Ates Ilker, Suzen H Sinan, Yucesoy Berran, Tekin Ishak Ozel, Karakaya Asuman
Faculty of Pharmacy, Department of Toxicology, Ankara University, Ankara, Turkey.
Am J Ind Med. 2008 Oct;51(10):741-7. doi: 10.1002/ajim.20632.
Cytokines appear to play a key role in some inflammatory reactions affecting the interactions among pro- and anti-inflammatory mechanisms that result in several diseases such as coal workers' pneumoconiosis (CWP). In this study, to determine the cytokine gene profiles of Turkish coal miners, we performed genotyping analysis to investigate the polymorphisms of CWP-related pro-inflammatory (TNFA, IL1A, IL1B, and IL6) and anti-inflammatory cytokines (IL-1RN and TGFB1). An additional goal was to observe whether these cytokine gene polymorphisms influence the development risk and severity of.
Genotyping was carried out by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) technique.
TNFA (-238) gene polymorphism principally affected CWP development and severity (OR = 3.47: 95% CI, 1.12-10.77 and OR = 4.30: 95% CI, 1.25-14.74, respectively) and also risk of CWP (OR = 3.79: 95% CI, 1.37-10.46). The TNFA (-308) variant was associated with a risk for the CWP severity (OR = 2.84: 95% CI, 1.08-7.39). A protective effect of IL6 was found on the development (OR = 0.48: 95% CI, 0.21-0.93) and severity of CWP (OR = 0.37: 95% CI, 0.15-0.91).
We suggest that TNFA (-238) variant may be a risk factor in both development and the severity of CWP, while TNFA (-308) variant seems to be important only in disease severity. On the other hand, IL6 variant may have a protective effect on the development and disease severity.
细胞因子似乎在一些炎症反应中起关键作用,这些炎症反应会影响促炎和抗炎机制之间的相互作用,从而导致多种疾病,如煤工尘肺(CWP)。在本研究中,为了确定土耳其煤矿工人的细胞因子基因谱,我们进行了基因分型分析,以研究与CWP相关的促炎细胞因子(TNFA、IL1A、IL1B和IL6)和抗炎细胞因子(IL-1RN和TGFB1)的多态性。另一个目标是观察这些细胞因子基因多态性是否会影响CWP的发病风险和严重程度。
采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)技术进行基因分型。
TNFA(-238)基因多态性主要影响CWP的发生和严重程度(OR = 3.47:95%CI,1.12 - 10.77和OR = 4.30:95%CI,1.25 - 14.74),也影响CWP的发病风险(OR = 3.79:95%CI,1.37 - 10.46)。TNFA(-308)变异与CWP严重程度风险相关(OR = 2.84:95%CI,1.08 - 7.39)。发现IL6对CWP的发生(OR = 0.48:95%CI,0.21 - 0.93)和严重程度具有保护作用(OR = 0.37:95%CI,0.15 - 0.91)。
我们认为TNFA(-238)变异可能是CWP发生和严重程度的危险因素,而TNFA(-308)变异似乎仅在疾病严重程度方面具有重要意义。另一方面,IL6变异可能对疾病的发生和严重程度具有保护作用。