Association of interleukin (IL)-4 gene intron 3 VNTR polymorphism with multiple sclerosis in Turkish population


Karakus N., YİĞİT S., Kurt G. S., Cevik B., Demir O., Ates O.

HUMAN IMMUNOLOGY, sa.9, ss.1157-1160, 2013 (SCI-Expanded, Scopus) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Basım Tarihi: 2013
  • Doi Numarası: 10.1016/j.humimm.2013.05.011
  • Dergi Adı: HUMAN IMMUNOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.1157-1160
  • Ondokuz Mayıs Üniversitesi Adresli: Hayır

Özet

Objective: Genetic risk factors are known to contribute to the etiology of multiple sclerosis (MS). Interleukin (IL)-4 gene polymorphisms have been associated with immune-mediated diseases. The aim of this study was to explore the frequency of IL-4 gene intron 3 VNTR (variable number tandem repeat) polymorphism in a cohort of Turkish patients with MS. Methods: The study included 125 patients with MS and 160 healthy controls. Genomic DNA was isolated and genotyped using polymerase chain reaction (PCR) analyses for the IL-4 gene intron 3 VNTR polymorphism. Results: The distribution of genotype and allele frequencies of IL-4 gene intron. 3 VNTR polymorphism was statistically different between MS patients and control group (p = 0.003 and p = 0.002, respectively). There were no statistically significant association between IL-4 VNTR polymorphism and clinical and demographical characteristics of MS patients. Conclusion: The results of this study suggest that intron 3 VNTR polymorphism of the 1L-4 gene was positively associated with predisposition to develop MS in Turkish population. (C) 2013 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.