Ph.D. Program in Pharmaceutic Biotechnology, Graduate Institute of Biomedical and Pharmaceutical Science, School of Medicine, Fu Jen Catholic University, New Taipei City, Taiwan.
School of Medicine, Fu Jen Catholic University, New Taipei City, Taiwan.
Front Endocrinol (Lausanne). 2023 Aug 10;14:1173079. doi: 10.3389/fendo.2023.1173079. eCollection 2023.
Angiogenesis in folliculogenesis contributes to oocyte developmental competence in natural and fertilization (IVF) cycles. Therefore, the identification of key angiogenic factors in follicular fluid (FF) during folliculogenesis is clinically significant and important for fertilization. This study aims to identify the key angiogenic factors in FF for predicting oocyte maturity during fertilization.
Forty participants who received ovarian stimulation using a GnRH antagonist protocol in their first fertilization treatment were recruited. From each patient, two follicular samples (one preovulatory follicle, > 18 mm; one mid-antral follicle, < 14 mm) were collected without flushing during oocyte retrieval. In total, 80 FF samples were collected from 40 patients. The expression profiles of angiogenesis-related proteins in FF were analyzed Luminex high-performance assays. Recorded patient data included antral follicle count, anti-müllerian hormone, age, and BMI. Serum samples were collected on menstrual cycle day 2, the trigger day, and the day of oocyte retrieval. Hormone concentrations including day 2 FSH/LH/E2/P4, trigger day E2/LH/P4, and retrieval day E2/LH/P4 were measured by chemiluminescence assay.
Ten angiogenic factors were highly expressed in FF: eotaxin, Gro-α, IL-8, IP-10, MCP-1, MIG, PAI-1 (Serpin), VEGF-A, CXCL-6, and HGF. The concentrations of eotaxin, IL-8, MCP1, PAI-1, and VEGF-A were significantly higher in preovulatory follicles than those in mid-antral follicles, while the Gro-α and CXCL-6 expressional levels were lower in preovulatory than in mid-antral follicles ( < 0.05). Logistic regression and receiver operating characteristic (ROC) analysis revealed that VEGF-A, eotaxin, and CXCL-6 were the three strongest predictors of oocyte maturity. The combination of VEGF-A and CXCL-6 predicted oocyte maturity with a higher sensitivity (91.7%) and specificity (72.7%) than other combinations.
Our findings suggest that VEGF-A, eotaxin, and CXCL-6 concentrations in FF strongly correlate with oocyte maturity from the mid-antral to preovulatory stage. The combination of VEGF-A and CXCL-6 exhibits a relatively good prediction rate of oocyte maturity during fertilization.
卵泡发生中的血管生成有助于自然和受精(IVF)周期中的卵母细胞发育能力。因此,鉴定卵泡液(FF)中卵泡发生过程中的关键血管生成因子对于受精具有重要的临床意义。本研究旨在鉴定 FF 中的关键血管生成因子,以预测受精过程中的卵母细胞成熟度。
招募了 40 名接受 GnRH 拮抗剂方案进行首次受精治疗的患者。从每位患者中,在取卵时不冲洗的情况下采集两个卵泡样本(一个排卵前卵泡,>18mm;一个中窦卵泡,<14mm)。总共从 40 名患者中采集了 80 个 FF 样本。使用 Luminex 高通量检测分析 FF 中与血管生成相关的蛋白表达谱。记录的患者数据包括窦卵泡计数、抗苗勒管激素、年龄和 BMI。在月经周期第 2 天、扳机日和取卵日采集血清样本。通过化学发光法测量第 2 天 FSH/LH/E2/P4、扳机日 E2/LH/P4 和取卵日 E2/LH/P4 的激素浓度。
FF 中高度表达了 10 种血管生成因子:嗜酸性粒细胞趋化因子、Gro-α、IL-8、IP-10、MCP-1、MIG、PAI-1(Serpin)、VEGF-A、CXCL-6 和 HGF。排卵前卵泡中的 eotaxin、IL-8、MCP1、PAI-1 和 VEGF-A 浓度明显高于中窦卵泡,而 Gro-α 和 CXCL-6 的表达水平则低于排卵前卵泡(<0.05)。逻辑回归和接收器操作特征(ROC)分析显示,VEGF-A、eotaxin 和 CXCL-6 是预测卵母细胞成熟度的三个最强预测因子。VEGF-A 和 CXCL-6 的组合预测卵母细胞成熟度的敏感性(91.7%)和特异性(72.7%)均高于其他组合。
我们的研究结果表明,FF 中的 VEGF-A、eotaxin 和 CXCL-6 浓度与从中窦卵泡到排卵前阶段的卵母细胞成熟度密切相关。VEGF-A 和 CXCL-6 的组合对受精过程中卵母细胞成熟度具有相对较好的预测率。