Y chromosome microdeletions in Mexican males of couples with idiopathic recurrent pregnancy loss

Journal of Obstetrics and Gynaecology Research

Volumn 38, Issue 6, 2012, Pages 912-917

  Pina Aguilar, Raul E ^a,b,e   Martínez Garza, Sandra G ^a,d   Kohls, Graciela ^a   Vargas Maciel, Marco A ^a   De Lara, Luis G Vázquez ^c   González Ortega, Claudia ^a   Cancino Villarreal, Patricia ^a   Gutiérrez Gutiérrez, Antonio M ^a  

^a Faculties of Medicine   (Mexico)

^b UNIVERSIDAD AUTÓNOMA DE YUCATÁN   (Mexico)

^c BENEMÉRITA UNIVERSIDAD AUTÓNOMA DE PUEBLA   (Mexico)

^d Inst de Cie en Reprod Humana   (Mexico)

^e INSTITUTO MEXICANO DEL SEGURO SOCIAL   (Mexico)

Author keywords

Abortion; Infertility; Male contribution; Recurrent miscarriage; Y chromosome

Indexed keywords

ADULT; ARTICLE; CHROMOSOME ANALYSIS; CHROMOSOME DELETION Y; CONTROLLED STUDY; HUMAN; HUMAN CELL; HUMAN TISSUE; IDIOPATHIC DISEASE; MAJOR CLINICAL STUDY; MALE; MEXICO; MULTIPLEX POLYMERASE CHAIN REACTION; PERIPHERAL LYMPHOCYTE; POWER ANALYSIS; RECURRENT DISEASE; SEQUENCE TAGGED SITE; SPONTANEOUS ABORTION;

EID: 84864591956     PISSN: 13418076     EISSN: 14470756     Source Type: Journal    
DOI: 10.1111/j.1447-0756.2011.01809.x     Document Type: Article

References (37)

1. Jauniaux E, Farquharson RG, Christiansen OB et al. Evidencebased guidelines for the investigation and medical treatment of recurrent miscarriage. Hum Reprod 2006; 21: 2216-2222.
2. Puscheck EE, Jeyendran RS. The impact of male factor on recurrent pregnancy loss. Curr Opin Obstet Gynecol 2007; 19: 222-228.
3. Sugiura-Ogasawara M, Ozaki Y, Sato T et al. Poor prognosis of recurrent aborters with either maternal or paternal reciprocal translocations. Fertil Steril 2004; 81: 367-373.
4. Rubio C, Simón C, Blanco J et al. Implications of sperm chromosome abnormalities in recurrent miscarriage. J Assist Reprod Genet 1999; 16: 253-258.
5. Carrell DT, Wilcox AL, Lowy L et al. Elevated sperm chromosome aneuploidy and apoptosis in patients with unexplained recurrent pregnancy loss. Obstet Gynecol 2003; 101: 1229-1235.
6. Bhattacharya SM. Hypo-osmotic swelling test and unexplained repeat early pregnancy loss. J Obstet Gynaecol Res 2010; 36: 119-122.
7. Carrell DT, Liu L, Peterson CM et al. Sperm DNA fragmentation is increased in couples with unexplained recurrent pregnancy loss. Arch Androl 2003; 49: 49-55.
8. Collodel G, Giannerini V, Antonio Pascarelli N et al. TEM and FISH studies in sperm from men of couples with recurrent pregnancy loss. Andrologia 2009; 41: 352-360.
9. Dewan S, Puscheck EE, Coulam CB et al. Y-chromosome microdeletions and recurrent pregnancy loss. Fertil Steril 2006; 85: 441-445.
10. Asghari-Roodsari A, Kariminejad A, Najmabadi H. Polymerase chain reaction for detection of Yq microdeletion among unexplained recurrent pregnancy loss couples. Int J Androl 2008; 31 (Suppl 1): 12.
11. Karaer A, Karaer K, Ozaksit G et al. Y chromosome azoospermia factor region microdeletions and recurrent pregnancy loss. Am J Obstet Gynecol 2008; 199: 662e1-662e5.
12. Aldrich CL, Stephenson MD, Karrison T et al. HLA-G genotypes and pregnancy outcome in couples with unexplained recurrent miscarriage. Mol Hum Reprod 2001; 7: 1167-1172.
13. Hiby SE, Regan L, Lo W et al. Association of maternal killercell immunoglobulin-like receptors and parental HLA-C genotypes with recurrent miscarriage. Hum Reprod 2008; 23: 972-976.
14. Jivraj S, Rai R, Underwood J et al. Genetic thrombophilic mutations among couples with recurrent miscarriage. Hum Reprod 2006; 21: 1161-1165.
15. Govindaiah V, Naushad SM, Prabhakara K et al. Association of parental hyperhomocysteinemia and C677T Methylene tetrahydrofolate reductase (MTHFR) polymorphism with recurrent pregnancy loss. Clin Biochem 2009; 42: 380-386.
16. Kilpatrick DC, Starrs L, Moore S et al. Mannan binding lectin concentration and risk of miscarriage. Hum Reprod 1999; 14: 2379-2380.
17. Foresta C, Moro E, Ferlin A. Y chromosome microdeletions and alterations of spermatogenesis. Endocr Rev 2001; 22: 226-239.
18. Krausz C, Degl'Innocenti S. Y chromosome and male infertility: Update 2006. Front Biosci 2006; 11: 3049-3061.
19. Bhasin S. Approach to the infertile man. J Clin Endocrinol Metab 2007; 92: 1995-2004.
20. McLachlan RI, O'Bryan MK. State of the art for genetic testing of infertile men. J Clin Endocrinol Metab 2010; 95: 1013-1024.
21. Simoni M, Bakker E, Krausz C. EAA/EMQN best practice guidelines for molecular diagnosis of y-chromosomal microdeletions. State of the art 2004. Int J Androl 2004; 27: 240-249.
22. Ferlin A, Arredi B, Speltra E et al. Molecular and clinical characterization of Y chromosome microdeletions in infertile men: A 10-year experience in Italy. J Clin Endocrinol Metab 2007; 92: 762-770.
23. Simoni M, Tüttelmann F, Gromoll J et al. Clinical consequences of microdeletions of the Y chromosome: The extended Münster experience. Reprod Biomed Online 2008; 16: 289-303.
24. Martínez-Garza SG, Gallegos-Rivas MC, Vargas-Maciel M et al. Genetic screening in infertile Mexican men: Chromosomal abnormalities, Y chromosome deletions, and androgen receptor CAG repeat length. J Androl 2008; 29: 654-660.
25. Nani JM, Brasch JG, Summers R et al. Microdeletions in the Y chromosome and recurrent reproductive loss. Fertil Steril 2001; 76: (3 Suppl): s13.
26. Noordam MJ, van der Veen F, Repping S. Techniques and reasons to remain interested in the Y chromosome. Fertil Steril 2006; 86: 1801-1802.
27. Kaare M, Painter JN, UlanderVMet al. Sex chromosome characteristics and recurrent miscarriage. Fertil Steril 2008; 90: 2328-2333.
28. Piña-Aguilar RE, Martínez-Garza SG, Gutiérrez- Gutiérrez AM. Are Y chromosome microdeletions and recurrent pregnancy loss really associated? Am J Obstet Gynecol 2009; 201: e9.
29. Bellver J, Meseguer M, Muriel L et al. Y chromosome microdeletions, sperm DNA fragmentation and sperm oxidative stress as causes of recurrent spontaneous abortion of unknown etiology. Hum Reprod 2010; 25: 1713-1721.
30. Wettasinghe TK, Jayasekara RW, Dissanayake VH. Y chromosome microdeletions are not associated with spontaneous recurrent pregnancy loss in a Sinhalese population in Sri Lanka. Hum Reprod 2010; 25: 3152-3156.
31. Faul F, Erdfelder E, Buchner A et al. Statistical power analyses using G Power 3.1: Tests for correlation and regression analyses. Behav Res Methods 2009; 41: 1149-1160.
32. De la Fuente-Cortés BE, Cerda-Flores RM, Dávila- Rodríguez MI et al. Chromosomal abnormalities and polymorphic variants in couples with repeated miscarriage in Mexico. Reprod Biomed Online 2009; 18: 543-548.
33. Meza-Espinoza JP, Anguiano LO, Rivera H. Chromosomal abnormalities in couples with reproductive disorders. Gynecol Obstet Invest 2008; 66: 237-240.
34. Silva-Zolezzi I, Hidalgo-Miranda A, Estrada-Gil J et al. Analysis of genomic diversity in Mexican Mestizo populations to develop genomic medicine in Mexico. Proc Natl Acad Sci U S A 2009; 106: 8611-8616.
35. Karafet TM, Mendez FL, Meilerman MB et al. New binary polymorphisms reshape and increase resolution of the human Y chromosomal haplogroup tree. Genome Res 2008; 18: 830-838.
36. Rangel-Villalobos H, Muñoz-Valle JF, González-Martín A et al. Genetic admixture, relatedness, and structure patterns among Mexican populations revealed by the Y-chromosome. Am J Phys Anthropol 2008; 135: 448-461.
37. Salazar-Flores J, Dondiego-Aldape R, Rubi-Castellanos R et al. Population structure and paternal admixture landscape on present-day Mexican-Mestizos revealed by Y-STR haplotypes. Am J Hum Biol 2010; 22: 401-409.