Sleep Spindles in Epilepsy
Spindles are a ubiquitous phenomenon in sleep, but their physiology and the effects of neurologic disorder on their frequency and amplitude are incompletely understood. We compared the incidence of three commonly defined spindle types (14-15 Hz, 12-13 Hz, and 10 Hz) and the frequency and amplitude o...
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Veröffentlicht in: | Clinical EEG and neuroscience 1991-07, Vol.22 (3), p.144-149 |
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description | Spindles are a ubiquitous phenomenon in sleep, but their physiology and the effects of neurologic disorder on their frequency and amplitude are incompletely understood. We compared the incidence of three commonly defined spindle types (14-15 Hz, 12-13 Hz, and 10 Hz) and the frequency and amplitude of spindles during Stage II sleep in 50 patients with complex partial, partial and secondarily generalized, and primary generalized seizures, with and without interictal behavioral symptoms. All patients had 12-13 Hz and 14-15 Hz spindles of symmetric character in C3-A1 and C4-A2 derivations during prolonged sleep-deprived EEG recordings, which were normal except for partial or generalized epileptiform activity. Seventy-one per cent of complex partial seizure patients had 10 Hz spindles, and they occurred in 50% of the other two groups, predominating among those with interictal behavioral symptoms in all groups. Spindle frequency was significantly less in patients with generalized epilepsy than with partial seizures, and patients with complex partial seizures and partial seizures with secondary generalization differed significantly in spindle frequency. Spindle frequency was significantly lower with polypharmacy than with monotherapy. Patients whose regimens included phenobarbital had significantly lower spindle frequencies and spindle frequencies differed significantly between phenytoin and carbamazepine. Differences in spindle frequency may be due to residual medication effects, underlying encephalopathy or physiological differences between partial and generalized epilepsy. |
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We compared the incidence of three commonly defined spindle types (14-15 Hz, 12-13 Hz, and 10 Hz) and the frequency and amplitude of spindles during Stage II sleep in 50 patients with complex partial, partial and secondarily generalized, and primary generalized seizures, with and without interictal behavioral symptoms. All patients had 12-13 Hz and 14-15 Hz spindles of symmetric character in C3-A1 and C4-A2 derivations during prolonged sleep-deprived EEG recordings, which were normal except for partial or generalized epileptiform activity. Seventy-one per cent of complex partial seizure patients had 10 Hz spindles, and they occurred in 50% of the other two groups, predominating among those with interictal behavioral symptoms in all groups. Spindle frequency was significantly less in patients with generalized epilepsy than with partial seizures, and patients with complex partial seizures and partial seizures with secondary generalization differed significantly in spindle frequency. Spindle frequency was significantly lower with polypharmacy than with monotherapy. Patients whose regimens included phenobarbital had significantly lower spindle frequencies and spindle frequencies differed significantly between phenytoin and carbamazepine. Differences in spindle frequency may be due to residual medication effects, underlying encephalopathy or physiological differences between partial and generalized epilepsy.</description><identifier>ISSN: 0009-9155</identifier><identifier>ISSN: 1550-0594</identifier><identifier>EISSN: 2169-5202</identifier><identifier>DOI: 10.1177/155005949102200305</identifier><identifier>PMID: 1879053</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Activity patterns ; Adolescent ; Adult ; Aged ; Biological and medical sciences ; Carbamazepine - administration & dosage ; Carbamazepine - therapeutic use ; Convulsions & seizures ; Drug Therapy, Combination ; Electroencephalography ; Epilepsy ; Epilepsy - drug therapy ; Epilepsy - physiopathology ; Epilepsy, Temporal Lobe - drug therapy ; Epilepsy, Temporal Lobe - physiopathology ; Female ; Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy ; Humans ; Male ; Medical sciences ; Middle Aged ; Nervous system (semeiology, syndromes) ; Neurology ; Phenytoin - administration & dosage ; Phenytoin - therapeutic use ; Physiology ; Polypharmacy ; Seizures ; Sleep ; Sleep - physiology</subject><ispartof>Clinical EEG and neuroscience, 1991-07, Vol.22 (3), p.144-149</ispartof><rights>1991 EEG and Clinical Neuroscience Society</rights><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c395t-8dd9ef2cb87c7a18005286ba23c2341861263c2e1c1c26ae2e5758d64ec57b183</citedby><cites>FETCH-LOGICAL-c395t-8dd9ef2cb87c7a18005286ba23c2341861263c2e1c1c26ae2e5758d64ec57b183</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1988358604/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$H</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1988358604?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,780,784,21389,21819,27924,27925,33530,43621,43622,43659,64385,64389,72469,74104</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4939197$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1879053$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Drake, Miles E.</creatorcontrib><creatorcontrib>Pakalnis, Ann</creatorcontrib><creatorcontrib>Padamadan, Hosi</creatorcontrib><creatorcontrib>Weate, Steven M.</creatorcontrib><creatorcontrib>Cannon, Patricia A.</creatorcontrib><title>Sleep Spindles in Epilepsy</title><title>Clinical EEG and neuroscience</title><addtitle>Clin Electroencephalogr</addtitle><description>Spindles are a ubiquitous phenomenon in sleep, but their physiology and the effects of neurologic disorder on their frequency and amplitude are incompletely understood. We compared the incidence of three commonly defined spindle types (14-15 Hz, 12-13 Hz, and 10 Hz) and the frequency and amplitude of spindles during Stage II sleep in 50 patients with complex partial, partial and secondarily generalized, and primary generalized seizures, with and without interictal behavioral symptoms. All patients had 12-13 Hz and 14-15 Hz spindles of symmetric character in C3-A1 and C4-A2 derivations during prolonged sleep-deprived EEG recordings, which were normal except for partial or generalized epileptiform activity. Seventy-one per cent of complex partial seizure patients had 10 Hz spindles, and they occurred in 50% of the other two groups, predominating among those with interictal behavioral symptoms in all groups. Spindle frequency was significantly less in patients with generalized epilepsy than with partial seizures, and patients with complex partial seizures and partial seizures with secondary generalization differed significantly in spindle frequency. Spindle frequency was significantly lower with polypharmacy than with monotherapy. Patients whose regimens included phenobarbital had significantly lower spindle frequencies and spindle frequencies differed significantly between phenytoin and carbamazepine. Differences in spindle frequency may be due to residual medication effects, underlying encephalopathy or physiological differences between partial and generalized epilepsy.</description><subject>Activity patterns</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Carbamazepine - administration & dosage</subject><subject>Carbamazepine - therapeutic use</subject><subject>Convulsions & seizures</subject><subject>Drug Therapy, Combination</subject><subject>Electroencephalography</subject><subject>Epilepsy</subject><subject>Epilepsy - drug therapy</subject><subject>Epilepsy - physiopathology</subject><subject>Epilepsy, Temporal Lobe - drug therapy</subject><subject>Epilepsy, Temporal Lobe - 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>Nervous system (semeiology, syndromes)</subject><subject>Neurology</subject><subject>Phenytoin - administration & dosage</subject><subject>Phenytoin - therapeutic use</subject><subject>Physiology</subject><subject>Polypharmacy</subject><subject>Seizures</subject><subject>Sleep</subject><subject>Sleep - physiology</subject><issn>0009-9155</issn><issn>1550-0594</issn><issn>2169-5202</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp1kE9Lw0AQxRdRaqn9AgWhoHiLndnNZnePIvUPFDxUz2GzmUhKmsRsc-i3d0uKiuJpZni_mXk8xmYIt4hKLVBKAGlig8A5gAB5wsYcExNJDvyUjQHARCZg52zq_QYOswIEM2Ij1MqAFGM2W1dE7XzdlnVekZ-X9XzZlhW1fn_BzgpbeZoe64S9PSxf75-i1cvj8_3dKnLCyF2k89xQwV2mlVMWdTDFdZJZLhwXMeoEeRJaQoeOJ5Y4SSV1nsTkpMpQiwm7Ge62XfPRk9-l29I7qipbU9P7VHGQEiUE8OoXuGn6rg7eUjRaC6kTiAPFB8p1jfcdFWnblVvb7VOE9JBc-je5sHR5PN1nW8q_V4acgn591K13tio6W7vSf2GxEQaNCthiwLx9px_u_n_8CRX-fiw</recordid><startdate>19910701</startdate><enddate>19910701</enddate><creator>Drake, Miles E.</creator><creator>Pakalnis, Ann</creator><creator>Padamadan, Hosi</creator><creator>Weate, Steven M.</creator><creator>Cannon, Patricia A.</creator><general>SAGE Publications</general><general>ECNS</general><general>SAGE PUBLICATIONS, INC</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>3V.</scope><scope>4T-</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</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>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>19910701</creationdate><title>Sleep Spindles in Epilepsy</title><author>Drake, Miles E. ; Pakalnis, Ann ; Padamadan, Hosi ; Weate, Steven M. ; Cannon, Patricia A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c395t-8dd9ef2cb87c7a18005286ba23c2341861263c2e1c1c26ae2e5758d64ec57b183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Activity patterns</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Carbamazepine - administration & dosage</topic><topic>Carbamazepine - therapeutic use</topic><topic>Convulsions & seizures</topic><topic>Drug Therapy, Combination</topic><topic>Electroencephalography</topic><topic>Epilepsy</topic><topic>Epilepsy - drug therapy</topic><topic>Epilepsy - physiopathology</topic><topic>Epilepsy, Temporal Lobe - drug therapy</topic><topic>Epilepsy, Temporal Lobe - 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>Nervous system (semeiology, syndromes)</topic><topic>Neurology</topic><topic>Phenytoin - administration & dosage</topic><topic>Phenytoin - therapeutic use</topic><topic>Physiology</topic><topic>Polypharmacy</topic><topic>Seizures</topic><topic>Sleep</topic><topic>Sleep - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Drake, Miles E.</creatorcontrib><creatorcontrib>Pakalnis, Ann</creatorcontrib><creatorcontrib>Padamadan, Hosi</creatorcontrib><creatorcontrib>Weate, Steven M.</creatorcontrib><creatorcontrib>Cannon, Patricia 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>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</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 & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</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>Clinical EEG and neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Drake, Miles E.</au><au>Pakalnis, Ann</au><au>Padamadan, Hosi</au><au>Weate, Steven M.</au><au>Cannon, Patricia A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sleep Spindles in Epilepsy</atitle><jtitle>Clinical EEG and neuroscience</jtitle><addtitle>Clin Electroencephalogr</addtitle><date>1991-07-01</date><risdate>1991</risdate><volume>22</volume><issue>3</issue><spage>144</spage><epage>149</epage><pages>144-149</pages><issn>0009-9155</issn><issn>1550-0594</issn><eissn>2169-5202</eissn><abstract>Spindles are a ubiquitous phenomenon in sleep, but their physiology and the effects of neurologic disorder on their frequency and amplitude are incompletely understood. We compared the incidence of three commonly defined spindle types (14-15 Hz, 12-13 Hz, and 10 Hz) and the frequency and amplitude of spindles during Stage II sleep in 50 patients with complex partial, partial and secondarily generalized, and primary generalized seizures, with and without interictal behavioral symptoms. All patients had 12-13 Hz and 14-15 Hz spindles of symmetric character in C3-A1 and C4-A2 derivations during prolonged sleep-deprived EEG recordings, which were normal except for partial or generalized epileptiform activity. Seventy-one per cent of complex partial seizure patients had 10 Hz spindles, and they occurred in 50% of the other two groups, predominating among those with interictal behavioral symptoms in all groups. Spindle frequency was significantly less in patients with generalized epilepsy than with partial seizures, and patients with complex partial seizures and partial seizures with secondary generalization differed significantly in spindle frequency. Spindle frequency was significantly lower with polypharmacy than with monotherapy. Patients whose regimens included phenobarbital had significantly lower spindle frequencies and spindle frequencies differed significantly between phenytoin and carbamazepine. Differences in spindle frequency may be due to residual medication effects, underlying encephalopathy or physiological differences between partial and generalized epilepsy.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>1879053</pmid><doi>10.1177/155005949102200305</doi><tpages>6</tpages></addata></record> |
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subjects | Activity patterns Adolescent Adult Aged Biological and medical sciences Carbamazepine - administration & dosage Carbamazepine - therapeutic use Convulsions & seizures Drug Therapy, Combination Electroencephalography Epilepsy Epilepsy - drug therapy Epilepsy - physiopathology Epilepsy, Temporal Lobe - drug therapy Epilepsy, Temporal Lobe - physiopathology Female Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy Humans Male Medical sciences Middle Aged Nervous system (semeiology, syndromes) Neurology Phenytoin - administration & dosage Phenytoin - therapeutic use Physiology Polypharmacy Seizures Sleep Sleep - physiology |
title | Sleep Spindles in Epilepsy |
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