PMID- 9547685 OWN - NLM STAT- MEDLINE DCOM- 19980611 LR - 20190515 IS - 1058-0468 (Print) IS - 1573-7330 (Electronic) IS - 1058-0468 (Linking) VI - 15 IP - 3 DP - 1998 Mar TI - Chromosome 21 detection in human oocyte fluorescence in situ hybridization: possible effect of maternal age. PG - 105-10 AB - PURPOSE: The purpose of this study was to evaluate, among 100 uncleaved oocytes, the incidence of numerical and structural chromosome 21 and X abnormalities and to analyze the influence of various factors, such as in vitro (IVF) indications, follicle stimulation protocols, and women's age. METHODS: We investigated 150 uncleaved oocytes from 128 patients after an IVF attempt. After cytogenetic analysis (Giemsa) 100 oocytes (66%) were selected for fluorescence in situ hybridization (FISH). Fluorescent probes for human chromosomes X and 21 were used simultaneously according to standard procedures for their hybridization and detection. RESULTS AND CONCLUSIONS: We analyzed by the FISH protocol 100 metaphase II oocytes with 22 to 25 chromosomes. Our results demonstrate a high rate of disomy for chromosome 21 in human oocytes. Among them, eight were disomic (8%) and three were nullosomic (3%) for chromosome 21. Only one disomy of chromosome X was noted. The various indications of IVF and the different folliculogenesis stimulating protocols did not seem to influence the results but suggested a correlation between the maternal age and the aneuploidy rate of chromosome 21. FAU - Benzacken, B AU - Benzacken B AD - Service d'Histologie, Embryologie, Cytogenetique et Biologie de la Reproduction, Hopital Jean Verdier, Bondy, France. FAU - Martin-Pont, B AU - Martin-Pont B FAU - Bergere, M AU - Bergere M FAU - Hugues, J N AU - Hugues JN FAU - Wolf, J P AU - Wolf JP FAU - Selva, J AU - Selva J LA - eng PT - Journal Article PL - Netherlands TA - J Assist Reprod Genet JT - Journal of assisted reproduction and genetics JID - 9206495 RN - 0 (Fluorescent Dyes) SB - IM MH - Adult MH - Aneuploidy MH - Chromosome Aberrations/*pathology MH - Chromosome Disorders MH - *Chromosomes, Human, Pair 21 MH - Female MH - Fertilization in Vitro MH - Fluorescent Dyes MH - Humans MH - In Situ Hybridization, Fluorescence MH - Infertility, Female/pathology MH - Infertility, Male/pathology MH - Male MH - *Maternal Age MH - Metaphase MH - Oocytes/*ultrastructure MH - Ovarian Follicle/physiology MH - Pregnancy MH - Sex Chromosome Aberrations/*pathology MH - *X Chromosome PMC - PMC3454976 EDAT- 1998/04/21 00:00 MHDA- 1998/04/21 00:01 PMCR- 1999/03/01 CRDT- 1998/04/21 00:00 PHST- 1998/04/21 00:00 [pubmed] PHST- 1998/04/21 00:01 [medline] PHST- 1998/04/21 00:00 [entrez] PHST- 1999/03/01 00:00 [pmc-release] AID - 421880 [pii] AID - 10.1023/a:1023056502731 [doi] PST - ppublish SO - J Assist Reprod Genet. 1998 Mar;15(3):105-10. doi: 10.1023/a:1023056502731.