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与使用解冻精子的密度梯度离心法相比,基于设备的精子分离技术的胚胎学结果——一项同胞供体卵母细胞研究

Embryology outcomes of a device-based sperm separation technique compared to density gradient centrifugation using thawed spermatozoa-a sibling donor oocyte study.

作者信息

Gavriil Eleftherios, Desli Anastasia, Geladaris Vasileios, Kachpani Elli, Neofytou Eirini, Tatsi Petroula, Dovas Dimitrios

机构信息

Department of Embryology and Andrology, Newlife IVF Greece, 171 Ethnikis Antistaseos Str, Kalamaria, 55134, Thessaloniki, Greece.

Department of Obstetrics and Gynecology, Newlife IVF Greece, 171 Ethnikis Antistaseos Str, Kalamaria, 55134, Thessaloniki, Greece.

出版信息

J Assist Reprod Genet. 2025 Jan;42(1):97-105. doi: 10.1007/s10815-024-03336-x. Epub 2024 Nov 30.

Abstract

OBJECTIVE

To evaluate whether the ZyMōt™ Multi 850 μl sperm separation device (SSD) effectively recovers motile spermatozoa from cryopreserved ejaculates and compare its effect on key embryology outcomes including fertilization, cleavage stage, and total and top-quality blastocyst formation rates to the traditional Density Gradient Centrifugation (DGC) method.

METHODS

In this prospective, single-center, controlled study, we used fresh sibling donor oocytes and non-donor cryopreserved ejaculates. In total, 150 couples participated in this study. At least eight MII donor oocytes were allocated to each couple split into two arms. One arm underwent ICSI with the control DGC-processed sample, and the other arm processed with SSD.

RESULTS

No significant difference on fertilization and cleavage stage embryo rates was observed between the two techniques. We observed a significant increase in the percentage of total (SSD: 74.03 ± 23.47% vs. DGC: 67.86 ± 23.92%; p = 0.016) and top-quality (SSD: 66.38 ± 24.94% vs. DGC: 60.98 ± 24.40%; p = 0.035) blastocysts formed post-SSD processing. Sub-analysis showed that this increase remained significant for the WHO-normal group (n = 118), but not for the WHO-abnormal group (n = 32).

CONCLUSION

The SSD was successfully applied in all 150 cases, providing adequate numbers of spermatozoa to undergo ICSI. Additionally, SSD significantly improved blastocyst development rates; however, this was of limited clinical impact considering the minor improvement on the average number of top-quality blastocysts. It can be hypothesized that this positive contribution may be stronger and clinically significant when a larger number of oocytes is used or in homologous oocyte ICSI cycles, where the repair mechanisms of the oocytes may insufficient for promoting healthy embryo development.

摘要

目的

评估ZyMōt™ Multi 850微升精子分离装置(SSD)能否有效地从冷冻保存的精液中回收活动精子,并将其对包括受精、卵裂期以及优质囊胚形成率等关键胚胎学指标的影响与传统密度梯度离心法(DGC)进行比较。

方法

在这项前瞻性、单中心对照研究中,我们使用了新鲜的同胞供体卵母细胞和非供体冷冻保存的精液。共有150对夫妇参与了本研究。每对夫妇至少分配8个MII期供体卵母细胞,分为两组。一组采用经对照DGC处理的样本进行卵胞浆内单精子注射(ICSI),另一组采用SSD处理的样本进行ICSI。

结果

两种技术在受精率和卵裂期胚胎率方面未观察到显著差异。我们观察到,经SSD处理后,优质囊胚的形成率显著提高(SSD:74.03±23.47% vs. DGC:67.86±23.92%;p = 0.016),优质囊胚的形成率也显著提高(SSD:66.38±24.94% vs. DGC:60.98±24.40%;p = 0.035)。亚组分析显示,对于世界卫生组织(WHO)精液正常组(n = 118),这一提高仍然显著,但对于WHO精液异常组(n = 32)则不然。

结论

SSD在所有150例病例中均成功应用,为进行ICSI提供了足够数量的精子。此外,SSD显著提高了囊胚发育率;然而,考虑到优质囊胚平均数量的微小改善,这一结果的临床影响有限。可以推测,当使用更多数量的卵母细胞或在同源卵母细胞ICSI周期中,由于卵母细胞的修复机制可能不足以促进健康胚胎发育,SSD的这种积极作用可能会更强且具有临床意义。

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