Biological variation of total testosterone, free androgen index and bioavailable testosterone in polycystic ovarian syndrome: implications for identifying hyperandrogenaemia

Authors: Cho, L. W.1; Kilpatrick, E. S.2; Jayagopal, V.3; Diver, M. J.4; Atkin, S. L.1

Source: Clinical Endocrinology, Volume 68, Number 3, March 2008 , pp. 390-394(5)

Publisher: Blackwell Publishing

Key:
Free Content - Free Content
New Content - New Content
Subscribed Content - Subscribed Content
Free Trial Content - Free Trial Content

Abstract:

Summary Objective 

Hyperandrogenaemia is one of the three Rotterdam consensus diagnostic criteria for polycystic ovarian syndrome (PCOS) and may be measured by estimation of total testosterone, free androgen index (FAI) or bioavailable testosterone (BioT). The aim of this study was to compare the biological variability of total testosterone with that of the biological variability of both the FAI and BioT, to determine the least variable measurement for clinical practice. Design 

Comparative study. Patients 

Blood samples were collected after an overnight fast at 4-day intervals on 10 consecutive occasions from 12 PCOS patients and 11 weight- and age-matched control women. Measurements 

Duplicate samples of stored serum were analysed for total testosterone, SHBG and BioT in a single batch. Results 

The PCOS group had a significantly higher median BioT, FAI and total testosterone than controls. In both the PCOS and control groups, the intraindividual variance was small and similar for BioT and FAI. There was no significant difference between the within-subject biological coefficient of variation (CVI) for BioT, FAI and total testosterone. The maximum and minimum critical differences were +58% and -37% for BioT and +70% and -40% for FAI, respectively. Conclusion 

FAI appears to be the better diagnostic marker to distinguish hyperandrogenism in patients with PCOS, but once diagnosis has been made, all three methods should be equally good in monitoring further changes in the androgen status.

Document Type: Research article

DOI: 10.1111/j.1365-2265.2007.03053.x

Affiliations: 1: Department of Medicine, University of Hull, 2: Department of Clinical Biochemistry, Hull Royal Infirmary, 3: Department of Medicine, York Hospital and 4: Department of Clinical Biochemistry, Royal Liverpool University Hospital, Liverpool, UK

The full text electronic article is available for purchase. You will be able to download the full text electronic article after payment.

$50.16 plus tax      Refund Policy

 

OR

Back to top

Key:
Free Content - Free Content
New Content - New Content
Subscribed Content - Subscribed Content
Free Trial Content - Free Trial Content
Share this item with others: These icons link to social bookmarking sites where readers can share and discover new web pages.
Page Help Click here for Page Help
Shopping cart
Tools
Sign in






Need to register?
Sign up here
Text size: A | A | A | A