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 in | Reproductive biology and endocrinology Vol. 15; no. 1; p. 13 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
England
BioMed Central
10.02.2017
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Subjects | |
Online Access | Get full text |
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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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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 1477-7827 1477-7827 |
DOI: | 10.1186/s12958-017-0230-0 |