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Cryopreservation time does not decrease follicular viability in ovarian tissue frozen for fertility preservation

机译:冷冻保存时间不会降低冷冻保存生育力的卵巢组织中的卵泡活力

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OBJECTIVE: To determine the effect of storage duration on cryopreserved ovarian tissue using fresh and frozenthawed samples. METHODS: Seventeen fertile patients underwent an ovarian biopsy during elective laparoscopic tubal ligation. The tissue sample was divided into three parts: one part was processed fresh (FG), and two were slowly frozen, cryopreserved for 30 (G30) or 180 days (G180), thawed and analyzed. Follicular density, follicular viability, and steroidogenic capacity were assessed. RESULTS: We observed no differences between the groups in follicular density, which was assessed in hematoxylin and eosin-stained tissue sections. A heterogeneous follicular distribution was observed in the parenchyma, with a mean density of 361.3±255.4, 454.9±676.3, and 296.8±269.0 follicles/mm3 for FG, G30 and G180, respectively (p = 0.46). Follicular viability was greater in FG (93.4%) when compared with the cryopreserved tissues (70.8% for G30 (p
机译:目的:使用新鲜和冷冻融化的样品,测定保存时间对冷冻保存的卵巢组织的影响。方法:十七名可育患者在选择性腹腔镜输卵管结扎术中接受了卵巢活检。将组织样品分为三部分:一份新鲜加工(FG),两份缓慢冷冻,冷冻保存30天(G30)或180天(G180),解冻并分析。评估卵泡密度,卵泡生存力和类固醇生成能力。结果:我们观察到两组之间的卵泡密度没有差异,这是在苏木精和曙红染色的组织切片中评估的。 FG,G30和G180的薄壁组织中的卵泡分布不均,平均密度分别为361.3±255.4、454.9±676.3和296.8±269.0卵泡/ mm3(p = 0.46)。与冷冻保存的组织相比,FG的卵泡生存力更高(93.4%)(G30的卵囊活力为70.8%(p

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