Frontiers in Neurology (Aug 2021)

Multidimensional Approach Assessing the Role of Interleukin 1 Beta in Mesial Temporal Lobe Epilepsy

  • Renato O. Santos,
  • Renato O. Santos,
  • Rodrigo Secolin,
  • Rodrigo Secolin,
  • Patrícia G. Barbalho,
  • Patrícia G. Barbalho,
  • Mariana S. Silva-Alves,
  • Mariana S. Silva-Alves,
  • Marina K. M. Alvim,
  • Marina K. M. Alvim,
  • Clarissa L. Yasuda,
  • Clarissa L. Yasuda,
  • Fábio Rogerio,
  • Fábio Rogerio,
  • Tonicarlo R. Velasco,
  • Americo C. Sakamoto,
  • Antonio L. Teixeira,
  • Fernando Cendes,
  • Fernando Cendes,
  • Claudia V. Maurer-Morelli,
  • Claudia V. Maurer-Morelli,
  • Iscia Lopes-Cendes,
  • Iscia Lopes-Cendes

DOI
https://doi.org/10.3389/fneur.2021.690847
Journal volume & issue
Vol. 12

Abstract

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We aimed to investigate the role of interleukin-1 beta (IL-1β) in the mechanisms underlying mesial temporal lobe epilepsy with hippocampal sclerosis (MTLE+HS). We assessed a cohort of 194 patients with MTLE+HS and 199 healthy controls. Patients were divided into those with positive and negative antecedent febrile seizures (FS). We used a multidimensional approach, including (i) genetic association with single nucleotide polymorphisms (SNPs) in the IL1B gene; (ii) quantification of the IL1B transcript in the hippocampal tissue of patients with refractory seizures; and (iii) quantification of the IL-1β protein in the plasma. We found a genetic association signal for two SNPs, rs2708928 and rs3730364*C in the IL1B gene, regardless of the presence of FS (adjusted p = 9.62e–11 and 5.14e–07, respectively). We found no difference between IL1B transcript levels when comparing sclerotic hippocampal tissue from patients with MTLE+HS, without FS, and hippocampi from autopsy controls (p > 0.05). Nevertheless, we found increased IL-1β in the plasma of patients with MTLE+HS with FS compared with controls (p = 0.0195). Our results support the hypothesis of a genetic association between MTLE+HS and the IL1B gene

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