Espectroscopia por ressonância magnética de prótons em epilepsia mioclônica juvenil sugere o comprometimento de uma rede neuronal específica

Detalhes bibliográficos
Autor(a) principal: Lin, Katia [UNIFESP]
Data de Publicação: 2008
Outros Autores: Carrete Junior, Henrique [UNIFESP], Lin, Jaime [UNIFESP], Peruchi, M.m. [UNIFESP], Araujo Filho, Gerardo Maria de [UNIFESP], Pascalicchio, T.f. [UNIFESP], Guaranha, Mirian Salvadori Bittar [UNIFESP], Guilhoto, Laura Maria de Figueiredo Ferreira [UNIFESP], Yacubian, Elza Márcia Targas [UNIFESP]
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/handle/11600/4538
http://dx.doi.org/10.1590/S1676-26492008000300003
Resumo: OBJECTIVES: The neuroanatomical basis and the neurochemical abnormalities that underlay juvenile myoclonic epilepsy (JME) are not fully defined. While the thalamus plays a central role in synchronization of widespread regions of the cerebral cortex during a seizure, emerging evidence suggests that all cortical neurons may not be homogeneously involved. The purpose of this study was to investigate the cerebral metabolic differences between patients with JME and normal controls. METHODS: All patients had a JME diagnosis based on seizure history and semiology, EEG recording, normal magnetic resonance neuroimaging (MRI) and video-EEG. Forty JME patients (JME-P) were submitted to 1.5 T MRI proton spectroscopy (1H-MRS), multi-voxel with PRESS sequence (TR/TE = 1500/30 ms) over the following locations: prefrontal cortex (PC), frontal cortex (FC), thalamus, basal nuclei, posterior cingulate gyrus (PCG), insular, parietal and occipital cortices. We determined ratios for integral values of N-acetyl aspartate (NAA) and glutamine-glutamate (GLX) over creatine-phosphocreatine (Cr). The control group (CTL) consisted of 20 age and sex-matched healthy volunteers. RESULTS: Group analysis demonstrated a tendency for lower NAA/Cr ratio of JME-P compared to CTL predominantly on FC, PC, thalamus and occipital cortex. When compared to CTL, JME-P had a statistically significant difference in GLX/Cr on FC, PC, insula, basal nuclei, PCG and on thalamus. When evaluating the relationship among the various components of this epileptic network among JME-P, the strongest correlation occurred between thalamus and PC. Also, we found a significant negative correlation between NAA/Cr and duration of epilepsy. CONCLUSION: Reductions in NAA may represent loss or injury of neurons and/or axons, as well as metabolic dysfunction while glutamate is considered to be an excitatory neurotransmitter in the brain which is involved in the pathogenesis of epileptogenic seizures.
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spelling Lin, Katia [UNIFESP]Carrete Junior, Henrique [UNIFESP]Lin, Jaime [UNIFESP]Peruchi, M.m. [UNIFESP]Araujo Filho, Gerardo Maria de [UNIFESP]Pascalicchio, T.f. [UNIFESP]Guaranha, Mirian Salvadori Bittar [UNIFESP]Guilhoto, Laura Maria de Figueiredo Ferreira [UNIFESP]Yacubian, Elza Márcia Targas [UNIFESP]Universidade Federal de São Paulo (UNIFESP)2015-06-14T13:38:42Z2015-06-14T13:38:42Z2008-09-01Journal of Epilepsy and Clinical Neurophysiology. Liga Brasileira de Epilepsia (LBE), v. 14, n. 3, p. 99-100, 2008.1676-2649http://repositorio.unifesp.br/handle/11600/4538http://dx.doi.org/10.1590/S1676-26492008000300003S1676-26492008000300003.pdfS1676-2649200800030000310.1590/S1676-26492008000300003OBJECTIVES: The neuroanatomical basis and the neurochemical abnormalities that underlay juvenile myoclonic epilepsy (JME) are not fully defined. While the thalamus plays a central role in synchronization of widespread regions of the cerebral cortex during a seizure, emerging evidence suggests that all cortical neurons may not be homogeneously involved. The purpose of this study was to investigate the cerebral metabolic differences between patients with JME and normal controls. METHODS: All patients had a JME diagnosis based on seizure history and semiology, EEG recording, normal magnetic resonance neuroimaging (MRI) and video-EEG. Forty JME patients (JME-P) were submitted to 1.5 T MRI proton spectroscopy (1H-MRS), multi-voxel with PRESS sequence (TR/TE = 1500/30 ms) over the following locations: prefrontal cortex (PC), frontal cortex (FC), thalamus, basal nuclei, posterior cingulate gyrus (PCG), insular, parietal and occipital cortices. We determined ratios for integral values of N-acetyl aspartate (NAA) and glutamine-glutamate (GLX) over creatine-phosphocreatine (Cr). The control group (CTL) consisted of 20 age and sex-matched healthy volunteers. RESULTS: Group analysis demonstrated a tendency for lower NAA/Cr ratio of JME-P compared to CTL predominantly on FC, PC, thalamus and occipital cortex. When compared to CTL, JME-P had a statistically significant difference in GLX/Cr on FC, PC, insula, basal nuclei, PCG and on thalamus. When evaluating the relationship among the various components of this epileptic network among JME-P, the strongest correlation occurred between thalamus and PC. Also, we found a significant negative correlation between NAA/Cr and duration of epilepsy. CONCLUSION: Reductions in NAA may represent loss or injury of neurons and/or axons, as well as metabolic dysfunction while glutamate is considered to be an excitatory neurotransmitter in the brain which is involved in the pathogenesis of epileptogenic seizures.UNIFESP-EPM Hospital São PauloUNIFESP, EPM, Hospital São PauloSciELO99-100porLiga Brasileira de Epilepsia (LBE)Journal of Epilepsy and Clinical NeurophysiologyEpilepsia mioclônica juvenilespectroscopia por ressonância magnéticaimagem por ressonância magnéticaJuvenile myoclonic epilepsymagnetic resonance spectroscopymagnetic resonance imagingEspectroscopia por ressonância magnética de prótons em epilepsia mioclônica juvenil sugere o comprometimento de uma rede neuronal específicaProton magnetic resonance spectroscopy study of juvenile myoclonic epilepsy patients suggests involvement of a specific neuronal networkinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESPORIGINALS1676-26492008000300003.pdfapplication/pdf69482${dspace.ui.url}/bitstream/11600/4538/1/S1676-26492008000300003.pdf18dd5ce1b2d80e4c596234f5288b591aMD51open accessTEXTS1676-26492008000300003.pdf.txtS1676-26492008000300003.pdf.txtExtracted texttext/plain8913${dspace.ui.url}/bitstream/11600/4538/2/S1676-26492008000300003.pdf.txt390ed97614d470540e4b0901e2516925MD52open access11600/45382022-11-04 15:31:40.622open accessoai:repositorio.unifesp.br:11600/4538Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652023-05-25T12:29:21.041523Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.pt.fl_str_mv Espectroscopia por ressonância magnética de prótons em epilepsia mioclônica juvenil sugere o comprometimento de uma rede neuronal específica
dc.title.alternative.en.fl_str_mv Proton magnetic resonance spectroscopy study of juvenile myoclonic epilepsy patients suggests involvement of a specific neuronal network
title Espectroscopia por ressonância magnética de prótons em epilepsia mioclônica juvenil sugere o comprometimento de uma rede neuronal específica
spellingShingle Espectroscopia por ressonância magnética de prótons em epilepsia mioclônica juvenil sugere o comprometimento de uma rede neuronal específica
Lin, Katia [UNIFESP]
Epilepsia mioclônica juvenil
espectroscopia por ressonância magnética
imagem por ressonância magnética
Juvenile myoclonic epilepsy
magnetic resonance spectroscopy
magnetic resonance imaging
title_short Espectroscopia por ressonância magnética de prótons em epilepsia mioclônica juvenil sugere o comprometimento de uma rede neuronal específica
title_full Espectroscopia por ressonância magnética de prótons em epilepsia mioclônica juvenil sugere o comprometimento de uma rede neuronal específica
title_fullStr Espectroscopia por ressonância magnética de prótons em epilepsia mioclônica juvenil sugere o comprometimento de uma rede neuronal específica
title_full_unstemmed Espectroscopia por ressonância magnética de prótons em epilepsia mioclônica juvenil sugere o comprometimento de uma rede neuronal específica
title_sort Espectroscopia por ressonância magnética de prótons em epilepsia mioclônica juvenil sugere o comprometimento de uma rede neuronal específica
author Lin, Katia [UNIFESP]
author_facet Lin, Katia [UNIFESP]
Carrete Junior, Henrique [UNIFESP]
Lin, Jaime [UNIFESP]
Peruchi, M.m. [UNIFESP]
Araujo Filho, Gerardo Maria de [UNIFESP]
Pascalicchio, T.f. [UNIFESP]
Guaranha, Mirian Salvadori Bittar [UNIFESP]
Guilhoto, Laura Maria de Figueiredo Ferreira [UNIFESP]
Yacubian, Elza Márcia Targas [UNIFESP]
author_role author
author2 Carrete Junior, Henrique [UNIFESP]
Lin, Jaime [UNIFESP]
Peruchi, M.m. [UNIFESP]
Araujo Filho, Gerardo Maria de [UNIFESP]
Pascalicchio, T.f. [UNIFESP]
Guaranha, Mirian Salvadori Bittar [UNIFESP]
Guilhoto, Laura Maria de Figueiredo Ferreira [UNIFESP]
Yacubian, Elza Márcia Targas [UNIFESP]
author2_role author
author
author
author
author
author
author
author
dc.contributor.institution.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Lin, Katia [UNIFESP]
Carrete Junior, Henrique [UNIFESP]
Lin, Jaime [UNIFESP]
Peruchi, M.m. [UNIFESP]
Araujo Filho, Gerardo Maria de [UNIFESP]
Pascalicchio, T.f. [UNIFESP]
Guaranha, Mirian Salvadori Bittar [UNIFESP]
Guilhoto, Laura Maria de Figueiredo Ferreira [UNIFESP]
Yacubian, Elza Márcia Targas [UNIFESP]
dc.subject.por.fl_str_mv Epilepsia mioclônica juvenil
espectroscopia por ressonância magnética
imagem por ressonância magnética
topic Epilepsia mioclônica juvenil
espectroscopia por ressonância magnética
imagem por ressonância magnética
Juvenile myoclonic epilepsy
magnetic resonance spectroscopy
magnetic resonance imaging
dc.subject.eng.fl_str_mv Juvenile myoclonic epilepsy
magnetic resonance spectroscopy
magnetic resonance imaging
description OBJECTIVES: The neuroanatomical basis and the neurochemical abnormalities that underlay juvenile myoclonic epilepsy (JME) are not fully defined. While the thalamus plays a central role in synchronization of widespread regions of the cerebral cortex during a seizure, emerging evidence suggests that all cortical neurons may not be homogeneously involved. The purpose of this study was to investigate the cerebral metabolic differences between patients with JME and normal controls. METHODS: All patients had a JME diagnosis based on seizure history and semiology, EEG recording, normal magnetic resonance neuroimaging (MRI) and video-EEG. Forty JME patients (JME-P) were submitted to 1.5 T MRI proton spectroscopy (1H-MRS), multi-voxel with PRESS sequence (TR/TE = 1500/30 ms) over the following locations: prefrontal cortex (PC), frontal cortex (FC), thalamus, basal nuclei, posterior cingulate gyrus (PCG), insular, parietal and occipital cortices. We determined ratios for integral values of N-acetyl aspartate (NAA) and glutamine-glutamate (GLX) over creatine-phosphocreatine (Cr). The control group (CTL) consisted of 20 age and sex-matched healthy volunteers. RESULTS: Group analysis demonstrated a tendency for lower NAA/Cr ratio of JME-P compared to CTL predominantly on FC, PC, thalamus and occipital cortex. When compared to CTL, JME-P had a statistically significant difference in GLX/Cr on FC, PC, insula, basal nuclei, PCG and on thalamus. When evaluating the relationship among the various components of this epileptic network among JME-P, the strongest correlation occurred between thalamus and PC. Also, we found a significant negative correlation between NAA/Cr and duration of epilepsy. CONCLUSION: Reductions in NAA may represent loss or injury of neurons and/or axons, as well as metabolic dysfunction while glutamate is considered to be an excitatory neurotransmitter in the brain which is involved in the pathogenesis of epileptogenic seizures.
publishDate 2008
dc.date.issued.fl_str_mv 2008-09-01
dc.date.accessioned.fl_str_mv 2015-06-14T13:38:42Z
dc.date.available.fl_str_mv 2015-06-14T13:38:42Z
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dc.identifier.citation.fl_str_mv Journal of Epilepsy and Clinical Neurophysiology. Liga Brasileira de Epilepsia (LBE), v. 14, n. 3, p. 99-100, 2008.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/handle/11600/4538
http://dx.doi.org/10.1590/S1676-26492008000300003
dc.identifier.issn.none.fl_str_mv 1676-2649
dc.identifier.file.none.fl_str_mv S1676-26492008000300003.pdf
dc.identifier.scielo.none.fl_str_mv S1676-26492008000300003
dc.identifier.doi.none.fl_str_mv 10.1590/S1676-26492008000300003
identifier_str_mv Journal of Epilepsy and Clinical Neurophysiology. Liga Brasileira de Epilepsia (LBE), v. 14, n. 3, p. 99-100, 2008.
1676-2649
S1676-26492008000300003.pdf
S1676-26492008000300003
10.1590/S1676-26492008000300003
url http://repositorio.unifesp.br/handle/11600/4538
http://dx.doi.org/10.1590/S1676-26492008000300003
dc.language.iso.fl_str_mv por
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dc.relation.ispartof.none.fl_str_mv Journal of Epilepsy and Clinical Neurophysiology
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eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 99-100
dc.publisher.none.fl_str_mv Liga Brasileira de Epilepsia (LBE)
publisher.none.fl_str_mv Liga Brasileira de Epilepsia (LBE)
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
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