Fluorodeoxyglucose–Positron Emission Tomographic Imaging for the Diagnosis of Mesial Temporal Lobe Epilepsy

Abstract OBJECTIVE Fluorodeoxyglucose (FDG)-positron emission tomographic (PET) imaging plays an important role in the evaluation of intractable epilepsy. The metabolic defect has proven utility in the lateralization of temporal lobe epilepsy. However, the role of FDG–PET imaging in the localization...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Neurosurgery 2008-12, Vol.63 (6), p.1130-1138
Hauptverfasser: Boling, Warren W., Lancaster, Melissa, Kraszpulski, Michal, Palade, Adriana, Marano, Gary, Puce, Aina
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1138
container_issue 6
container_start_page 1130
container_title Neurosurgery
container_volume 63
creator Boling, Warren W.
Lancaster, Melissa
Kraszpulski, Michal
Palade, Adriana
Marano, Gary
Puce, Aina
description Abstract OBJECTIVE Fluorodeoxyglucose (FDG)-positron emission tomographic (PET) imaging plays an important role in the evaluation of intractable epilepsy. The metabolic defect has proven utility in the lateralization of temporal lobe epilepsy. However, the role of FDG–PET imaging in the localization of a seizure focus within the temporal lobe is uncertain. We evaluated FDG–PET imaging for the capability to localize a temporal seizure focus within the mesial structures. METHODS Twenty-eight patients who underwent selective amygdalohippocampectomy for intractable temporal lobe epilepsy were studied. Patients were divided into 2 groups: those who were free of seizures (FS) and those with persisting seizures postoperatively. FS patients were defined by having mesial temporal lobe epilepsy (MTLE). Preoperative FDG–PET activity was evaluated in temporal lobe structures and contrasted with magnetic resonance imaging (MRI) for usefulness in identifying MTLE in an individual. RESULTS Pathology of the hippocampus revealed mesial temporal sclerosis in all but 1 patient. Qualitative visual inspection of the MRI scan was not reliable in the identification of MTLE (P = 0.15). MRI volumetry found smaller mesial temporal structures (P = 0.04) in FS patients. Mesial temporal metabolic activity was reduced in the FS group (hippocampus, P = 0.001). However, a combination of imaging modalities was found to be the best predictor of MTLE. PET imaging plus MRI qualitative inspection identified all patients with and without MTLE correctly and was superior to MRI alone (P = 0.01 and P = 0.02, respectively). CONCLUSION MRI volumetry and PET imaging were comparable (P = 0.73) and able to identify MTLE in most patients, but a combination of PET imaging and MRI visual inspection was superior in the recognition of MTLE.
doi_str_mv 10.1227/01.NEU.0000334429.15867.3B
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_69877124</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><oup_id>10.1227/01.NEU.0000334429.15867.3B</oup_id><sourcerecordid>1985683807</sourcerecordid><originalsourceid>FETCH-LOGICAL-c306t-1a6fe81d874a1699830f3d926cd4fe3cc87e6c4b588069e687b1c2bf6dd8e0853</originalsourceid><addsrcrecordid>eNqVkc1u1DAQxy0EokvhFZAFErcEO3b8wY22W1pp-ThsJW6W40xSV0kc7I3UvfEOvCFPgumuVIkbc_Ecfv-ZsX4IvaGkpFUl3xNaflnflCQXY5xXuqS1ErJkZ0_QitYVLzjh5ClaEcpVwbT4foJepHRHCBVcqufohGpSS1bVKzReDkuIoYVwv--HxYUEv3_--haS38Uw4fXoU_K52YYx9NHOt97h69H2fupxFyLe3QK-8LafciLh0OHPkLwd8BbGOcTcbEIDeD37Aea0f4medXZI8Or4nqKby_X2_KrYfP10ff5xUzhGxK6gVnSgaKskt1RorRjpWKsr4VreAXNOSRCON7VSRGgQSjbUVU0n2lYBUTU7Re8Oc-cYfiyQdib_w8Ew2AnCkozQSkpa8Qy-_Qe8C0uc8m2GalULxRSRmfpwoFwMKUXozBz9aOPeUGL-KjGEmqzEPCoxD0oMO8vh18cVSzNC-xg9OshAfQDCMv_P4D9-_ZmA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1985683807</pqid></control><display><type>article</type><title>Fluorodeoxyglucose–Positron Emission Tomographic Imaging for the Diagnosis of Mesial Temporal Lobe Epilepsy</title><source>MEDLINE</source><source>Journals@Ovid Complete</source><creator>Boling, Warren W. ; Lancaster, Melissa ; Kraszpulski, Michal ; Palade, Adriana ; Marano, Gary ; Puce, Aina</creator><creatorcontrib>Boling, Warren W. ; Lancaster, Melissa ; Kraszpulski, Michal ; Palade, Adriana ; Marano, Gary ; Puce, Aina</creatorcontrib><description>Abstract OBJECTIVE Fluorodeoxyglucose (FDG)-positron emission tomographic (PET) imaging plays an important role in the evaluation of intractable epilepsy. The metabolic defect has proven utility in the lateralization of temporal lobe epilepsy. However, the role of FDG–PET imaging in the localization of a seizure focus within the temporal lobe is uncertain. We evaluated FDG–PET imaging for the capability to localize a temporal seizure focus within the mesial structures. METHODS Twenty-eight patients who underwent selective amygdalohippocampectomy for intractable temporal lobe epilepsy were studied. Patients were divided into 2 groups: those who were free of seizures (FS) and those with persisting seizures postoperatively. FS patients were defined by having mesial temporal lobe epilepsy (MTLE). Preoperative FDG–PET activity was evaluated in temporal lobe structures and contrasted with magnetic resonance imaging (MRI) for usefulness in identifying MTLE in an individual. RESULTS Pathology of the hippocampus revealed mesial temporal sclerosis in all but 1 patient. Qualitative visual inspection of the MRI scan was not reliable in the identification of MTLE (P = 0.15). MRI volumetry found smaller mesial temporal structures (P = 0.04) in FS patients. Mesial temporal metabolic activity was reduced in the FS group (hippocampus, P = 0.001). However, a combination of imaging modalities was found to be the best predictor of MTLE. PET imaging plus MRI qualitative inspection identified all patients with and without MTLE correctly and was superior to MRI alone (P = 0.01 and P = 0.02, respectively). CONCLUSION MRI volumetry and PET imaging were comparable (P = 0.73) and able to identify MTLE in most patients, but a combination of PET imaging and MRI visual inspection was superior in the recognition of MTLE.</description><identifier>ISSN: 0148-396X</identifier><identifier>EISSN: 1524-4040</identifier><identifier>DOI: 10.1227/01.NEU.0000334429.15867.3B</identifier><identifier>PMID: 19057325</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Adolescent ; Adult ; Epilepsy ; Epilepsy, Temporal Lobe - diagnostic imaging ; Epilepsy, Temporal Lobe - pathology ; Female ; Fluorodeoxyglucose F18 ; Humans ; Magnetic Resonance Imaging ; Male ; Metabolism ; Middle Aged ; NMR ; Nuclear magnetic resonance ; Positron-Emission Tomography - methods ; Radiopharmaceuticals ; Reproducibility of Results ; Sensitivity and Specificity ; Tomography ; Young Adult</subject><ispartof>Neurosurgery, 2008-12, Vol.63 (6), p.1130-1138</ispartof><rights>2008 by the Congress of Neurological Surgeons</rights><rights>Copyright © Congress of Neurological Surgeons</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c306t-1a6fe81d874a1699830f3d926cd4fe3cc87e6c4b588069e687b1c2bf6dd8e0853</citedby><cites>FETCH-LOGICAL-c306t-1a6fe81d874a1699830f3d926cd4fe3cc87e6c4b588069e687b1c2bf6dd8e0853</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19057325$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Boling, Warren W.</creatorcontrib><creatorcontrib>Lancaster, Melissa</creatorcontrib><creatorcontrib>Kraszpulski, Michal</creatorcontrib><creatorcontrib>Palade, Adriana</creatorcontrib><creatorcontrib>Marano, Gary</creatorcontrib><creatorcontrib>Puce, Aina</creatorcontrib><title>Fluorodeoxyglucose–Positron Emission Tomographic Imaging for the Diagnosis of Mesial Temporal Lobe Epilepsy</title><title>Neurosurgery</title><addtitle>Neurosurgery</addtitle><description>Abstract OBJECTIVE Fluorodeoxyglucose (FDG)-positron emission tomographic (PET) imaging plays an important role in the evaluation of intractable epilepsy. The metabolic defect has proven utility in the lateralization of temporal lobe epilepsy. However, the role of FDG–PET imaging in the localization of a seizure focus within the temporal lobe is uncertain. We evaluated FDG–PET imaging for the capability to localize a temporal seizure focus within the mesial structures. METHODS Twenty-eight patients who underwent selective amygdalohippocampectomy for intractable temporal lobe epilepsy were studied. Patients were divided into 2 groups: those who were free of seizures (FS) and those with persisting seizures postoperatively. FS patients were defined by having mesial temporal lobe epilepsy (MTLE). Preoperative FDG–PET activity was evaluated in temporal lobe structures and contrasted with magnetic resonance imaging (MRI) for usefulness in identifying MTLE in an individual. RESULTS Pathology of the hippocampus revealed mesial temporal sclerosis in all but 1 patient. Qualitative visual inspection of the MRI scan was not reliable in the identification of MTLE (P = 0.15). MRI volumetry found smaller mesial temporal structures (P = 0.04) in FS patients. Mesial temporal metabolic activity was reduced in the FS group (hippocampus, P = 0.001). However, a combination of imaging modalities was found to be the best predictor of MTLE. PET imaging plus MRI qualitative inspection identified all patients with and without MTLE correctly and was superior to MRI alone (P = 0.01 and P = 0.02, respectively). CONCLUSION MRI volumetry and PET imaging were comparable (P = 0.73) and able to identify MTLE in most patients, but a combination of PET imaging and MRI visual inspection was superior in the recognition of MTLE.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Epilepsy</subject><subject>Epilepsy, Temporal Lobe - diagnostic imaging</subject><subject>Epilepsy, Temporal Lobe - pathology</subject><subject>Female</subject><subject>Fluorodeoxyglucose F18</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Metabolism</subject><subject>Middle Aged</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Positron-Emission Tomography - methods</subject><subject>Radiopharmaceuticals</subject><subject>Reproducibility of Results</subject><subject>Sensitivity and Specificity</subject><subject>Tomography</subject><subject>Young Adult</subject><issn>0148-396X</issn><issn>1524-4040</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqVkc1u1DAQxy0EokvhFZAFErcEO3b8wY22W1pp-ThsJW6W40xSV0kc7I3UvfEOvCFPgumuVIkbc_Ecfv-ZsX4IvaGkpFUl3xNaflnflCQXY5xXuqS1ErJkZ0_QitYVLzjh5ClaEcpVwbT4foJepHRHCBVcqufohGpSS1bVKzReDkuIoYVwv--HxYUEv3_--haS38Uw4fXoU_K52YYx9NHOt97h69H2fupxFyLe3QK-8LafciLh0OHPkLwd8BbGOcTcbEIDeD37Aea0f4medXZI8Or4nqKby_X2_KrYfP10ff5xUzhGxK6gVnSgaKskt1RorRjpWKsr4VreAXNOSRCON7VSRGgQSjbUVU0n2lYBUTU7Re8Oc-cYfiyQdib_w8Ew2AnCkozQSkpa8Qy-_Qe8C0uc8m2GalULxRSRmfpwoFwMKUXozBz9aOPeUGL-KjGEmqzEPCoxD0oMO8vh18cVSzNC-xg9OshAfQDCMv_P4D9-_ZmA</recordid><startdate>20081201</startdate><enddate>20081201</enddate><creator>Boling, Warren W.</creator><creator>Lancaster, Melissa</creator><creator>Kraszpulski, Michal</creator><creator>Palade, Adriana</creator><creator>Marano, Gary</creator><creator>Puce, Aina</creator><general>Oxford University Press</general><general>Wolters Kluwer Health, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20081201</creationdate><title>Fluorodeoxyglucose–Positron Emission Tomographic Imaging for the Diagnosis of Mesial Temporal Lobe Epilepsy</title><author>Boling, Warren W. ; Lancaster, Melissa ; Kraszpulski, Michal ; Palade, Adriana ; Marano, Gary ; Puce, Aina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c306t-1a6fe81d874a1699830f3d926cd4fe3cc87e6c4b588069e687b1c2bf6dd8e0853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Epilepsy</topic><topic>Epilepsy, Temporal Lobe - diagnostic imaging</topic><topic>Epilepsy, Temporal Lobe - pathology</topic><topic>Female</topic><topic>Fluorodeoxyglucose F18</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Metabolism</topic><topic>Middle Aged</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Positron-Emission Tomography - methods</topic><topic>Radiopharmaceuticals</topic><topic>Reproducibility of Results</topic><topic>Sensitivity and Specificity</topic><topic>Tomography</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Boling, Warren W.</creatorcontrib><creatorcontrib>Lancaster, Melissa</creatorcontrib><creatorcontrib>Kraszpulski, Michal</creatorcontrib><creatorcontrib>Palade, Adriana</creatorcontrib><creatorcontrib>Marano, Gary</creatorcontrib><creatorcontrib>Puce, Aina</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Neurosurgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Boling, Warren W.</au><au>Lancaster, Melissa</au><au>Kraszpulski, Michal</au><au>Palade, Adriana</au><au>Marano, Gary</au><au>Puce, Aina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fluorodeoxyglucose–Positron Emission Tomographic Imaging for the Diagnosis of Mesial Temporal Lobe Epilepsy</atitle><jtitle>Neurosurgery</jtitle><addtitle>Neurosurgery</addtitle><date>2008-12-01</date><risdate>2008</risdate><volume>63</volume><issue>6</issue><spage>1130</spage><epage>1138</epage><pages>1130-1138</pages><issn>0148-396X</issn><eissn>1524-4040</eissn><abstract>Abstract OBJECTIVE Fluorodeoxyglucose (FDG)-positron emission tomographic (PET) imaging plays an important role in the evaluation of intractable epilepsy. The metabolic defect has proven utility in the lateralization of temporal lobe epilepsy. However, the role of FDG–PET imaging in the localization of a seizure focus within the temporal lobe is uncertain. We evaluated FDG–PET imaging for the capability to localize a temporal seizure focus within the mesial structures. METHODS Twenty-eight patients who underwent selective amygdalohippocampectomy for intractable temporal lobe epilepsy were studied. Patients were divided into 2 groups: those who were free of seizures (FS) and those with persisting seizures postoperatively. FS patients were defined by having mesial temporal lobe epilepsy (MTLE). Preoperative FDG–PET activity was evaluated in temporal lobe structures and contrasted with magnetic resonance imaging (MRI) for usefulness in identifying MTLE in an individual. RESULTS Pathology of the hippocampus revealed mesial temporal sclerosis in all but 1 patient. Qualitative visual inspection of the MRI scan was not reliable in the identification of MTLE (P = 0.15). MRI volumetry found smaller mesial temporal structures (P = 0.04) in FS patients. Mesial temporal metabolic activity was reduced in the FS group (hippocampus, P = 0.001). However, a combination of imaging modalities was found to be the best predictor of MTLE. PET imaging plus MRI qualitative inspection identified all patients with and without MTLE correctly and was superior to MRI alone (P = 0.01 and P = 0.02, respectively). CONCLUSION MRI volumetry and PET imaging were comparable (P = 0.73) and able to identify MTLE in most patients, but a combination of PET imaging and MRI visual inspection was superior in the recognition of MTLE.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>19057325</pmid><doi>10.1227/01.NEU.0000334429.15867.3B</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0148-396X
ispartof Neurosurgery, 2008-12, Vol.63 (6), p.1130-1138
issn 0148-396X
1524-4040
language eng
recordid cdi_proquest_miscellaneous_69877124
source MEDLINE; Journals@Ovid Complete
subjects Adolescent
Adult
Epilepsy
Epilepsy, Temporal Lobe - diagnostic imaging
Epilepsy, Temporal Lobe - pathology
Female
Fluorodeoxyglucose F18
Humans
Magnetic Resonance Imaging
Male
Metabolism
Middle Aged
NMR
Nuclear magnetic resonance
Positron-Emission Tomography - methods
Radiopharmaceuticals
Reproducibility of Results
Sensitivity and Specificity
Tomography
Young Adult
title Fluorodeoxyglucose–Positron Emission Tomographic Imaging for the Diagnosis of Mesial Temporal Lobe Epilepsy
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-22T20%3A01%3A44IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Fluorodeoxyglucose%E2%80%93Positron%20Emission%20Tomographic%20Imaging%20for%20the%20Diagnosis%20of%20Mesial%20Temporal%20Lobe%20Epilepsy&rft.jtitle=Neurosurgery&rft.au=Boling,%20Warren%20W.&rft.date=2008-12-01&rft.volume=63&rft.issue=6&rft.spage=1130&rft.epage=1138&rft.pages=1130-1138&rft.issn=0148-396X&rft.eissn=1524-4040&rft_id=info:doi/10.1227/01.NEU.0000334429.15867.3B&rft_dat=%3Cproquest_cross%3E1985683807%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1985683807&rft_id=info:pmid/19057325&rft_oup_id=10.1227/01.NEU.0000334429.15867.3B&rfr_iscdi=true