PMID- 20095908 OWN - NLM STAT- MEDLINE DCOM- 20120410 LR - 20100222 IS - 1931-843X (Electronic) IS - 1540-9996 (Linking) VI - 19 IP - 2 DP - 2010 Feb TI - Estrogen receptor-1 genetic polymorphisms for the risk of premature ovarian failure and early menopause. PG - 297-304 LID - 10.1089/jwh.2008.1317 [doi] AB - BACKGROUND: The aim of this study was to investigate the role of the estrogen receptor 1 (ESR1) genetic polymorphisms for early menopause that was classified as premature ovarian failure (POF) and early menopause (EM) and to examine whether the associations of ESR1 genetic variants are different for POF and EM. METHODS: We selected 100 POF cases and matched 100 EM cases and 200 normal menopause (NM) controls from the Korean Multi-Center Cohort. Among them, we restricted idiopathic POF and EM cases vs NM controls by excluding POF/EM cases with medical/surgical causes. The XbaI (rs9340799) and PvuII (rs2234693) in the ESR1 gene were genotyped. The single-nucleotide polymorphism (SNP) and haplotype effects were analyzed by multivariate logistic regression and haplotype analysis. Also nominal polytomous logistic regression was used to find whether ESR1 genetic variants are differently associated with POF and EM. RESULTS: The global p values for idiopathic POF and EM were 0.08 and 0.39 (SNP-based), and <0.001 and 0.12 (haplotype-based), respectively. The XbaI genetic variant containing the X allele was marginally significantly associated with a reduced risk of idiopathic POF (OR = 0.6, 95% CI 0.3-1.0). The P-x haplotype and diplotypes significantly decreased the risk of idiopathic POF (OR = 0.5, 95% CI 0.2-0.9; OR = 0.4, 95% CI 0.2-0.9, respectively). In contrast from POF, the P-x haplotypes and diplotypes insignificantly increased the risk for both idiopathic EM (p(polytomous) = 0.009 for P-x haplotype; p(polytomous) = 0.02 for P-x diplotypes). CONCLUSION: Our results suggest that the ESR1 gene including PvuII and XbaI polymorphisms may modify the risk of idiopathic premature ovarian failure (POF) but not idiopathic early menopause (EM) risk. FAU - Yang, Jae Jeong AU - Yang JJ AD - Department of Preventive Medicine, Seoul National University College of Medicine, Seoul, Korea. FAU - Cho, Lisa Y AU - Cho LY FAU - Lim, Yun Jeong AU - Lim YJ FAU - Ko, Kwang-Pil AU - Ko KP FAU - Lee, Kun-Sei AU - Lee KS FAU - Kim, Hyeongsu AU - Kim H FAU - Yim, Sung Vin AU - Yim SV FAU - Chang, Soung Hoon AU - Chang SH FAU - Park, Sue K AU - Park SK LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - J Womens Health (Larchmt) JT - Journal of women's health (2002) JID - 101159262 RN - 0 (Estrogen Receptor alpha) SB - IM MH - Adult MH - Cohort Studies MH - Estrogen Receptor alpha/*genetics MH - Female MH - Humans MH - Menopause, Premature/*genetics MH - Middle Aged MH - *Polymorphism, Genetic MH - Primary Ovarian Insufficiency/*genetics MH - Prospective Studies MH - Republic of Korea MH - Risk EDAT- 2010/01/26 06:00 MHDA- 2012/04/11 06:00 CRDT- 2010/01/26 06:00 PHST- 2010/01/26 06:00 [entrez] PHST- 2010/01/26 06:00 [pubmed] PHST- 2012/04/11 06:00 [medline] AID - 10.1089/jwh.2008.1317 [doi] PST - ppublish SO - J Womens Health (Larchmt). 2010 Feb;19(2):297-304. doi: 10.1089/jwh.2008.1317.