[母体和胎儿 ERAP-1 基因多态性与先兆子痫的关系]。

C Ma, X W Liu, Y Y Zheng, W Y Zhang
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引用次数: 0

摘要

研究目的研究内质网氨肽酶 1(ERAP-1)基因多态性与子痫前期(PE)发生的关系。研究方法2018年10月至2021年10月在北京妇产医院进行病例对照研究。结果:(1)通过单变量分析,共筛选出母体ERAP-1基因的13个目标SNP位点。其中,96096828、96121524、96121715、96122260 和 96122281 基因型的频率分布在 PE 组和对照组之间有显著统计学差异(所有 PCI:0.687-5.831,P=0.020)。(2)单变量分析共筛选出 4 个胎儿 ERAP-1 基因的目标 SNP 位点,PE 组与对照组在这 4 个位点的基因多态性上差异无统计学意义(均 P>0.05)。多变量逻辑回归分析显示,位点 96121406 基因型为 AA 的胎儿发生 PE 的风险是基因型为 GG 的胎儿的 0.236 倍(95%CI:0.055-1.025,P=0.016)。结论母亲ERAP-1基因96121524位点的TC基因型和胎儿96121406位点的GG基因型可能与PE的发病率有关。
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[Relationship between maternal and fetal ERAP-1 gene polymorphism and pre-eclampsia].

Objective: To investigate the relationship between the polymorphism of endoplasmic reticulum aminopeptidase 1 (ERAP-1) gene and the occurrence of pre-eclampsia (PE). Methods: A case-control study was conducted in Beijing Obstetrics and Gynecology Hospital from October 2018 to October 2021. A total of 51 PE pregnant women with onset gestational age<34 weeks were selected as the PE group, and 48 normal pregnant women during the same period were selected as the control group. Venous blood samples were collected from the pregnant women before delivery and umbilical cord within 5 minutes after delivery. Single nucleotide polymorphisms (SNP) of ERAP-1 gene in the pregnant women and their fetus were detected by next-generation sequencing. Univariate analysis and multivariate logistic regression analysis were used to analyze all the SNP loci and alleles detected in the two groups, and the significant SNP were screened. Results: (1) A total of 13 target SNP loci of maternal ERAP-1 gene were selected by univariate analysis. Among them, the frequency distribution of genotypes at 96096828, 96121524, 96121715, 96122260 and 96122281 showed statistically significant differences between PE group and control group (all P<0.05). Multivariate logistic regression analysis showed that the risk of PE in pregnant women with TC genotype at locus 96121524 was 2.002 times higher than those with TT genotype (95%CI: 0.687-5.831, P=0.020). (2) A total of 4 target SNP loci of ERAP-1 gene in fetal were selected by univariate analysis, and there was no statistical significance in gene polymorphism of the 4 loci between PE group and control group (all P>0.05). Multivariate logistic regression analysis showed that the risk of PE in fetus with genotype AA at locus 96121406 was 0.236 times that of fetus with genotype GG (95%CI: 0.055-1.025, P=0.016). Conclusion: ERAP-1 gene with TC genotype at 96121524 in the mother and GG genotype at 96121406 in the fetus might be related to the incidence of PE.

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