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Hum. Reprod. Advance Access published online on January 7, 2005

Human Reproduction, doi:10.1093/humrep/deh726
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Human Reproduction © European Society of Human Reproduction and Embryology 2005; all rights reserved
Received November 17, 2004
Accepted December 8, 2004

Article

Association between endometriosis and genetic polymorphisms of the estradiol-synthesizing enzyme genes HSD17B1 and CYP19

M. Tsuchiya 1, H. Nakao 2, T. Katoh 2*, H. Sasaki 3, M. Hiroshima 3, T. Tanaka 3, T. Matsunaga 4, T. Hanaoka 5, S. Tsugane 5, and T. Ikenoue 6

1 Department of Public Health, Miyazaki Medical College, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki, Japan; Department of Obstetrics and Gynecology, Miyazaki Medical College, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki, Japan
2 Department of Public Health, Miyazaki Medical College, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki, Japan
3 Department of Obstetrics and Gynecology, The Jikei University School of Medicine, 3-25-8 Nishi-shinbashi, Minato-ku, Tokyo, Japan
4 Department of Biotechnology, Tokyo University of Agriculture and Technology, 2-24-16 Naka-cho, Koganei, Tokyo, Japan
5 Epidemiology and Prevention Division, Research Center for Cancer Prevention and Screening, National Cancer Center, 5-1-1 Tsukiji, Chuo-ku, Tokyo, Japan
6 Department of Obstetrics and Gynecology, Miyazaki Medical College, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki, Japan

* To whom correspondence should be addressed.
T. Katoh, E-mail: katoht{at}med.miyazaki-u.ac.jp


   Abstract

BACKGROUND: Endometriosis, an estrogen-dependent disease, is believed to be influenced by multiple genetic and environmental factors. Here, we evaluated whether the risk and severity of endometriosis are associated with polymorphisms in estradiol-synthesizing enzyme genes: the Ser312Gly polymorphism in 17-beta-hydroxysteroid dehydrogenase type 1 (HSD17B1) and the Arg264Cys polymorphism in cytochrome P450, subfamily XIX (CYP19). METHODS: All participants underwent diagnostic laparoscopy, and the stage of endometriosis was determined according to the Revised American Fertility Society classification. Of the 138 women enrolled, 59 had no endometriosis, 21 had stage I, 10 had stage II, 23 had stage III and 25 had stage IV. SNPs were discriminated by allele-specific oligonucleotide hybridization. RESULTS: Individuals having at least one A-allele (A/G or A/A genotype) of HSD17B1 showed a significantly increased risk of endometriosis (A/G genotype: adjusted OR, 3.06; 95%CI 1.21-7.74; A/A genotype: adjusted OR, 3.02; 95%CI 1.08-8.43). There was a significant trend associating A/G + A/A genotypes with severity of endometriosis (P for trend <0.01). No statistically significant association was found for the CYP19 polymorphism. CONCLUSIONS: Evidence for association between the Ser312Gly polymorphism in HSD17B1 and endometriosis was found in a Japanese population. The A-allele of HSD17B1 appears to confer higher risk for endometriosis.

Keywords: CYP19; endometriosis; estrogen synthesis; genetic polymorphism; HSD17B1.
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