Haidari M, Hajilooi M, Rezazadeh M, Rafiei A, Alavi S A, Keramat F
Department of Biotechnology, University of Texas-Houston Health Science Center, Houston, Texas 77030, USA.
Immunol Invest. 2006;35(2):239-45. doi: 10.1080/08820130600634568.
A single-nucleotide polymorphism in the promoter region of the CD14 gene at position 159 has been implicated in susceptibility to infectious diseases. We sought to determine the association between CD14 C-159 T functional promoter polymorphism and brucellosis in Western Iranian population where the disease is endemic. The CD14 genotype was determined in 228 patients with brucellosis from a rural area and 129 healthy volunteers from the same area. The prevalence of genotype TT was significantly higher in the patients while the controls showed higher prevalence of genotype CC (34.5% vs 15.5%, 15.4% vs 25.6%, P = 0.009). Multiple logistic regression analysis after adjustment for gender demonstrated that the patients who were homozygous for allele T of promoter of CD14 gene had a significantly higher risk for developing brucellosis with odds ratio of 3.03 (95% CI, 5.2, 1.75 P = 0.0004). The existence of homozygous genotype of allele T of CD14 was an independent determinant for occurrence of arthritis among the patients with brucellosis (odds ratio of 3.92 (95% CI, 2.93, 5.88, P = 0.001).Our findings provide suggestive evidence of association of the CD14 gene polymorphism with susceptibility to development of brucellosis in Iranian populations.
CD14基因启动子区域第159位的单核苷酸多态性与传染病易感性有关。我们试图确定CD14基因C-159T功能性启动子多态性与伊朗西部布鲁氏菌病流行地区人群布鲁氏菌病之间的关联。对来自农村地区的228例布鲁氏菌病患者和来自同一地区的129名健康志愿者进行了CD14基因分型。患者中基因型TT的患病率显著更高,而对照组中基因型CC的患病率更高(34.5%对15.5%,15.4%对25.6%,P = 0.009)。在对性别进行校正后的多因素逻辑回归分析表明,CD14基因启动子T等位基因纯合的患者患布鲁氏菌病的风险显著更高,比值比为3.03(95%可信区间,5.2,1.75;P = 0.0004)。CD14基因T等位基因纯合基因型的存在是布鲁氏菌病患者发生关节炎的独立决定因素(比值比为3.92(95%可信区间,2.93,5.88,P = 0.001)。我们的研究结果为CD14基因多态性与伊朗人群布鲁氏菌病易感性之间的关联提供了提示性证据。