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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Main Authors: Jadranka Sertić, Darija Mahović Lakušić, Tomislav Babić, Davor Sporiš, Silvio Bašić
Format: Article
Language:English
Published: Sestre Milosrdnice University hospital, Institute of Clinical Medical Research 2017-01-01
Series:Acta Clinica Croatica
Subjects:
Online Access:http://hrcak.srce.hr/file/271526
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spelling 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
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