Association of TGFB, but not IL10, single nucleotide polymorphisms with febrile seizures

作者:Shahrokhi Amin; Zare Shahabadi Ameneh; Soltani Samaneh; Soleimani Farin; Vameghi Roshanak; Konjkav Arian Rahimi; Karimi Parviz; Katibeh Pegah; Vafaei Mohammad; Zoghi Samaneh; Ashrafi Mahmoud Reza; Rezaei Nima*
来源:Seizure-European Journal of Epilepsy, 2015, 29: 148-152.
DOI:10.1016/j.seizure.2015.05.001

摘要

Purpose: Febrile seizures (FS) are the most common convulsive event in children. Inflammatory elements and genetics seem to have major roles in their pathogenesis. Methods: Seventy nine patients with FS were enrolled in this study and compared with 140 controls. Cytokine genotyping was performed, using polymerase chain reaction with sequence-specific primers. The allele and genotype frequency of three single nucleotide polymorphisms (SNPs) within the IL-10 gene at -1082, -819 and -592 positions (rs1800896, rs1800871, rs1800872), and two SNPs within the TGFB at codons 10 and 25 (rs1982037, rs1800471) were determined. Results: No significant difference was detected in allelic frequency of IL-10 at -1082, -819 and -592 positions (rsl 800896, rsl 800871, rsl 800872) and TGFB at codon 25 (rsl 800471), between patients and controls. A significant negative association was observed at the codon 10/CT (rs1982037) in the patient group (OR, 0.5; 95%CI, 0.27-0.93; p = 0.026). Further, a negative association was detected in patients with simple FS at same position (OR, 0.41; 95%CI, 0.18-0.93; p = 0.03), thus revealing a protective effects in FS patients. There was no significant difference in allelic and genotype frequency between simple and complex FS samples. Furthermore, haplotype analysis revealed significant difference in frequency of TGFB/TC haplotype in comparison between complex FS patients and controls (p = 0.048). Conclusion: Certain alleles, genotypes, and haplotypes in TGFB genes were over represented in patients with FS, which possibly could predispose individuals to this disease.

  • 出版日期2015-7