Data mining neocortical high-frequency oscillations in epilepsy and controls
Transient high-frequency (100-500 Hz) oscillations of the local field potential have been studied extensively in human mesial temporal lobe. Previous studies report that both ripple (100-250 Hz) and fast ripple (250-500 Hz) oscillations are increased in the seizure-onset zone of patients with mesial...
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description | Transient high-frequency (100-500 Hz) oscillations of the local field potential have been studied extensively in human mesial temporal lobe. Previous studies report that both ripple (100-250 Hz) and fast ripple (250-500 Hz) oscillations are increased in the seizure-onset zone of patients with mesial temporal lobe epilepsy. Comparatively little is known, however, about their spatial distribution with respect to seizure-onset zone in neocortical epilepsy, or their prevalence in normal brain. We present a quantitative analysis of high-frequency oscillations and their rates of occurrence in a group of nine patients with neocortical epilepsy and two control patients with no history of seizures. Oscillations were automatically detected and classified using an unsupervised approach in a data set of unprecedented volume in epilepsy research, over 12 terabytes of continuous long-term micro- and macro-electrode intracranial recordings, without human preprocessing, enabling selection-bias-free estimates of oscillation rates. There are three main results: (i) a cluster of ripple frequency oscillations with median spectral centroid = 137 Hz is increased in the seizure-onset zone more frequently than a cluster of fast ripple frequency oscillations (median spectral centroid = 305 Hz); (ii) we found no difference in the rates of high frequency oscillations in control neocortex and the non-seizure-onset zone neocortex of patients with epilepsy, despite the possibility of different underlying mechanisms of generation; and (iii) while previous studies have demonstrated that oscillations recorded by parenchyma-penetrating micro-electrodes have higher peak 100-500 Hz frequencies than penetrating macro-electrodes, this was not found for the epipial electrodes used here to record from the neocortical surface. We conclude that the relative rate of ripple frequency oscillations is a potential biomarker for epileptic neocortex, but that larger prospective studies correlating high-frequency oscillations rates with seizure-onset zone, resected tissue and surgical outcome are required to determine the true predictive value. |
doi_str_mv | 10.1093/brain/awr212 |
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Previous studies report that both ripple (100-250 Hz) and fast ripple (250-500 Hz) oscillations are increased in the seizure-onset zone of patients with mesial temporal lobe epilepsy. Comparatively little is known, however, about their spatial distribution with respect to seizure-onset zone in neocortical epilepsy, or their prevalence in normal brain. We present a quantitative analysis of high-frequency oscillations and their rates of occurrence in a group of nine patients with neocortical epilepsy and two control patients with no history of seizures. Oscillations were automatically detected and classified using an unsupervised approach in a data set of unprecedented volume in epilepsy research, over 12 terabytes of continuous long-term micro- and macro-electrode intracranial recordings, without human preprocessing, enabling selection-bias-free estimates of oscillation rates. There are three main results: (i) a cluster of ripple frequency oscillations with median spectral centroid = 137 Hz is increased in the seizure-onset zone more frequently than a cluster of fast ripple frequency oscillations (median spectral centroid = 305 Hz); (ii) we found no difference in the rates of high frequency oscillations in control neocortex and the non-seizure-onset zone neocortex of patients with epilepsy, despite the possibility of different underlying mechanisms of generation; and (iii) while previous studies have demonstrated that oscillations recorded by parenchyma-penetrating micro-electrodes have higher peak 100-500 Hz frequencies than penetrating macro-electrodes, this was not found for the epipial electrodes used here to record from the neocortical surface. We conclude that the relative rate of ripple frequency oscillations is a potential biomarker for epileptic neocortex, but that larger prospective studies correlating high-frequency oscillations rates with seizure-onset zone, resected tissue and surgical outcome are required to determine the true predictive value.</description><identifier>ISSN: 0006-8950</identifier><identifier>EISSN: 1460-2156</identifier><identifier>DOI: 10.1093/brain/awr212</identifier><identifier>PMID: 21903727</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Adult ; Biological and medical sciences ; Brain Mapping - methods ; Brain Waves - physiology ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Electrodes, Implanted ; Electroencephalography - methods ; Epilepsy - physiopathology ; Female ; Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy ; Humans ; Male ; Medical sciences ; Middle Aged ; Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis ; Neocortex - physiopathology ; Nervous system (semeiology, syndromes) ; Neurology ; Original ; Prospective Studies</subject><ispartof>Brain (London, England : 1878), 2011-10, Vol.134 (10), p.2948-2959</ispartof><rights>The Author (2011). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For Permissions, please email: journals.permissions@oup.com 2011</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c543t-5375a444817e71b97cdfd49042a208764ec59d3d8edc7995cec24787c6c149793</citedby><cites>FETCH-LOGICAL-c543t-5375a444817e71b97cdfd49042a208764ec59d3d8edc7995cec24787c6c149793</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,1578,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24606652$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21903727$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Blanco, Justin A.</creatorcontrib><creatorcontrib>Stead, Matt</creatorcontrib><creatorcontrib>Krieger, Abba</creatorcontrib><creatorcontrib>Stacey, William</creatorcontrib><creatorcontrib>Maus, Douglas</creatorcontrib><creatorcontrib>Marsh, Eric</creatorcontrib><creatorcontrib>Viventi, Jonathan</creatorcontrib><creatorcontrib>Lee, Kendall H.</creatorcontrib><creatorcontrib>Marsh, Richard</creatorcontrib><creatorcontrib>Litt, Brian</creatorcontrib><creatorcontrib>Worrell, Gregory A.</creatorcontrib><title>Data mining neocortical high-frequency oscillations in epilepsy and controls</title><title>Brain (London, England : 1878)</title><addtitle>Brain</addtitle><description>Transient high-frequency (100-500 Hz) oscillations of the local field potential have been studied extensively in human mesial temporal lobe. Previous studies report that both ripple (100-250 Hz) and fast ripple (250-500 Hz) oscillations are increased in the seizure-onset zone of patients with mesial temporal lobe epilepsy. Comparatively little is known, however, about their spatial distribution with respect to seizure-onset zone in neocortical epilepsy, or their prevalence in normal brain. We present a quantitative analysis of high-frequency oscillations and their rates of occurrence in a group of nine patients with neocortical epilepsy and two control patients with no history of seizures. Oscillations were automatically detected and classified using an unsupervised approach in a data set of unprecedented volume in epilepsy research, over 12 terabytes of continuous long-term micro- and macro-electrode intracranial recordings, without human preprocessing, enabling selection-bias-free estimates of oscillation rates. There are three main results: (i) a cluster of ripple frequency oscillations with median spectral centroid = 137 Hz is increased in the seizure-onset zone more frequently than a cluster of fast ripple frequency oscillations (median spectral centroid = 305 Hz); (ii) we found no difference in the rates of high frequency oscillations in control neocortex and the non-seizure-onset zone neocortex of patients with epilepsy, despite the possibility of different underlying mechanisms of generation; and (iii) while previous studies have demonstrated that oscillations recorded by parenchyma-penetrating micro-electrodes have higher peak 100-500 Hz frequencies than penetrating macro-electrodes, this was not found for the epipial electrodes used here to record from the neocortical surface. We conclude that the relative rate of ripple frequency oscillations is a potential biomarker for epileptic neocortex, but that larger prospective studies correlating high-frequency oscillations rates with seizure-onset zone, resected tissue and surgical outcome are required to determine the true predictive value.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Brain Mapping - methods</subject><subject>Brain Waves - physiology</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Electrodes, Implanted</subject><subject>Electroencephalography - methods</subject><subject>Epilepsy - physiopathology</subject><subject>Female</subject><subject>Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</subject><subject>Neocortex - physiopathology</subject><subject>Nervous system (semeiology, syndromes)</subject><subject>Neurology</subject><subject>Original</subject><subject>Prospective Studies</subject><issn>0006-8950</issn><issn>1460-2156</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkTtPwzAURi0EgvLYmFEWxELAdvxckBBvqRILzJbrOK1Ragc7BfXfY2hpYYHJg4--e797ADhE8AxBWZ2Ponb-XL9HjPAGGCDCYIkRZZtgACFkpZAU7oDdlF4gRKTCbBvsYCRhxTEfgOG17nUxdd75ceFtMCH2zui2mLjxpGyifZ1Zb-ZFSMa1re5d8KlwvrCda22X5oX2dWGC72No0z7YanSb7MHy3QPPtzdPV_fl8PHu4epyWBpKqr6kFaeaECIQtxyNJDd1UxMJCdYYCs6INVTWVS1sbbiU1FiDCRfcMIOI5LLaAxeL3G42mmbI5vG6VV10Ux3nKminfv94N1Hj8KYqJDglMAecLANiyAVTr6YuGZsL5hPMkpIYckkZ4v-SQjKBBcQ0k6cL0sSQUrTNah8E1acp9WVKLUxl_OhnhxX8rSYDx0tApyykidobl9Zc9swYxesNw6z7e-QHttusCw</recordid><startdate>20111001</startdate><enddate>20111001</enddate><creator>Blanco, Justin A.</creator><creator>Stead, Matt</creator><creator>Krieger, Abba</creator><creator>Stacey, William</creator><creator>Maus, Douglas</creator><creator>Marsh, Eric</creator><creator>Viventi, Jonathan</creator><creator>Lee, Kendall H.</creator><creator>Marsh, Richard</creator><creator>Litt, Brian</creator><creator>Worrell, Gregory A.</creator><general>Oxford University Press</general><scope>IQODW</scope><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>7X8</scope><scope>7TK</scope><scope>5PM</scope></search><sort><creationdate>20111001</creationdate><title>Data mining neocortical high-frequency oscillations in epilepsy and controls</title><author>Blanco, Justin A. ; Stead, Matt ; Krieger, Abba ; Stacey, William ; Maus, Douglas ; Marsh, Eric ; Viventi, Jonathan ; Lee, Kendall H. ; Marsh, Richard ; Litt, Brian ; Worrell, Gregory A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c543t-5375a444817e71b97cdfd49042a208764ec59d3d8edc7995cec24787c6c149793</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Brain Mapping - methods</topic><topic>Brain Waves - physiology</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Electrodes, Implanted</topic><topic>Electroencephalography - methods</topic><topic>Epilepsy - physiopathology</topic><topic>Female</topic><topic>Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</topic><topic>Neocortex - physiopathology</topic><topic>Nervous system (semeiology, syndromes)</topic><topic>Neurology</topic><topic>Original</topic><topic>Prospective Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Blanco, Justin A.</creatorcontrib><creatorcontrib>Stead, Matt</creatorcontrib><creatorcontrib>Krieger, Abba</creatorcontrib><creatorcontrib>Stacey, William</creatorcontrib><creatorcontrib>Maus, Douglas</creatorcontrib><creatorcontrib>Marsh, Eric</creatorcontrib><creatorcontrib>Viventi, Jonathan</creatorcontrib><creatorcontrib>Lee, Kendall H.</creatorcontrib><creatorcontrib>Marsh, Richard</creatorcontrib><creatorcontrib>Litt, Brian</creatorcontrib><creatorcontrib>Worrell, Gregory A.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Brain (London, England : 1878)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Blanco, Justin A.</au><au>Stead, Matt</au><au>Krieger, Abba</au><au>Stacey, William</au><au>Maus, Douglas</au><au>Marsh, Eric</au><au>Viventi, Jonathan</au><au>Lee, Kendall H.</au><au>Marsh, Richard</au><au>Litt, Brian</au><au>Worrell, Gregory A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Data mining neocortical high-frequency oscillations in epilepsy and controls</atitle><jtitle>Brain (London, England : 1878)</jtitle><addtitle>Brain</addtitle><date>2011-10-01</date><risdate>2011</risdate><volume>134</volume><issue>10</issue><spage>2948</spage><epage>2959</epage><pages>2948-2959</pages><issn>0006-8950</issn><eissn>1460-2156</eissn><abstract>Transient high-frequency (100-500 Hz) oscillations of the local field potential have been studied extensively in human mesial temporal lobe. Previous studies report that both ripple (100-250 Hz) and fast ripple (250-500 Hz) oscillations are increased in the seizure-onset zone of patients with mesial temporal lobe epilepsy. Comparatively little is known, however, about their spatial distribution with respect to seizure-onset zone in neocortical epilepsy, or their prevalence in normal brain. We present a quantitative analysis of high-frequency oscillations and their rates of occurrence in a group of nine patients with neocortical epilepsy and two control patients with no history of seizures. Oscillations were automatically detected and classified using an unsupervised approach in a data set of unprecedented volume in epilepsy research, over 12 terabytes of continuous long-term micro- and macro-electrode intracranial recordings, without human preprocessing, enabling selection-bias-free estimates of oscillation rates. There are three main results: (i) a cluster of ripple frequency oscillations with median spectral centroid = 137 Hz is increased in the seizure-onset zone more frequently than a cluster of fast ripple frequency oscillations (median spectral centroid = 305 Hz); (ii) we found no difference in the rates of high frequency oscillations in control neocortex and the non-seizure-onset zone neocortex of patients with epilepsy, despite the possibility of different underlying mechanisms of generation; and (iii) while previous studies have demonstrated that oscillations recorded by parenchyma-penetrating micro-electrodes have higher peak 100-500 Hz frequencies than penetrating macro-electrodes, this was not found for the epipial electrodes used here to record from the neocortical surface. We conclude that the relative rate of ripple frequency oscillations is a potential biomarker for epileptic neocortex, but that larger prospective studies correlating high-frequency oscillations rates with seizure-onset zone, resected tissue and surgical outcome are required to determine the true predictive value.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>21903727</pmid><doi>10.1093/brain/awr212</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Biological and medical sciences Brain Mapping - methods Brain Waves - physiology Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Electrodes, Implanted Electroencephalography - methods Epilepsy - physiopathology Female Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy Humans Male Medical sciences Middle Aged Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis Neocortex - physiopathology Nervous system (semeiology, syndromes) Neurology Original Prospective Studies |
title | Data mining neocortical high-frequency oscillations in epilepsy and controls |
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