Eur J Endocrinol
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DOI: 10.1530/eje.1.02195
European Journal of Endocrinology, Vol 155, Issue 1, 127-130
Copyright © 2006 by European Society of Endocrinology
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CLINICAL STUDY

The androgen receptor CAG repeat modifies the impact of testosterone on insulin resistance in women with polycystic ovary syndrome

Matthias Möhlig1,2, Annette Jürgens4, Joachim Spranger1,2, Kurt Hoffmann3, Martin O Weickert1,2, Hans W Schlösser6, Thilo Schill6, Georg Brabant7, Andreas Schüring5, Andreas F H Pfeiffer1,2, Jörg Gromoll4 and Christof Schöfl1

1 Department of Endocrinology, Diabetes and Nutrition, Charité-University Medicine Berlin, Berlin, Germany, 2 Departments of Clinical Nutrition and 3 Epidemiology, German Institute of Human Nutrition, Potsdam-Rehbruecke, 14558 Nuthetal, Germany, 4 Institute of Reproductive Medicine, and 5 Department of Obstetrics and Gynecology, University of Münster, 48129 Münster, Germany, and 6 Departments of Gynecological Endocrinology and 7 Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, 30625 Hannover, Germany

(Correspondence should be addressed to C Schöfl; Email: christof.schoefl{at}charite.de)

Objective: Hyperandrogenism is a central feature of the polycystic ovary syndrome (PCOS) and might worsen insulin resistance (IR) often seen in PCOS. Androgens act through the androgen receptor (AR). A polymorphic CAG repeat sequence within the AR gene was reported to modulate its transactivation activity. Therefore, we investigated a putative interaction between testosterone and the CAG repeat length polymorphism with respect to IR.

Design: In 63 PCOS women with normal glucose tolerance free testosterone, the biallelic CAG repeat length and a multiplicative interaction term were investigated by multiple linear regression analysis for an association with IR as indicated by the homeostasis model assessment of IR (HOMA-IR).

Results: Free testosterone was correlated with HOMA-IR. The impact of testosterone on HOMA-IR was modified by the AR CAG length as indicated by an interaction term. This interaction remained significant after adjustment for smoking, age and body mass index. While there was a positive association of free testosterone with HOMA-IR, the interaction term was inversely associated. The model, which explained 42.5% of the variation of HOMA-IR predicted that in carriers of short CAG lengths, an increase in testosterone increased IR. This effect attenuated with rising biallelic CAG length until it turns into the opposite at a CAG length longer than 23. The results were confirmed by using CIGMA as another measure of IR.

Conclusions: The association between testosterone and IR is modified by the CAG repeat polymorphism within the AR. Therefore, the evaluation of testosterone effects on IR seems to require consideration of the AR CAG repeat polymorphism in PCOS women.




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