Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Mais filtros








Base de dados
Intervalo de ano de publicação
1.
Akush Ginekol (Sofiia) ; 53(6): 15-21, 2014.
Artigo em Búlgaro | MEDLINE | ID: mdl-25672133

RESUMO

Approximately 7-12% of women in reproductive age are affected by PCOS[2] and 40 to 70 percent of them are overweight contributing to the clinical picture of PCOS and increased reproductive and metabolic disorder. In order to investigate the role of PAl-1 as a possible risk factor for the development of PCOS a group of 67 women with polycystic ovarian disease and 70 healthy controls were investigated for levels of PAl-1 and carriage of the promoter polymorphism 675 4G/5G in gene of PAI-1. The correlation with BMI was checked. The results of the DNA analysis showed a high carriage of polymorphism 675 4G/4G in promoter of PAl-1 gene in women with PCOS but not significant (OR = 1.655; p = 0.141), as well in the total group of the patient (OR =1.474; p>0.05). Serum levels of PAI-1 were significantly higher in total group of patients compared to controls. The levels of PAI-1 is correlated with carriage of 675 4G/5G polymorphism in the gene for PAI-1 (r=0.534; p=0.03) as well as with BMI, like correlation coefficients were higherin the group with PCOS (0.572; p=0.04). Data from the disease history showed a higher percentage of women with reproductive problems: early pregnancy loss 48.5% and infertility 23.2%, significantly higher in the group with PCOS (58.1% compared to 32.4%). The carriers of polymorphism 4G are at greater risk for early pregnancy loss than those with 5G (61.45% as compared to 36.8%), which confirms that carriage of the polymorphism 4G/5G 675 gene PAl-1 has a specific in multifactorial pathogenesis and expression of PCOS.


Assuntos
Aborto Espontâneo/etiologia , Índice de Massa Corporal , Infertilidade Feminina/etiologia , Inibidor 1 de Ativador de Plasminogênio/genética , Síndrome do Ovário Policístico/complicações , Polimorfismo de Nucleotídeo Único , Aborto Espontâneo/sangue , Aborto Espontâneo/genética , Adulto , Feminino , Humanos , Infertilidade Feminina/sangue , Infertilidade Feminina/genética , Inibidor 1 de Ativador de Plasminogênio/sangue , Síndrome do Ovário Policístico/sangue , Síndrome do Ovário Policístico/genética , Gravidez , Regiões Promotoras Genéticas , Fatores de Risco , Adulto Jovem
2.
Akush Ginekol (Sofiia) ; 53(5): 3-9, 2014.
Artigo em Búlgaro | MEDLINE | ID: mdl-25558663

RESUMO

Approximately 7-12% of women in reproductive age are affected by PCOS[2] and 40 to 70 percent of them are overweight contributing to the clinical picture of PCOS and increased reproductive and metabolic disorder. In order to investigate the role of PAl-1 as a possible risk factor for the development of PCOS a group of 67 women with polycystic ovarian disease and 70 healthy controls were investigated for levels of PAI-1 and carriage of the promoter polymorphism 675 4G/5G in gene of PAl-1. The results of the DNA analysis showed a high carriage of polymorphism 675 4G/4G in promoter of PAI-1 gene in women with PCOS but not as significant (OR = 1.6645, p = 0.141). Serum levels of PAI-1 were significantly higher in total group of patients compared to controls. The levels of PAI-1 is correlated with carriage of 675 4G/5G polymorphism in the gene for PAI-1 (R = 0.534, p = 0.03) as well as wih BMI, like correlation coefficients were higher in the group with PCOS (0.572, p = 0.04). Data from the disease history showed a higher percentage of women with reproductive problems: 61.5% (early pregnancy loss and infertility) significantly higher in the group with PCOS (70.1% compared to 54.1%). The carriers of polymorphism 4G are at greater risk for early pregnancy loss than those with 5G (61.45% as compared to 36.8%), which confirms that carriage of the polymorphism 4G/5G 675 gene PAI-1 has a specific in multifactorial pathogenesis and expression of PCOS.


Assuntos
Perda do Embrião/etiologia , Perda do Embrião/genética , Inibidor 1 de Ativador de Plasminogênio/genética , Síndrome do Ovário Policístico/complicações , Síndrome do Ovário Policístico/genética , Polimorfismo de Nucleotídeo Único , Adulto , Índice de Massa Corporal , Perda do Embrião/sangue , Feminino , Humanos , Inibidor 1 de Ativador de Plasminogênio/sangue , Síndrome do Ovário Policístico/sangue , Gravidez , Regiões Promotoras Genéticas , Reprodução , Adulto Jovem
3.
Akush Ginekol (Sofiia) ; 52(6): 11-4, 2013.
Artigo em Búlgaro | MEDLINE | ID: mdl-24501874

RESUMO

A plenty of factors have been connected with embryo implantation and further fetus development. Recurrent implantation failure (RIF) after assisted reproductive technology (ART) forces seeking the causes of decreased endometrial receptivity. A non-haemostatic function of thrombophilic mutations such as Factor V Leiden (FVL) was considered a factor related with endometrial receptivity. One hundred eighty eight women with two or more RIF after in vitro fertilization procedures investigated for carrier status for FVL was compared with carrier status of 97 women without reproductive failure who give a birth of at least one health child. There was no significant difference in carrier status for FVL in patients and controls (5.9% and 7.2% respectively, OR 0.80, 95% CI (0.26-2.73, p>0.05). Negligible higher prevalence of FVL was fond in health subjects compared with women with RIF A slightly positive relationship was found between FVL and embryo implantation. A preliminary determination of thrombophilic status in RIF women could specify needing or rejection of anticoagulant therapy during implantation period.


Assuntos
Implantação do Embrião , Fator V/genética , Fertilização in vitro , Adulto , Feminino , Humanos , Trombofilia/genética
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA