Exon 6 and 2 Peroxisome Proliferator-Activated Receptor-γ Polymorphisms in Polycystic Ovary Syndrome

Author:

Orio Francesco1,Matarese Giuseppe2,Di Biase Sebastiano3,Palomba Stefano4,Labella Donato3,Sanna Veronica2,Savastano Silvia1,Zullo Fulvio4,Colao Annamaria1,Lombardi Gaetano1

Affiliation:

1. Department of Molecular & Clinical Endocrinology and Oncology (F.O., S.S., A.C., G.L.), University “Federico II”, 80131 Naples, Italy;

2. Immunoendocrinology Group (G.M., V.S.), Institute of Endocrinology and Experimental Oncology, National Research Council, 80131 Naples, Italy;

3. MeriGen Molecular Biology Laboratory (S.D.B., D.L.), 80131 Naples, Italy;

4. Chair of Obstetrics and Gynecology (S.P., F.Z.), University of Catanzaro “Magna Graecia”, 88100 Catanzaro, Italy

Abstract

Abstract Obesity affects about 44% of women with polycystic ovary syndrome (PCOS). Peroxisome proliferator-activated receptor-γ (PPAR-γ) is one of the genes involved in the differentiation of adipose tissue. In an attempt to shed light on the high percentage of obesity in PCOS, we examined polymorphisms at exons 6 and 2 of the PPAR-γ gene in 100 PCOS patients and in 100 healthy controls matched for age and body mass index (BMI). The T allele frequency of exon 6 was significantly higher (P < 0.05) in PCOS patients compared with control women. In addition, the BMI and leptin levels were significantly higher (P < 0.05) in PCOS patients carrying the C→T substitution than in controls. There was no significant difference in leptin levels after normalization for BMI. The Pro12Ala polymorphism at exon 2 was unrelated to BMI and/or leptin levels in PCOS women. In conclusion, the higher frequency of the C→T substitution in exon 6 of the PPAR-γ gene in PCOS women suggests that it plays a role in the complex pathogenetic mechanism of obesity in PCOS, whereas the Pro12Ala polymorphism does not seem to affect BMI in PCOS women.

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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