Literature DB >> 1761653

Premature chromosome condensation as a sign of oocyte immaturity.

J M Calafell1, J Badenas, J Egozcue, J Santaló.   

Abstract

In this work we report the possibility that oocyte immaturity is associated with premature chromosome condensation (PCC) after in-vitro fertilization (IVF). Using a murine model, we have related PCC and endoreduplicated-like oocytes to oocyte immaturity as a basis for a prognosis in oocyte immaturity problems. The cytogenetic analysis was performed in 511 embryos obtained from immature oocytes that were directly fertilized in vitro and in 1363 embryos obtained from immature oocytes that were matured in vitro with different concentrations of human chorionic gonadotrophin (HCG) added to the culture medium. As a control we used 507 embryos obtained from freshly ovulated oocytes. PCC at the G1-phase-(G1-PCC) was observed only when immature oocytes were immediately fertilized in vitro (45.4%) and PCC at the S-phase (S-PCC) only when using in-vitro matured oocytes with the highest HCG concentration (3.3%). Neither G1-PCC nor S-PCC were found in the control group. Endoreduplicated-like oocytes appeared in a significant percentage (27.3%) only in the immature group. Immature oocytes yielded a low fertilization rate (16.6%) while in-vitro maturation seemed to confer a higher fertilization capacity compared to the control group (90.1% versus 78.2%). The possible correlation between PCC and oocyte immaturity provides new prospects in the determination of human IVF failures of unknown origin. Thus, when a problem of oocyte immaturity is diagnosed through the presence of PCC, a special programme of in vitro oocyte maturation, such as a longer preincubation time or addition of hormones to the media, would be recommended.

Entities:  

Mesh:

Year:  1991        PMID: 1761653     DOI: 10.1093/oxfordjournals.humrep.a137452

Source DB:  PubMed          Journal:  Hum Reprod        ISSN: 0268-1161            Impact factor:   6.918


  6 in total

1.  Assessment of maximal fertilization rates with intracytoplasmic sperm injection.

Authors:  S Ma; B Ho Yuen
Journal:  J Assist Reprod Genet       Date:  2000-02       Impact factor: 3.412

2.  The genetic risks of in vitro fertilization techniques: the use of an animal model.

Authors:  J Santaló; J Badenas; J M Calafell; V Català; S Munné; J Egozcue; A M Estop
Journal:  J Assist Reprod Genet       Date:  1992-10       Impact factor: 3.412

3.  Factors associated with premature chromosome condensation (PCC) following in vitro fertilization.

Authors:  M I Tejada; M R Mendoza; B Corcóstegui; J A Benito
Journal:  J Assist Reprod Genet       Date:  1992-02       Impact factor: 3.412

4.  Fertilization, embryo quality, and cryosurvival in in vitro fertilization and intracytoplasmic sperm injection cycles.

Authors:  J M Moilanen; M Tulppala; I Reima; O Hovatta
Journal:  J Assist Reprod Genet       Date:  1999-01       Impact factor: 3.412

5.  Cytogenetic analysis of uncleaved oocytes after intracytoplasmic sperm injection.

Authors:  M Bergère; J Selva; M Volante; M Dumont; A Hazout; F Olivennes; R Frydman
Journal:  J Assist Reprod Genet       Date:  1995-05       Impact factor: 3.412

6.  Late fertilization of unfertilized human oocytes in in vitro fertilization and intracytoplasmic sperm injection cycles: conventional insemination versus ICSI.

Authors:  K S Park; H B Song; S S Chun
Journal:  J Assist Reprod Genet       Date:  2000-09       Impact factor: 3.412

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.