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Fertil Steril ; 91(2): 489-99, 2009 Feb.
Article in English | MEDLINE | ID: mdl-18353318

ABSTRACT

OBJECTIVE: To characterize possible endometrial defects in infertile women with isolated PCO morphology. DESIGN: Prospective study. SETTING: An academic hospital with an IVF unit. PATIENT(S): Women with primary unexplained infertility and isolated PCO, fertile women, and women with infertility secondary to male factor. INTERVENTION(S): Thirty-one women (fertile and with male factor infertility) had endometrial sampling across the menstrual cycle. Nine fertile women and 10 infertile women with isolated PCO had sampling on day LH +7, adjusted for histologic dating. MAIN OUTCOME MEASURE(S): Expression of alphavbeta3 and its ligand, osteopontin, were determined using real-time quantitative polymerase chain reaction and immunohistochemistry. In vitro regulation of osteopontin was assessed using the Ishikawa cell line. RESULT(S): Cyclic variations revealed a fall in integrin alphavbeta3 mRNA during the secretory phase with concomitant up-regulation of osteopontin mRNA. Immunohistochemistry on day LH +7 demonstrated a significant reduction in expression of osteopontin in the isolated PCO group with no difference in expression of alphavbeta3. In vitro studies confirmed up-regulation of osteopontin by estrogen with no apparent effect of androgen. CONCLUSION(S): These results demonstrate an apparent reduction of osteopontin expression, important in cell-cell adhesion, during the window of implantation in infertile women with isolated PCO morphology.


Subject(s)
Embryo Implantation , Endometrium/metabolism , Infertility, Female/metabolism , Integrin alphaVbeta3/metabolism , Osteopontin/metabolism , Polycystic Ovary Syndrome/metabolism , Adult , Cell Line , Down-Regulation , Estradiol/metabolism , Female , Humans , Immunohistochemistry , Infertility, Female/etiology , Infertility, Female/physiopathology , Integrin alphaVbeta3/genetics , Male , Metribolone/pharmacology , Osteopontin/genetics , Polycystic Ovary Syndrome/complications , Polycystic Ovary Syndrome/physiopathology , Progesterone/metabolism , Prospective Studies , RNA, Messenger/metabolism , Reverse Transcriptase Polymerase Chain Reaction , Testosterone Congeners/pharmacology , Time Factors
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