Nuclear status and cytogenetics of embryos derived from in vitro-matured oocytes

Citation
D. Nogueira et al., Nuclear status and cytogenetics of embryos derived from in vitro-matured oocytes, FERT STERIL, 74(2), 2000, pp. 295-298
Citations number
4
Categorie Soggetti
Reproductive Medicine","da verificare
Journal title
FERTILITY AND STERILITY
ISSN journal
00150282 → ACNP
Volume
74
Issue
2
Year of publication
2000
Pages
295 - 298
Database
ISI
SICI code
0015-0282(200008)74:2<295:NSACOE>2.0.ZU;2-B
Abstract
Objective: To analyze embryos after in vitro maturation by investigating th eir nuclear status and cytogenetic constitution. Design: Prospective randomized laboratory study. Setting: Reproductive medicine unit in an academic hospital. Patient(s): Patients with male and tubal factor infertility undergoing fert ility treatment. Intervention(s): Denuded immature oocytes (n = 75) were matured in vitro fo r 24-30 hours, and intracytoplasmic sperm injection was performed 30 hours after oocyte retrieval. Fluorescence in situ hybridization was performed on the produced embryos. Main Outcome Measure(s): Blastomere content of the total embryo. Result(s): The in vitro-matured oocytes showed a similar fertilization rate as the in vivo-matured oocytes, but with a higher incidence of noncleavage (21.0%). In addition, 26.7% of these embryos arrested at the first mitotic division. Thirty embryos were processed for fluorescence in situ hybridiza tion; only 6.7% had all mononuclear blastomeres, 30.0% had at least one bin uclear blastomere, 43.3% had at least one multinuclear blastomere, and 56.6 % contained anuclear cells. The chromosomal constitution was analyzed in 14 embryos, and chromosomal anomalies were found in 11 (78.5%). Conclusion(s): Germinal vesicle oocytes retrieved from superovulated patien ts and cultured in vitro for a short time had the ability to resume meiosis and achieve fertilization. However, arrest of embryo development was commo n. These embryos showed a high incidence of multinuclear blastomeres and an euploidy, suggesting abnormal cytokinesis or genetic abnormalities. (C) 200 0 by American Society for Reproductive Medicine.