Web of Science: 45 cites, Scopus: 55 cites, Google Scholar: cites,
Role of sperm fluorescent in situ hybridization studies in infertile patients : indications, study approach, and clinical relevance
Sarrate Navas, Zaida (Universitat Autònoma de Barcelona. Departament de Biologia Cel·lular, de Fisiologia i d'Immunologia)
Vidal, Francesca (Universitat Autònoma de Barcelona. Departament de Biologia Cel·lular, de Fisiologia i d'Immunologia)
Blanco, Joan (Universitat Autònoma de Barcelona. Departament de Biologia Cel·lular, de Fisiologia i d'Immunologia)

Data: 2010
Resum: Objective: To determine the group of infertile patients that would benefit from sperm fluorescent in situ hybridization (FISH) analysis, the number of chromosomes to be analyzed, and the diagnostic interpretation of the results obtained. Design: A retrospective study of sperm FISH analyses. Setting: Universitat Autònoma de Barcelona. Patient(s): Three hundred nineteen infertile men. Intervention(s): Semen samples were processed for FISH. Main Outcome Measure(s): The frequencies of chromosomal abnormalities for chromosomes 13, 18, 21, X, and Y were compared to the seminogram, the somatic and meiotic karyotype, and the age. Result(s): The highest percentages of patients with an increased rate of sperm chromosome abnormalities were found in the oligozoospermic (50%), oligoasthenozoospermic (33. 3%), and oligoasthenoteratozoospermic (21%) individuals. Low sperm count was the only parameter correlated with the percentage of chromosome abnormalities. The 14% of the individuals with a normal somatic karyotype had an increased rate of sperm chromosome abnormalities. This percentage was higher in the group with an altered somatic karyotype (36%) and in patients with meiotic abnormalities (26%). Conclusion(s): Sperm FISH studies are indicated when the oligo condition is present and in individuals with an abnormal somatic or meiotic karyotype. The analysis of chromosomes 21, X, and Y is enough to identify at-risk individuals. Significant differences in the rates of chromosome abnormalities should be taken into consideration regardless of the numerical value.
Drets: Tots els drets reservats.
Llengua: Anglès
Document: Article ; recerca ; Versió acceptada per publicar
Matèria: Chromosome abnormalities ; Clinical relevance ; Indications ; Male infertility ; Sperm FISH ; Study approach
Publicat a: Fertility and Sterility, Vol. 93 Núm. 6 (April 2010) , p. 1892-1902, ISSN 1556-5653

DOI: 10.1016/j.fertnstert.2008.12.139


36 p, 766.7 KB

El registre apareix a les col·leccions:
Articles > Articles de recerca
Articles > Articles publicats

 Registre creat el 2024-02-09, darrera modificació el 2024-03-24



   Favorit i Compartir