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Journal of Cellular and Molecular Medicine logoLink to Journal of Cellular and Molecular Medicine
. 2007 May 1;9(3):698–703. doi: 10.1111/j.1582-4934.2005.tb00500.x

Association of refractory complex partial seizures with a polymorphism of ApoE genotype

Davor Sporiš 1,, Jadranka Sertic 2, Neven Henigsberg 3, Darija Mahovic 1, Nenad Bogdanovic 4, Tomislav Babic 1
PMCID: PMC6741410  PMID: 16202217

Abstract

Apolipoprotein E (ApoE) is a constituent of many types of lipoproteins that play a role in metabolism of cholesterol and lipids in the body as well as in the brain. ApoE is synthesised in astrocytes and microglia and enter to neurons through LDL, LRP and VLDL receptors. Recently it was shown that ApoE is also produced in neurons. ApoE has a role in modulating learning and memory, structural plasticity, mobilization of cholesterol in repair, growth and maintenance of myelin and neuronal membranes during development and aging, and cell death after ischemic, convulsive, or other type of brain injury. The aim of this research was to investigate the possible association of ApoE gene polymorphism with the development of resistance to pharmacological therapy in patients with partial complex seizures with or without secondary generalization. In this prospective matched‐pair controlled study, 60 patients with cryptogenic epilepsy with complex partial seizures, with or without secondary generalization, who have been suffering for five or more years, were studied. The first group comprised 30 patients refractory to the current therapy, while the second group consisted of patients with well‐controlled seizures. The refractory and non‐refractory groups of patients differed significantly in their phenotypes. Phenotype E3/4 was six times more frequent in refractory group than among non‐refractory group. The lack of response was shown to be significantly associated with the presence of β allele. This study provided evidence that the presence of β4 allele is more often associated with a lack of response to current antiepileptic drugs as compared to β2 and β3 alleles.

Keywords: ApoE polymorphism, refractory epilepsy, complex partial seizures, ischaemia/reperfusion, non‐responders, pharmacotherapy

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