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Vitrification versus slow freezing for human ovarian tissue cryopreservation: a systematic review and meta-anlaysis

机译:玻璃化与慢速冷冻对人类卵巢组织的冷冻保存:系统评价和荟萃分析

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摘要

Vitrification is a well-accepted procedure for cryopreservation of gametes and embryos. Less is known, however, about its performance in preserving ovarian tissue, for which slow freezing is the current convention. Increasing interest is being focused on vitrification, but there are as yet no standard protocols for its use with ovarian tissue. In part, this is because of the variety of cell types and complex nature of ovarian tissue. We performed a meta-analysis of 14 studies that compared vitrification with slow freezing for cryopreservation of ovarian tissue. In the pooled analysis, there was no significant difference between the two methods in terms of the proportion of intact primordial follicles, but vitrification was associated with significantly less DNA damage. Secondary endpoints included the number of stromal cells, significantly higher with vitrification, and primordial follicle density, which did not differ between the two methods. The present meta-analysis suggests that vitrification may be more effective than slow freezing, with less primordial follicular DNA strand breaks and better preservation of stromal cells. These advantages should lead to improved ovarian function after transplantation.
机译:玻璃化是冷冻保存配子和胚胎的公认方法。然而,关于其在保存卵巢组织中的性能知之甚少,目前的常规做法是缓慢冷冻。人们越来越关注玻璃化,但是目前尚无用于卵巢组织的标准方案。部分原因是由于细胞类型的多样性和卵巢组织的复杂性。我们对14项研究进行了荟萃分析,比较了玻璃化与慢速冷冻对卵巢组织进行冷冻保存的情况。在合并分析中,两种方法之间在完整原始卵泡的比例方面没有显着差异,但是玻璃化与DNA损伤显着相关。次要终点包括基质细胞的数量(玻璃化显着更高)和原始卵泡密度,这两种方法之间没有差异。目前的荟萃分析表明,玻璃化可能比慢速冷冻更有效,原始卵泡DNA链断裂更少,基质细胞保存更好。这些优点应导致移植后卵巢功能的改善。

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