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HERO ID
7398068
Reference Type
Journal Article
Title
Age, body mass index, and serum level of DHEA-S can predict glucocorticoid receptor function in women with polycystic ovary syndrome
Author(s)
Macut, D; Milutinovic, DV; Bozic, I; Matic, G; Brkljacic, J; Panidis, D; Petakov, M; Spanos, N; Bjekic, J; Stanojlovic, O; Milinkovic, AP; Radojicic, Z; Damjanovic, S
Year
2010
Is Peer Reviewed?
Yes
Journal
Endocrine
ISSN:
1355-008X
EISSN:
1559-0100
Volume
37
Issue
1
Page Numbers
129-134
Language
English
PMID
20963561
DOI
10.1007/s12020-009-9277-9
Web of Science Id
WOS:000273851800016
Abstract
Glucocorticoid receptor (GR) transduces the glucocorticoid (GC) signal that could lead to metabolic derangements depending on the tissue responsiveness to GC. We aimed to investigate possible causative relation of the GR functional properties in peripheral blood mononuclear cells of women with polycystic ovary syndrome (PCOS), with their clinical and biochemical characteristics. Thirty women with PCOS [mean age: 26.5 ± 5.1 years, mean body mass index (BMI) 24.5 ± 5 kg/m(2)], and thirty respective controls were analyzed for the number of GR sites per cell (B (max)), apparent equilibrium dissociation constant (K (d)), and binding potency (GR potency). A strong association between B (max) and K (d) (r = 0.70, P < 0.0001), and GR potency with age (r = 0.49, P = 0.009) was observed in PCOS women. The multiple regression analyses within the PCOS group revealed that independent predictors for K (d) were BMI, total cholesterol, and dehydroepiandrosterone-sulfate (DHEA-S) (r = 0.58, P = 0.038), while for GR potency (r = 0.687, P = 0.013) were age, BMI, DHEA-S, and basal cortisol concentration. The results suggest that PCOS pathophysiology may be related to alterations of a cross stalk between glucocorticoid signaling, age, and metabolic parameters. These findings should be further explored in studies on the role of GR in PCOS-related metabolic derangements.
Keywords
PCOS; Glucocorticoid receptor; Glucocorticoid-receptor-binding characteristics; DHEA-S
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