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Exp Clin Endocrinol Diabetes 2012; 120(02): 73-79
DOI: 10.1055/s-0031-1291343
Article
© J. A. Barth Verlag in George Thieme Verlag KG Stuttgart · New York

Role of the CAG Repeat Polymorphism of the Androgen Receptor Gene in Polycystic Ovary Syndrome (PCOS)

A. N. Schüring   *
1   Department of Obstetrics and Gynecology, Münster University Hospital, Münster, Germany
,
A. Welp   *
1   Department of Obstetrics and Gynecology, Münster University Hospital, Münster, Germany
,
J. Gromoll
2   Institute of Reproductive Medicine, Münster University Hospital, Münster, Germany
,
M. Zitzmann
2   Institute of Reproductive Medicine, Münster University Hospital, Münster, Germany
,
B. Sonntag
1   Department of Obstetrics and Gynecology, Münster University Hospital, Münster, Germany
,
E. Nieschlag
2   Institute of Reproductive Medicine, Münster University Hospital, Münster, Germany
,
R. R. Greb
1   Department of Obstetrics and Gynecology, Münster University Hospital, Münster, Germany
,
L. Kiesel
1   Department of Obstetrics and Gynecology, Münster University Hospital, Münster, Germany
› Author Affiliations
Further Information

Publication History

received 12 April 2011
first decision 15 September 2011

accepted 18 October 2011

Publication Date:
08 November 2011 (online)

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Abstract

Background:

Polycystic ovary syndrome (PCOS) is a frequent heterogenic disorder with a familial background. Androgenic effects, determining the clinical features of the syndrome, are mediated by the androgen receptor (AR), whose activity is modulated by a genetic polymorphism. We investigated the role of the CAG repeat polymorphism of the androgen receptor in PCOS.

Methods:

In the infertility unit of a university clinic, 72 PCOS patients were compared with 179 ovulatory controls undergoing a standardized diagnostic work-up. The number of CAG repeats was determined by PCR, labelling with IR-800 and PAGE. X-chromosome inactivation was assessed by a methylation-sensitive assay.

Results:

Compared to controls, PCOS patients displayed a shorter mean CAG repeat length, encoding for higher AR activity (P=0.001). CAG repeat length correlated inversely with oligomenorrhea, a central androgen dependent feature of the syndrome (P=0.005). In a binomial regression analysis including BMI, LH and free testosterone, CAG repeat length was identified as an independent risk factor for PCOS (P=0.002).

Conclusions:

The CAG repeat polymorphism could constitute one of the genetic factors modulating the syndrome’s phenotype, contributing to its clinical heterogeneity and associated metabolic consequences.

Key words

polycystic ovary syndrome - hyperandrogenemia - luteinizing hormone - androgen receptor - genetic polymorphism
* 

* Both authors contributed equally.


 

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