Cytokine Polymorphism and HLA Genotyping in Patients with Temporal Lobe Epilepsy Related to Hippocampal Sclerosis.
Mesial temporal lobe epilepsy (MTLE) is a form of intractable epilepsy that may highly benefit from surgery in which hippocampal sclerosis (HS) is the most frequent pathological substrate. Histopathology of human epileptic hippocampi shows a specific neuronal loss in the areas of CA and gliosis (1). Formerly the relationship between prolonged febrile seizures (FS) and the development of MTLE has been shown with regard to cytokine gene expression (2), although other studies have failed to replicate it (3,4,5). Because altered immunity due to the etiopathogenesis of HS has been a point of interest, the role of proinflammatory cytokines and growth factors in the signaling process leading to a glial reaction have been investigated in animal models and human epilepsy (2,6,7,8). Despite recent studies, the pathogenesis of HS remains obscure, probably because of multifactorial reasons, including both environmental and genetic factors (9,10).
Previously we performed HLA typing in patients with MTLE and found a significant difference in DR2, DR4, and DQ2 antigen distributions between the MTLE group and healthy population (11). Moreover IL-I[beta]/[alpha] gene polymorphism has been investigated in another group of patients with MTLE, but no significant difference has been observed (12).
To study the role of the immune system, we aimed to investigate other cytokine gene polymorphisms, including both pro- and anti-inflammatory cytokines (IL-6, IL-10, TNF-[alpha], TGF-[beta]1, IFN-[gamma]), and HLA-DRBI genotyping in patients with MTLE--HS.
In total, 100 consecutive patients with MTLE--HS who were admitted to the epilepsy outpatient clinic of Cerrahpasa School of Medicine were studied. All these patients were surgical candidates because of medically intractable seizures and evaluated according to a standard protocol that included interictal and ictal video EEG recordings, cranial magnetic resonance imaging (MRI), and neuropsychological and psychiatric investigations. There were 68 female and 32 male patients, with a mean age of 25.8 years (range: 10-43) (Table 1). A history of FS was evident in 68% of the patients. HS was histopathologically confirmed in 70 patients who underwent anterior temporal lobectomy (the remaining were either under evaluation or in the waiting list for surgery). Informed consent was obtained from all the patients. The control group consisted of 201 healthy volunteers. This research was approved by the ethics committee of Istanbul University Cerrahpasa Faculty of Medicine (2006:18105).
DNA was extracted from the peripheral blood by using a standard method (13). Genotyping analysis of DRBI loci and cytokine genes was performed at the Department of Medical Biology Istanbul University Cytokine genotypes were determined by the polymerase chain reaction (PCR)-SSP method using a commercial kit (One Lambda, Inc., Canoga Park, CA, USA) that contains sequence-specific primers for determining the following polymorphisms: TNF-a (-308 G/A), TGF-[beta]1 (C/T codon 10, C/G codon 25), IL10 (-1082 G/A, -819 T/C, -592 A/C), IL-6 (-174 G/C), and IFN-[delta] (+874 A/T). DNA fragments corresponding to each cytokine were amplified. The allele frequencies of specified cytokines were analyzed. In patients with MTLE, the correlations between the genotype of cytokines and the presence of FS were also investigated.
For analysis of HLA-DRBI, all the samples were typed at the DRBI loci by PCR-based methods (PCR-SSO) at low resolution (14,I5,I6).
Statistical analysis was performed using Statistical Packages for the Social Sciences (SPSS Inc., Chicago, IL, USA) 12.0 version. Chi-square ([chi square]) test with Bonferroni correction and binary logistic regression models were also utilized for analysis.
Our results did not reveal any significant difference in the genotyping of pro- and anti-inflammatory cytokines between patients and controls. Further allele distribution was not different in patients with or without FS. However, analyses of HLA-DRBI showed a significant difference, where the DRBI (*) I3 allele was found to be more frequent in patients (p<0.05), and it remained significant after Bonferroni correction.
Although previous studies have suggested a role of genetic, immunological, and environmental factors (9,10,I7), the etiopathogenesis of MTLE remains obscure. In this study, we aimed to enhance the understanding of the etiology and identify potential immune markers in the susceptibility of disease.
Evaluation of Cytokines
Recent studies on epilepsy have suggested that the immune and inflammatory mechanisms play roles in some subgroups (18). In our study, the expressions of different cytokine genes (IL-6, IL-10, TNF-a, TGF-[beta]1, and IFN-[gamma]) and HLA-DR genotypes in Turkish patients with MTLE--HS were investigated to reveal the role of the immune system.
Cells in the central nervous system can produce cytokines upon activation (19), which may influence the transport systems by opening the blood-brain barrier (BBB). The administration of IL-I, IL-6, TNF-a, and IFN-[gamma] may also increase the endothelial permeability (20,21,22,23). Impaired BBB and inflammatory states are common features of neurological diseases associated with late-onset epilepsy (24). The involvement of inflammation in the pathogenesis of epilepsy and seizure-induced brain damage have been emphasized in many studies (17,18,25). Vezzani et al. (25) showed that the manipulation of pro- and anti-inflammatory cytokines can modify the outcome as well as the neuropathological consequences of experimentally induced seizures. Moreover, in patients with treatment-resistant epilepsy, increased levels of IL-6 and decreased levels of anti-inflammatory cytokine IL-IRA have been demonstrated (26). Recently, it has been shown that IL-1[beta], among others, is upregulated in pediatric patients with MTLE during the developmental phase of refractory seizures related to HS (27). The role of IL-1[beta], in the pathogenesis of MTLE has been supported by the finding that the inflammatory effects of IL-1[beta], lead to the upregulation of the P13K/Akt/mTor signaling pathway and could be suppressed by the administration of specific pathway inhibitors (28). The genetic susceptibility to inflammation has been found to be correlated with an increased risk of epilepsy (29). Weinberg et al. (30) explored the role of TNF-[alpha] and its two signaling receptors. They described a pro-ictogenic role of TNF-[alpha] mediated by TNFR1 and an anti-ictogenic role of this cytokine, probably mediated by TNFR2. The authors demonstrated that chronic induction of TNF-[alpha], although inducing glial activation and BBB damage, did not provoke cell loss or seizures but enhanced the pathological consequences of seizures.
In many epilepsy models, acute seizures cause glial activation and increased expression of transcription factors and cytokines (31,32). The activated glia and elevated cytokines contribute to seizure-related hippocampal pathology such as neuronal death, reactive gliosis, and mossy fiber sprouting (33,34,35,36).
Differences in cytokine production are related to sequence variants in cytokine genes. Many of these polymorphisms occur in the regulatory regions, resulting in high or low cytokine production (37,38). We investigated different allelic variants in the promoter regions in pro-inflammatory (TNF-[alpha], IFN-[gamma], and IL6) and anti-inflammatory (IL10 and TGF[beta]1) cytokine genes that have been identified previously (39). However we did not find significant differences between patients with MTLE--HS and controls with regard to the genotype frequencies of IFN-[gamma], TNF-[alpha], TGF-[beta]1, IL-6, and IL-10.
Evaluation of HLA Genotype
HLA antigens and haplotypes have been described in connection with different epilepsies since the early 1970s; however the results of such studies have been contradictory (40). We have reported a significantly high frequency of the HLA class II antigens DR4, DR7, and DQ2 in Turkish patients with MTLE--HS (11). Both our previous studies and several other studies have shown that HLA may play a role in different types of epilepsies (11,12,41). Moreover, the HLA-B (*) 1502 allele has been found to be strongly associated with carbamazepine-induced Stevens-Johnson syndrome and its related disease, toxic epidermal necrolysis, in Southeast Asian countries (42).
In this study, we investigated the polymorphic exons of the HLA-DR locus (exon 2 of the class II HLA locus) in patients with MTLE--HS based on our previous results, which suggested that DR4, DR7, and DQ2 are independent risk factors for MTLE--HS (11). In correlation with previous results, the present results revealed that the DRBI (*) 13 allele is more frequent in patients (p<0.05) than in healthy subjects (Table 2). Although the sample size is limited, our findings may suggest that a high frequency of HLA-DRBI (*) 13 allele plays a role in the induction of hyperexcitability of the epileptic tissue. Recently, the HLA-DRBI (*) 13:02 allele was found to be elevated in patients with MTLE--HS in comparison with controls, although the statistical significance was lost after Bonferroni correction (43). These findings may be taken into consideration as further evidence for immune-dependent genetic factors in the etiology of HS.
This study did not reveal any relationship between cytokine polymorphisms and human MTLE. However the findings on HLA may suggest its role in the pathogenesis of HS, although this needs to be verified and requires further investigations, including a larger number of patients.
Ethics Committee Approval: Ethics committee approval was received for this study from the ethics committee of Istanbul University Cerrahpasa School of Medicine.
Informed Consent: Written informed consent was obtained from patients who participated in this study.
Peer-review: Externally peer-reviewed.
Conflict of Interest: No conflict of interest was declared by the authors.
Financial Disclosure: The authors declared that this study has received no financial support.
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Ayse ALTINTAS (1), Cigdem OZKARA (1), Melis SOHTAOGLU SEVINDIK (1), Mustafa UZAN (2), Cigdem KEKIK CINAR (3), Omer UYSAL (4), Fatma SAVRAN OGUZ (3)
(1) Department of Neurology, Istanbul University Cerrahpasa School of Medicine, Istanbul, Turkey
(2) Department of Neurosurgery, Istanbul University Cerrahpaja School of Medicine, Istanbul, Turkey
(3) Department of Medical Biology, Istanbul University Istanbul School of Medicine, Istanbul, Turkey
(4) Department of Biostatistics and Medicine Informatics, Bezmialem Vakif University School of Medicine, Istanbul, Turkey
Correspondence Address: Ayse Altintas, Istanbul Universitesi Istanbul Tip Fakultesi, Noroloji Anabilim Dali, Istanbul, Turkiye E-mail: altintasI3@gmail.com
Author Contributions: Concept - A.A., C.O., M.U., F.S.O.; Design--A.A., C.O., M.U., F.S.O.; Supervision - A.A., C.O., F.S.O.; Resources--A.A., C.O., M.S.S., C.K.C., F.S.O.; Materials--A.A., C.O., M.U., F.S.O.; Data Collection and/or Processing--A.A., C.O., M.S.S., C.K.C., O.Y., F.S.O.; Analysis and/or Interpretation--A.A., C.O., M.U., F.S.O.; Literature Search--A.A., C.O., M.S.S., C.K.C., F.S.O.; Writing Manuscript--A.A., C.O., F.S.O.; Critical Review--A.A., C.O., F.S.O.; Other--A.A., C.O., M.U., F.S.O.
Cite this article as: Altintaj A, Ozkara C, Sohtaoglu Sevindik M, Uzan M, Kekik Cmar C, Uysal O, Savran Oguz F, Cytokine Polymorphism and HLA Genotyping in Patients with Temporal Lobe Epilepsy Related to Hippocampal Sclerosis. Arch Neuropsychiatry 2017; 54:350-353.
Received: 29.12.2015 Accepted: 10.04.2016 Available Online Date:15.07.2016
Table 1. Demographics and clinical characteristics of patients Number of patients 100 Age (years) 25.8 (range:10-43) Gender 68 females (68%) 32 male (32%) Presence of febrile seizures 68 (68%) Age at onset (years) 8.9[+ or -]5.8 (range: 1-28) Disease duration (years) 18.4[+ or -]8.1 (range: 1-41) Operation 70 patients (70%) Age at operation (years) 25.4 (range:12-44) Seizure characteristics Presence of GTCS 47 patients (47%) Status epilepticus 13 patients (13%) Presence of aura 65 patients (65%) GTCS: generalized tonic--clonic seizures Table 2. HLA-DRB genotyping in patients and controls Patient Control n=200 n=402 [chi square] test p DRBI (*) 01 9 21 0.189 0.664 DRBI (*) 03 26 30 3.770 0.052 DRBI (*) 04 37 63 1.387 0.239 DRBI (*) 07 21 35 0.376 0.540 DRBI (*) 08 3 13 1.995 0.158 DRBI (*) 09 0 7 fisher 0.100 DRBI (*) 10 3 9 fisher 0.757 DRBI (*) 11 40 87 0.307 0.579 DRBI (*) 12 3 16 2.747 0.097 DRBI (*) 13 22 27 5.199 0.037 (*) DRBI (*) 14 17 29 0.169 0.681 DRBI (*) 15 11 41 3.986 0.046 DRBI (*) 16 8 24 1.091 0.296 n refers to the number of HLA alleles. (*) p value was obtained from chi-square test and Bonferroni correction.
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|Author:||Altintas, Ayse; Ozkara, Cigdem; Sevindik, Melis Sohtaoglu; Uzan, Mustafa; Cinar, Cigdem Kekik; Uysal|
|Publication:||Archives of Neuropsychiatry|
|Date:||Dec 1, 2017|
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