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首页> 外文期刊>American Journal of BioScience >Healthy Monozygotic Twins Born from a Vitrified Blastocyst Derived from a Vitrified Oocyte, and a Highly Efficient Vitrification for Freezing Human Oocytes and Blastsocysts
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Healthy Monozygotic Twins Born from a Vitrified Blastocyst Derived from a Vitrified Oocyte, and a Highly Efficient Vitrification for Freezing Human Oocytes and Blastsocysts

机译:从衍生自玻璃卵母细胞的玻璃状胚泡中出生的健康单卵锥双胞胎,以及用于冷冻人卵母细胞和囊细胞的高效玻璃化

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We used simplified oocyte/embryo vitrification and warming protocols (Irvine Scientific) combined with vitristraws (SciTech Invention) to freeze and thaw human oocytes and blastsocysts. Throughout the year of 2014, twelve recipients were transferred embryos developed from vitrified donor oocytes, and fourteen recipients were transferred embryos developed from fresh donor oocytes at the North Carolina center for reproductive medicine (NCCRM). There were no statistically significant differences in donor age (25.9 3.6 vs 24.9 3.2) and recipient age (43.0 5.4 vs 41.4 6.8), fertilization rates (86.2% vs 87.0%), blastocyst development rates (50.0% vs 53.8%), number of embryo transferred (1.7 0.8 vs 1.9 0.4), clinical pregnancy rates per transfer (75.0% vs 71.4%) and live birth rates per transfer (66.7% vs 57.1%) between vitrified and fresh oocyte cycles, respectively. The results demonstrate that vitrification techniques can be used to cryopreserve human oocytes for future use. We are also reporting the live birth of healthy monozygotic twins resulted from a re-vitrified blastocyst derived from a vitrified oocyte. Oocytes from a 30-year-old donor were vitrified in vitristraws. Seven out of eight oocytes survived after thawing on November 16, 2013. Those seven oocytes were inseminated by intracytoplasmic sperm injection (ICSI) at about 2 hours post thawing. All seven oocytes were tested as fertilized by pronuclear check at 18 hours after ICSI. Those fertilized oocytes showed normal cleavage on day 2 and day 3. Four of them developed to blastsocysts by culturing in continuous single culture medium in a tri-gas incubator for 5 days. Two blastsocysts were transferred to a 43-year-old recipient, but that did not result in a pregnancy. The other two blastsocysts were re-vitrified in a vitristraw. The re-vitrified blastsocysts were thawed and then transferred to the same recipient on May 8, 2014. The patient achieved a normal pregnancy on her second transfer. On June 14, 2014, an ultrasound scan detected two heartbeats in one gestational sac. Two healthy monozygotic boys (weighing 2466g and 2353g) were born on January 13, 2015. To our knowledge, this is the first report of monozygotic twins born from an embryo by twice vitrification at oocyte and blastocyst stage.
机译:我们使用简化的卵母细胞/胚胎玻璃化和升温方案(Irvine Scientific)与Vitriristraws(Scitech发明)结合冻结和解冻的人卵母细胞和囊胚。整个2014年,十二名受者被转移从玻璃供体卵母细胞产生的胚胎,并在北卡罗来纳州生殖医学中心(NCCRM)的新鲜供体卵母细胞中产生了14个受体。捐助年龄没有统计学意义(25.9 3.6 vs 24.9 3.2)和受体年龄(43.0 5.4 vs 41.4 6.8),施肥率(86.2%vs 87.0%),胚泡发展率(50.0%vs 53.8%),数量胚胎转移(1.7 0.8 Vs 1.9 0.4),每次转移临床妊娠率(75.0%vs 71.4%)和诸如玻璃化和新鲜卵母细胞循环之间的每转移(66.7%vs 57.1%)的活率。结果表明,玻璃化技术可用于冷冻保存人卵母细胞以供将来使用。我们还报告了来自衍生自玻璃卵母细胞的重新玻璃胚泡产生的健康单卵锥双胞胎的活诞生。来自30岁的供体的卵母细胞在蒸料玻璃之下玻璃化。在2013年11月16日之后解冻后,七种卵母细胞中的七个幸存下来。在解冻后约2小时内,这些七个卵母细胞受到脊髓内膜精子注射(ICSI)的潜行。在ICSI后18小时后,所有七个卵母细胞都被称为经核检查所施肥。这些受精卵母细胞在第2天和第3天显示正常的裂解3.通过在三气培养箱中培养在三气体培养箱中培养5天,它们为囊细胞培养。两种囊状腺转移到43岁的受体,但这并没有导致怀孕。另外两个囊体在蒸料渣中重新玻璃化。再玻璃囊细胞被解冻然后于2014年5月8日转移到同一受体中。患者对她的第二次转移达到正常妊娠。 2014年6月14日,超声扫描在一个妊娠囊中检测到两个心跳。两个健康的单一男孩(体重2466G和2353G)于2015年1月13日出生。对于我们的知识,这是从卵母细胞和胚泡阶段的两次玻璃化从胚胎中出生的单吞咽双胞胎的第一报告。

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