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Biological and Clinical Rationale for Androgen Priming in Ovarian Stimulation

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@article{2978bd0d5b7b494b8e8c9acb0455896f,
title = "Biological and Clinical Rationale for Androgen Priming in Ovarian Stimulation",
abstract = "Androgen receptors are expressed by all stages of growing follicles, and follicular fluid androgen levels are positively correlated to granulosa cell androgen receptor and follicle-stimulating hormone (FSH) receptor expression. Thus, androgens may promote follicular growth, accumulation and/or responsiveness to gonadotropins. This is explored therapeutically in the concept of androgen priming, to improve the ovarian response to stimulation in assisted reproduction. Androgen effects may be achieved in two different ways, either directly by providing exogenous androgen or by providing luteinizing hormone (LH) activity [i.e., LH or human chorionic gonadotropin (hCG)] to stimulate local ovarian production of androgen. The androgen concentrations in follicular fluid by far exceed the levels in female circulation and it has recently been shown that there was no correlation between serum testosterone levels and follicular fluid androgen levels. There is some evidence that administration of exogenous dehydroepiandrosterone or testosterone increases live birth rates, but an optimal protocol has not been established and such adjuvant treatment should be considered experimental. Furthermore, studies exploring long-term administration of LH activity, achieving LH levels comparable to those seen in women with polycystic ovary syndrome, are awaited. The aim of the present review is to discuss critically the most suitable approach for androgen priming from a biological and clinical standpoint, and to evaluate current approaches and results obtained in clinical trials.",
keywords = "androgen priming, follicular recruitment, follicular responsiveness, IVF, LH activity, local androgen production, testosterone",
author = "Kristine L{\o}ssl and Freiesleben, {Nina la Cour} and Wissing, {Marie Louise} and {Birch Petersen}, Kathrine and Holt, {Marianne Dreyer} and Mamsen, {Linn Salto} and Anderson, {Richard A} and Andersen, {Claus Yding}",
note = "Copyright {\textcopyright} 2020 L{\o}ssl, Freiesleben, Wissing, Birch Petersen, Holt, Mamsen, Anderson and Andersen.",
year = "2020",
month = sep,
day = "4",
doi = "10.3389/fendo.2020.00627",
language = "English",
volume = "11",
pages = "627",
journal = "Frontiers in Endocrinology",
issn = "1664-2392",
publisher = "Frontiers Research Foundation",

}

RIS

TY - JOUR

T1 - Biological and Clinical Rationale for Androgen Priming in Ovarian Stimulation

AU - Løssl, Kristine

AU - Freiesleben, Nina la Cour

AU - Wissing, Marie Louise

AU - Birch Petersen, Kathrine

AU - Holt, Marianne Dreyer

AU - Mamsen, Linn Salto

AU - Anderson, Richard A

AU - Andersen, Claus Yding

N1 - Copyright © 2020 Løssl, Freiesleben, Wissing, Birch Petersen, Holt, Mamsen, Anderson and Andersen.

PY - 2020/9/4

Y1 - 2020/9/4

N2 - Androgen receptors are expressed by all stages of growing follicles, and follicular fluid androgen levels are positively correlated to granulosa cell androgen receptor and follicle-stimulating hormone (FSH) receptor expression. Thus, androgens may promote follicular growth, accumulation and/or responsiveness to gonadotropins. This is explored therapeutically in the concept of androgen priming, to improve the ovarian response to stimulation in assisted reproduction. Androgen effects may be achieved in two different ways, either directly by providing exogenous androgen or by providing luteinizing hormone (LH) activity [i.e., LH or human chorionic gonadotropin (hCG)] to stimulate local ovarian production of androgen. The androgen concentrations in follicular fluid by far exceed the levels in female circulation and it has recently been shown that there was no correlation between serum testosterone levels and follicular fluid androgen levels. There is some evidence that administration of exogenous dehydroepiandrosterone or testosterone increases live birth rates, but an optimal protocol has not been established and such adjuvant treatment should be considered experimental. Furthermore, studies exploring long-term administration of LH activity, achieving LH levels comparable to those seen in women with polycystic ovary syndrome, are awaited. The aim of the present review is to discuss critically the most suitable approach for androgen priming from a biological and clinical standpoint, and to evaluate current approaches and results obtained in clinical trials.

AB - Androgen receptors are expressed by all stages of growing follicles, and follicular fluid androgen levels are positively correlated to granulosa cell androgen receptor and follicle-stimulating hormone (FSH) receptor expression. Thus, androgens may promote follicular growth, accumulation and/or responsiveness to gonadotropins. This is explored therapeutically in the concept of androgen priming, to improve the ovarian response to stimulation in assisted reproduction. Androgen effects may be achieved in two different ways, either directly by providing exogenous androgen or by providing luteinizing hormone (LH) activity [i.e., LH or human chorionic gonadotropin (hCG)] to stimulate local ovarian production of androgen. The androgen concentrations in follicular fluid by far exceed the levels in female circulation and it has recently been shown that there was no correlation between serum testosterone levels and follicular fluid androgen levels. There is some evidence that administration of exogenous dehydroepiandrosterone or testosterone increases live birth rates, but an optimal protocol has not been established and such adjuvant treatment should be considered experimental. Furthermore, studies exploring long-term administration of LH activity, achieving LH levels comparable to those seen in women with polycystic ovary syndrome, are awaited. The aim of the present review is to discuss critically the most suitable approach for androgen priming from a biological and clinical standpoint, and to evaluate current approaches and results obtained in clinical trials.

KW - androgen priming

KW - follicular recruitment

KW - follicular responsiveness

KW - IVF

KW - LH activity

KW - local androgen production

KW - testosterone

UR - http://www.scopus.com/inward/record.url?scp=85091241293&partnerID=8YFLogxK

U2 - 10.3389/fendo.2020.00627

DO - 10.3389/fendo.2020.00627

M3 - Review

C2 - 33013703

VL - 11

SP - 627

JO - Frontiers in Endocrinology

JF - Frontiers in Endocrinology

SN - 1664-2392

M1 - 627

ER -

ID: 60978749