Basal insulin-like factor 3 levels predict functional ovarian hyperandrogenism in the polycystic ovary syndrome

被引:20
作者
Gambineri, A. [1 ,2 ]
Patton, L. [1 ,2 ]
Prontera, O. [1 ,2 ]
Fanelli, F. [1 ,2 ]
Ciampaglia, W. [3 ]
Cognigni, G. E. [3 ]
Pagotto, U. [1 ,2 ]
Pasquali, R. [1 ,2 ]
机构
[1] Univ Bologna, Div Endocrinol, Dept Internal Med, S Orsola M Malpighi Hosp, I-40138 Bologna, Italy
[2] Univ Bologna, Ctr Appl Biomed Res CRBA, S Orsola M Malpighi Hosp, I-40138 Bologna, Italy
[3] Day Surg Ctr, Bologna, Italy
关键词
FOH; hyperandrogenism; INSL3; insulin; LH; LUTEINIZING-HORMONE; CIRCULATING HORMONE; OBESE WOMEN; RESISTANCE; TESTOSTERONE; METFORMIN; ANDROGEN; DYSREGULATION; EXPRESSION; RESPONSES;
D O I
10.3275/7726
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim: The aims of the study were to understand the association between insulin-like factor 3 (INSL3) and functional ovarian hyperandrogenism (FOH) in PCOS and the regulatory role played by LH. Subjects and methods: Fifteen PCOS women were classified as FOH (FOH-PCOS, no.=8) and non-FOR (NFOH-PCOS, no.=7) according to the response of 17OH-progesterone to buserelin (a GnRH analogue) with respect to 15 controls. FOH-PCOS and NFOH-PCOS were compared for basal INSL3 levels. In addition, the effect of buserelin on INSL3 concentrations and the relationship between basal and buserelin-stimulated LH and 17OH-progesterone and INSL3 were evaluated. Results: Basal INSL3 levels were higher in FOH-PCOS than NFOH-PCOS (p=0.001) and controls (p=0.001), whereas they did not differ between NFOH-PCOS and controls. In addition, FOH-PCOS had a higher response of LH to buserelin with respect to NFOH-PCOS. Within all PCOS women the levels of INSL3 positively correlated with free testosterone (p=0.022) and negatively with SHBG (r= p=0.031). Moreover, positive correlations with the absolute increase of 17OH-progesterone (p<0.001) and with the LH area under the curve (p=0.001) after buserelin administration were found. In the multiple regression analysis INSL3 persisted significantly correlated only with 17OH-progesterone response to buserelin. Finally, INSL3 was not significantly modified after buserelin administration either in FOH-PCOS or in NFOH-PCOS. Conclusions: These data suggest that INSL3 is related to FOH in PCOS women, but this association seems not to be mediated by LH, further reinforcing the concept that a pathophysiological heterogeneity for ovarian hyperandrogenism in PCOS exists. (J. Endocrinol. Invest. 34: 685-691, 2011) (C) 2011, Editrice Kurtis
引用
收藏
页码:685 / 691
页数:7
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