Relationship between follicle stimulating hormone and AZF microdeletion on Y chromosome in patients with azoospermia or severe oligozoospermia / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
;
(6): 559-561, 2011.
Artigo
em Chinês
| WPRIM
| ID: wpr-326891
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the relationship between follicle stimulating hormone (FSH) and AZF microdeletion on Y chromosome.</p><p><b>METHODS</b>Fifteen loci of 4 regions of the AZF gene were investigated by multiplex PCR in 100 patients with azoospermia or severe oligozoospermia. The reproductive hormone FSH was detected by access 2 immunoassay system from BECKMAN COULTER. Epidata was set up and analyzed for means. F test of anova was performed.</p><p><b>RESULTS</b>The rate of microdeletion was 13% (13 out of 100 patients). The deletion was on AZFa in 1 patient, AZFb+c+d in 4 patients, AZFc+d in 7 patients, AZFd in 1 patient, respectively. The level of FSH (40.8±11.3 U/L) in the AZFb+c+d deletion group was significantly higher than that in the group without Y chromosome deletion (16.7±14.3 U/L) and the other types of deletion (11.8±6.7 U/L) (P<0.01).</p><p><b>CONCLUSION</b>The common microdeletion regions were AZFc and AZFd on Y chromosome in azoospermia or severe oligozoospermia. The microdeletion of AZFb+c+d was one of the important causes of the high level of FSH.</p>
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Oligospermia
/
Sangue
/
Deleção Cromossômica
/
Cromossomos Humanos Y
/
Azoospermia
/
Estudos de Associação Genética
/
Loci Gênicos
/
Hormônio Foliculoestimulante
/
Genética
Limite:
Adulto
/
Humanos
/
Masculino
Idioma:
Chinês
Revista:
Chinese Journal of Medical Genetics
Ano de publicação:
2011
Tipo de documento:
Artigo
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