低氧诱导因子1α基因多态性与重症感染急性肾损伤的关系

Analysis of relationship between hypoxia-inducible factor 1α gene polymorphism and acute kidney injury in patients with severe infection

  • 摘要: 目的 分析身体质量指数(BMI)及低氧诱导因子1α(HIF-1α)基因多态性与重症感染患者急性肾损伤(AKI)的关系。方法 选择2017年1月-2019年6月廊坊市人民医院诊治的122例重症感染患者,根据是否并发AKI将患者分为AKI组(n=53)和非AKI组(n=69),比较两组患者BMI,检测HIF-1α基因单核苷酸多态性(SNP)位点多态性,并分析BMI以及HIF-1α基因多态性与重症感染患者并发AKI的关系。结果 AKI组BMI高于非AKI组(P<0.05);AKI组HIF-1α基因rs11549465位点CC基因型分布频率和C等位基因频率低于非AKI组(P<0.05),CT+TT基因型分布频率和T等位基因频率高于非AKI组(P<0.05);AKI组HIF-1α基因rs11549467位点GG基因型分布频率和G等位基因频率低于非AKI组(P<0.05),GA+AA基因型分布频率和A等位基因频率高于非AKI组(P<0.05);在超显性、显性模型下,AKI组HIF-1α基因rs11549465、rs11549467位点各基因型分布频率与非AKI组比较,差异有统计学意义(P<0.05),分别与CC、GG基因型比较,CT+TT、GA+AA基因型重症感染患者并发AKI风险增加;多因素Logistic回归分析显示,BMI、HIF-1α基因rs11549465位点CT+TT基因型、rs11549467位点GA+AA基因型是影响重症感染患者AKI发生的危险因素。结论 BMI指数以及HIF-1α基因rs11549465位点CT+TT基因型和rs11549467位点GA+AA基因型可能会增加重症感染患者并发AKI的风险。

     

    Abstract: OBJECTIVE To analyze the relationship between body mass index(BMI) and hypoxia-inducible factor 1α(HIF-1α) gene polymorphisms and acute kidney injury(AKI) in patients with severe infection. METHODS A total of 122 patients with severe infection diagnosed and treated in the People’s Hospital of Langfang from Jan 2017 to Jun 2019 were recruited. The patients were divided into the AKI group(n=53) and non-AKI group(n=69) according to whether they were complicated with AKI. The BMI index was compared between the two groups, and the locus polymorphism of single nucleotide polymorphism(SNP) of HIF-1α gene was detected. The relationship between BMI index and HIF-1α gene polymorphism and AKI in patients with severe infection was analyzed. RESULTS The BMI index in the AKI group was significantly higher than that in the non-AKI group(P<0.05). The CC genotype distribution frequency and C allele frequency at rs11549465 locus of HIF-1α gene in the AKI group were significantly lower than those in the non-AKI group(P<0.05) while the CT+TT genotype distribution frequency and T allele frequency were significantly higher than those in the non-AKI group(P<0.05). The GG genotype distribution frequency and G allele frequency at rs11549467 locus of HIF-1α gene in the AKI group were significantly lower than those in the non-AKI group(P<0.05) while the GA+AA genotype distribution frequency and A allele frequency were significantly higher than those in the non-AKI group(P<0.05). Under the superdominant or dominant model, there were significant differences in the distribution frequencies of genotypes at rs11549465 locus and rs11549467 locus of HIF-1α gene between the AKI group and non-AKI group(P<0.05). Compared with CC and GG genotypes, patients with severe infection carrying CT+TT and GA+AA genotypes had higher risk of AKI. Multivariate Logistic regression analysis showed that BMI index, CT+TT genotype at rs11549465 locus and GA+AA genotype at rs11549467 locus of HIF-1α gene were risk factors affecting the occurrence of AKI in patients with severe infection. CONCLUSION BMI index and CT+TT genotype at rs11549465 locus and GA+AA genotype at rs11549467 locus of HIF-1α gene may increase the risk of AKI in patients with severe infection.

     

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