Division of Orthopaedics & Traumatology, Department of Orthopaedics, Southern Medical University Nanfang Hospital, Guangzhou 510515, China.
Guangdong Provincial Key Laboratory of Bone and Cartilage Regenerative Medicine, Southern Medical University Nanfang Hospital, Guangzhou 510515, China.
J Immunol Res. 2022 Feb 10;2022:9025354. doi: 10.1155/2022/9025354. eCollection 2022.
Variations in the vitamin D receptor () gene are related to several inflammatory disorders. However, the potential links between such alternations and the risk of developing late fracture-related infection (FRI) remain unclear. This study investigated associations between genetic variations in the and susceptibility to late FRI in the Chinese Han population. Between January 2016 and December 2019, 336 patients with late FRI and 368 healthy controls were genotyped six genetic variations, including (rs7975232), (rs1544410), (rs2228570), (rs731236), (rs4516035), and (rs11568820). Significant associations were observed between rs7975232 and FRI susceptibility in the recessive ( = 0.019, OR = 0.530, 95% CI 0.310-0.906) model. Patients with AA genotype had a relatively higher level of serological vitamin D (20.6 vs. 20.3 vs. 17.9 ng/ml) ( = 0.021) than those of AC and CC genotypes. Although no statistical differences were observed, potential correlations may exist between rs1544410 (dominant model: = 0.079, OR = 0.634), rs2228570 (dominant model: = 0.055, OR = 0.699), and rs4516035 (dominant model: = 0.065, OR = 1.768) and the risk of FRI development. In the Chinese cohort, was associated with a decreased risk of developing FRI, and patients with the AA genotype had a higher vitamin D level. Further studies are required to assess the role of genetic variations in , , and in the pathogenesis of late FRI.
维生素 D 受体 () 基因的变异与几种炎症性疾病有关。然而,这些改变与发生晚期骨折相关感染 (FRI) 的风险之间的潜在联系尚不清楚。本研究调查了中国汉族人群中 基因变异与晚期 FRI 易感性之间的关系。2016 年 1 月至 2019 年 12 月,共纳入 336 例晚期 FRI 患者和 368 例健康对照者,对 6 个 基因的遗传变异(rs7975232、rs1544410、rs2228570、rs731236、rs4516035 和 rs11568820)进行了基因分型。在隐性模型中( = 0.019,OR = 0.530,95%CI 0.310-0.906),rs7975232 与 FRI 易感性显著相关。与 AC 和 CC 基因型相比,AA 基因型患者的血清维生素 D 水平相对较高(20.6 vs. 20.3 vs. 17.9 ng/ml)( = 0.021)。尽管未观察到统计学差异,但 rs1544410(显性模型: = 0.079,OR = 0.634)、rs2228570(显性模型: = 0.055,OR = 0.699)和 rs4516035(显性模型: = 0.065,OR = 1.768)可能与 FRI 发病风险之间存在潜在关联。在中国人群中, 与 FRI 发病风险降低相关,AA 基因型患者维生素 D 水平较高。需要进一步研究以评估 、 、 和 基因变异在晚期 FRI 发病机制中的作用。