Skip to main content Accessibility help
×
Hostname: page-component-586b7cd67f-t8hqh Total loading time: 0 Render date: 2024-11-28T02:08:59.622Z Has data issue: false hasContentIssue false

11 - Treatment of hyperandrogenism in polycystic ovary syndrome

Published online by Cambridge University Press:  05 July 2014

Adam Balen
Affiliation:
University of Leeds
Stephen Franks
Affiliation:
St Mary’s Hospital, London
Roy Homburg
Affiliation:
Homerton Fertility Centre, London
Sean Kehoe
Affiliation:
John Radcliffe Hospital, Oxford
Get access

Summary

Introduction

Hyperandrogenism is the most common endocrinopathy seen in women and may result from ovarian or adrenal overproduction of androgens, altered peripheral metabolism and/or end-organ hypersensitivity. Androgen excess can have profound effects on human skin, especially the skin appendages, sebaceous glands and hair follicles, which are strongly dependent on biologically active androgens.

The development of sudden-onset acne and/or hirsutism, female-pattern hair loss, irregular menses, increased libido, acanthosis nigricans, deepening voice, clitoromegaly or other signs of hyperandrogenism such as cushingoid features requires further investigation. It is important to recognise that women with hyperandrogenism may also have insulin resistance that puts them at increased risk of developing diabetes and cardiovascular disease. The treatment of these women should be managed by an endocrinologist and a gynaecologist to ensure that a comprehensive approach is adopted. The most common cause of hyperandrogenism in women is polycystic ovary syndrome (PCOS) but congenital adrenal hyperplasia as well as ovarian and adrenal tumours may need to be considered.

In the sebaceous gland, androgens stimulate sebocyte proliferation. This is most pronounced in facial sebocytes and leads to increased sebum production. Within the intrafollicular duct of the pilosebaceous unit, androgens increase the rate of mitosis and epithelial proliferation, leading to hyperkeratosis. These events contribute to the pathogenesis and subsequent development of clinical acne.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2010

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Save book to Kindle

To save this book to your Kindle, first ensure [email protected] is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×