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Serum adiponectin concentrations are decreased in women with endometriosis.

Authors :
Takemura Y
Osuga Y
Harada M
Hirata T
Koga K
Morimoto C
Hirota Y
Yoshino O
Yano T
Taketani Y
Source :
Human reproduction (Oxford, England) [Hum Reprod] 2005 Dec; Vol. 20 (12), pp. 3510-3. Date of Electronic Publication: 2005 Jul 29.
Publication Year :
2005

Abstract

Background: Adiponectin is a pleiotropic cytokine originally discovered as an adipocyte-specific gene product. Serum adiponectin concentrations have been reported to be low in women with endometrial cancer, breast cancer and uterine leiomyoma, suggesting possible involvement of adiponectin in these estrogen-related diseases. We thus addressed the relevance of adiponectin to endometriosis, an estrogen-dependent disease, in the present study.<br />Methods: Women with (n = 48) and without (n = 30) endometriosis undergoing laparoscopy were recruited in this study. Blood samples were collected, and serum adiponectin concentrations were measured using a specific enzyme-linked immunosorbent assay. The relationship between laparoscopic findings and serum adiponectin concentrations was analysed.<br />Results: The adiponectin concentrations in the serum of the women with endometriosis (median, 13.1 microg/ml; interquartile range, 10.2 - 16.7) were significantly lower than those of the women without endometriosis (15.9 microg/ml, 13.5 - 19.5; P = 0.008). A significant negative correlation was found between serum adiponectin concentrations and both endometriosis scores (R = - 0.307, P = 0.006) and adhesion scores (R = - 0.254, P = 0.026) of the revised American Society for Reproductive Medicine classification of endometriosis.<br />Conclusions: The present findings suggest that adiponectin is implicated in the pathophysiology of endometriosis.

Details

Language :
English
ISSN :
0268-1161
Volume :
20
Issue :
12
Database :
MEDLINE
Journal :
Human reproduction (Oxford, England)
Publication Type :
Academic Journal
Accession number :
16055459
Full Text :
https://doi.org/10.1093/humrep/dei233