4.7 Article

Defining the proliferative phase endometrial defect

期刊

FERTILITY AND STERILITY
卷 91, 期 3, 页码 698-704

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.fertnstert.2007.12.066

关键词

Endometrium; endometrial development; proliferative phase; clomiphene; FSH; endometriosis; polycystic ovary syndrome; recurrent pregnancy loss

资金

  1. NICHD NIH HHS [U54 HD052668, R01 HD036887-06, R01 HD036887, U54 HD052668-01A10001] Funding Source: Medline

向作者/读者索取更多资源

Objective: To evaluate proliferative phase endometrial development in a heterogeneous infertility population. Design: Retrospective study. Setting: University-based infertility practice. Patient(s): Two hundred forty-six treatment cycles. Intervention(s): Clomiphene citrate or FSH ovarian stimulation, followed by IUI or IVF. Main Outcome Measure(s): Endometrial thickness according to transvaginal ultrasonography; clinical pregnancy rate. Result(s): Endometrial growth began from a nadir of approximately 4.5 mm on cycle day 4 and increased linearly to a plateau of approximately 10 mm on cycle day 9. This same pattern was observed in all cycles, regardless of pregnancy, drug, or underlying diagnosis. Follicle-stimulating hormone-stimulated cycles showed a significantly increased endometrial thickness compared with clomiphene citrate cycles (10.1 vs. 8.3 mm). Maximum endometrial 2 level. Subjects who trial thickness achieved showed a correlation with age, body mass index, and maximum E-2 level. Subjects who carried a primary diagnosis of polycystic ovary syndrome, endometriosis, or recurrent pregnancy loss all achieved a significantly lower peak endometrial thickness than control subjects. There was a trend toward increased endometrial thickness in cycles resulting in pregnancy compared with those not (10.1 vs. 9.6 mm, respectively). Conclusion(s): Endometrial development follows a predictable pattern, with a plateau in growth at cycle day 9. Diseases associated with infertility manifest a proliferative phase defect that can be recognized clinically. (Fertil Steril (R) 2009;91:698-704. (C) 2009 by American Society for Reproductive Medicine.)

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