Cryopreservation of human germinal vesicle stage and in vitro matured M II oocytes: influence of cryopreservation media on the survival, fertilization, and early cleavage divisions

Cryopreservation of human germinal vesicle stage and in vitro matured M II oocytes: influence of cryopreservation media on the survival, fertilization, and early cleavage divisions
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DOI:
10.1016/s0015-0282(00)00672-5
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发表时间:
2000-09-01
影响因子:
6.7
通讯作者:
Dhont, M
Dhont, M
中科院分区:
医学2区
文献类型:
--
作者:
Goud, A;Goud, P;Dhont, M

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目的:研究低钠冷冻对冻融期和体外成熟人卵母细胞存活和发育的影响。设计:前瞻性实验研究。地点:学术医院生育中心。患者(S):实验组:卵母细胞冷冻保存在生发泡期(A组,n=63)和生发泡期(C组,n=62),同时使用常规(A组)或低钠(B组,C组)卵母细胞。对照组:同胞GV期卵母细胞体外成熟(IVM;对照组A,n=;对照组B,n=)。干预组(S):体外成熟、卵母细胞浆内单精子注射及后续培养。主要观察指标(S):存活率、成熟率、受精率和卵裂率。结果(S):A组和B组的解冻后存活率(57.1%)和B组(48.4%)显著低于C组(84.4%)。A组成熟率和卵裂率显著低于对照组,受精率与对照组相似(GVBD:72.2%比90.6%;进展到M II:33.3%比76.6%;卵裂:42.9%比88.2%;受精率:58.3%比69.4%)。B组则无明显差异。在C组中,尽管2个卵母细胞卵裂率略低于B组(47.4%vs.70.2%),3个卵母细胞卵裂率(3PN:15.8%vs.3.2%)显著高于A组(4.8%),但与B组(15.6%)相比差异不显著。B组GV期卵母细胞的成熟率和卵裂率显著高于A组(S)。结论:低钠液有利于MⅡ期卵母细胞的体外成熟,明显优于传统的钠基液。(Fertil Steril(R)2000;74:487-93.(C)2000年美国生殖医学学会。)。
Objective: To study the influence of low-sodium cryopreservation media (CPM) on the survival and development of frozen-thawed germinal vesicle (GV) stage and in vitro matured human oocytes.Design: Prospective experimental study.Setting: Academic hospital-based fertility center.Patient(s): Experimental groups: Oocytes cryopreserved at the GV (group A, n = 63 and group B, n = 64) or M II stage (group C, n = 62) With use Of conventional (group A) or low-sodium CPM (groups B and C). Control groups: Sibling GV stage oocytes subjected to in vitro maturation (IVM; control group A, n = 64; control group B, n = 64).Intervention(s): IVM, intracytoplasmic sperm injection and subsequent culture.Main Outcome Measure(s): Rates of survival, maturation, fertilization, and cleavage.Result(s): The postthaw survival was significantly lower in groups A (57.1%) and B (48.4%) compared to C (84.4%). In group A, maturation and cleavage rates were significantly lower, and fertilization rate was similar to controls (GVBD: 72.2% vs. 90.6%; progression to M II: 33.3% vs. 76.6%; cleavage: 42.9% vs. 88.2%; and fertilization: 58.3% vs. 69.4% in group A vs, control group A, respectively). There was no such difference in group B. In group C, despite a slight but significant lowering of the rate of 2 PN and an increase in that of 3 PN (2 PN: 47.4% vs. 70.2% and 3 PN: 15.8% vs. 3.2% in group C vs. total controls, respectively), embryonic cleavage per GV oocyte was significantly higher (25.8%) compared to group A (4.8%) but not to group B (15.6%). The rate of maturation and cleavage per surviving GV oocyte was significantly higher in group B than group A.Conclusion(s): Low-sodium-based CPM is beneficial for in vitro matured M II stage oocytes and is significantly better than the conventional sodium-based media for the GV stage oocytes. (Fertil Steril(R) 2000; 74:487-93. (C) 2000 by American Society for Reproductive Medicine.).