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1.
Andrologia ; 49(5)2017 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-27484294

RESUMO

Association of hepatitis C virus (HCV) with autoimmune phenomena and impaired semen parameters has been previously reported. The aim of this study was to investigate the influence of HCV infection on the development of antisperm antibodies (ASAs) in HCV-positive males. The study was conducted on 30 HCV-infected individuals and 30 healthy control subjects. In both patients and control groups, liver enzymes and reproductive hormones were measured; computer-assisted semen analysis (CASA) was performed; HCV-RNA in serum was measured and IgG and IgA ASAs in semen were determined. Free testosterone, sperm concentration, progressive and total motility were significantly lower in HCV patients than in the control group, whereas ASAs of the IgG and IgA classes were significantly higher in HCV patients. However, correlations between viral load and the examined semen parameters and ASAs were nonsignificant. In conclusion, HCV may be responsible for the increased ASAs detected in HCV patients in the present study, possibly providing another plausible explanation for the decreased sperm motility reported in HCV patients. These findings could be of value in fertility management of HCV patients.


Assuntos
Autoanticorpos/análise , Hepatite C/imunologia , Espermatozoides/imunologia , Adulto , Alanina Transaminase/sangue , Aspartato Aminotransferases/sangue , Egito , Hepatite C/fisiopatologia , Humanos , Imunoglobulina A/análise , Imunoglobulina G/análise , Masculino , Pessoa de Meia-Idade , Sêmen/imunologia , Análise do Sêmen , Contagem de Espermatozoides , Motilidade dos Espermatozoides , Carga Viral
2.
Andrologia ; 47(5): 587-93, 2015 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-25130880

RESUMO

The aim of this study was to examine whether an association exists between glutathione S-transferase Mu-1 (GSTM1) gene polymorphism and idiopathic male infertility. Sixty men with primary idiopathic infertility and 60 fertile men, serving as controls, were recruited for the study. The polymorphism was analysed using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) technique. The frequency of GSTM1 null genotype was observed to be higher in infertile men 40% in comparison with 33.3% in the fertile men, but this difference was not statistically significant. There was statistically significant difference between cases and controls as regards GSTM1 genotype distribution ((MC) P = 0.006*) in GSTM1-positive men. Patients with the GSTM1 null genotype had significantly lower sperm concentrations and total sperm count when compared with patients with GSTM1-positive genotype. In the control group, men with GSTM1 null genotype had significantly lower sperm concentrations but not total sperm count when compared with men with GSTM1-positive genotype. The results of this study suggest a possible negative effect of GSTM1 null genotype on the spermatogenic potential of the testis.


Assuntos
Glutationa Transferase/genética , Infertilidade Masculina/genética , Espermatogênese/genética , Adulto , Egito , Predisposição Genética para Doença , Genótipo , Humanos , Masculino , Pessoa de Meia-Idade , Reação em Cadeia da Polimerase , Polimorfismo Genético , Polimorfismo de Fragmento de Restrição , Contagem de Espermatozoides
3.
Andrologia ; 43(1): 16-22, 2011 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-21219377

RESUMO

The aim of this study was to assess the prevalence of Δ-F508 mutation and 5T allele in a sample of Egyptian patients having congenital bilateral absent vas deferens (CBAVD), to correlate between genotype and phenotypic genital pattern, and to demonstrate the value of micro-assisted reproduction in them. The study included thirty patients with CBAVD and 30 fertile controls. Clinical, laboratory and radiological examinations of the patients were performed. Genetic assessment of patients and controls as regards Δ-F508 mutation and 5T allele was done. Trials of testicular sperm extraction (TESE) and intracytoplasmic sperm injection (ICSI) were carried out for the patients. Δ-F508 mutation was present in 40% and 5T allele was detected in 46.6% of the patients. On the other hand, all the control group was negative as regards Δ-F508 mutation, while 5T allele was detected in 10% of them. The total fertilisation rate was 75% and pregnancy rate was 60% with no significant difference in fertilisation and pregnancy rates between cases positive for Δ-F508 or 5T allele and others. It is evident that Δ-F508 mutation and 5T allele play important roles in the pathogenesis of CBAVD in Egyptians. TESE/ICSI is a beneficial method to enable these patients to father children of their own.


Assuntos
Alelos , Regulador de Condutância Transmembrana em Fibrose Cística/genética , Mutação/genética , Fenótipo , Ducto Deferente/anormalidades , Adulto , Estudos de Casos e Controles , Egito/epidemiologia , Aconselhamento Genético , Genótipo , Humanos , Infertilidade Masculina/epidemiologia , Infertilidade Masculina/genética , Infertilidade Masculina/terapia , Masculino , Pessoa de Meia-Idade , Prevalência , Injeções de Esperma Intracitoplásmicas/métodos , Recuperação Espermática
4.
Andrologia ; 40(5): 312-7, 2008 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-18811922

RESUMO

The aim of this work was to study the possible beneficial effect of repeated sequential ejaculation on sperm DNA integrity in subfertile males and its possible implementation in assisted reproduction. The study included 20 infertile males with idiopathic asthenozoospermia or oligoasthenozoospermia. They underwent detailed history taking, complete clinical assessment and hormonal assessment. Patients were asked to bring two semen samples (taken within 1-3 h). Two consecutive samples were assessed with regard to semen volume, sperm count, motility grading, and morphology and sperm DNA integrity using the comet assay. There was a significant improvement in the sperm motility pattern and DNA integrity in the second sample in comparison with the first sample. Therefore, it is concluded that due to its positive impact on sperm motility and DNA integrity, repeated sequential ejaculation is recommended in subfertile males with idiopathic asthenozoospermia who pursue assisted reproduction.


Assuntos
Astenozoospermia/fisiopatologia , Dano ao DNA/fisiologia , Ejaculação/fisiologia , Espermatozoides/fisiologia , Adulto , Estudos de Casos e Controles , Humanos , Masculino , Técnicas de Reprodução Assistida , Contagem de Espermatozoides , Motilidade dos Espermatozoides/fisiologia
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