Incidence of chromosome 8, 10, X and Y aneuploidies in sperm nucleus of infertile men detected by FISH

Urologia Internationalis

Volumn 64, Issue 4, 2000, Pages 202-208

  Acar, Hasan ^a,b   Kilinç, Mehmet ^a   Çora, Tülin ^a   Aktan, Murat ^a   Taşkapu, Hakan ^a  

^a SELCUK UNIVERSITY   (Turkey)

^b UNIVERSITY OF MINNESOTA   (United States)

Author keywords

Aneuploidy; FISH; Infertility; Sperm

Indexed keywords

ANEUPLOIDY; ARTICLE; CHROMOSOME 10; CHROMOSOME 8; CONTROLLED STUDY; CYTOGENETICS; DISOMY; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; MALE; MALE INFERTILITY; PRIORITY JOURNAL; X CHROMOSOME; Y CHROMOSOME;

EID: 0033940448     PISSN: 00421138     EISSN: None     Source Type: Journal    
DOI: 10.1159/000030531     Document Type: Article

References (40)

1. Hecht F, Hecht BK: Aneuploidy in humans: Dimensions, demongraphy and danger abnormal numbers of chromosomes; in Sandberg AA (ed): Aneuploidy. A Incidence and Etiology. New York, Liss, 1987, pp 9-49.
2. Whiteman DAH, Klinger K: Efficacy of rapid in situ hybridization methods for prenatal diagnosis of chromosome abnormalities causing birth defect. Am J Hum Genet 1995; 49(suppl).
3. Jacobs PA: The chromosomal complement of human gametes; in Milligan SR (ed): Oxford Review of Reproductive Biology, New York, Oxford University Press, 1992, vol 14, pp 47-72.
4. Rudak E, Jacobs PA, Yanagimachi R: Direct analysis of the chromosome constitution of human spermatozoa. Nature 1978;274:911-913.
5. Pellestor F: Frequency and distribution of aneuploidy in human female gametes. Hum Genet 1991;86:283-288.
6. Martin RH, Ko E, Rademarker A: Distribution of aneuploidy in human gametes: Comparison between human sperm and oocytes. Am J Med Genet 1991;39:321-331.
7. Kruger TF, Menkveld V, Stander FSH, Lonbanrt CF, Vander Werve Van YIJ, Smith K: Sperm morphologie features as a prognostic factor in in vitro fertilization. Fert Steril 1986; 4:1118-1122.
8. Griffin D, Abruzzo M, Millie EA, Sheean LA, Feingold E, Sherman SL, Hassold TJ: Non-disjunction in human sperm: Evidence for an effect of increasing age. Hum Mol Genet 1995; 4:2227-2232.
9. Dauwerse JG, Weigant J, Raap AK, Breuning MH, Van Ommen GJB: Multiple colour by fluorescence in situ using ratio-labeled DNA probes create a molecular karyotype, Hum Mol Gen 1992;1:593-598.
10. Acar H, Acar A: Application of the multicolour FISH to interphase nuclei and metaphase spreads for simultaneous examination of monosomy 7 and trisomies 8 and 11 in acute myelocytic leukaemia (AML). Clin Lab Haematol 1997;19:33-38.
11. Chevret E, Rousseaux S, Monteil M, Usson Y, Cozzi J, Pelletier R, Sele B: Increase incidence of hyperhaploid 24,XY spermatozoa detected by three-color FISH in a 46,XY/47,XXY male. Hum Genet 1996;96:171-175.
12. Lu PY, Hammitt DG, Zinsmeister AR, Dewald GW: Dual color fluorescence in situ hybridization to investigate aneuploidy in sperm from 36 normal males and a men with a t(2;4:8)(q23;q27;p21). Fertil Steril 1994;62: 394-399.
13. Rousseaux S, Chevret E, Monteil M, Cozzi J, Pelletier R, Delafontaine D, Sele B: Sperm nuclei analysis of a Robertsonian t(14q21q) carrier, by FISH, using three plasmids and two YAC probes. Hum Genet 1995;96:655-660.
14. Mercier S, Morel F, Fellman F, Roux C, Bresson JL: Molecular analysis of the chromosomal equipment in spermatozoa of a 46,XY, t(7;8)(q11.21;cen) carrier by using fluorescence in situ hybridization. Hum Genet 1995;102: 446-451.
15. Martini E, von Bergh AR, Coonen E, de Die-Smulders CE, Hopman AH, Ramaekers FC, Geraedts JP: Detection of structural abnormalities in spermatozoa of a translocation carrier t(3;11)(q27.3;q24.3) by triple FISH. Hum Genet 1995;102:157-165.
16. Colls P, Martinez-Pasarell O, Perez MM, Egozcue J, Templado C: Sperm chromosome analysis in the father of a child with a de-novo reciprocal translocation t(11;15)(q12;q22) by G-banding and fluorescence in-situ hybridization. Hum Reprod 1998;13:60-64.
17. Martin RH, Spriggs E, Ko E, Rademaker AW: The relationship between paternal age, sex ratios, and aneuploidy frequencies in human sperm, as assessed by multicolor FISH. Am J Hum Genet 1995;57:1395-1399.
18. Robbins WA, Baulch JE, Moore D, Weier HU, Blakey D, Wyrobek AJ: Three-probe fluorescence in situ hybridization to assess chromosome X, Y, and 8 aneuploidy in sperm of 14 men from two healthy groups: Evidence for a paternal age effect on sperm aneuploidy. Reprod Fertil Dev 1995;7:799-809.
19. Kinakin B, Rademaker A, Martin R: Paternal age effect of YY aneuploidy in human sperm, as assessed by fluorescence in situ hybridization. Cytogenet Cell Genet 1997;78:116-1 19.
20. McInnes B, Rademarker A, Martin R: Donor age and the frequency of disomy for chromosomes 1, 13, 21 and structural abnormalities in human spermatozoa using multicolour fluorescence in situ hybridization. Hum Reprod 1998; 13:2494-2498.
21. Wyrobek AJ, Rubes J, Cassel M: Smokers produced more aneuploid sperm than non-smokers. Am J Hum Gen 1995;57:A131.
22. Rubes J, Lowe X, Moore D, Perrenault S, Slott V, Evenson D, Selevan SG, Wyrobek AJ: Smoking cigarettes is associated with increased sperm disomy in teenage men. Fert Steril 1998; 70:715-723.
23. William BJ, Ballenger CA, Malter HE, Bishop F, Tucker M, Zwingman TA, Hassold TJ: Non-disjunction in human sperm: Results of fluorescence in situ hybridization studies using two and three probes. Hum Mol Genet 1993;2: 1929-1936.
24. Bischoff FZ, Nguyen DD, Burt KJ, Shaffer LG: Estimates of aneuploidy using multicolor fluorescence in situ hybridization on human sperm. Cytogenet Cell Genet 1994;66:237-243.
25. Blanco J, Egozcue J, Vidai F: Incidence of chromosome 21 disomy in human spermatozoa as determined by fluorescent in situ hybridization. Hum Reprod 1996;11:722-726.
26. Spriggs EL, Rademaker AW, Martin RH: Aneuploidy in human sperm: the use of multicolor FISH to test various theories of nondisjunction. Am J Hum Genet 1996;58:356-362.
27. Martin RH, Spriggs E, Rademaker AW: Multicolor fluorescence in situ hybridization analysis of aneuploidy and diploidy frequencies in 225,846 sperm from 10 normal men. Biol Reprod 1996;54:394-398.
28. Spriggs EL, Rademark AW, Martin RH: Aneuploidy in human sperm: results of two- and three-color fluorescence in situ hybridization using centromeric probes for chromosomes 1, 12, 15, 18, X and Y, Cytogenet Cell Genet 1995;71:47-53.
29. Miharu N, Best RG, Young SR: Numerical chromosome abnormalities in spermatozoa of fertile and infertile men detected by fluorescence in situ hybridization. Hum Genet 1994; 93:502-506.
30. Guttenbach M, Expositio JM, Michelmann H, Engel W, Schmid M: Incidence of diploid and disomic sperm nuclei in 45 infertile men. Hum Reprod 1997;12:468-473.
31. Moosoni N, Pattinso HA, Carter MD, Cox DM, Rademarker AW, Martin RH: Chromosomal analysis of sperm from men with idiopathic infertility using karyotypingand fluorescence in situ hybridization. Fertil Steril 1995; 64:811-817.
32. Martin RH: The risk of chromosomal abnormalities following ICSI. Hum Reprod 1996;11: 924-925.
33. Lahdetie J, Saari N, Saari MA, Mykkanen J: Incidence of aneuploid spermatozoa among infertile men studied by multicolor fluorescence in situ hybridization. Am J Med Gen 1997;71: 115-121.
34. Bernardini L, Martini E, Geraedts J, Hopman AHN, Lanteri S, Cont N, Capitani GL: Comparison of gonosomal aneuploidy in spermatozoa of normal fertile men and those with severe male factor detected by in-situ hybridization. Mol Hum Reprod 1997;3:341-438.
35. McInnes B, Rademark A, Greene CA, Ko E, Barclay L, Martin RH: Abnormalities for chromosome 13 and 21 detected in spermatozoa from infertile men. Hum Reprod 1998;13: 2787-2790.
36. Griffin DK, Abruzzo MA, Millie EA, Feingold E, Hassold TJ: Sex ratio in normal and disomic sperm: Evidence that the extra chromosome 21 preferentially segregates with the Y chromosome. Am J Hum Genet 1996;59:1108-1113.
37. Hixon M, Millie E, Judis LA, Sherman S, Allran K, Taft L, Hassold T: FISH studies of the sperm of fathers of paternally derived cases of trisomy 21: No evidence for an increase in aneuploidy. Hum Genet 1998;103:654-657.
38. Pellestor MF, Girardet A, Coignet L, Andreo B, Charlieu JP: Assessment of aneuploidy for chromosomes 8, 9, 13, 16, and 21 in human sperm by using prime in situ labeling technique. Am J Hum Genet 1996;58:797-802.
39. Acar H, Connor MJ: Detection of trisomy 12 and centrometric alterations in CLL by interphase- and metaphase-FISH. Cancer Genet Cytogenet 1998;100:148-151.
40. Cora T, Acar H, Oran B: A partial trisomy 15q due to 15:17 translocation detected by converntional cytogenetic and FISH techniques. Genet Counsel 2000;11:25-32.