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Peroxisome Proliferator-Activated Receptor-gamma and Its Coactivator-1 alpha Gene Polymorphisms in Korean Women with Polycystic Ovary Syndrome

Cited 20 time in Web of Science Cited 20 time in Scopus
Authors

Chae, Soo Jin; Kim, Jin Ju; Choi, Young Min; Kim, Jong Mee; Moon, Shin Yong; Cho, Young Min

Issue Date
2010
Publisher
KARGER
Citation
GYNECOLOGIC AND OBSTETRIC INVESTIGATION; Vol.70 1; 1-7
Keywords
Peroxisome proliferator-activated receptor-gammaPPAR-gamma coactivator-1 alphaPolycystic ovary syndrome
Abstract
Background/Aims: To investigate whether the peroxisome proliferator-activated receptor-gamma (PPAR-gamma) Pro12Ala and the PPAR-gamma coactivator-1 alpha (PGC-1 alpha) Gly482Ser polymorphisms were associated with polycystic ovary syndrome (PCOS). Methods: Genetic analyses of the PPAR-gamma Pro12Ala and the PGC-1 alpha Gly482Ser polymorphisms were performed in 184 patients with PCOS and 256 controls. Hormone levels, biochemical and clinical features were analyzed according to these polymorphisms. Results: Neither the PPAR-gamma Pro12Ala nor the PGC-1 alpha Gly482Ser polymorphism showed significant differences in genotypic distribution between women with PCOS and controls. In PCOS patients, women with the non-Pro/Pro genotypes of the PPAR-gamma Pro12Ala polymorphism showed statistically significantly higher HDL levels than those with the Pro/Pro genotype (p = 0.002). PCOS patients who had the Ser/Ser genotype of the PGC-1 alpha Gly482Ser polymorphism had significantly higher levels of postprandial 2-hour insulin than those with the Gly/Ser genotype (p = 0.045). Conclusions: Neither the PPAR-gamma Pro12Ala nor the P GC-1 alpha Gly482Ser polymorphism were supposed to be susceptible genes in PCOS. However, in PCOS patients, the PPAR-gamma Pro12Ala and the PGC-1 alpha Gly482Ser polymorphism may modulate the concentrations of serum HDL levels and postprandial 2-hour insulin level, respectively. Copyright (C) 2010 S. Karger AG, Basel
ISSN
0378-7346
Language
English
URI
https://hdl.handle.net/10371/76548
DOI
https://doi.org/10.1159/000279309
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