Cerebral glucose metabolism in corticobasal degeneration: Comparison with progressive supranuclear palsy and normal controls
Identifieur interne : 005391 ( Main/Exploration ); précédent : 005390; suivant : 005392Cerebral glucose metabolism in corticobasal degeneration: Comparison with progressive supranuclear palsy and normal controls
Auteurs : Yasuhiro Nagahama [Japon] ; Fukuyama [Japon] ; Nora Turjanski [Royaume-Uni] ; Angus Kennedy [Royaume-Uni] ; Hiroshi Yamauchi [Japon] ; Yasuomi Ouchi [Japon] ; Jun Kimura [Japon] ; David J. Brooks [Royaume-Uni] ; Hiroshi Shibasaki [Japon]Source :
- Movement Disorders [ 0885-3185 ] ; 1997-09.
Descripteurs français
- Pascal (Inist)
- Wicri :
English descriptors
- KwdEn :
- Aged, Analysis of Variance, Atrophy, Basal Ganglia Diseases (metabolism), Basal ganglion, Brain (metabolism), Brain (pathology), Brain (vertebrata), Case-Control Studies, Cerebral Cortex (metabolism), Cerebral Cortex (pathology), Cerebral cortex, Cerebral glucose metabolism, Comparative study, Corticobasal degeneration, Degeneration, Emission tomography, Exploration, Female, Glucose, Glucose (metabolism), Human, Humans, Male, Metabolism, Middle Aged, Neurodegenerative Diseases (metabolism), Positron, Positron‐emission tomography, Progressive, Progressive supranuclear palsy, Supranuclear Palsy, Progressive (metabolism), Supranuclear ophthalmoplegia, Tomography, Emission-Computed.
- MESH :
- chemical , metabolism : Glucose.
- metabolism : Basal Ganglia Diseases, Brain, Cerebral Cortex, Neurodegenerative Diseases, Supranuclear Palsy, Progressive.
- pathology : Brain, Cerebral Cortex.
- Aged, Analysis of Variance, Atrophy, Case-Control Studies, Female, Humans, Male, Middle Aged, Tomography, Emission-Computed.
Abstract
The regional metabolic rate of glucose was estimated using 18F‐labeled 2‐deoxyglucose and positron‐emission tomography (PET) in eight patients with corticobasal degeneration (CBD). Measures of cerebral glucose metabolism in these patients were compared with those for nine age‐matched normal controls and eight patients with progressive supranuclear palsy (PSP). Compared with that in the normal controls, the CBD patients showed significantly reduced cerebral glucose metabolism in the contralateral hemisphere to the clinically most affected side in the dorsolateral frontal, medial frontal, inferior parietal, sensorimotor, and lateral temporal cortex, as well as in the corpus striatum and the thalamus. In comparison with that in PSP, in CBD the glucose metabolism in the contralateral hemisphere was significantly decreased in the in ferior parietal, sensorimotor, lateral temporal cortex, and the corpus striatum. These results confirm the marked asymmetric cerebral involvement in CBD and suggest that there are significant differences between CBD and PSP in the cerebral metabolism in some cerebral regions such as the inferior parietal cortex and sensorimotor cortex, which might reflect the differences in their clinical characteristics.
Url:
DOI: 10.1002/mds.870120510
Affiliations:
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sort="Turjanski, Nora" uniqKey="Turjanski N" first="Nora" last="Turjanski">Nora Turjanski</name><affiliation wicri:level="2"><country>Royaume-Uni</country><placeName><region type="country">Angleterre</region></placeName><wicri:cityArea>MRC Cyclotron Unit, Hammersmith Hospital, London</wicri:cityArea></affiliation></author><author><name sortKey="Kennedy, Angus" sort="Kennedy, Angus" uniqKey="Kennedy A" first="Angus" last="Kennedy">Angus Kennedy</name><affiliation wicri:level="2"><country>Royaume-Uni</country><placeName><region type="country">Angleterre</region></placeName><wicri:cityArea>MRC Cyclotron Unit, Hammersmith Hospital, London</wicri:cityArea></affiliation></author><author><name sortKey="Yamauchi, Hiroshi" sort="Yamauchi, Hiroshi" uniqKey="Yamauchi H" first="Hiroshi" last="Yamauchi">Hiroshi Yamauchi</name><affiliation wicri:level="4"><country xml:lang="fr">Japon</country><wicri:regionArea>Department of Neurology, Kyoto University, Kyoto</wicri:regionArea><orgName 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Disord.</title><idno type="ISSN">0885-3185</idno><idno type="eISSN">1531-8257</idno><imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><date type="published" when="1997-09">1997-09</date><biblScope unit="vol">12</biblScope><biblScope unit="issue">5</biblScope><biblScope unit="page" from="691">691</biblScope><biblScope unit="page" to="696">696</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">3A0A2879B94B4D9CE473C40A55B5E760B2328D37</idno><idno type="DOI">10.1002/mds.870120510</idno><idno type="ArticleID">MDS870120510</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term><term>Analysis of Variance</term><term>Atrophy</term><term>Basal Ganglia Diseases (metabolism)</term><term>Basal ganglion</term><term>Brain (metabolism)</term><term>Brain (pathology)</term><term>Brain (vertebrata)</term><term>Case-Control Studies</term><term>Cerebral Cortex (metabolism)</term><term>Cerebral Cortex (pathology)</term><term>Cerebral cortex</term><term>Cerebral glucose metabolism</term><term>Comparative study</term><term>Corticobasal degeneration</term><term>Degeneration</term><term>Emission tomography</term><term>Exploration</term><term>Female</term><term>Glucose</term><term>Glucose (metabolism)</term><term>Human</term><term>Humans</term><term>Male</term><term>Metabolism</term><term>Middle Aged</term><term>Neurodegenerative Diseases (metabolism)</term><term>Positron</term><term>Positron‐emission tomography</term><term>Progressive</term><term>Progressive supranuclear palsy</term><term>Supranuclear Palsy, Progressive (metabolism)</term><term>Supranuclear ophthalmoplegia</term><term>Tomography, Emission-Computed</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Glucose</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Basal Ganglia Diseases</term><term>Brain</term><term>Cerebral Cortex</term><term>Neurodegenerative Diseases</term><term>Supranuclear Palsy, Progressive</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Brain</term><term>Cerebral Cortex</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Aged</term><term>Analysis of Variance</term><term>Atrophy</term><term>Case-Control Studies</term><term>Female</term><term>Humans</term><term>Male</term><term>Middle Aged</term><term>Tomography, Emission-Computed</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Cortex cérébral</term><term>Dégénérescence</term><term>Encéphale</term><term>Etude comparative</term><term>Exploration</term><term>Glucose</term><term>Homme</term><term>Métabolisme</term><term>Noyau gris central</term><term>Ophtalmoplégie supranucléaire</term><term>Positon</term><term>Progressif</term><term>Tomoscintigraphie</term></keywords><keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Glucose</term><term>Homme</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The regional metabolic rate of glucose was estimated using 18F‐labeled 2‐deoxyglucose and positron‐emission tomography (PET) in eight patients with corticobasal degeneration (CBD). Measures of cerebral glucose metabolism in these patients were compared with those for nine age‐matched normal controls and eight patients with progressive supranuclear palsy (PSP). Compared with that in the normal controls, the CBD patients showed significantly reduced cerebral glucose metabolism in the contralateral hemisphere to the clinically most affected side in the dorsolateral frontal, medial frontal, inferior parietal, sensorimotor, and lateral temporal cortex, as well as in the corpus striatum and the thalamus. In comparison with that in PSP, in CBD the glucose metabolism in the contralateral hemisphere was significantly decreased in the in ferior parietal, sensorimotor, lateral temporal cortex, and the corpus striatum. These results confirm the marked asymmetric cerebral involvement in CBD and suggest that there are significant differences between CBD and PSP in the cerebral metabolism in some cerebral regions such as the inferior parietal cortex and sensorimotor cortex, which might reflect the differences in their clinical characteristics.</div></front></TEI><affiliations><list><country><li>Japon</li><li>Royaume-Uni</li></country><region><li>Angleterre</li><li>Région du Kansai</li></region><settlement><li>Kyoto</li></settlement><orgName><li>Université de Kyoto</li></orgName></list><tree><country name="Japon"><region name="Région du Kansai"><name sortKey="Nagahama, Yasuhiro" sort="Nagahama, Yasuhiro" uniqKey="Nagahama Y" first="Yasuhiro" last="Nagahama">Yasuhiro Nagahama</name></region><name sortKey="Fukuyama" sort="Fukuyama" uniqKey="Fukuyama" last="Fukuyama">Fukuyama</name><name sortKey="Kimura, Jun" sort="Kimura, Jun" uniqKey="Kimura J" first="Jun" last="Kimura">Jun Kimura</name><name sortKey="Ouchi, Yasuomi" sort="Ouchi, Yasuomi" uniqKey="Ouchi Y" first="Yasuomi" last="Ouchi">Yasuomi Ouchi</name><name sortKey="Shibasaki, Hiroshi" sort="Shibasaki, Hiroshi" uniqKey="Shibasaki H" first="Hiroshi" last="Shibasaki">Hiroshi Shibasaki</name><name sortKey="Yamauchi, Hiroshi" sort="Yamauchi, Hiroshi" uniqKey="Yamauchi H" first="Hiroshi" last="Yamauchi">Hiroshi Yamauchi</name></country><country name="Royaume-Uni"><region name="Angleterre"><name sortKey="Turjanski, Nora" sort="Turjanski, Nora" uniqKey="Turjanski N" first="Nora" last="Turjanski">Nora Turjanski</name></region><name sortKey="Brooks, David J" sort="Brooks, David J" uniqKey="Brooks D" first="David J." last="Brooks">David J. Brooks</name><name sortKey="Kennedy, Angus" sort="Kennedy, Angus" uniqKey="Kennedy A" first="Angus" last="Kennedy">Angus Kennedy</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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