| Literature DB >> 26405555 |
Serdal Arslan1, Özge Korkmaz2, Nil Özbilüm3, Öcal Berkan2.
Abstract
Coronary artery disease (CAD) is the leading cause of fatalities worldwide. Nuclear factor (NF)-κB is a transcription factor that controls cell proliferation, differentiation and immunity. To the best of our knowledge, the present study is the first investigation of the association between CAD and NF-κB1 -94 W/D/NF-κBIA 3'-untranslated region (3'-UTR) A→G polymorphisms. The study population comprised 226 CAD patients and 201 controls. There was no significant difference in NF-κB1A 3'-UTR A→G in the allele and genotype frequencies between case and control populations. The D allele frequency of NF-κB1 -94 in the case group was significantly higher compared to the control group (P=0.028, odds ratio=1.37). The genotype frequency of NF-κB1 -94 DD in the case group was significantly higher compared to the controls (P=0.028). Linkage analysis showed a close linkage among these 2 genes (P<0.001 for case and control), and AD and GD haplotypes were associated with CAD (P<0.001; P=0.015, respectively). NF-κB1 -94 DD genotype can be a significant risk factor for the development of CAD.Entities:
Keywords: coronary artery disease; genetic polymorphism; nuclear factor-κB1; nuclear factor-κBIA
Year: 2015 PMID: 26405555 PMCID: PMC4576491 DOI: 10.3892/br.2015.499
Source DB: PubMed Journal: Biomed Rep ISSN: 2049-9434