Literature DB >> 24406619

Significant association of interleukin-4 gene intron 3 VNTR polymorphism with susceptibility to knee osteoarthritis.

Serbulent Yigit1, Ahmet Inanir2, Akın Tekcan3, Ercan Tural4, Gokhan Tuna Ozturk2, Gorkem Kismali5, Nevin Karakus1.   

Abstract

OBJECTIVE: Interleukin-4 (IL-4) is a strong chondroprotective cytokine and polymorphisms within this gene may be a risk factor for osteoarthritis (OA). We aimed to investigate genotype and allele frequencies of IL-4 gene intron 3 variable number of tandem repeats (VNTR) polymorphism in patients with knee OA in a Turkish population.
METHODS: The study included 202 patients with knee OA and 180 healthy controls. Genomic DNA was isolated and IL-4 gene 70 bp VNTR polymorphism determined by using polymerase chain reaction (PCR) with specific primers followed by restriction fragment length polymorphism (RFLP) analysis.
RESULTS: Our result show that there was statistically significant difference between knee OA patients and control group with respect to IL-4 genotype distribution and allele frequencies (p=0.000, OR: 0.20, 95% CI: 0.10-0.41, OR: 0.22, 95% CI: 0.12-0.42, respectively).
CONCLUSIONS: Our findings suggest that there is an association of IL-4 gene intron 3 VNTR polymorphism with susceptibility of a person for development of knee OA. As a result, IL-4 gene intron 3 VNTR polymorphism could be a genetic marker in OA in a Turkish study population. This is the first association study that evaluates the associations between IL-4 gene VNTR polymorphism and knee OA. Crown
Copyright © 2013. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  ESRD; IL-4; IL-4R; Interleukin-4 (IL-4); Knee osteoarthritis; MS; OA; PCR; Polymorphism; RA; RFLP; SLE; SM; VNTR; end-stage renal disease; interleukin 4; interleukin-4 receptor; multiple sclerosis; osteoarthritis; polymerase chain reaction; restriction fragment length polymorphism; rheumatoid arthritis; severe malaria; systemic lupus erythematosus; variable number tandem repeat

Mesh:

Substances:

Year:  2014        PMID: 24406619     DOI: 10.1016/j.gene.2013.12.060

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


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