Jm. Clyde et al., Demonstration of a mechanism of aneuploidy in human oocytes using Multifluor fluorescence in situ hybridization, FERT STERIL, 76(4), 2001, pp. 837-840
Objective: To evaluate the potential of Multifluor fluorescence in situ hyb
ridization (M-FISH) for karyotyping the human oocyte and first polar body.
Design: Prospective case study.
Setting: Research laboratories, university hospital.
Patient(s): A 33-year-old woman with polycystic ovary syndrome who was unde
rgoing ovarian stimulation and ICSI.
Main Outcome Measure(s): Karyotyping of all chromosomes within an oocyte an
d first polar body, using GV stage oocytes matured to metaphase II in vitro
.
Result(s): Oocyte hyperploidy was diagnosed by M-FISH to be 23, X + 15 cht
+ 19 cht +22 cht. The corresponding polar body was hypoploid, with a karyot
ype of 23, X - 15 cht - 19 cht -22 cht. Ms was due to unbalanced predivisio
n at meiosis I. Reprobing confirmed karyotype assignments for chromosomes X
, 13, 18, and 21.
Conclusion(s): The mechanism involved in maternally derived aneuploidy can
be defined by using M-FISH to simultaneously karyotype both oocyte and firs
t polar body chromosomes at metaphase II. Multifluor FISH may be useful for
investigative studies of maternally derived aneuploidy, which is a major c
ause of preimplantation waste in natural and assisted reproduction. (Fertil
Steril(R) 2001;76:837-40. (C) 2001 by American Society for Reproductive Me
dicine.).