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1.
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
2.
J Clin Endocrinol Metab ; 92(5): 1975-8, 2007 May.
Article in English | MEDLINE | ID: mdl-17341570

ABSTRACT

CONTEXT: In polycystic ovary syndrome (PCOS), an increased proportion of follicles leave the primordial (resting) pool and initiate growth. However, there is little evidence for a reduced reproductive life span (early menopause) in women with PCOS, suggesting that the dynamics of follicle growth, and of follicle loss by atresia, is altered in PCOS. OBJECTIVE: The aim of this study was to investigate the possibility that loss of preantral follicles by atresia is reduced in PCOS, leading to prolonged follicle survival. DESIGN: We compared follicle growth in normal and polycystic ovaries using cultures of small ovarian biopsies. SETTING: Tissue samples were obtained at routine laparoscopy from 12 patients with anovulatory PCOS and 16 controls and processed in an ovarian physiology laboratory. MAIN OUTCOME MEASURES: We performed morphometric analysis of follicle population in tissue fixed at time of biopsy (d 0) or after 5, 10, or 15 d in culture. Analyses included assessment of follicle and oocyte diameter, number and proportion of primordial and growing follicles, and number and proportion of atretic follicles. RESULTS: In tissue fixed on d 0, the proportion of healthy growing follicles was, as expected, greater in ovaries from PCOS patients than in normal ovaries (64 vs. 28%; P = 0.0005), but there were no differences between PCOS and normal tissue during culture. The rate of atresia throughout the period of culture in follicles was, however, significantly lower in PCOS tissue (P < 0.0001). After culture, 80% of follicles in normal ovarian tissue were atretic compared with 53% in PCOS biopsies. CONCLUSION: Follicles from polycystic ovaries demonstrate a decreased rate of atresia in culture, suggesting a mechanism for maintaining a larger follicle pool throughout reproductive life.


Subject(s)
Ovarian Follicle/pathology , Polycystic Ovary Syndrome/pathology , Adult , Cell Survival/physiology , Cells, Cultured , Female , Follicular Atresia/physiology , Humans , Laparoscopy , Tissue Culture Techniques
3.
Fertil Steril ; 82(3): 735-7, 2004 Sep.
Article in English | MEDLINE | ID: mdl-15374723

ABSTRACT

OBJECTIVE: To present the first report of massive hemoperitoneum in a case of essential thrombocythemia after transvaginal oocyte retrieval for IVF and review the relevant literature related to the management of patients with this condition. DESIGN: Case report. SETTING: Assisted conception unit of a tertiary care university hospital in the United Kingdom. PATIENT(S): A 37-year-old woman with essential thrombocythemia who developed massive intra-abdominal bleeding after transvaginal oocyte retrieval for IVF. INTERVENTION(S): Emergency laparotomy and right salpingoophorectomy. RESULT(S): Resuscitation of the patient. MAIN OUTCOME MEASURE(S): Overall management of the patient is discussed. CONCLUSION(S): The management of patients with essential thrombocythemia at the childbearing period poses a difficult problem. Fertility may be reduced, and an adverse outcome of pregnancy due to thrombotic or bleeding complications is a matter of concern. A multidisciplinary approach with close and early cooperation with the hematologists before initiation of IVF therapy for patients with essential thrombocythemia is essential. Efforts should be made to reduce the platelet count and assess the platelet function before embarking on IVF, keeping in mind the double jeopardy from bleeding and thrombosis in these cases.


Subject(s)
Fertilization in Vitro/adverse effects , Hemoperitoneum/etiology , Oocytes/cytology , Thrombocytosis/etiology , Adult , Blood Transfusion , Female , Hemoperitoneum/surgery , Humans , Salpingostomy , Thrombocytosis/surgery
5.
Biochem Biophys Res Commun ; 292(1): 102-8, 2002 Mar 22.
Article in English | MEDLINE | ID: mdl-11890678

ABSTRACT

Scanning immunoelectron microscopy was applied to human endometrial epithelium for the first time to simultaneously determine epitope localisation and cellular architecture. The method was established using HMFG1, an antibody to a glycoform of the MUC1 mucin. This was chosen because of the potential importance of MUC1 in connection with endometrial receptivity. Biopsies of mid-secretory phase endometrium were labelled using HMFG1 and silver-enhanced, gold-conjugated secondary antibody was then visualised by back-scattered electron imaging. The method provided a highly specific localisation of the HMFG1 epitope to the ciliated and "ciliogenic" cells of the endometrial surface. In contrast, no reactivity was evident on the microvillous cells and endometrial pinopodes. The potential to integrate the study of the molecular and ultrastructural changes that occur in the endometrium by using scanning immunoelectron microscopy offers a powerful means of expanding our understanding of the adaptation of the endometrium in preparation for embryo implantation.


Subject(s)
Endometrium/chemistry , Endometrium/ultrastructure , Microscopy, Electron, Scanning/methods , Microscopy, Immunoelectron/methods , Mucin-1/immunology , Adult , Endometrium/physiology , Epithelium/chemistry , Epithelium/ultrastructure , Epitopes/analysis , Female , Humans , Menstrual Cycle , Mucin-1/analysis
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