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The association between male infertility and sperm disomy: evidence for variation in disomy levels among individuals and a correlation between particular semen parameters and disomy of specific chromosome pairs.
Tempest, Helen G; Homa, Sheryl T; Dalakiouridou, Maria; Christopikou, Dimitra; Wright, David; Zhai, Xiao P; Griffin, Darren K.
Afiliação
  • Tempest HG; Cell and Chromosome Biology Group, Department of Biological Sciences, Brunel University, Uxbridge, UK. helen.tempest@brunel.ac.uk <helen.tempest@brunel.ac.uk>
Reprod Biol Endocrinol ; 2: 82, 2004 Dec 14.
Article em En | MEDLINE | ID: mdl-15598347
BACKGROUND: The association between infertility and sperm disomy is well documented. Results vary but most report that men with severely compromised semen parameters have a significantly elevated proportion of disomic sperm. The relationship between individual semen parameters and segregation of specific chromosome pairs is however less well reported as is the variation of disomy levels in individual men. METHODS: In order to address these questions the technique of fluorescent in-situ hybridisation (FISH) was utilised to determine the disomy levels of chromosomes X, Y and 21 in 43 sperm samples from 19 infertile males. The results generated from this study were analysed using logistic regression. RESULTS: In this study we compared levels of sperm concentration, motility and morphology with levels of sperm disomy for chromosome 21 and the sex chromosomes. Our results suggest that there is considerable variation in disomy levels for certain men. They also suggest that oligozoospermic males have significantly elevated levels of sex chromosome disomy but not disomy 21; they suggest that severe asthenozoospermic males have significantly elevated levels of disomy 21 but not sex chromosome disomy. Surprisingly, severe teratozoopsermic males appeared to have significantly lower levels of sperm disomy for both the sex chromosomes and chromosome 21. CONCLUSION: We suggest that the association between sex chromosome disomy and oligozoospermia may be due to reduced recombination in the XY pairing region and discuss the relevance of our findings for the correlations between sperm disomy and sperm motility and morphology.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 21 / Dissomia Uniparental / Cromossomos Humanos X / Cromossomos Humanos Y / Infertilidade Masculina Tipo de estudo: Diagnostic_studies / Risk_factors_studies Limite: Humans / Male Idioma: En Ano de publicação: 2004 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 21 / Dissomia Uniparental / Cromossomos Humanos X / Cromossomos Humanos Y / Infertilidade Masculina Tipo de estudo: Diagnostic_studies / Risk_factors_studies Limite: Humans / Male Idioma: En Ano de publicação: 2004 Tipo de documento: Article