Aneuploidy study in sperm and preimplantation embryos from nonmosaic 47,XYY men

Fertility and Sterility

Volumn 88, Issue 3, 2007, Pages 600-606

  Gonzalez Merino, Eric ^a   Hans, Christine ^a   Abramowicz, Marc ^a   Englert, Yvon ^a   Emiliani, Serena ^a  

^a ERASME HOSPITAL   (Belgium)

Author keywords

Early embryo; fluorescence in situ hybridization; preimplantation genetic diagnosis; sperm analysis; XYY

Indexed keywords

ADULT; ANEUPLOIDY; ARTICLE; BLASTOMERE; CASE REPORT; CHROMOSOME 13; CHROMOSOME 16; CHROMOSOME 18; CHROMOSOME 21; CHROMOSOME 22; CHROMOSOME STRUCTURE; DATA ANALYSIS; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; MALE; MALE FERTILITY; MALE INFERTILITY; OLIGOSPERMIA; OUTCOME ASSESSMENT; PREIMPLANTATION EMBRYO; PRIORITY JOURNAL; SEMEN ANALYSIS; SEX CHROMOSOME; SEX CHROMOSOME ABERRATION; SPERM; STATISTICAL SIGNIFICANCE; X CHROMOSOME; Y CHROMOSOME;

ADULT; ANEUPLOIDY; BLASTOCYST; FEMALE; FERTILIZATION IN VITRO; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; SEX CHROMOSOME ABERRATIONS; SPERMATOZOA;

EID: 34548473343     PISSN: 00150282     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.fertnstert.2006.12.020     Document Type: Article

References (36)

1. Hauschka T.S., Hasson J.E., Goldstein M.N., Koepf G.F., and Sandberg A.A. An XYY man with progeny indicating familial tendency to non-disjunction. Am J Hum Genet 14 (1962) 22-30
2. Chandley A.C., Fletcher J., and Robinson J.A. Normal meiosis in two 47,XYY men. Hum Genet 33 (1976) 231-240
3. Morel F., Roux C., and Bresson J.L. Sex chromosome aneuploidies in sperm of 47,XYY men. Arch Androl 43 (1999) 27-36
4. Thompson H., Melnyk J., and Hecht F. Reproduction and meiosis in XYY. Lancet (1967) 2:831
5. Martini E., Geraedts J.P., Liebaers I., Land J.A., Capitanio G.L., Ramaekers F.C., et al. Constitution of semen samples from XYY and XXY males as analysed by in-situ hybridization. Hum Reprod 11 (1996) 1638-1643
6. Blanco J., Rubio C., Simon C., Egozcue J., and Vidal F. Increased incidence of disomic sperm nuclei in a 47,XYY male assessed by fluorescent in situ hybridization (FISH). Hum Genet 99 (1997) 413-416
7. Mercier S., Morel F., Roux C., Clavequin M.C., and Bresson J.L. Analysis of the sex chromosomal equipment in spermatozoa of a 47,XYY male using two-colour fluorescence in-situ hybridization. Mol Hum Reprod 2 (1996) 485-488
8. Chevret E., Rousseaux S., Monteil M., Usson Y., Cozzi J., Pelletier R., et al. Meiotic behaviour of sex chromosomes investigated by three-colour FISH on 35,142 sperm nuclei from two 47,XYY males. Hum Genet 99 (1997) 407-412
9. Bielanska M., Tan S.L., and Ao A. Fluorescence in-situ hybridization of sex chromosomes in spermatozoa and spare preimplantation embryos of a Klinefelter 46,XY/47,XXY male. Hum Reprod 15 (2000) 440-444
10. Escudero T., Lee M., Carrel D., Blanco J., and Munne S. Analysis of chromosome abnormalities in sperm and embryos from two 45,XY,t(13;14)(q10;q10) carriers. Prenat Diagn 20 (2000) 599-602
11. Gianaroli L., Magli M.C., and Ferraretti A.P. Sperm and blastomere aneuploidy detection in reproductive genetics and medicine. J Histochem Cytochem 53 (2005) 261-267
12. Emiliani S., Gonzalez-Merino E., Van den Bergh M., Abramowicz M., Vassart G., Englert Y., et al. Re-analysis by fluorescence in situ hybridisation of spare embryos cultured until Day 5 after preimplantation genetic diagnosis for a 47, XYY infertile patient demonstrates a high incidence of diploid mosaic embryos: a case report. Prenat Diagn 20 (2000) 1063-1066
13. Van den Bergh M., Baszo I., Biramane J., Bertrand E., Devreker F., and Englert Y. Quality control in IVF with mouse bioassays: a four years' experience. J Assist Reprod Genet 13 (1996) 733-738
14. Coonen E., Harper J.C., Ramaekers F.C., Delhanty J.D., Hopman A.H., Geraedts J.P., et al. Presence of chromosomal mosaicism in abnormal preimplantation embryos detected by fluorescence in situ hybridisation. Hum Genet 94 (1994) 609-615
15. Staessen C., Van Assche E., Joris H., Bonduelle M., Vandervorst M., Liebaers I., et al. Clinical experience of sex determination by fluorescent in-situ hybridization for preimplantation genetic diagnosis. Mol Hum Reprod 5 (1999) 382-389
16. Gonzalez-Merino E., Emiliani S., Vassart G., Van den Bergh M., Vanin A.S., Abramowicz M., et al. Incidence of chromosomal mosaicism in human embryos at different developmental stages analyzed by fluorescence in situ hybridization. Genet Test 7 (2003) 85-95
17. Hopman A.H., Ramaekers F.C., Raap A.K., Beck J.L.M., Devilee P., van der Ploeg M., et al. In situ hybridization as a tool to study numerical chromosome aberrations in solid bladder tumors. Histochemistry 89 (1988) 307-316
18. Munné S., Marquez C., Magli C., Morton P., and Morrison L. Scoring criteria for preimplantation genetic diagnosis of numerical abnormalities for chromosomes X, Y, 13, 16, 18 and 21. Mol Hum Reprod 4 (1998) 863-870
19. Faed M., Robertson J., MacIntosh W.G., and Grieve J. Spermatogenesis in an infertile XYY man. Hum Genet 33 (1976) 341-347
20. Benet J., and Martin R.H. Sperm chromosome complements in a 47,XYY man. Hum Genet 78 (1988) 313-315
21. Solari A.J., and Rey Valzacchi G. The prevalence of a YY synaptonemal complex over XY synapsis in an XYY man with exclusive XYY spermatocytes. Chromosome Res 5 (1997) 467-474
22. Martin R.H., McInnes B., and Rademaker A.W. Analysis of aneuploidy for chromosomes 13, 21, X and Y by multicolour fluorescence in situ hybridisation (FISH) in a 47,XYY male. Zygote 7 (1999) 131-134
23. Giltay J.C., van Golde R.J., and Kastrop P.M. Analysis of spermatozoa from seven ICSI males with constitutional sex chromosomal abnormalities by fluorescent in situ hybridization. J Assist Reprod Genet 17 (2000) 151-155
24. Shi Q., and Martin R.H. Multicolor fluorescence in situ hybridization analysis of meiotic chromosome segregation in a 47,XYY male and a review of the literature. Am J Med Genet 93 (2000) 40-46
25. Rives N., Simeon N., Milazzo J.P., Barthelemy C., and Mace B. Meiotic segregation of sex chromosomes in mosaic and non-mosaic XYY males: case reports and review of the literature. Int J Androl 26 (2003) 242-249
26. Han T.H., Ford J.H., Flaherty S.P., Webb G.C., and Matthews C.D. A fluorescent in situ hybridization analysis of the chromosome constitution of ejaculated sperm in a 47,XYY male. Clin Genet 45 (1994) 67-70
27. Petit F.M., Frydman N., Benkhalifa M., Le Du A., Aboura A., Fanchin R., et al. Could sperm aneuploidy rate determination be used as a predictive test before intracytoplasmic sperm injection?. J Androl 26 (2005) 235-241
28. Pang M.G., Hoegerman S.F., Cuticchia A.J., Moon S.Y., Doncel G.F., Acosta A.A., et al. Detection of aneuploidy for chromosomes 4, 6, 7, 8, 9, 10, 11, 12, 13, 17, 18, 21, X and Y by fluorescence in-situ hybridization in spermatozoa from nine patients oligoasthenoteratospermia undergoing intracytoplasmic sperm injection. Hum Reprod 14 (1999) 1266-1273
29. Pfeffer J., Pang M.G., Hoegerman S.F., Osgood C.J., Stacey M.W., Mayer J., et al. Aneuploidy frequencies in semen fractions from ten oligoasthenoteratospermic patients donating sperm for intracytoplasmic sperm injection. Fertil Steril 72 (1999) 472-478
30. Martin R.H., Rademaker A.W., Greene C., Ko E., Hoang T., Barclay L., et al. A comparison of the frequency of sperm chromosome abnormalities in men with mild, moderate, and severe oligozoospermia. Biol Reprod 69 (2003) 535-539
31. Pang M.G., Kim Y.J., Lee S.H., and Kim C.K. The high incidence of meiotic errors increases with decreased sperm count in severe male factor infertilities. Hum Reprod 20 (2005) 1688-1694
32. Gianaroli L., Magli M.C., Cavallini G., Crippa A., Nadalini M., Bernardini L., et al. Frequency of aneuploidy in sperm from patients with extremely severe male factor infertility. Hum Reprod 20 (2005) 2140-2152
33. Miharu N., Best R.G., and Young S.R. Numerical chromosome abnormalities in spermatozoa of fertile and infertile men detected by fluorescence in-situ hybridization. Hum Genet 93 (1994) 502-506
34. Samura O., Miharu N., He H., Okamoto E., and Ohama K. Assessment of sex chromosome ratio and aneuploidy rate in motile spermatozoa selected by three different methods. Hum Reprod 12 (1997) 2437-2442
35. Staessen C., Coonen E., Van Assche E., Tournaye H., Joris H., Devroey P., et al. Preimplantation diagnosis for X and Y normality in embryos from three Klinefelter patients. Hum Reprod 11 (1996) 1650-1653
36. Reubinoff B.E., Abeliovich D., Werner M., Schenker J.G., Safran A., and Lewin A. A birth in non-mosaic Klinefelter's syndrome after testicular fine needle aspiration, intracytoplasmic sperm injection and preimplantation genetic diagnosis. Hum Reprod 13 (1998) 1887-1892