Yang Fengjiao, Gu Yun, Yan Ya, Wang Pengyu, Wang Min, Chen Jianjie, Du Xiaoshan, Wang Guangming
School of Clinical Medicine, Dali University, Dali, 671000, Yunnan, People's Republic of China.
Department of Pharmacy, The People's Hospital of Baoshan, Baoshan, 678000, Yunnan Province, People's Republic of China.
Sci Rep. 2025 Apr 26;15(1):14600. doi: 10.1038/s41598-025-99418-6.
Hypoxia-inducible factor 1 A (HIF1A) is considered as a potential marker gene for ischemic stroke (IS), its gene polymorphism may affect IS risk and may be related to the IS pathological process. In this study, a total of 159 IS patients and 141 healthy controls were enrolled by case-control study method. HIF1A three single nucleotide polymorphisms (SNPs: rs10873142, rs11549465, rs11549467) were genotyped by SNaPshot method and HIF1A protein levels was detected by enzyme-linked immunosorbent assay (ELISA), then the correlation between HIF-1 A SNPs and IS was analyzed by statistical analysis method. The genotype of HIF1A SNPs can affect the expression levels of clinical and laboratory parameters in IS patients, such as high-density lipoproteincholesterol (HDL-C), apolipoprotein A1, reactive oxygen species (ROS). HIF1A TCG haplotype is a protective factor for IS, HIF1A CCG haplotype is a risk factor for IS. However, the association between HIF1A rs10873142, rs11549465, rs11549467 genotypes and the IS risk was not statistically significant. ELISA analysis showed that the HIF1A expression of IS patients is higher than the healthy controls. Therefore, the gene polymorphism and expression of HIF1A may be related to IS pathological process, but the relationship between HIF1A gene polymorphism and the IS risk still needs further study.
缺氧诱导因子1A(HIF1A)被认为是缺血性中风(IS)的潜在标志物基因,其基因多态性可能影响IS风险,并可能与IS的病理过程相关。在本研究中,采用病例对照研究方法共纳入159例IS患者和141例健康对照。通过SNaPshot方法对HIF1A的三个单核苷酸多态性(SNPs:rs10873142、rs11549465、rs11549467)进行基因分型,并采用酶联免疫吸附测定(ELISA)检测HIF1A蛋白水平,然后通过统计分析方法分析HIF-1A SNPs与IS之间的相关性。HIF1A SNPs的基因型可影响IS患者临床和实验室参数的表达水平,如高密度脂蛋白胆固醇(HDL-C)、载脂蛋白A1、活性氧(ROS)。HIF1A TCG单倍型是IS的保护因素,HIF1A CCG单倍型是IS的危险因素。然而,HIF1A rs10873142、rs11549465、rs11549467基因型与IS风险之间的关联无统计学意义。ELISA分析显示,IS患者的HIF1A表达高于健康对照。因此,HIF1A的基因多态性和表达可能与IS的病理过程相关,但HIF1A基因多态性与IS风险之间的关系仍需进一步研究。