Quantitative EEG abnormalities in persons with “pure” epileptic predisposition without epilepsy: A low resolution electromagnetic tomography (LORETA) study
Summary Objective Epileptic predisposition means genetically determined, increased seizure susceptibility. Neurophysiological evaluation of this condition is still lacking. In order to investigate “pure epileptic predisposition” (without epilepsy) in this pilot study the authors prospectively recrui...
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description | Summary Objective Epileptic predisposition means genetically determined, increased seizure susceptibility. Neurophysiological evaluation of this condition is still lacking. In order to investigate “pure epileptic predisposition” (without epilepsy) in this pilot study the authors prospectively recruited ten persons who displayed generalized tonic–clonic seizures precipitated by 24 or more hours of sleep deprivation but were healthy in any other respects. Methods 21-channel EEGs were recorded in the morning, in the waking state, after a night of sufficient sleep in the interictal period. For each person, a total of 120 s artifact-free EEG was processed to low resolution electromagnetic tomography (LORETA) analysis. LORETA activity (Ampers/meters squared) was computed for 2394 voxels, 19 active electrodes and 1 Hz very narrow bands from 1 to 25 Hz. The data were compressed into four frequency bands ( δ : 0.5–4.0 Hz, : 4.5–8.0 Hz, α : 8.5–12.0 Hz, β : 12.5–25.0 Hz) and projected onto the MRI figures of a digitized standard brain atlas. The band-related LORETA results were compared to those of ten, age- and sex-matched healthy persons using independent t -tests. p < 0.01 differences were accepted as statistically significant. Results Statistically significant decrease of α activity was found in widespread, medial and lateral parts of the cortex above the level of the basal ganglia. Maximum α decrease and statistically significant β decrease were found in the left precuneus. Statistically not significant differences were δ increase in the medial-basal frontal area and increase in the same area and in the basal temporal area. Discussion The significance of α decrease in the patient group remains enigmatic. β decrease presumably reflects non-specific dysfunction of the cortex. Prefrontal δ and increase might have biological meaning despite the lack of statistical significance: these findings are topographically similar to those reported in idiopathic generalized epilepsy in previous investigations. Significance Quantitative EEG characteristics of the genetically determined epilepsy predisposition were given in terms of frequency bands and anatomical distribution. |
doi_str_mv | 10.1016/j.eplepsyres.2010.07.001 |
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Neurophysiological evaluation of this condition is still lacking. In order to investigate “pure epileptic predisposition” (without epilepsy) in this pilot study the authors prospectively recruited ten persons who displayed generalized tonic–clonic seizures precipitated by 24 or more hours of sleep deprivation but were healthy in any other respects. Methods 21-channel EEGs were recorded in the morning, in the waking state, after a night of sufficient sleep in the interictal period. For each person, a total of 120 s artifact-free EEG was processed to low resolution electromagnetic tomography (LORETA) analysis. LORETA activity (Ampers/meters squared) was computed for 2394 voxels, 19 active electrodes and 1 Hz very narrow bands from 1 to 25 Hz. The data were compressed into four frequency bands ( δ : 0.5–4.0 Hz, : 4.5–8.0 Hz, α : 8.5–12.0 Hz, β : 12.5–25.0 Hz) and projected onto the MRI figures of a digitized standard brain atlas. The band-related LORETA results were compared to those of ten, age- and sex-matched healthy persons using independent t -tests. p < 0.01 differences were accepted as statistically significant. Results Statistically significant decrease of α activity was found in widespread, medial and lateral parts of the cortex above the level of the basal ganglia. Maximum α decrease and statistically significant β decrease were found in the left precuneus. Statistically not significant differences were δ increase in the medial-basal frontal area and increase in the same area and in the basal temporal area. Discussion The significance of α decrease in the patient group remains enigmatic. β decrease presumably reflects non-specific dysfunction of the cortex. Prefrontal δ and increase might have biological meaning despite the lack of statistical significance: these findings are topographically similar to those reported in idiopathic generalized epilepsy in previous investigations. Significance Quantitative EEG characteristics of the genetically determined epilepsy predisposition were given in terms of frequency bands and anatomical distribution.</description><identifier>ISSN: 0920-1211</identifier><identifier>EISSN: 1872-6844</identifier><identifier>DOI: 10.1016/j.eplepsyres.2010.07.001</identifier><identifier>PMID: 20674273</identifier><identifier>CODEN: EPIRE8</identifier><language>eng</language><publisher>Kidlington: Elsevier B.V</publisher><subject>Adolescent ; Adult ; Anticonvulsants. Antiepileptics. Antiparkinson agents ; Biological and medical sciences ; EEG ; Electroencephalography - methods ; Electromagnetic Phenomena ; Epilepsy ; Epilepsy, Tonic-Clonic - diagnosis ; Epilepsy, Tonic-Clonic - physiopathology ; Epileptic predisposition ; Female ; Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy ; Humans ; LORETA ; Male ; Medical sciences ; Nervous system (semeiology, syndromes) ; Neurology ; Neuropharmacology ; Pharmacology. Drug treatments ; Pilot Projects ; Prospective Studies ; Tomography, X-Ray Computed - methods ; Young Adult</subject><ispartof>Epilepsy research, 2010-09, Vol.91 (1), p.94-100</ispartof><rights>Elsevier B.V.</rights><rights>2010 Elsevier B.V.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright 2010 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c508t-2abb1d0d19123c1692fe0f704abaf6b2e4dbb0492de2bab4010af44e688e4b483</citedby><cites>FETCH-LOGICAL-c508t-2abb1d0d19123c1692fe0f704abaf6b2e4dbb0492de2bab4010af44e688e4b483</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0920121110001634$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23239585$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20674273$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Puskás, S</creatorcontrib><creatorcontrib>Bessenyei, M</creatorcontrib><creatorcontrib>Fekete, I</creatorcontrib><creatorcontrib>Hollódy, K</creatorcontrib><creatorcontrib>Clemens, B</creatorcontrib><title>Quantitative EEG abnormalities in persons with “pure” epileptic predisposition without epilepsy: A low resolution electromagnetic tomography (LORETA) study</title><title>Epilepsy research</title><addtitle>Epilepsy Res</addtitle><description>Summary Objective Epileptic predisposition means genetically determined, increased seizure susceptibility. Neurophysiological evaluation of this condition is still lacking. In order to investigate “pure epileptic predisposition” (without epilepsy) in this pilot study the authors prospectively recruited ten persons who displayed generalized tonic–clonic seizures precipitated by 24 or more hours of sleep deprivation but were healthy in any other respects. Methods 21-channel EEGs were recorded in the morning, in the waking state, after a night of sufficient sleep in the interictal period. For each person, a total of 120 s artifact-free EEG was processed to low resolution electromagnetic tomography (LORETA) analysis. LORETA activity (Ampers/meters squared) was computed for 2394 voxels, 19 active electrodes and 1 Hz very narrow bands from 1 to 25 Hz. The data were compressed into four frequency bands ( δ : 0.5–4.0 Hz, : 4.5–8.0 Hz, α : 8.5–12.0 Hz, β : 12.5–25.0 Hz) and projected onto the MRI figures of a digitized standard brain atlas. The band-related LORETA results were compared to those of ten, age- and sex-matched healthy persons using independent t -tests. p < 0.01 differences were accepted as statistically significant. Results Statistically significant decrease of α activity was found in widespread, medial and lateral parts of the cortex above the level of the basal ganglia. Maximum α decrease and statistically significant β decrease were found in the left precuneus. Statistically not significant differences were δ increase in the medial-basal frontal area and increase in the same area and in the basal temporal area. Discussion The significance of α decrease in the patient group remains enigmatic. β decrease presumably reflects non-specific dysfunction of the cortex. Prefrontal δ and increase might have biological meaning despite the lack of statistical significance: these findings are topographically similar to those reported in idiopathic generalized epilepsy in previous investigations. Significance Quantitative EEG characteristics of the genetically determined epilepsy predisposition were given in terms of frequency bands and anatomical distribution.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Anticonvulsants. Antiepileptics. Antiparkinson agents</subject><subject>Biological and medical sciences</subject><subject>EEG</subject><subject>Electroencephalography - methods</subject><subject>Electromagnetic Phenomena</subject><subject>Epilepsy</subject><subject>Epilepsy, Tonic-Clonic - diagnosis</subject><subject>Epilepsy, Tonic-Clonic - physiopathology</subject><subject>Epileptic predisposition</subject><subject>Female</subject><subject>Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy</subject><subject>Humans</subject><subject>LORETA</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Nervous system (semeiology, syndromes)</subject><subject>Neurology</subject><subject>Neuropharmacology</subject><subject>Pharmacology. Drug treatments</subject><subject>Pilot Projects</subject><subject>Prospective Studies</subject><subject>Tomography, X-Ray Computed - methods</subject><subject>Young Adult</subject><issn>0920-1211</issn><issn>1872-6844</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNks1u1DAUhSMEoqXwCsgbBCxmsB1PflggDdVQkEaqgLK2bOem9ZDYqa_TKrs-CIh365Pg6QxUYsXKkvWd-3POzTLC6JxRVrzZzGHoYMApAM45Td-0nFPKHmSHrCr5rKiEeJgd0prTGeOMHWRPEDeU0pIK8Tg74LQoBS_zw-zX51G5aKOK9grIanVClHY-9Kqz0QIS68gAAb1Dcm3jBbm9-TGMAW5vfhIYbJohWkOGAI3FwWPSeHcH-jHuAZzekiXp_DVJw_puvEOgAxOD79W5g22F6Ht_HtRwMZFX69Mvq7Pla4JxbKan2aNWdQjP9u9R9u3D6uz442x9evLpeLmemQWt4owrrVlDG1YznhtW1LwF2qZtlVZtoTmIRmsqat4A10qLZJlqhYCiqkBoUeVH2ctd3SH4yxEwyt6iga5TDvyIslzkdV0u6iKR1Y40wSMGaOUQbK_CJBmV23TkRt6nI7fpSFrKlE6SPt83GXUPzV_hnzgS8GIPKDSqa4NyxuI9l_O8XlSLxL3fcZAsubIQJBoLzqQYQjJWNt7-zzTv_iliOuts6vsdJsCNH4NLlksmkUsqv26vaXtMLN0RK3KR_wYYbM5y</recordid><startdate>20100901</startdate><enddate>20100901</enddate><creator>Puskás, S</creator><creator>Bessenyei, M</creator><creator>Fekete, I</creator><creator>Hollódy, K</creator><creator>Clemens, B</creator><general>Elsevier B.V</general><general>Elsevier</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></search><sort><creationdate>20100901</creationdate><title>Quantitative EEG abnormalities in persons with “pure” epileptic predisposition without epilepsy: A low resolution electromagnetic tomography (LORETA) study</title><author>Puskás, S ; Bessenyei, M ; Fekete, I ; Hollódy, K ; Clemens, B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c508t-2abb1d0d19123c1692fe0f704abaf6b2e4dbb0492de2bab4010af44e688e4b483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Anticonvulsants. Antiepileptics. Antiparkinson agents</topic><topic>Biological and medical sciences</topic><topic>EEG</topic><topic>Electroencephalography - methods</topic><topic>Electromagnetic Phenomena</topic><topic>Epilepsy</topic><topic>Epilepsy, Tonic-Clonic - diagnosis</topic><topic>Epilepsy, Tonic-Clonic - physiopathology</topic><topic>Epileptic predisposition</topic><topic>Female</topic><topic>Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy</topic><topic>Humans</topic><topic>LORETA</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Nervous system (semeiology, syndromes)</topic><topic>Neurology</topic><topic>Neuropharmacology</topic><topic>Pharmacology. Drug treatments</topic><topic>Pilot Projects</topic><topic>Prospective Studies</topic><topic>Tomography, X-Ray Computed - methods</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Puskás, S</creatorcontrib><creatorcontrib>Bessenyei, M</creatorcontrib><creatorcontrib>Fekete, I</creatorcontrib><creatorcontrib>Hollódy, K</creatorcontrib><creatorcontrib>Clemens, B</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><jtitle>Epilepsy research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Puskás, S</au><au>Bessenyei, M</au><au>Fekete, I</au><au>Hollódy, K</au><au>Clemens, B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantitative EEG abnormalities in persons with “pure” epileptic predisposition without epilepsy: A low resolution electromagnetic tomography (LORETA) study</atitle><jtitle>Epilepsy research</jtitle><addtitle>Epilepsy Res</addtitle><date>2010-09-01</date><risdate>2010</risdate><volume>91</volume><issue>1</issue><spage>94</spage><epage>100</epage><pages>94-100</pages><issn>0920-1211</issn><eissn>1872-6844</eissn><coden>EPIRE8</coden><abstract>Summary Objective Epileptic predisposition means genetically determined, increased seizure susceptibility. Neurophysiological evaluation of this condition is still lacking. In order to investigate “pure epileptic predisposition” (without epilepsy) in this pilot study the authors prospectively recruited ten persons who displayed generalized tonic–clonic seizures precipitated by 24 or more hours of sleep deprivation but were healthy in any other respects. Methods 21-channel EEGs were recorded in the morning, in the waking state, after a night of sufficient sleep in the interictal period. For each person, a total of 120 s artifact-free EEG was processed to low resolution electromagnetic tomography (LORETA) analysis. LORETA activity (Ampers/meters squared) was computed for 2394 voxels, 19 active electrodes and 1 Hz very narrow bands from 1 to 25 Hz. The data were compressed into four frequency bands ( δ : 0.5–4.0 Hz, : 4.5–8.0 Hz, α : 8.5–12.0 Hz, β : 12.5–25.0 Hz) and projected onto the MRI figures of a digitized standard brain atlas. The band-related LORETA results were compared to those of ten, age- and sex-matched healthy persons using independent t -tests. p < 0.01 differences were accepted as statistically significant. Results Statistically significant decrease of α activity was found in widespread, medial and lateral parts of the cortex above the level of the basal ganglia. Maximum α decrease and statistically significant β decrease were found in the left precuneus. Statistically not significant differences were δ increase in the medial-basal frontal area and increase in the same area and in the basal temporal area. Discussion The significance of α decrease in the patient group remains enigmatic. β decrease presumably reflects non-specific dysfunction of the cortex. Prefrontal δ and increase might have biological meaning despite the lack of statistical significance: these findings are topographically similar to those reported in idiopathic generalized epilepsy in previous investigations. Significance Quantitative EEG characteristics of the genetically determined epilepsy predisposition were given in terms of frequency bands and anatomical distribution.</abstract><cop>Kidlington</cop><pub>Elsevier B.V</pub><pmid>20674273</pmid><doi>10.1016/j.eplepsyres.2010.07.001</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Anticonvulsants. Antiepileptics. Antiparkinson agents Biological and medical sciences EEG Electroencephalography - methods Electromagnetic Phenomena Epilepsy Epilepsy, Tonic-Clonic - diagnosis Epilepsy, Tonic-Clonic - physiopathology Epileptic predisposition Female Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy Humans LORETA Male Medical sciences Nervous system (semeiology, syndromes) Neurology Neuropharmacology Pharmacology. Drug treatments Pilot Projects Prospective Studies Tomography, X-Ray Computed - methods Young Adult |
title | Quantitative EEG abnormalities in persons with “pure” epileptic predisposition without epilepsy: A low resolution electromagnetic tomography (LORETA) study |
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