`FRE`	`@0 Système nerveux central pathologie @5 40`
C07	`04`	`X`	`ENG`	`@0 Central nervous system disease @5 40`
C07	`04`	`X`	`SPA`	`@0 Sistema nervosio central patología @5 40`
N21				`@1 057`
N44	`01`			`@1 OTO`
N82				`@1 OTO`

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Pascal:07-0090867

Le document en format XML

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<author><name sortKey="Oda, Masaya" sort="Oda, Masaya" uniqKey="Oda M" first="Masaya" last="Oda">Masaya Oda</name>
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<author><name sortKey="Kubori, Tamotsu" sort="Kubori, Tamotsu" uniqKey="Kubori T" first="Tamotsu" last="Kubori">Tamotsu Kubori</name>
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<author><name sortKey="Udaka, Fukashi" sort="Udaka, Fukashi" uniqKey="Udaka F" first="Fukashi" last="Udaka">Fukashi Udaka</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Hypoperfusion of the visual pathway in parkinsonian patients with visual hallucinations</title>
<author><name sortKey="Matsui, Hideaki" sort="Matsui, Hideaki" uniqKey="Matsui H" first="Hideaki" last="Matsui">Hideaki Matsui</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurology, Sumitomo Hospital</s1>
<s2>Kita-ku, Osaka</s2>
<s3>JPN</s3>
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<author><name sortKey="Nishinaka, Kazuto" sort="Nishinaka, Kazuto" uniqKey="Nishinaka K" first="Kazuto" last="Nishinaka">Kazuto Nishinaka</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurology, Sumitomo Hospital</s1>
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<author><name sortKey="Oda, Masaya" sort="Oda, Masaya" uniqKey="Oda M" first="Masaya" last="Oda">Masaya Oda</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurology, Sumitomo Hospital</s1>
<s2>Kita-ku, Osaka</s2>
<s3>JPN</s3>
<sZ>1 aut.</sZ>
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<sZ>3 aut.</sZ>
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<country>Japon</country>
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<author><name sortKey="Hara, Narihiro" sort="Hara, Narihiro" uniqKey="Hara N" first="Narihiro" last="Hara">Narihiro Hara</name>
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<s2>Kita-ku, Osaka</s2>
<s3>JPN</s3>
<sZ>4 aut.</sZ>
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</author>
<author><name sortKey="Komatsu, Kenichi" sort="Komatsu, Kenichi" uniqKey="Komatsu K" first="Kenichi" last="Komatsu">Kenichi Komatsu</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurology, Sumitomo Hospital</s1>
<s2>Kita-ku, Osaka</s2>
<s3>JPN</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
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<country>Japon</country>
</affiliation>
</author>
<author><name sortKey="Kubori, Tamotsu" sort="Kubori, Tamotsu" uniqKey="Kubori T" first="Tamotsu" last="Kubori">Tamotsu Kubori</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurology, Sumitomo Hospital</s1>
<s2>Kita-ku, Osaka</s2>
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<author><name sortKey="Udaka, Fukashi" sort="Udaka, Fukashi" uniqKey="Udaka F" first="Fukashi" last="Udaka">Fukashi Udaka</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurology, Sumitomo Hospital</s1>
<s2>Kita-ku, Osaka</s2>
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<series><title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Human</term>
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<term>Single photon emission tomography</term>
<term>Visual hallucination</term>
<term>Visual pathway</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Système nerveux pathologie</term>
<term>Parkinson maladie</term>
<term>Hallucination visuelle</term>
<term>Voie visuelle</term>
<term>Homme</term>
<term>Tomoscintigraphie émission monophotonique</term>
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<front><div type="abstract" xml:lang="en">Little is known about the developing mechanisms of visual hallucinations in Parkinson's disease. This study aimed to investigate perfusion changes in parkinsonian patients with visual hallucinations using n-isopropyl-p-[<sup>123</sup>
I]iodoamphetamine ([<sup>123</sup>
I]IMP) single photon emission computed tomography imaging. A total of 70 consecutive patients, including 31 patients with visual hallucinations, and 39 patients without hallucinations, participated in this study. Patients with severe cognitive impairment (Mini-Mental State Examination score < 20), nonvisual hallucinations, or confusion were excluded. We compared brain perfusion changes between the two groups. We found that hallucinatory patients had significant perfusion reductions in the bilateral inferior parietal lobule, inferior temporal gyrus, precuneus gyrus, and occipital cortex compared to nonhallucinatory patients. These results suggested that hypoperfusion of the visual pathway was closely related to visual hallucinations in Parkinson's disease.</div>
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<fA11 i1="01" i2="1"><s1>MATSUI (Hideaki)</s1>
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<fA14 i1="01"><s1>Department of Neurology, Sumitomo Hospital</s1>
<s2>Kita-ku, Osaka</s2>
<s3>JPN</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
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<fA14 i1="02"><s1>Department of Radiology, Sumitomo Hospital</s1>
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<fC01 i1="01" l="ENG"><s0>Little is known about the developing mechanisms of visual hallucinations in Parkinson's disease. This study aimed to investigate perfusion changes in parkinsonian patients with visual hallucinations using n-isopropyl-p-[<sup>123</sup>
I]iodoamphetamine ([<sup>123</sup>
I]IMP) single photon emission computed tomography imaging. A total of 70 consecutive patients, including 31 patients with visual hallucinations, and 39 patients without hallucinations, participated in this study. Patients with severe cognitive impairment (Mini-Mental State Examination score < 20), nonvisual hallucinations, or confusion were excluded. We compared brain perfusion changes between the two groups. We found that hallucinatory patients had significant perfusion reductions in the bilateral inferior parietal lobule, inferior temporal gyrus, precuneus gyrus, and occipital cortex compared to nonhallucinatory patients. These results suggested that hypoperfusion of the visual pathway was closely related to visual hallucinations in Parkinson's disease.</s0>
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<fC03 i1="06" i2="X" l="SPA"><s0>Tomografía emisión fotón único</s0>
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<fC07 i1="02" i2="X" l="ENG"><s0>Extrapyramidal syndrome</s0>
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<s5>40</s5>
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<fC07 i1="04" i2="X" l="SPA"><s0>Sistema nervosio central patología</s0>
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<fN21><s1>057</s1>
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<fN82><s1>OTO</s1>
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   |texte=   Hypoperfusion of the visual pathway in parkinsonian patients with visual hallucinations
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	Movement Disorders (revue)
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Movement Disorders (revue)

Hypoperfusion of the visual pathway in parkinsonian patients with visual hallucinations

Hypoperfusion of the visual pathway in parkinsonian patients with visual hallucinations

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