a Department of Orthopaedics and Traumatology , Nanfang Hospital, Southern Medical University , Guangzhou , PR China.
b Guangdong Provincial Key Laboratory of Bone and Cartilage Regenerative Medicine , Nanfang Hospital, Southern Medical University , Guangzhou , PR China.
Infect Dis (Lond). 2017 Nov-Dec;49(11-12):817-823. doi: 10.1080/23744235.2017.1347816. Epub 2017 Jul 6.
Cyclooxygenase-2 (COX-2) enzyme is one of the major mediators during inflammation reactions, and COX-2 gene polymorphisms of rs20417 and rs689466 have been reported to be associated with several inflammatory diseases. However, potential links between the two polymorphisms and risk of developing post-traumatic osteomyelitis remain unclear. The present study aimed to investigate associations between the rs20417 and rs689466 polymorphisms and susceptibility to post-traumatic osteomyelitis in Chinese population.
A total of 189 patients with definite diagnosis of post-traumatic osteomyelitis and 220 healthy controls were genotyped for rs20417 and rs689466 using the SNaPshot genotyping method. Chi-square test was used to compare differences of genotype distributions as well as outcomes of five different genetic models between the two groups.
Significant association was found between rs689466 and post-traumatic osteomyelitis by recessive model (GG vs. AA + AG) (OR = 1.74, 95% CI: 1.098-2.755, p = .018). Although no statistical differences were identified of rs689466 between the two groups by allele model (p = .098) or homozygous model (p = .084), outcomes revealed a tendency that allele G may be a risk factor and people of GG genotype may be in a higher risk to develop post-traumatic osteomyelitis in Chinese population. However, no significant link was found between rs20417 and susceptibility to post-traumatic osteomyelitis in this Chinese cohort.
To our knowledge, we reported for the first time that COX-2 gene polymorphism rs689466 may contribute to the increased susceptibility to post-traumatic osteomyelitis in Chinese population.
环氧化酶-2(COX-2)酶是炎症反应过程中的主要介质之一,COX-2 基因的 rs20417 和 rs689466 多态性已被报道与多种炎症性疾病相关。然而,这两种多态性与创伤后骨髓炎风险之间的潜在联系尚不清楚。本研究旨在探讨 COX-2 基因 rs20417 和 rs689466 多态性与中国人群创伤后骨髓炎易感性的关系。
采用 SNaPshot 基因分型法对 189 例确诊为创伤后骨髓炎患者和 220 例健康对照者进行 rs20417 和 rs689466 基因型检测。采用卡方检验比较两组间不同遗传模型的基因型分布和 5 种不同遗传模型的结果差异。
在隐性模型(GG 与 AA+AG)中,rs689466 与创伤后骨髓炎显著相关(OR=1.74,95%CI:1.098-2.755,p=0.018)。虽然在等位基因模型(p=0.098)或纯合模型(p=0.084)中 rs689466 两组间无统计学差异,但结果显示等位基因 G 可能是一个危险因素,GG 基因型的人在中国人群中发生创伤后骨髓炎的风险可能更高。然而,在这个中国队列中,rs20417 与创伤后骨髓炎易感性之间没有发现显著联系。
据我们所知,我们首次报道 COX-2 基因多态性 rs689466 可能导致中国人群创伤后骨髓炎易感性增加。