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1.
Gynecol Endocrinol ; 32(9): 709-713, 2016 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-26951881

RESUMO

This prospective study aimed to determine the status of circulating levels of C-reactive protein (CRP), tumor necrosis factor α (TNF-α), IL-27, IL-35, IL-37, α-1 acid glycoprotein in patients with polycystic ovary syndrome (PCOS) compared with controls and to evaluate their relation with hyperandrogenism and obesity. Forty-eight patients with PCOS (29 obese, 19 lean) and 40 healthy controls (20 obese, 20 lean) were enrolled. CRP, TNF-α, IL-27, IL-35, IL-37, α-1 acid glycoprotein, sex hormone-binding globulin (SHBG), dehydroepiandrosterone sulfate (DHEA-S) levels were measured. Levels of total testosterone, A4, DHEA-S were significantly higher in patients with PCOS than in controls both in the obese and lean groups, while levels of SHBG were significantly lower in all patients with PCOS than in all (p < 0.05). Free androgen index (FAI) values were significantly higher in all patients with PCOS than in all controls (all p < 0.05). Levels of CRP, TNF-α, α-1 acid glycoprotein were significantly increased in all patients with PCOS compared with all controls (all p < 0.001). FAI had a positive correlation with CRP, TNF-α, α-1 acid glycoprotein, a negative correlation with IL-27, IL-25, IL-37 (all p < 0.01). Body mass index had a negative correlation with IL-27, IL-35, IL-37, a positive correlation with α-1 acid glycoprotein, FAI (p < 0.05). The findings confirm the proinflammatory state of PCOS. Moreover, obesity along with PCOS significantly elevates the inflammatory status and hyperandrogenism.


Assuntos
Hiperandrogenismo/sangue , Inflamação/sangue , Obesidade/sangue , Síndrome do Ovário Policístico/sangue , Adulto , Comorbidade , Feminino , Humanos , Hiperandrogenismo/epidemiologia , Inflamação/epidemiologia , Obesidade/epidemiologia , Síndrome do Ovário Policístico/epidemiologia , Estudos Prospectivos , Adulto Jovem
2.
Fertil Steril ; 103(4): 1059-1064.e2, 2015 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-25747132

RESUMO

OBJECTIVE: To evaluate and compare the levels of Mucin 1 (MUC-1) and Glycodelin A (GdA) in precisely timed endometrial biopsies and blood samples taken from women with recurrent implantation failure, and women with proven fertility, in a control group. DESIGN: Molecular studies in human blood and tissue. SETTING: University hospital. PATIENT(S): Women with recurrent implantation failure and women with proven fertility. INTERVENTION(S): Primary endometrial cells and blood samples during the implantation "window" (between day 7 and day 9 after the surge in luteinizing hormone). MAIN OUTCOME MEASURE(S): Expression of MUC-1 and GdA in the human endometrium and in blood during the implantation window were analyzed by enzyme-linked immunosorbent assay. Additionally, MUC-1 and GdA levels in tissue were analyzed by western blot during the same period. RESULT(S): Both blood and tissue measurements of MUC-1 and GdA were significantly lower in women with recurrent implantation failure than in fertile women during the implantation window. In addition, we found a highly significant correlation between blood vs. tissue measurements of both MUC-1 and GdA. CONCLUSION(S): The present study reveals that blood and tissue levels of MUC-1 and GdA are much lower in women with RIF, compared with those in fertile women. Receptivity can be evaluated with noninvasive blood sampling, rather than more-invasive endometrium sampling, as the blood and tissue measurements of MUC-1 and GdA are correlated.


Assuntos
Aborto Habitual/metabolismo , Implantação do Embrião , Glicoproteínas/fisiologia , Infertilidade Feminina/metabolismo , Mucina-1/fisiologia , Aborto Habitual/sangue , Aborto Habitual/patologia , Adulto , Estudos de Casos e Controles , Endométrio/metabolismo , Endométrio/patologia , Ensaio de Imunoadsorção Enzimática , Feminino , Glicodelina , Glicoproteínas/sangue , Glicoproteínas/metabolismo , Humanos , Infertilidade Feminina/sangue , Infertilidade Feminina/patologia , Ciclo Menstrual/sangue , Ciclo Menstrual/metabolismo , Mucina-1/sangue , Mucina-1/metabolismo
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