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Ovarian Response to Recombinant Follicle Stimulating Hormone in Women With PCOS

Phase 4
Completed
Conditions
Healthy
Hyperandrogenism
Anovulation
Polycystic Ovary Syndrome
Interventions
Registration Number
NCT03252223
Lead Sponsor
University of California, San Diego
Brief Summary

Women with PCOS suffer from anovulation and, as a result, infertility. Efforts to clinically induce ovulation in these women using follicle stimulating hormone (FSH) administered subcutaneously seemingly requires prolonged administration compared to that of ovulatory women without PCOS. The apparent differing ovarian responsiveness to FSH between PCOS and normal women has not been carefully studied. We propose to address this issue by performing a dose-response study and examine ovarian follicle (estrogen, E2) responses to FSH administered subcutaneously in women with PCOS compared to responses observed in normal women.

Detailed Description

In women with polycystic ovary syndrome (PCOS) androgen excess is fundamental to the clinical and physiological alterations of this disorder. In particular, androgen overproduction induces distinctive PCO morphology and appears to influence follicle function. Studies conducted in animals and nonhuman primates have demonstrated that androgens increase follicle number and in small antral follicles enhance granulosa cell (GC) responsiveness to gonadotropin stimulation. However, androgens also have been shown to clearly inhibit GC aromatase activity, and in PCOS follicular fluid, androgen content is abnormally increased. Efforts to reconcile these differences are nonexistent. Moreover, appropriate clinical studies to examine the effects of androgen on follicle health in women are lacking. Excessive androgen exposure in women due to functional tumors or high-dose testosterone treatment in F-M transsexuals has been associated with PCO morphology. Use of androgen therapy to promote follicle growth prior to ovarian hyperstimulation in women undergoing in vitro fertilization has not provided consistent results. However, in these studies GC responses to FSH were not carefully assessed, study populations were exclusively women with previously poor ovarian responses to FSH, and women with PCOS were not included. In fact, there are essentially no clinical studies that have addressed in detail the impact of androgen on follicle function in normal or PCOS women. We hypothesize that androgen facilitates GC responses to FSH in normal women and androgen excess further amplifies follicle growth and function in women with PCOS. We propose to study the effect of increased ovarian androgen on follicle function by increasing intraovarian androgen accumulation using aromatase inhibition followed by FSH stimulation. The experiments in this project are designed to provide insight into whether androgen excess facilitates or interferes with follicle function and ovulation in women with PCOS.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
33
Inclusion Criteria
  • Subjects determined to have PCOS based on clinical history of irregular menses and clinical or laboratory evidence of hyperandrogenism and polycystic ovaries on ultrasound OR
  • Subjects determined to have a clinical history of regular periods.
Exclusion Criteria
  1. Women with hemoglobin less than 11 gm/dl at screening evaluation
  2. Women with untreated thyroid abnormalities
  3. Pregnant women or women who are nursing
  4. Women with BMI > 37
  5. Women with known sensitivity to the agents being used
  6. Women with diabetes, or renal, liver, or heart disease
  7. Women with any hormonal therapy or metformin for at least 2 months prior to study start.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Women with normal mensesRecombinant Follicle Stimulating Hormone-
Women with Polycystic Ovary SyndromeRecombinant Follicle Stimulating Hormone-
Primary Outcome Measures
NameTimeMethod
Change in follicle count in following FSH administrationWith each dose tested, a pelvic ultrasound will be done before and 3 days after commencing FSH

Number of ovarian follicles will be assessed by pelvic ultrasound

Change in granulosa cell function in 24 hours intervals following FSH administrationSerum levels will be assessed daily during each 3 day FSH stimulation test and for five days following the initial FSH administration

Granulosa function will be assessed using estradiol and inhibin levels

Change in follicular size in following FSH administrationWith each dose tested, a pelvic ultrasound will be done before and 3 days after commencing FSH

Size of ovarian follicles will be assessed by pelvic ultrasound

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of California, San Diego

🇺🇸

La Jolla, California, United States

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