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Cytogenetic and andrological status and ICSI-results in couples with severe male factor infertility 被引量:1

Cytogenetic and andrological status and ICSI-results in couples with severe male factor infertility
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摘要 Aim: To pursue whether cytogenetic aberrations correlate with specific spermatological or hormonal abnormalities.Methods: 305 infertile couples were investigated. All male partners were referred to a complete andrological work-up with physical examination, determination of hormones, HIV testing and semen analysis. Cytogenetic analysis wascarded out in both partners by means of standard techniques using cultured lymphocytes from peripheral blood. Re-suits: Among the 305 couples, 10 men (3.2%) and 10 women (3.2%) showed constitutional chromosomal aber-rations, including reciprocal translocations (n = 7), Robertsonian translocations (n = 3), inversions (n = 3), otherstructural aberrations (n = 4) and sex chromosome aberrations (n = 3). In addition to the impaired sperm count inmost of the patients, a tendency to an increased proportion of spermatozoa with acrosome defect was observed. Con-clusion: Chromosomal aberrations may contribute to the low fertilization and pregnancy rates in the infertile couples.(Asian J Androl 2000 Dec; 2: 293-296) Aim: To pursue whether cytogenetic aberrations correlate with specific spermatological or hormonal abnormalities.Methods: 305 infertile couples were investigated. All male partners were referred to a complete andrological work-up with physical examination, determination of hormones, HIV testing and semen analysis. Cytogenetic analysis wascarded out in both partners by means of standard techniques using cultured lymphocytes from peripheral blood. Re-suits: Among the 305 couples, 10 men (3.2%) and 10 women (3.2%) showed constitutional chromosomal aber-rations, including reciprocal translocations (n = 7), Robertsonian translocations (n = 3), inversions (n = 3), otherstructural aberrations (n = 4) and sex chromosome aberrations (n = 3). In addition to the impaired sperm count inmost of the patients, a tendency to an increased proportion of spermatozoa with acrosome defect was observed. Con-clusion: Chromosomal aberrations may contribute to the low fertilization and pregnancy rates in the infertile couples.(Asian J Androl 2000 Dec; 2: 293-296)
出处 《Asian Journal of Andrology》 SCIE CAS CSCD 2000年第4期293-296,共4页 亚洲男性学杂志(英文版)
关键词 male infertility intracytoplasmic sperm injection chromosome aberrations male infertility intracytoplasmic sperm injection chromosome aberrations
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同被引文献19

  • 1Nathalie Rives,Marion Jarnot,Nathalie Mousset-Siméon,Géraldine Joly,Bertrand Macé.Fluorescence in situ hybridisation (FISH) analysis of chromosome segregation and interchromosomal effect in spermatozoa of a reciprocal translocation t(9,10)(q11;p11.1) carrier[J].Journal of Human Genetics.2003(10)
  • 2S. Egozcue,J. M. Vendrell,F. Garcia,A. Veiga,B. Aran,P. N. Barri,J. Egozcue.Increased Incidence of Meiotic Anomalies in Oligoasthenozoospermic Males Preselected for Intracytoplasmic Sperm Injection[J].Journal of Assisted Reproduction and Genetics.2000(6)
  • 3Anna M. Estop,Kathy Cieply,Santiago Munne,Urvashi Surti,Anthony Wakim,Eleanor Feingold.Is there an interchromosomal effect in reciprocal translocation carriers? Sperm FISH studies[J].Human Genetics.2000(5)
  • 4Joan Blanco,Josep Egozcue,Francesca Vidal.Interchromosomal effects for chromosome?21 in carriers of structural chromosome reorganizations determined by fluorescence in situ hybridization on sperm nuclei[J].Human Genetics.2000(5)
  • 5Naomi Nishikawa,Isamu Murakami,Katsuo Ikuta,Kaoru Suzumori.Sex Chromosomal Analysis of Spermatozoa from Infertile Men Using Fluorescence In Situ Hybridization[J].Journal of Assisted Reproduction and Genetics.2000(2)
  • 6H. Honda,N. Miharu,O. Samura,H. He,K. Ohama.Meiotic segregation analysis of a 14;21 Robertsonian translocation carrier by fluorescence in situ hybridization[J].Human Genetics.2000(2)
  • 7H. Honda,N. Miharu,Y. Ohashi,N. Honda,T. Hara,K. Ohama.Analysis of segregation and aneuploidy in two reciprocal translocation carriers, t(3;9)(q26.2;q32) and t(3;9)(p25;q32), by triple-color fluorescence in situ hybridization[J].Human Genetics.1999(5)
  • 8Nathalie Rives,Alexia Saint Clair,Sophie Mazurier,Louis Sibert,Nathalie Siméon,Géraldine Joly,Bertrand Macé.Relationship between clinical phenotype, semen parameters and aneuploidy frequency in sperm nuclei of 50 infertile males[J].Human Genetics.1999(3)
  • 9Alvin Soon Tiong Lim,Yang Fong,Su Ling Yu.Estimates of sperm sex chromosome disomy and diploidy rates in a 47,XXY/46,XY mosaic Klinefelter patient[J].Human Genetics.1999(5)
  • 10Anna M. Estop,Kathy M. Cieply,Santiago Munne,Eleanor Feingold.Multicolor fluorescence in situ hybridization analysis of the spermatozoa of a male heterozygous for a reciprocal translocation t(11;22)(q23;q11)[J].Human Genetics.1999(5)

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