Late-Onset Focal Epilepsy: Electroclinical Features and Prognostic Role of Leukoaraiosis
The aim of this study was to describe the electroclinical and prognostic characteristics, and to investigate the role of leukoaraiosis in outpatients with new-onset elderly focal epilepsy aged ≥60 years, referred to a tertiary epilepsy center between 2005 and December 31, 2020. Among the 720 patient...
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Published in | Frontiers in neurology Vol. 13; p. 828493 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Frontiers Media S.A
23.02.2022
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ISSN | 1664-2295 1664-2295 |
DOI | 10.3389/fneur.2022.828493 |
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Abstract | The aim of this study was to describe the electroclinical and prognostic characteristics, and to investigate the role of leukoaraiosis in outpatients with new-onset elderly focal epilepsy aged ≥60 years, referred to a tertiary epilepsy center between 2005 and December 31, 2020. Among the 720 patients who were referred to the center, we retrospectively selected 162 consecutive outpatients, with a first referral for recent-onset focal epilepsy of unknown cause (UC) or structural cause (SC), and collected a clinical and standard-Electroencephalogram (S-EEG), 24-h ambulatory EEG (A-EEG), and neuroimaging data. We also analyzed the seizure prognosis after titration of the first antiseizure medication (ASM). One hundred and four UC and 58 SC patients, followed up for 5.8 ± 5.3 years (mean ± SD), were included. Compared with the SC group, the patients with UC showed a predominance of focal seizures with impaired awareness (51.9% of cases) and focal to bilateral tonic-clonic seizures during sleep (25%); conversely, the SC group, more frequently, had focal to bilateral tonic-clonic seizures during wakefulness (39.6%) and focal aware seizures (25.8%) (
p
< 0.0001). Oral or gestural automatisms were prevalent in UC epilepsy (20.2 vs. 6.9% in the SC group,
p
= 0.04). In UC compared to patients with SC, interictal epileptiform discharges showed a preferential temporal lobe localization (
p
= 0.0007), low expression on S-EEG, and marked activation during deep Non-Rapid Eye Movement (NREM) sleep (
p
= 0.003). An overall good treatment response was found in the whole sample, with a probability of seizure freedom of 68.9% for 1 year. The cumulative probability of seizure freedom was significantly higher in the UC compared with the SC group (
p
< 0.0001). The prognosis was worsened by leukoaraiosis (
p
= 0.012). In the late-onset focal epilepsy of unknown cause, electroclinical findings suggest a temporal lobe origin of the seizures. This group showed a better prognosis compared with the patients with structural epilepsy. Leukoaraiosis,
per se
, negatively impacted on seizure prognosis. |
---|---|
AbstractList | The aim of this study was to describe the electroclinical and prognostic characteristics, and to investigate the role of leukoaraiosis in outpatients with new-onset elderly focal epilepsy aged ≥60 years, referred to a tertiary epilepsy center between 2005 and December 31, 2020. Among the 720 patients who were referred to the center, we retrospectively selected 162 consecutive outpatients, with a first referral for recent-onset focal epilepsy of unknown cause (UC) or structural cause (SC), and collected a clinical and standard-Electroencephalogram (S-EEG), 24-h ambulatory EEG (A-EEG), and neuroimaging data. We also analyzed the seizure prognosis after titration of the first antiseizure medication (ASM). One hundred and four UC and 58 SC patients, followed up for 5.8 ± 5.3 years (mean ± SD), were included. Compared with the SC group, the patients with UC showed a predominance of focal seizures with impaired awareness (51.9% of cases) and focal to bilateral tonic-clonic seizures during sleep (25%); conversely, the SC group, more frequently, had focal to bilateral tonic-clonic seizures during wakefulness (39.6%) and focal aware seizures (25.8%) (p < 0.0001). Oral or gestural automatisms were prevalent in UC epilepsy (20.2 vs. 6.9% in the SC group, p = 0.04). In UC compared to patients with SC, interictal epileptiform discharges showed a preferential temporal lobe localization (p = 0.0007), low expression on S-EEG, and marked activation during deep Non-Rapid Eye Movement (NREM) sleep (p = 0.003). An overall good treatment response was found in the whole sample, with a probability of seizure freedom of 68.9% for 1 year. The cumulative probability of seizure freedom was significantly higher in the UC compared with the SC group (p < 0.0001). The prognosis was worsened by leukoaraiosis (p = 0.012). In the late-onset focal epilepsy of unknown cause, electroclinical findings suggest a temporal lobe origin of the seizures. This group showed a better prognosis compared with the patients with structural epilepsy. Leukoaraiosis, per se, negatively impacted on seizure prognosis.The aim of this study was to describe the electroclinical and prognostic characteristics, and to investigate the role of leukoaraiosis in outpatients with new-onset elderly focal epilepsy aged ≥60 years, referred to a tertiary epilepsy center between 2005 and December 31, 2020. Among the 720 patients who were referred to the center, we retrospectively selected 162 consecutive outpatients, with a first referral for recent-onset focal epilepsy of unknown cause (UC) or structural cause (SC), and collected a clinical and standard-Electroencephalogram (S-EEG), 24-h ambulatory EEG (A-EEG), and neuroimaging data. We also analyzed the seizure prognosis after titration of the first antiseizure medication (ASM). One hundred and four UC and 58 SC patients, followed up for 5.8 ± 5.3 years (mean ± SD), were included. Compared with the SC group, the patients with UC showed a predominance of focal seizures with impaired awareness (51.9% of cases) and focal to bilateral tonic-clonic seizures during sleep (25%); conversely, the SC group, more frequently, had focal to bilateral tonic-clonic seizures during wakefulness (39.6%) and focal aware seizures (25.8%) (p < 0.0001). Oral or gestural automatisms were prevalent in UC epilepsy (20.2 vs. 6.9% in the SC group, p = 0.04). In UC compared to patients with SC, interictal epileptiform discharges showed a preferential temporal lobe localization (p = 0.0007), low expression on S-EEG, and marked activation during deep Non-Rapid Eye Movement (NREM) sleep (p = 0.003). An overall good treatment response was found in the whole sample, with a probability of seizure freedom of 68.9% for 1 year. The cumulative probability of seizure freedom was significantly higher in the UC compared with the SC group (p < 0.0001). The prognosis was worsened by leukoaraiosis (p = 0.012). In the late-onset focal epilepsy of unknown cause, electroclinical findings suggest a temporal lobe origin of the seizures. This group showed a better prognosis compared with the patients with structural epilepsy. Leukoaraiosis, per se, negatively impacted on seizure prognosis. The aim of this study was to describe the electroclinical and prognostic characteristics, and to investigate the role of leukoaraiosis in outpatients with new-onset elderly focal epilepsy aged ≥60 years, referred to a tertiary epilepsy center between 2005 and December 31, 2020. Among the 720 patients who were referred to the center, we retrospectively selected 162 consecutive outpatients, with a first referral for recent-onset focal epilepsy of unknown cause (UC) or structural cause (SC), and collected a clinical and standard-Electroencephalogram (S-EEG), 24-h ambulatory EEG (A-EEG), and neuroimaging data. We also analyzed the seizure prognosis after titration of the first antiseizure medication (ASM). One hundred and four UC and 58 SC patients, followed up for 5.8 ± 5.3 years (mean ± SD), were included. Compared with the SC group, the patients with UC showed a predominance of focal seizures with impaired awareness (51.9% of cases) and focal to bilateral tonic-clonic seizures during sleep (25%); conversely, the SC group, more frequently, had focal to bilateral tonic-clonic seizures during wakefulness (39.6%) and focal aware seizures (25.8%) (p < 0.0001). Oral or gestural automatisms were prevalent in UC epilepsy (20.2 vs. 6.9% in the SC group, p = 0.04). In UC compared to patients with SC, interictal epileptiform discharges showed a preferential temporal lobe localization (p = 0.0007), low expression on S-EEG, and marked activation during deep Non-Rapid Eye Movement (NREM) sleep (p = 0.003). An overall good treatment response was found in the whole sample, with a probability of seizure freedom of 68.9% for 1 year. The cumulative probability of seizure freedom was significantly higher in the UC compared with the SC group (p < 0.0001). The prognosis was worsened by leukoaraiosis (p = 0.012). In the late-onset focal epilepsy of unknown cause, electroclinical findings suggest a temporal lobe origin of the seizures. This group showed a better prognosis compared with the patients with structural epilepsy. Leukoaraiosis, per se, negatively impacted on seizure prognosis. The aim of this study was to describe the electroclinical and prognostic characteristics, and to investigate the role of leukoaraiosis in outpatients with new-onset elderly focal epilepsy aged ≥60 years, referred to a tertiary epilepsy center between 2005 and December 31, 2020. Among the 720 patients who were referred to the center, we retrospectively selected 162 consecutive outpatients, with a first referral for recent-onset focal epilepsy of unknown cause (UC) or structural cause (SC), and collected a clinical and standard-Electroencephalogram (S-EEG), 24-h ambulatory EEG (A-EEG), and neuroimaging data. We also analyzed the seizure prognosis after titration of the first antiseizure medication (ASM). One hundred and four UC and 58 SC patients, followed up for 5.8 ± 5.3 years (mean ± SD), were included. Compared with the SC group, the patients with UC showed a predominance of focal seizures with impaired awareness (51.9% of cases) and focal to bilateral tonic-clonic seizures during sleep (25%); conversely, the SC group, more frequently, had focal to bilateral tonic-clonic seizures during wakefulness (39.6%) and focal aware seizures (25.8%) ( < 0.0001). Oral or gestural automatisms were prevalent in UC epilepsy (20.2 vs. 6.9% in the SC group, = 0.04). In UC compared to patients with SC, interictal epileptiform discharges showed a preferential temporal lobe localization ( = 0.0007), low expression on S-EEG, and marked activation during deep Non-Rapid Eye Movement (NREM) sleep ( = 0.003). An overall good treatment response was found in the whole sample, with a probability of seizure freedom of 68.9% for 1 year. The cumulative probability of seizure freedom was significantly higher in the UC compared with the SC group ( < 0.0001). The prognosis was worsened by leukoaraiosis ( = 0.012). In the late-onset focal epilepsy of unknown cause, electroclinical findings suggest a temporal lobe origin of the seizures. This group showed a better prognosis compared with the patients with structural epilepsy. Leukoaraiosis, , negatively impacted on seizure prognosis. The aim of this study was to describe the electroclinical and prognostic characteristics, and to investigate the role of leukoaraiosis in outpatients with new-onset elderly focal epilepsy aged ≥60 years, referred to a tertiary epilepsy center between 2005 and December 31, 2020. Among the 720 patients who were referred to the center, we retrospectively selected 162 consecutive outpatients, with a first referral for recent-onset focal epilepsy of unknown cause (UC) or structural cause (SC), and collected a clinical and standard-Electroencephalogram (S-EEG), 24-h ambulatory EEG (A-EEG), and neuroimaging data. We also analyzed the seizure prognosis after titration of the first antiseizure medication (ASM). One hundred and four UC and 58 SC patients, followed up for 5.8 ± 5.3 years (mean ± SD), were included. Compared with the SC group, the patients with UC showed a predominance of focal seizures with impaired awareness (51.9% of cases) and focal to bilateral tonic-clonic seizures during sleep (25%); conversely, the SC group, more frequently, had focal to bilateral tonic-clonic seizures during wakefulness (39.6%) and focal aware seizures (25.8%) ( p < 0.0001). Oral or gestural automatisms were prevalent in UC epilepsy (20.2 vs. 6.9% in the SC group, p = 0.04). In UC compared to patients with SC, interictal epileptiform discharges showed a preferential temporal lobe localization ( p = 0.0007), low expression on S-EEG, and marked activation during deep Non-Rapid Eye Movement (NREM) sleep ( p = 0.003). An overall good treatment response was found in the whole sample, with a probability of seizure freedom of 68.9% for 1 year. The cumulative probability of seizure freedom was significantly higher in the UC compared with the SC group ( p < 0.0001). The prognosis was worsened by leukoaraiosis ( p = 0.012). In the late-onset focal epilepsy of unknown cause, electroclinical findings suggest a temporal lobe origin of the seizures. This group showed a better prognosis compared with the patients with structural epilepsy. Leukoaraiosis, per se , negatively impacted on seizure prognosis. |
Author | Paoletti, Matteo Scanziani, Sofia Galimberti, Carlo Andrea Micalizzi, Elisa Ballante, Elena Tartara, Elena |
AuthorAffiliation | 2 Department of Brain and Behavioral Sciences, University of Pavia , Pavia , Italy 3 BioData Center, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Mondino Foundation , Pavia , Italy 1 Epilepsy Center, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Mondino Foundation , Pavia , Italy 5 Department of Neuroradiology, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Mondino Foundation , Pavia , Italy 4 Department of Mathematics, University of Pavia , Pavia , Italy |
AuthorAffiliation_xml | – name: 3 BioData Center, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Mondino Foundation , Pavia , Italy – name: 1 Epilepsy Center, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Mondino Foundation , Pavia , Italy – name: 5 Department of Neuroradiology, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Mondino Foundation , Pavia , Italy – name: 2 Department of Brain and Behavioral Sciences, University of Pavia , Pavia , Italy – name: 4 Department of Mathematics, University of Pavia , Pavia , Italy |
Author_xml | – sequence: 1 givenname: Elena surname: Tartara fullname: Tartara, Elena – sequence: 2 givenname: Elisa surname: Micalizzi fullname: Micalizzi, Elisa – sequence: 3 givenname: Sofia surname: Scanziani fullname: Scanziani, Sofia – sequence: 4 givenname: Elena surname: Ballante fullname: Ballante, Elena – sequence: 5 givenname: Matteo surname: Paoletti fullname: Paoletti, Matteo – sequence: 6 givenname: Carlo Andrea surname: Galimberti fullname: Galimberti, Carlo Andrea |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35295838$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1111/epi.13709 10.1212/WNL.0000000000007010 10.1046/j.1528-1157.2001.0420081025.x 10.1111/j.1528-1157.1997.tb01075.x 10.1016/j.nicl.2015.07.016 10.1111/j.1528-1167.2007.01164.x 10.1016/j.eplepsyres.2014.10.012 10.1016/j.clinimag.2017.06.011 10.1016/j.yebeh.2019.06.039 10.1016/j.seizure.2013.06.005 10.1016/j.seizure.2019.02.004 10.1016/j.clineuro.2012.07.009 10.1212/WNL.62.5_suppl_2.S24 10.1001/jamaneurol.2018.1935 10.1016/j.yebeh.2005.11.007 10.1111/j.1528-1157.1997.tb01219.x 10.1016/j.eplepsyres.2013.08.009 10.1111/j.1528-1167.2009.02303.x 10.1016/0013-4694(80)90396-X 10.1111/j.1528-1157.1996.tb00007.x 10.1016/j.eplepsyres.2016.08.023 10.1111/ane.12398 10.1016/j.clinph.2014.10.155 10.1016/j.seizure.2016.03.011 10.1212/WNL.43.2.425 10.1111/j.1528-1157.1998.tb01329.x 10.1212/WNL.41.2_Part_1.290 10.1111/j.1528-1167.2009.02285.x 10.1177/155005949903000403 10.1016/j.seizure.2004.09.003 10.1111/j.1528-1157.1992.tb06222.x 10.1017/S0317167100035411 10.1097/MD.0000000000007682 10.1016/j.yebeh.2012.11.041 10.1016/j.biopsych.2008.03.024 10.1111/epi.13670 10.1016/S0013-4694(97)00158-2 10.1007/s10072-019-03913-4 10.1016/S1059-1311(05)80005-6 10.1155/2017/8724503 10.2307/2530904 10.1016/S1388-2457(00)00404-1 10.1111/j.1468-1331.2006.01205.x 10.1111/j.0013-9580.2004.29003.x 10.1177/1073858412462747 |
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Keywords | epilepsy sleep interictal epileptiform discharges leukoaraiosis elderly |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 European Reference Network for Rare and Complex Epilepsies (ERN EpiCARE) Full Member Reviewed by: Vincenzo Belcastro, Lodi Hospital, Italy; Melissa Barker-Haliski, University of Washington, United States These authors have contributed equally to this work This article was submitted to Epilepsy, a section of the journal Frontiers in Neurology Edited by: Filippo Sean Giorgi, University of Pisa, Italy |
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Title | Late-Onset Focal Epilepsy: Electroclinical Features and Prognostic Role of Leukoaraiosis |
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