Department of Obstetrics and Women's Diseases, Poznan University of Medical Sciences, Polna 33, 60-535 Poznan, Poland.
Chair and Department of Cell Biology, Poznan University of Medical Sciences, Rokietnicka 5D, 60-806 Poznan, Poland.
Int J Mol Sci. 2023 Feb 21;24(5):4267. doi: 10.3390/ijms24054267.
Recurrent implantation failure (RIF) is a global health issue affecting a significant number of infertile women who undergo in vitro fertilization (IVF) cycles. Extensive vasculogenesis and angiogenesis occur in both maternal and fetal placental tissues, and vascular endothelial growth factor (VEGF) and fibroblast growth factor (FGF) family molecules and their receptors are potent angiogenic mediators in the placenta. Five single nucleotide polymorphisms (SNPs) in the genes encoding angiogenesis-related factors were selected and genotyped in 247 women who had undergone the ART procedure and 120 healthy controls. Genotyping was conducted by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). A variant of the kinase insertion domain receptor () gene (rs2071559) was associated with an increased risk of infertility after adjusting for age and BMI (OR = 0.64; 95% CI: 0.45-0.91, = 0.013 in a log-additive model). Vascular endothelial growth factor A () rs699947 was associated with an increased risk of recurrent implantation failures under a dominant (OR = 2.34; 95% CI: 1.11-4.94, p = 0.022) and a log-additive model (OR = 0.65; 95% CI 0.43-0.99, p = 0.038). Variants of the gene (rs1870377, rs2071559) in the whole group were in linkage equilibrium (D' = 0.25, r = 0.025). Gene-gene interaction analysis showed the strongest interactions between the gene SNPs rs2071559-rs1870377 ( = 0.004) and rs1870377- rs699947 ( = 0.030). Our study revealed that the gene rs2071559 variant may be associated with infertility and rs699947 with an increased risk of recurrent implantation failures in infertile ART treated Polish women.
复发性植入失败 (RIF) 是一个全球性的健康问题,影响了大量接受体外受精 (IVF) 周期的不孕妇女。母体和胎儿胎盘组织中广泛发生血管生成和血管生成,血管内皮生长因子 (VEGF) 和成纤维细胞生长因子 (FGF) 家族分子及其受体是胎盘内强有力的血管生成介质。选择编码血管生成相关因子的基因中的 5 个单核苷酸多态性 (SNP),并对 247 名接受 ART 程序的妇女和 120 名健康对照者进行基因分型。基因分型通过聚合酶链反应-限制性片段长度多态性 (PCR-RFLP) 进行。激酶插入结构域受体 () 基因 (rs2071559) 的变体与调整年龄和 BMI 后不孕的风险增加相关 (OR = 0.64;95%CI:0.45-0.91,log-additive 模型中 = 0.013)。血管内皮生长因子 A () rs699947 在显性 (OR = 2.34;95%CI:1.11-4.94,p = 0.022) 和 log-additive 模型下与复发性植入失败的风险增加相关 (OR = 0.65;95%CI 0.43-0.99,p = 0.038)。整个组中基因 () rs1870377、rs2071559 的变体处于连锁平衡 (D' = 0.25,r = 0.025)。基因-基因相互作用分析显示基因 SNPs rs2071559-rs1870377 ( = 0.004) 和 rs1870377-rs699947 ( = 0.030) 之间的相互作用最强。我们的研究表明,基因 rs2071559 变体可能与不孕有关,rs699947 与波兰接受 ART 治疗的不孕妇女复发性植入失败的风险增加有关。