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Human Reproduction, Vol. 18, No. 11, 2413-2419, November 2003
© 2003 European Society of Human Reproduction and Embryology

The effect of pronuclear morphology on early development and chromosomal abnormalities in cleavage-stage embryos

Pilar Gámiz1, Carmen Rubio1,3, M. José de los Santos1, Amparo Mercader1, Carlos Simón1,2, José Remohí1,2 and Antonio Pellicer1,2

1 Instituto Valenciano de Infertilidad (IVI), Plaza Policía Local, Valencia and 2 Department of Paediatrics, Obstetrics and Gynaecology, University of Valencia, Valencia, Spain

3 To whom correspondence should be addressed at: Instituto Valenciano de Infertilidad, Policía Local 3, 46015 Valencia, Spain. e-mail: c.rubio{at}ivi.es

BACKGROUND: Pronuclear (PN) zygote morphology has been proposed as a useful tool for selecting the best embryos for transfer. METHODS: PN morphology was recorded in 888 zygotes and classified according to similar/different PN size [groups A (n = 816) and B (n = 72)] and to the number, distribution and synchrony of nucleolar precursor bodies (NPB): subgroup I, pronuclei with 3–4 polarized NPB; subgroup II, 5–7 synchronic polarized NPB or 7–10 NPB distributed randomly; and subgroup III, morphologies other than those of groups I or II. Embryo development and chromosomal abnormalities were evaluated for each PN pattern. RESULTS: In patients aged <=37 years, the number of zygotes reaching morula and blastocyst stage was significantly (P = 0.0003) higher in group A than in group B. In group A, the incidence of chromosomal abnormalities was significantly (P = 0.0247) lower than in group B, and significant differences were observed when pattern AI was compared with pattern AII (P = 0.0280), AIII (P = 0.0024), BIII (P = 0.0077) and total B (P = 0.0247). In patients aged >37 years, statistical differences among groups were not observed. CONCLUSIONS: In patients aged <=37 years, zygotes with similar PN size and with polarized NPB present the best prognosis based on embryo development and the incidence of chromosomal abnormalities, whereas in patients aged >37 years, this correlation does not exist.

Key words: age/chromosomal abnormalities/ pronuclear morphology/nucleolar precursor bodies


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