The effect of estradiol on granulosa cell responses to FSH in women with polycystic ovary syndrome

The influence of estradiol (E ) on granulosa cell (GC) function has not been tested clinically in women with polycystic ovary syndrome (PCOS). The objective of this study is to determine if E influences GC responses to FSH in women with PCOS. This is a two phase, single cohort study conducted over a...

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Published inReproductive biology and endocrinology Vol. 15; no. 1; p. 13
Main Authors Homer, Michael V, Rosencrantz, Marcus A, Shayya, Rana F, Chang, R Jeffrey
Format Journal Article
LanguageEnglish
Published England BioMed Central 10.02.2017
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Summary:The influence of estradiol (E ) on granulosa cell (GC) function has not been tested clinically in women with polycystic ovary syndrome (PCOS). The objective of this study is to determine if E influences GC responses to FSH in women with PCOS. This is a two phase, single cohort study conducted over a 2-year period at a single academic center. Nine women with PCOS according to NIH criteria. In Phase 1, FSH stimulation of GC responses as measured by E and Inhibin B (Inh B) were assessed before and at 5 and 6 weeks after GnRH agonist administration. In Phase 2, the same protocol was employed with the addition of an aromatase inhibitor (letrozole, LET) administered daily beginning at week 4 for 2 weeks. In Phase 1, recovery of FSH, E and Inh B from ovarian suppression occurred at 5 and 6 weeks after GnRH agonist injection and preceded resumption of LH and androgen secretion. In Phase 2, hormone recovery after GnRH agonist was characterized by elevated FSH and suppressed E levels whereas recovery of LH and androgen levels were unchanged. In Phase 1, FSH stimulated E and Inh B responses were unaltered during recovery from ovarian suppression. In Phase 2, E and Inh B fold changes after FSH were significantly reduced at weeks 5 (p < 0.04) and 6 (p < 0.01), respectively. In anovulatory women with PCOS, chronic, unopposed E secretion may contribute, at least in part, to enhanced ovarian responsiveness to FSH. NCT02389088.
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ISSN:1477-7827
1477-7827
DOI:10.1186/s12958-017-0230-0