Tehran University of Medical Sciences

Science Communicator Platform

Stay connected! Follow us on X network (Twitter):
Share this content! On (X network) By
Association of the Single Nucleotide Polymorphisms of the Genes Encoding Il-2 and Ifn-Γ With Febrile Seizure Pubmed



Shahrokhi A1, 2 ; Zareshahabadi A3, 4 ; Poor MN5 ; Sajedi F1 ; Soltani S6 ; Zoghi S7, 8 ; Badv RS2 ; Ashrafi MR2 ; Rezaei N3, 7, 9
Authors
Show Affiliations
Authors Affiliations
  1. 1. Pediatric Neurorehabilitation Research Center, The University of Social Welfare and Rehabilitation Sciences, Tehran, Iran
  2. 2. Pediatrics Center of Excellence, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Research Center for Immunodeficiencies, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. NeuroImmunology Research Association (NIRA), Universal Scientific Education and Research Network (USERN), Tehran, Iran
  5. 5. Noor Afshar Hospital, Iranian Red Crescent Society, Tehran, Iran
  6. 6. Molecular Immunology Research Center, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
  7. 7. Department of Immunology, School of Medicine, Molecular Immunology Research Center, Tehran University of Medical Sciences, Tehran, Iran
  8. 8. Medical Genetics Network (MeGeNe), Universal Scientific Education and Research Network (USERN), Vienna, Austria
  9. 9. Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA), Universal Scientific Education and Research Network (USERN), Sheffield, United Kingdom

Source: Acta Medica Iranica Published:2017


Abstract

Inflammatory elements and genetics have major roles in febrile seizures (FS) pathogenesis. Seventy patients were enrolled and compared with 139 controls. The allele and genotype frequency of the IL- 2 gene at -330 and +166 positions and the IFN-γ at +874 position were determined. A significant positive association with GG genotype at position -330 in the patient group was found (P=0.003). Further, a positive association was detected in simple and complex FS groups at the same position (P=0.03, P=0.004). IL-2 GT haplotype was significantly more common in the patients compared to controls (P=0.0008). Higher frequency of GT haplotype was detected in simple FS patients in comparison to controls (P=0.0003). Contrary, IL-2 TG haplotype frequency was lower in complex FS group (P=0.005). Overrepresentation of certain alleles, genotypes and haplotypes in IL-2 gene in FS patients could predispose individuals to this disease. © 2017 Tehran University of Medical Sciences. All rights reserved.
Other Related Docs