Da. Gook et al., FERTILIZATION OF HUMAN OOCYTES FOLLOWING CRYOPRESERVATION - NORMAL KARYOTYPES AND ABSENCE OF STRAY CHROMOSOMES, Human reproduction, 9(4), 1994, pp. 684-691
Survival folllowing cryopreservation of fresh and aged human oocytes b
y the propanediol (PROH) procedure was observed in 51 and 73% of oocyt
es respectively, immediately after thawing. This survival was reduced
in both types of oocytes at the time of insemination (3-4 h) to 41% in
fresh and 61% in aged oocytes. Insemination of the cryopreserved and
control oocytes with spermatozoa from one donor resulted in total fert
ilization rates similar to our in-vitro fertilization (IVF) rate for n
on-male factor patients. The normal fertilization rate for fresh cryop
reserved oocytes was slightly lower (46%) than the rate for IVF oocyte
s (59%) (P < 0.05), while the abnormal fertilization rates were not si
gnificantly different (16 and 15% respectively). In contrast, a reduct
ion in the normal fertilization rate was observed for the aged cryopre
served oocytes (13%) compared to the IVF rate (P < 0.001). Associated
with this was an increase in the abnormal fertilization rate for the a
ged cryopreserved oocytes, which was significantly higher (47%) than t
he IVF rate (15%) (P < 0.001). Significant differences in the total an
d normal fertilization rates were observed between cryopreserve oocyte
s obtained from cohorts with less than or equal to 27 (total: 84%, nor
mal: 68%) and > 27 oocytes (total: 55%, normal: 33%) (P < 0.05). Ferti
lized oocytes and oocytes with abnormal or absent spindles were examin
ed for chromosomal loss and no stray chromosomes were observed in any
of these cryopreserved oocytes (n = 137). In the cryopreserved oocytes
which had undergone normal fertilization, four scorable karyotypes we
re achieved and in all of these two sets of 23 chromosomes were observ
ed.