Is Apolipoprotein E ε2 Associated with Delayed Onset of Non-Lesional Temporal Lobe Epilepsy?
The aim of the study was to evaluate the possible association between Apo E polymorphisms and age at seizure onset in patients with non-lesional temporal lobe epilepsy. Eighty patients with non-lesional temporal lobe epilepsy with or without bilateral tonic-clonic propagation were analyzed. Age at s...
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Sestre Milosrdnice University hospital, Institute of Clinical Medical Research
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doaj-b3225b22ec2d4357bd946c860e76e88f2020-11-24T21:59:01ZengSestre Milosrdnice University hospital, Institute of Clinical Medical Research Acta Clinica Croatica0353-94661333-94512017-01-0156.1.1014Is Apolipoprotein E ε2 Associated with Delayed Onset of Non-Lesional Temporal Lobe Epilepsy?Jadranka Sertić0Darija Mahović Lakušić1Tomislav Babić2Davor Sporiš3Silvio Bašić4Zagreb University Hospital Center, Clinical Institute of Laboratory DiagnosisDepartment of Neurology, Zagreb, CroatiaWorldwide Clinical Trials, London, UKOsijek School of Medicine, Josip Juraj Strossmayer University, Osijek; Dubrava University Hospital, Department of NeurologyOsijek School of Medicine, Josip Juraj Strossmayer University, Osijek; Dubrava University Hospital, Department of NeurologyThe aim of the study was to evaluate the possible association between Apo E polymorphisms and age at seizure onset in patients with non-lesional temporal lobe epilepsy. Eighty patients with non-lesional temporal lobe epilepsy with or without bilateral tonic-clonic propagation were analyzed. Age at seizure onset was defined as age at the first unequivocal seizure (excluding febrile convulsions). ApoE alleles were determined by a procedure where genome DNA was amplified by chain reaction along with polymerase, using the LightCycler kit (Roche) for ApoE mutations on codons 112 and 158. There was a statistically significant difference between the groups of patients with ApoE ε2/3 and ε3/4 genotypes (p=0.03), but not between patients with ApoE ε2/3 and ε3/3, and those with ApoE ε3/4 and ε3/3. In conclusion, the results of our study suggested positive association of a specific ApoE genotype and onset of non-lesional temporal lobe epilepsy.http://hrcak.srce.hr/file/271526Apolipoprotein E2Polymorphism, geneticEpilepsy, temporal lobeAge at onset |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jadranka Sertić Darija Mahović Lakušić Tomislav Babić Davor Sporiš Silvio Bašić |
spellingShingle |
Jadranka Sertić Darija Mahović Lakušić Tomislav Babić Davor Sporiš Silvio Bašić Is Apolipoprotein E ε2 Associated with Delayed Onset of Non-Lesional Temporal Lobe Epilepsy? Acta Clinica Croatica Apolipoprotein E2 Polymorphism, genetic Epilepsy, temporal lobe Age at onset |
author_facet |
Jadranka Sertić Darija Mahović Lakušić Tomislav Babić Davor Sporiš Silvio Bašić |
author_sort |
Jadranka Sertić |
title |
Is Apolipoprotein E ε2 Associated with Delayed Onset of Non-Lesional Temporal Lobe Epilepsy? |
title_short |
Is Apolipoprotein E ε2 Associated with Delayed Onset of Non-Lesional Temporal Lobe Epilepsy? |
title_full |
Is Apolipoprotein E ε2 Associated with Delayed Onset of Non-Lesional Temporal Lobe Epilepsy? |
title_fullStr |
Is Apolipoprotein E ε2 Associated with Delayed Onset of Non-Lesional Temporal Lobe Epilepsy? |
title_full_unstemmed |
Is Apolipoprotein E ε2 Associated with Delayed Onset of Non-Lesional Temporal Lobe Epilepsy? |
title_sort |
is apolipoprotein e ε2 associated with delayed onset of non-lesional temporal lobe epilepsy? |
publisher |
Sestre Milosrdnice University hospital, Institute of Clinical Medical Research |
series |
Acta Clinica Croatica |
issn |
0353-9466 1333-9451 |
publishDate |
2017-01-01 |
description |
The aim of the study was to evaluate the possible association between Apo E polymorphisms and age at seizure onset in patients with non-lesional temporal lobe epilepsy. Eighty patients with non-lesional temporal lobe epilepsy with or without bilateral tonic-clonic propagation were analyzed. Age at seizure onset was defined as age at the first unequivocal seizure (excluding febrile convulsions). ApoE alleles were determined by a procedure where genome DNA was amplified by chain reaction along with polymerase, using the LightCycler kit (Roche) for ApoE mutations on codons 112 and 158. There was a statistically significant difference between the groups of patients with ApoE ε2/3 and ε3/4 genotypes (p=0.03), but not between patients with ApoE ε2/3 and ε3/3, and those with ApoE ε3/4 and ε3/3. In conclusion, the results of our study suggested positive association of a specific ApoE genotype and onset of non-lesional temporal lobe epilepsy. |
topic |
Apolipoprotein E2 Polymorphism, genetic Epilepsy, temporal lobe Age at onset |
url |
http://hrcak.srce.hr/file/271526 |
work_keys_str_mv |
AT jadrankasertic isapolipoproteinee2associatedwithdelayedonsetofnonlesionaltemporallobeepilepsy AT darijamahoviclakusic isapolipoproteinee2associatedwithdelayedonsetofnonlesionaltemporallobeepilepsy AT tomislavbabic isapolipoproteinee2associatedwithdelayedonsetofnonlesionaltemporallobeepilepsy AT davorsporis isapolipoproteinee2associatedwithdelayedonsetofnonlesionaltemporallobeepilepsy AT silviobasic isapolipoproteinee2associatedwithdelayedonsetofnonlesionaltemporallobeepilepsy |
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1725849581564985344 |