Endometrial scratching in unexplained repeated implantation failure causes two competing forces, angiogenesis and anti-angiogenesis: An RCT study

S. Aghajanpour, Fereshteh Mehraein, F. Amjadi, Z. Zandieh, Firouzeh Ghaffari, K. Aflatoonian, Elham Hosseini, M. Bakhtiyari, Reza Aflatoonian
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Abstract

Background: A significant association between endometrial vascularity and pregnancy has been shown in previous research, while poor vascularization was attributed to repeated implantation failure (RIF). One possible approach to enhance angiogenesis for successful implantation is endometrial scratching (ES). Objective: The purpose was to investigate endometrial responses to scratching by profiling angiogenesis-related gene expression in unexplained RIF participants. Materials and Methods: In this randomized controlled trial study, 20 infertile women with unexplained RIF were assigned to 2 groups by the balanced block randomization method (n = 10/each group): the intervention group (group A) (who received ES in the follicular phase) and the control group (group B). Endometrial biopsy was performed in the secretory phase. Gene expression profiling was performed using a polymerase chain reaction-array kit for humanangiogenic growth factors. The implantation and clinical pregnancy rates were also assessed. Results: Among the angiogenesis-promoting genes, FGF1, FGF13, FGF2, TGFA, ANG, ANGPT1, and VEGFA were significantly upregulated (p < 0.05). IL12A (an angiogenesis-inhibiting cytokine) was significantly upregulated (p < 0.01). In contrast, 15 genes with angiogenesisrelated functions, including CXCL11, CXCL13, CXCL3, CXCL5, CXCL6, EREG, FIGF, FST, IL10, LEP, PPBP, PROK1, RHOB, TNF, and TYMP, were downregulated after ES. No significant differences were observed between the intervention (group A) and control (group B) groups in terms of implantation (43.75% vs. 28.57%) or clinical pregnancy rates (75% vs. 57.1%). Conclusion: ES induced significant alterations in the expression of angiogenesis-related genes, with notable up/downregulation of key angiogenic/antiangiogenic factors. These findings enhance our understanding of the molecular responses triggered by ES, underscoring the potential influence of ES on the complex processes of angiogenesis crucial for implantation. Key words: Endometrium, Angiogenesis, Embryo implantation, Polymerase chain reaction.
原因不明的反复种植失败中的子宫内膜搔抓会导致血管生成和抗血管生成两种相互竞争的力量:一项RCT研究
背景:以往的研究表明,子宫内膜血管与妊娠之间存在明显的关联,而血管生成不良则是反复种植失败(RIF)的原因。子宫内膜搔刮术(ES)是促进血管生成以成功着床的一种可行方法。目的:目的是通过分析原因不明的 RIF 参与者的血管生成相关基因表达,研究子宫内膜对搔刮的反应。材料与方法:在这项随机对照试验研究中,20 名患有不明原因 RIF 的不孕妇女通过平衡块随机法被分配到两组(n = 10/每组):干预组(A 组)(在卵泡期接受 ES 治疗)和对照组(B 组)。子宫内膜活检在分泌期进行。使用聚合酶链反应阵列试剂盒对人血管生长因子进行基因表达谱分析。此外,还对植入率和临床妊娠率进行了评估。结果在促进血管生成的基因中,FGF1、FGF13、FGF2、TGFA、ANG、ANGPT1 和 VEGFA 均显著上调(p < 0.05)。抑制血管生成的细胞因子 IL12A 则明显上调(p < 0.01)。相反,15 个具有血管生成相关功能的基因,包括 CXCL11、CXCL13、CXCL3、CXCL5、CXCL6、EREG、FIGF、FST、IL10、LEP、PPBP、PROK1、RHOB、TNF 和 TYMP 在 ES 后下调。干预组(A 组)和对照组(B 组)在植入率(43.75% 对 28.57%)和临床妊娠率(75% 对 57.1%)方面无明显差异。结论ES 会诱导血管生成相关基因的表达发生明显变化,其中关键的血管生成/血管生成因子的上调/下调效果显著。这些发现加深了我们对 ES 触发的分子反应的理解,强调了 ES 对植入所必需的复杂血管生成过程的潜在影响。关键词:子宫内膜 血管生成子宫内膜 血管生成 胚胎植入 聚合酶链反应
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