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Human Reproduction 2007 22(7):1824-1829; doi:10.1093/humrep/dem118
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© The Author 2007. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Serum visfatin in relation to insulin resistance and markers of hyperandrogenism in lean and obese women with polycystic ovary syndrome

Irina Kowalska1,3, Marek Straczkowski1, Agnieszka Nikolajuk1, Agnieszka Adamska1, Monika Karczewska-Kupczewska1, Elzbieta Otziomek1, Slawomir Wolczynski2 and Maria Gorska1

1 Department of Endocrinology, Diabetology and Internal Medicine, Medical University of Bialystok, M.C. Sklodowskiej 24a, 15-276 Bialystok, Poland 2 Department of Reproduction and Gynecological Endocrinology, Medical University of Bialystok, M.C. Sklodowskiej 24a, 15-276 Bialystok, Poland

3 Correspondence address. Tel: +48-85-7468239; Fax: +48-85-7447611; E-mail: irinak{at}poczta.onet.pl

BACKGROUND: Visfatin, a protein secreted by adipose tissue, is suggested to play a role in pathogenesis of insulin resistance. In polycystic ovary syndrome (PCOS), insulin resistance might be involved in the development of endocrine and metabolic abnormalities. The aim of the study was to asses the relation between serum visfatin concentration and insulin sensitivity and markers of hyperandrogenism in lean and obese PCOS patients.

METHODS: The study group consisted of 70 women with PCOS (23 lean and 47 obese) and 45 healthy women (25 lean and 20 obese). Euglycemic hyperinsulinemic clamp and the measurements of serum visfatin, sex hormones were performed.

RESULTS: The PCOS group had lower insulin sensitivity (P = 0.00049) and higher serum visfatin (P = 0.047) in comparison to the control group. The decrease in insulin sensitivity was present in both the lean (P = 0.019) and obese (P = 0.0077) PCOS subjects, whereas increase in serum visfatin was observed only in lean PCOS subjects (P = 0.012). In the whole group, serum visfatin was negatively correlated with insulin sensitivity (r = –0.27, P = 0.004). This relationship was also observed in the subgroup of lean (r = –0.30, P = 0.038), but not obese women. Additionally, in lean women, visfatin was associated with serum testosterone (r = 0.47, P = 0.002) and free androgen index (r = 0.48, P = 0.002), independently of other potential confounding factors.

CONCLUSIONS: Visfatin is associated with insulin resistance and markers of hyperandrogenism in lean PCOS patients.

Key words: hyperandrogenism/insulin resistance/polycystic ovary syndrome/visfatin

Submitted on December 5, 2006; resubmitted on March 31, 2007; accepted on April 13, 2007.


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