Aneuploidy study of human oocytes first polar body comparative genomic hybridization and metaphase II fluorescence in situ hybridization analysis

Human Reproduction

Volumn 19, Issue 12, 2004, Pages 2859-2868

  Gutiérrez Mateo, Cristina ^a   Benet, J ^a   Wells, D ^b   Colls, P ^c   Bermudez M G ^b   Sanchez Garcia J F ^a   Egozcue, J ^a   Navarro, Joaquinia ^a   Munne S ^b,c  

^a UNIVERSITAT AUTÒNOMA DE BARCELONA   (Spain)

^b SAINT BARNABAS MEDICAL CENTER   (United States)

^c Reprogenetics LLC   (United States)

Author keywords

Aneuploidy; CGH; First polar body; FISH; Oocyte

Indexed keywords

ADULT; ANEUPLOIDY; ARTICLE; CELL POLARITY; CHI SQUARE TEST; CHROMATID ABERRATION; CHROMOSOME 1; CHROMOSOME 13; CHROMOSOME 16; CHROMOSOME 22; CHROMOSOME 4; CHROMOSOME ANALYSIS; CHROMOSOME SIZE; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; DIAGNOSTIC ERROR; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; METAPHASE; NUMERICAL CHROMOSOME ABERRATION; OOCYTE; PATHOGENESIS; SCORING SYSTEM;

EID: 11144301234     PISSN: 02681161     EISSN: None     Source Type: Journal    
DOI: 10.1093/humrep/deh515     Document Type: Article

References (55)

1. Anahory T, Andréo B, Régnier-Vigouroux G, Soulie JP, Baudouin M, Demaille J and Pellestor F (2003) Sequential multiple probe fluorescence in-situ hybridization analysis of human oocytes and polar bodies by combining centromeric labelling and whole chromosome painting. Mol Hum Reprod 9,577-585.
2. Angell R (1997) First-meiotic-division nondisjunction in human oocytes. Am J Hum Genet 61,23-32.
3. Angell RR, Xian J and Keith J (1993) Chromosome anormalities in human oocytes in relation to age. Hum Reprod 8,1047-1054.
4. Bahçe M, Cohen J and Munné S (1999) Preimplantation genetic diagnosis of aneuploidy: were we looking at the wrong chromosomes? J Assist Reprod Genet 16,176-181.
5. Bartmann A, Romao G, Ramos E and Ferriani R (2004) Why do older women have poor implantation rates? A possible role of the mitochondria. J Assist Reprod Genet 21,79-83.
6. Benkhalifa M, Menezo Y, Yanny L, Pouly J and Qumsiyeh M (1996) Cytogenetics of uncleaved oocytes and arrested zygotes in IVF programs. J Assist Reprod Genet 13,140-148.
7. Boiso I, Márquez C, Veiga A and Munné S (1997) Cytogenetic and fluorescent in situ hybridization analysis of in vitro matured human oocytes. Assist Reprod Rev 7,160-164.
8. Boué A, Boué J and Gropp, A (1985) Cytogenetics of pregnancy wastage. Adv Hum Genet 14,1-57.
9. Clyde JM, Hogg JE, Rutherford AJ and Pincton HM (2003) Karyotyping of human metaphase II oocytes by Multifluor fluorescence in situ hybridization. Fertil Steril 80,1003-1011.
10. Cupisti S, Conn CM, Fragouli E, Whalley K, Mills JA, Faed MJW and Delhanty JDA (2003) Sequential FISH analysis of oocytes and polar bodies reveals aneuploidy mechanisms. Prenat Diagn 23,663-668.
11. Dailey T, Dale B, Cohen J and Munné S (1996) Association between nondisjunction and maternal age in meiosis-II human oocytes detected by FISH analysis. Am J Hum Genet 59,176-184.
12. Dyban A, Freidine M, Severova E, Cieslak J, Ivakhnenko V and Verlinsky Y (1996) Detection of aneuploidy in human oocytes and corresponding first polar bodies by fluorescent in situ hybridization. J Assist Reprod Genet 13,73-78.
13. Edirisinghe W, Murch A, Junk S and Yovich J (1997) Cytogenefic abnormalities of unfertilized oocytes generated from in-vitro fertilization and intracytoplasmic sperm injection: a double blind study. Hum Reprod 12,2784-2791.
14. Flaherty S, Payne D, Swann N and Matthews C (1995) Assessment of fertilization failure and abnormal fertilization after intracytoplasmic sperm injection (ICSI). Reprod Fertil Dev 7,197-210.
15. Gutierrez-Mateo C, Wells D, Benet J, Sánchez-García JF, Bermúdez MG, Belil I, Egozcue J, Munné S and Navarro J (2004) Reliability of comparative genomic hybridization to detect chromosome abnoramlities in first polar bodies and metaphase II oocytes. Hum Reprod 19,2118-2125.
16. Hanna J, Shires P and Matile G (1997) Trisomy 1 in a clinically recognized pregnancy. Am J Med Genet 68,98.
17. Hassold T and Hunt P (2001) To err (meiotically) is human: the genesis of human aneuploidy. Nature Rev Genet 2,280-291.
18. Hassold T, Sherman S and Hunt P (2000) Counting cross-overs: characterizing meiotic recombination in mammals. Hum Mol Genet 9,2409-2419.
19. Hunt P, LeMaire R, Embury P, Sheean L and Mroz K (1995) Analysis of chromosome behavior in intact mammalian oocytes: monitoring the segregation of a univalent chromosome during female meiosis. Hum Mol Genet 4,2007-2012.
20. Koehler K, Hawley R, Shreman S and Hassold T (1996) Recombination and nondisjunction in humans and flies. Hum Mol Genet,5.
21. Kuliev A, Cieslak J, Ilkevitch Y and Verlinsky Y (2003) Chromosomal abnormalities in a series of 6733 human oocytes in preimplantation diagnosis for age-related aneuploidies. Reprod Biomed Online 6,54-59.
22. LeMarie-Adkins R, Radke K and Hunt PA (1997) Lack of checkpoint control at the metaphase/anaphase transition: a mechanism of meiotic nondisjunction in mammalian females. J Cell Biol 139,1611-1619.
23. Mahmood R, Brierley CH, Faed MJW, Mills JA and Delhanty JDA (2000) Mechanisms of maternal aneuploidy: FISH analysis of oocytes and polar bodies in patients undergoing assisted conception. Hum Genet 106, 620-626.
24. Márquez C, Cohen J and Munné S (1998) Chromosome identification in human oocytes and polar bodies by spectral karyotyping. Cytogenet Cell Genet 81,254-258.
25. Márquez C, Sandalinas M, Bahçe M, Alikani M and Munné S (2000) Chromosome abnormalities in 1255 cleavage-stage human embryos. Reprod Biomed Online 1,17-27.
26. Martini E, Flaherty S, Swann N, Matthews C, Ramaekers F and Geraedts J (2000) FISH analysis of six chromosomes in unfertilized human oocytes after polar body removal. J Assist Reprod Genet 17,276-283.
27. Munné S and Weier U (1996) Simultaneous enumeration of chromosomes 13, 18, 21, X and Y in interphase cells for preimplantation genetic diagnosis of aneuploidy. Cytogenet Cell Genet 75,263-270.
28. Munné S, Alikani M, Tomkin G, Grifo J and Cohen J (1995a) Embryo morphology, development rates and maternal age are correlated with chromosome abnormalities. Fertil Steril 64,382-391.
29. Munné S, Dailey T, Sultan KM, Grifo J and Cohen J (1995b) The use of first polar bodies for preimplantation diagnosis of aneuploidy. Hum Reprod 10,1014-1020.
30. Munné S, Magli C, Bahçe M, Fung J, Legator M, Morrison L, Cohert J and Gianaroli L (1998a) Preimplantation diagnosis of the aneuploidies most commonly found in spontaneous abortions and live births: XY, 13, 14, 15, 16, 18, 21, 22. Prenat Diagn 18,1459-1466.
31. Munné S, Márquez C, Magli C, Morton P and Morrison L (1998b) Scoring criteria for preimplantation genetic diagnosis of numerical abnormalities for chromosomes X Y, 13, 16, 18 and 21. Mol Hum Reprod 4,863-870.
32. Munné S, Sandalinas M, Escudero T, Velilla E, Walmsley R, Sadowy S, Cohen J and Sable D (2003) Improved implantation after preimplantation genetic diagnosis of aneuploidy. Reprod Biomed Online 7,91-97.
33. Munné S, Bahçe M, Sandalinas M, Escudero T, Márquez C, Velilla E, Colls P, Oter M, Alikani M et al. (2004) Differences in chromosome susceptibility to aneuploidy and survival to first trimester. Reprod Biomed Online 8,81-90.
34. Nakaoka Y, Okamoto E, Miharu N and Ohama K (1998) Chromosome analysis in human oocytes remaining unfertilized after in-vitro insemination: effect of maternal age and fertilization rate. Hum Reprod 13,419-424.
35. Nicolaidis P and Petersen M (1998) Origin and mechanisms of nondisjunction in human autosomal trisomies. Hum Reprod 13,313-319.
36. Pellestor F (1991a) Differential distribution of aneuploidy in human gametes according to their sex. Hum Reprod 6,1252-1258.
37. Pellestor F (1991b) Frequency and distribution of aneuploidy in human female gametes. Hum Genet 86,283-288.
38. Pellestor F, Andréo B, Arnal F, Humeau C and Demaille J (2002) Mechanisms of non-disjunction in human female meiosis: the co-existence of two modes of malsegregation evidenced by the karyotyping of 1397 in-vitro unfertilized oocytes. Hum Reprod 17,2134-2145.
39. Pellestor F, Andréo B, Arnal F, Humeau C and Demaille J (2003) Maternal aging and chromosomal abnormalities: new data drawn from in vitro unfertilized human oocytes. Human Genetics 112,195-203.
40. Pickering S, Johnson M, Braude PR and Houliston E (1988) Cytoskeletal organization in fresh, aged and spontaneously activated human oocytes. Hum Reprod 3,978-989.
41. Pujol A, Boiso I, Beret J, Veiga A, Durban M, Campillo M, Egozcue J and Navarro J (2003) Analysis of nine chromosome probes in 1st polar bodies and metaphase II oocytes for the detection of aneuploidies. Eur J Hum Genet 11,325-336.
42. Sandalinas M, Márquez C and Munné S (2002) Spectral karyotyping of fresh, non-inseminated oocytes. Mol Hum Reprod 8,580-585.
43. Schmiady H, Tandler-Schneider A and Kentenich H (1996) Premature chromosome condensation of the sperm nucleus after intracytoplasmic sperm injection. Hum Reprod 11,2239-2245.
44. Schon E, Kim S, Ferreira J, Magalhaes P, Grace M, Wardburton D and Gross S (2000) Chromosomal non-disjunction in human oocytes: in there a mitochondrial connection? Hum Reprod 15,160-172.
45. Simpson J (1990) Incidence and timing of pregnancy losses: relevance to evaluating safety of prental diagnosis. Am J Med Genet 35,165-173.
46. Sun F, Oliver-Bonet M, Liehr T, Starke H, Ko E, Rademaker A, Navarro J, Benet J and Martin RH (2004) Human male recombinations maps for individual chromosomes. Am J Hum Genet 74,521-531.
47. Tarkowski A (1966) An air drying method for chromosome preparation from mouse eggs. Cytogenetics 5,394-400.
48. Uhlmann F (2004) The mechanism of sister chromatid cohesion. Exp Cell Res 296,80-85.
49. Verlinsky Y and Kuliev A (1996) Preimplantation diagnosis of common aneuploidies in fertile couples of advanced maternal age. Hum Reprod 11,2076-2077.
50. Verlinsky Y, Cieslak J, Ivakhnenko V, Evsikov S, Wolf G, White M, Lifchez A, Kaplan B, Moise J et al. (1999) Prevention of age-related anauploidies by polar body testing of oocytes. J Assist Reprod Genet 16,165-169.
51. Voullaire L, Wilton L, Slater H and Williamson R (1999) Detection of aneuploidy in single cells using comparative genomic hybridization. Prenat Diagn 19,846-851.
52. Wells D, Sherlock JK, Handyside AH and Delhanty JDA (1999) Detailed chromosomal and molecular genetic analysis of single cells by whole genome amplification, comparative genomic hybridisation. Nucleic Acids Res 27,1214-1218.
53. Wells D, Escudero, T, Levy B, Hirschhorn K, Delhanty JDA and Munné S (2002) First clinical application of comparative genomic hybridization and polar body testing for preimplantation genetic diagnosis of aneuploidy. Fertil Steril 78,543-549.
54. Wilton L, Voullaire L, Sargeant P, Williamson R and MeBain J (2003) Preimplantation aneuploidy screening using comparative genomic hybridization or fluorescence in situ hybridization of embryos from patients with recurrent implantation failure. Fertil Steril 80,860-868.
55. Zenzes M, Wang P and Casper R (1992) Evidence for maternal predisposition to chromosome aneuploidy in multiple oocytes of some in vitro fertilization patients. Fertil Steril 57,143-149.