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利用废弃胚胎进行体外受精实验室质控的可行性探讨 被引量:3

Feasibility of discarded embryos as a quality control in the IVF laboratory
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摘要 目的探讨废弃胚胎作为体外受精(IVF)实验室质控的可行性。方法通过囊胚序贯培养将无原核(0PN)、单原核(1PN)、3原核(3PN)和发育迟缓或停滞的2原核(2PN)的废弃胚胎进行囊胚培养,比较不同来源胚胎的囊胚形成情况。结果共收集396个废弃胚胎,经序贯培养形成98个囊胚(24.75%),0PN、2PN、1PN、3PN的囊胚形成率分别为50.50%(51/101)、24.59%(30/122)、1 7.07%(7/41)、7.58%(10/132),其中0PN、停滞的2PN的胚胎有孵出,孵出率分别为47.06%(24/51)和33.33%(10/30);有囊胚形成与无囊胚形成患者的临床妊娠率分别为30.28%(43/142)、1 9.72%(28/142),两者相比有统计学差异(P<0.05);特别是0PN+2PN患者的临床妊娠率为23.24%(33/142),显著高于无囊胚形成者的9.15%(13/142)(P<0.01)。结论废弃胚胎有不同程度的发育潜能,可部分发育成囊胚,特别是0PN+2PN囊胚形成率超过35%,可以作为IVF实验室质控的一种辅助方法,并可作为临床妊娠结局预测的参考指标。 Objective: To study the feasibility of discarded embryos as a quality control in the IVF laboratory. Methods: The embryos from 0PN, IPN, and 2PN were cultured in microdrops of sequenced medium and observed daily from Day 3 to Day 6. Results. A total of 396 abandoned embryos were cultured. Ninety eight blastocysts were formed from Day 4 to Day 6 and the blastocyst rate was 24.75%. The blastocyst formation rate from 0PN, 1PN, 2PN, 3PN was 50.5%(51/101), 24.59%(30/122), 17.07%(7/41)and 7.58%(10/132), respectively. The zy- gote with 2PN and 0PN could develope to embryos. The hatch rate was 30%(10/30)and 47.06%(24/51), respectively. The clinical pregnancy rate of the women with blastosphere formed was 30.98% (43/142), which was significantly higher than those without blastosphere formed(19.71%, 28/142)(P〈0.05). The clinical pregnancy rate of the women with 0PN and 2PN was 23.24% (33/142), which was significantly higher than those without formation of blastosphere(9.15%, 13/142)(P%0.01). Conclusions: The discarded embryos have different development potential. They can develop into blas- tospheres. The blastosphere formation rate of 0PN and 2PN can be more than 35 %. It can be used as a quality control for IVF laboratory and a predictor for clinical pregnancy outcome.
出处 《生殖医学杂志》 CAS 2013年第2期97-100,共4页 Journal of Reproductive Medicine
关键词 废弃胚胎 囊胚 异常受精 质量控制 Discarded embryos Blastocyst Abnormal infertility Quality control
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参考文献11

  • 1LerouPH, Yabuuehi A, Huo H, et al. Derivation and maintenance of human embryonic stem cells from poor-quality in vitro fertilization embryos [J]. Nat Protoc, 2008, 3: 923-933.
  • 2甄璟然,王雪,孙正怡,郁琦,邓成艳,周远征,何方方.人类低质量卵裂期胚胎体外发育至囊胚能力的研究[J].生殖医学杂志,2011,20(4):253-256. 被引量:7
  • 3温烯,李蓉,郝桂琴,杨伟洪,肖宇.低质量人类胚胎体外发育至囊胚能力的研究[J].现代妇产科进展,2010,19(4):286-288. 被引量:9
  • 4Brinsden PR. A textbook of in vitro fertilization and assisted reproduction[S]. Third edition. New York: The Parthenon Publishing Group Inc, 1999: 196.
  • 5Gardner DK, Lane M, Stevens J, et al. Blastocyst score affects implantation and pregnancy outcome: towards a single blastocyst transfer[J]. Fertil Steril, 2000, 73:1155-1158.
  • 6Chen H, Qian K, Hu J, et aI. The derivation of twoadditional human embryonic stem cell lines from day 3 embryos with low morphological seores[J]. Hum Reprod, 2005,20 : 2201-2206.
  • 7Shapiro BS, Harris DC, Richter KS, et al. Predictive value of 72-hour blastomere cell number on blastocyst development and success of subsequent transfer based on the degree of blastocyst development[J]. Fertil Steril, 2000,73 : 582-586.
  • 8Langley MT, Marek DM, Gardner DK, et al. Extended embryo culture in human assisted reproduction treatments [J]. HumReprod, 2001,16:902 908.
  • 9梁菊艳,王芳,孙莹璞,孔慧娟,金海霞,宋文妍,苏迎春,郭艺红.废弃胚胎继续囊胚培养研究[J].生殖与避孕,2008,28(10):598-601. 被引量:31
  • 10Sell E, Vergouw CG, Morita H, et al. Noninvasive metabolomic profiling as an adiunct to morphology for noninvasive embryo assessment in women undergoing single embryo transfer[J]. Ferfil Steril, 2010,94 : 535-542.

二级参考文献41

  • 1Mitalipova M, Calhoun J, Shin S, et al. Human embryonic stem cell lines derived from discarded embryos. Stem Cells, 2003, 21(5):521-6.
  • 2Suss-Toby E, Gerecht-Nir S, Amit M, et al. Derivation of a diploid human embryonic stem cell line from a mononuclear zygote. Hum Reprod, 2004, 19(3):670-5.
  • 3Lerou PH, Yabuuchi A, Huo H, et al. Derivation and maintenance of human embryonic stem cells from poorquality in vitro fertilization embryos. Nat Protoc, 2008, 3(5): 923-33.
  • 4Brinsden PR. A textbook of in vitro fertilization and assisted reproduction. New York: The Parthenon Publishing Group Inc, 1999:196.
  • 5Gardner DK, Lane M, Stevens J, et al. Blastocyst score affects implantation and pregnancy outcome :to wards a single blastocyst transfer. Fertil Steril, 2000, 73(6): 1 155-8.
  • 6Feng H, Hershlag A.Fertilization abnormalities following human in vitro fertilization and intracytoplasmic sperm injection. Microsc Res Tech, 2003, 61(4):358-61.
  • 7Racowsky C, Combelles CM, Nureddin A, et al. Day 3 and day 5 morphological predictors of embryo viability. Reprod Biomed Online, 2003, 6(3):323-31.
  • 8Alikani M, Calderon G, Tomikin G, et al. Cleavage anomalies in early human embryos and survival after prolonged culture in vitro. Hum Reprod, 2000, 15(12):2 634-43.
  • 9Neuber E, Rinaudo P, Trimarchi JR, et al. Sequential assessment of individually cultured human embyros as an indicator of subsequent good quality blastocyst development. Hum Reprod, 2003, 18(6):1 307-12.
  • 10Racowsky C, Katharine V, Jackson KV, et al. The number of eight-cell embryos is a key determinant for selecting day 3 or day 5 transfer. Fertil Steril, 2000, 73(3):558-64.

共引文献39

同被引文献48

  • 1Gardner DK, Lane M, Stevens J, et al. Noninvasive assessment of hu- man embryo nutrient consumption as a measure of developmental po- tential[ J]. Fertil Steri1,2001,76 ( 6 ) : 1175 - 1180.
  • 2Jones GM, Trounson AO, Vella PJ, et al. Glucose metabolism of hu- man mornla and blastocyst-stage embryos and its relationship to via- bility after transfer [ J ]. Reprod Biomed Online, 2001,3 2 ) : 124 - 132.
  • 3Houghton FD, Hawkhead JA, Humpherson PG, et al. Non-invasive a- mino acid turnover predicts human embryo developmental capacity [ J ]. Hum Reprod ,2002,17 (4) :999 - 1005.
  • 4Hardy K, Stark J, Winston RM. Maintenance of the inner cell mass in human blastocysts from fragmented embryos [ J ]. Biol Reprod, 2003, 68(4) :1165 - 1169.
  • 5Eftekhari-Yazdi P, Valojerdi MR, Ashtiani SK, et al. Effect of frag- ment removal on blastocyst formation and quality of human embryos [ J ]. Reprod Biomed Online, 2006,13 (6) :823 - 832.
  • 6Antczak M, Van BJ. Temporal and spatial aspects of fragmentation in early human embryos : possible effects on developmental competence and association with the differential elimination of regulatory proteins from polarized domains [ J ]. Hum Reprod, 1999,14 ( 2 ) :429 - 447.
  • 7Magli MC, Gianaroli L, Ferraretti AP, et al. Embryo morphology and development are dependent on the chromosomal complement [ J ]. Fer- til Steri1,2007,87 (3) :534 - 541.
  • 8Wang F, Kong H J, Karl QC, et al. Analysis of blastocyst culture of dis- carded embryos and its significance for establishing human embryonic stem cell lines [ J ]. J Cell Biochem,2012,113 ( 12 ) :3835 - 3842.
  • 9Racowsky C,Jaekson KV, Cekleniak NA,et al. The number of eight-cell embryos is a key determinant for selecting day 3 or day 5 transfer[J]. Fer- til Steril,2000,73(3) :558-564.
  • 10Luna M, Copperman AB, Duke M, et al. Human blastocyst morphologi- cal quality is significantly improved in embryos classified as fast on day 3 ( ≥10 cells), bringing into question current embryological dog- ma[ J ]. Fertil Steril,2008,89 (2) :358 - 363.

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