The role of male chromosomal polymorphism played in spermatogenesis and the outcome of IVF/ICSI-ET treatment

International Journal of Andrology

Volumn 35, Issue 6, 2012, Pages 802-809

  Guo, T ^a,b,c   Qin, Y ^a,b,c   Gao, X ^a,b,c   Chen, H ^a,b,c   Li, G ^a,b,c   Ma, J ^a,b,c   Chen, Z J ^a,b,c  

^a SHANDONG PROVINCIAL HOSPITAL AFFILIATED TO SHANDONG UNIVERSITY   (China)

^b National Research Center for Assisted Reproductive Technology   (China)

^c BEIJING UNIVERSITY OF POSTS AND TELECOMMUNICATIONS   (China)

Author keywords

Chromosomal polymorphism; Clinical outcome; IVF ICSI ET; Male infertility; Oligozoospermia

Indexed keywords

RECOMBINANT CHORIONIC GONADOTROPIN; RECOMBINANT FOLLITROPIN; TRIPTORELIN;

ADULT; ARTICLE; CHROMOSOME POLYMORPHISM; CONTROLLED STUDY; FEMALE; FEMALE INFERTILITY; FERTILIZATION; FERTILIZATION IN VITRO; HUMAN; INTRACYTOPLASMIC SPERM INJECTION; MAJOR CLINICAL STUDY; MALE; MALE INFERTILITY; NIDATION; OLIGOSPERMIA; PREGNANCY RATE; PRIORITY JOURNAL; SPERMATOGENESIS; SPONTANEOUS ABORTION; TREATMENT OUTCOME; Y CHROMOSOME;

FEMALE; FERTILIZATION IN VITRO; HUMANS; KARYOTYPING; MALE; POLYMORPHISM, GENETIC; PREGNANCY; PREGNANCY RATE; RETROSPECTIVE STUDIES; SPERM INJECTIONS, INTRACYTOPLASMIC; SPERMATOGENESIS;

EID: 84869878638     PISSN: 01056263     EISSN: 13652605     Source Type: Journal    
DOI: 10.1111/j.1365-2605.2012.01284.x     Document Type: Article

References (39)

1. Antonelli A, Gandini L, Petrinelli P, Marcucci L, Elli R, Lombardo F, Dondero F & Lenzi A. (2000) Chromosomal alterations and male infertility. J Endocrinol Invest 23, 677-683.
2. Choi JM, Chung P, Veeck L, Mielnik A, Palermo GD & Schlegel P N. (2004) AZF microdeletions of the Y chromosome and in vitro fertilization outcome. Fertil Steril 81, 337-341.
3. Codina-Pascual M. (2006) Behaviour of human heterochromatic regions during the synapsis of homologous chromosomes. Hum Reprod 21, 1490-1497.
4. Cryderman DE, Cuaycong MH, Elgin SC & Wallrath L L. (1998) Characterization of sequences associated with position-effect variegation at pericentric sites in Drosophila heterochromatin. Chromosoma 107, 277-285.
5. Eiben B, Leipoldt M, Rammelsberg O, Krause W & Engel W. (1987) High incidence of minor chromosomal variants in teratozoospermic males. Andrologia 19, 684-687.
6. Foresta C, Moro E & Ferlin A. (2001) Y chromosome microdeletions and alterations of spermatogenesis. Endocr Rev 22, 226-239.
7. Giglio S, Broman KW, Matsumoto N, Calvari V, Gimelli G, Neumann T et al. (2001) Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements. Am J Hum Genet 68, 874-883.
8. Hong Y, Zhou YW, Tao J, Wang SX & Zhao X M. (2011) Do polymorphic variants of chromosomes affect the outcome of in vitro fertilization and embryo transfer treatment? Hum Reprod 26, 933-940.
9. Humphray SJ, Oliver K, Hunt AR, Plumb RW, Loveland JE, Howe KL et al. (2004) DNA sequence and analysis of human chromosome 9. Nature 429, 369-374.
10. Iida R, Sawazaki K, Ikeda H, Miyamoto T, Tsubota E, Takatsuka H, Masuyama M, Matsuki T, Yasuda T & Kishi K. (2003) A novel multiplex PCR system consisting of Y-STRs DYS441, DYS442, DYS443, DYS444, and DYS445. J Forensic Sci 48, 1088-1090.
11. Kim IF, Mohammadi E & Huang RC. (1999) Isolation and characterization of IPP, a novel human gene encoding an actin-binding, kelch-like protein. Gene 228, 73-83.
12. Kondoh N, Nishina Y, Tsuchida J, Koga M, Tanaka H, Uchida K et al. (1997) Assignment of synaptonemal complex protein 1 (SCP1) to human chromosome 1p13 by fluorescence in situ hybridization and its expression in the testis. Cytogenet Cell Genet 78, 103-104.
13. Krausz C & Forti G. (2008) The Y chromosome and its fragility. Int J Androl 31, 374-375.
14. Krausz C, Forti G & McElreavey K. (2003) The Y chromosome and male fertility and infertility. Int J Androl 26, 70-75.
15. Kuroda-Kawaguchi T, Skaletsky H, Brown LG, Minx PJ, Cordum HS, Waterston RH et al. (2001) The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men. Nat Genet 29, 279-286.
16. Madon PF, Athalye AS & Parikh FR. (2005) Polymorphic variants on chromosomes probably play a significant role in infertility. Reprod Biomed Online 11, 726-732.
17. Matzuk MM & Lamb DJ. (2002) Genetic dissection of mammalian fertility pathways. Nat Cell Biol 4(Suppl), s41-s49.
18. Minocherhomji S, Athalye AS, Madon PF, Kulkarni D, Uttamchandani SA & Parikh FR. (2009) A case-control study identifying chromosomal polymorphic variations as forms of epigenetic alterations associated with the infertility phenotype. Fertil Steril 92, 88-95.
19. Mirfakhraie R, Mirzajani F, Kalantar SM, Montazeri M, Salsabili N, Pourmand GR & Houshmand M. (2010) High prevalence of AZFb microdeletion in Iranian patients with idiopathic non-obstructive azoospermia. Indian J Med Res 132, 265-270.
20. Mozdarani H, Meybodi AM & Zari-Moradi S. (2008) A cytogenetic study of couples with recurrent spontaneous abortions and infertile patients with recurrent IVF/ICSI failure. Indian J Hum Genet 14, 1-6.
21. Nagvenkar P, Desai K, Hinduja I & Zaveri K. (2005) Chromosomal studies in infertile men with oligozoospermia & non-obstructive azoospermia. Indian J Med Res 122, 34-42.
22. Nakamura Y, Kitamura M, Nishimura K, Koga M, Kondoh N, Takeyama M, Matsumiya K & Okuyama A. (2001) Chromosomal variants among 1790 infertile men. Int J Urol 8, 49-52.
23. Oates RD, Silber S, Brown LG & Page DC. (2002) Clinical characterization of 42 oligospermic or azoospermic men with microdeletion of the AZFc region of the Y chromosome, and of 18 children conceived via ICSI. Hum Reprod 17, 2813-2824.
24. Page DC, Silber S & Brown LG. (1999) Men with infertility caused by AZFc deletion can produce sons by intracytoplasmic sperm injection, but are likely to transmit the deletion and infertility. Hum Reprod 14, 1722-1726.
25. Paquis-Flucklinger V, Santucci-Darmanin S, Paul R, Saunieres A, Turc-Carel C & Desnuelle C. (1997) Cloning and expression analysis of a meiosis-specific MutS homolog: the human MSH4 gene. Genomics 44, 188-194.
26. Rodovalho RG, Arruda JT & Moura KK. (2008) Tracking microdeletions of the AZF region in a patrilineal line of infertile men. Genet Mol Res 7, 614-622.
27. Rusche LN & Rine J. (2001) Conversion of a gene-specific repressor to a regional silencer. Genes Dev 15, 955-967.
28. Sahin FI, Yilmaz Z, Yuregir OO, Bulakbasi T, Ozer O & Zeyneloglu H B. (2008) Chromosome heteromorphisms: an impact on infertility. J Assist Reprod Genet 25, 191-195.
29. Simoni M, Tuttelmann F, Gromoll J & Nieschlag E. (2008) Clinical consequences of microdeletions of the Y chromosome: the extended Munster experience. Reprod Biomed Online 16, 289-303.
30. Skaletsky H, Kuroda-Kawaguchi T, Minx PJ, Cordum HS, Hillier L, Brown LG et al. (2003) The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes. Nature 423, 825-837.
31. Tessari A, Salata E, Ferlin A, Bartoloni L, Slongo ML & Foresta C. (2004) Characterization of HSFY, a novel AZFb gene on the Y chromosome with a possible role in human spermatogenesis. Mol Hum Reprod 10, 253-258.
32. Tilford CA, Kuroda-Kawaguchi T, Skaletsky H, Rozen S, Brown LG, Rosenberg M et al. (2001) A physical map of the human Y chromosome. Nature 409, 943-945.
33. Van Assche E, Bonduelle M, Tournaye H, Joris H, Verheyen G, Devroey P, Van Steirteghem A & Liebaers I. (1996) Cytogenetics of infertile men. Hum Reprod 11(Suppl. 4), 1-24; discussion 25-26.
34. Velasco G, Pendas AM, Fueyo A, Knauper V, Murphy G & Lopez-Otin C. (1999) Cloning and characterization of human MMP-23, a new matrix metalloproteinase predominantly expressed in reproductive tissues and lacking conserved domains in other family members. J Biol Chem 274, 4570-4576.
35. Venkatesh S, Thilagavathi J, Kumar K, Deka D, Talwar P & Dada R. (2011) Cytogenetic, Y chromosome microdeletion, sperm chromatin and oxidative stress analysis in male partners of couples experiencing recurrent spontaneous abortions. Arch Gynecol Obstet 284, 1577-1584.
36. Verp MS, Rzeszotarski MS, Martin AO & Simpson JL. (1983) Relationship between Y-chromosome length and first-trimester spontaneous abortions. Am J Obstet Gynecol 145, 433-438.
37. Vinci G, Raicu F, Popa L, Popa O, Cocos R & McElreavey K. (2005) A deletion of a novel heat shock gene on the Y chromosome associated with azoospermia. Mol Hum Reprod 11, 295-298.
38. Yakin K, Balaban B & Urman B. (2005) Is there a possible correlation between chromosomal variants and spermatogenesis? Int J Urol 12, 984-989.
39. Yuce H, Tekedereli I & Elyas H. (2007) Cytogenetic results of recurrent spontaneous abortions in Turkey. Med Sci Monit 13, CR286-CR289.