| Literature DB >> 24657075 |
Lodovico Parmegiani1, Carla Tatone2, Graciela Estela Cognigni3, Silvia Bernardi3, Enzo Troilo3, Alessandra Arnone3, Antonio Manuel Maccarini3, Giovanna Di Emidio2, Maurizio Vitti2, Marco Filicori3.
Abstract
Nowadays, human oocytes/embryos are cryopreserved via slow freezing or vitrification. The aim of this study was to evaluate a rapid warming protocol for slow-frozen human oocytes based on the standard warming procedure for vitrification. This was a prospective study on 216 sibling oocytes randomized for either conventional rapid thawing or rapid warming with vitrification warming solution. The primary endpoint was morphological assessment of survival at 2h. Surviving oocytes were divided into two subgroups: (i) parthenogenetically activated; and (ii) fixed and observed for spindle/chromosome configuration. Secondary endpoints were parthenogenetic development and spindle/metaphase configuration. Survival rate with rapid warming was higher (92/102, 90.2%) than with rapid thawing (85/114, 74.6%; P=0.005), and after 3d of culture the rapidly warmed parthenotes had more blastomeres compared with those rapidly thawed (P=0.042). Meiotic spindle and chromosomal configuration were not significantly influenced by rapid warming or rapid thawing. The finding of this study allows IVF centres to increase the efficiency of oocyte slow freezing, enabling survival rates comparable to vitrification protocols, and potentially to optimize costs by using the same warming protocol for both slow-frozen and vitrified reproductive cells.Entities:
Keywords: oocyte slow freezing; oocyte vitrification; parthenogenetic activation; rapid thawing; universal warming protocol; warming
Mesh:
Year: 2014 PMID: 24657075 DOI: 10.1016/j.rbmo.2014.01.015
Source DB: PubMed Journal: Reprod Biomed Online ISSN: 1472-6483 Impact factor: 3.828