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Estrogen receptor beta gene haplotype is associated with pelvic organ prolapse
Authors:Chen Huey-Yi  Wan Lei  Chung Ya-Wen  Chen Wei-Chi  Tsai Fuu-Jen  Tsai Chang-Hai
Institution:

aDepartment of Obstetrics and Gynecology, China Medical University Hospital, College of Chinese Medicine, China Medical University, Taichung, Taiwan

bDepartment of Medical Genetics, China Medical University Hospital, College of Chinese Medicine, China Medical University, No. 2 Yu-Der Road, Taichung 404, Taiwan

cDepartment of Urology, China Medical University Hospital, College of Chinese Medicine, China Medical University, Taichung, Taiwan

dCollege of Life Science, National Chung Hsing University, Taichung, Taiwan

eAsia University, Taichung, Taiwan

Abstract:OBJECTIVE: Estrogen and estrogen receptors are known to play important roles in the pathophysiology of pelvic organ prolapse (POP). We investigated whether estrogen receptor beta (ERbeta) gene polymorphisms were associated with POP by conducting a case-control association study in 69 women with POP and 141 women without POP. STUDY DESIGN: Genotypes of the ERbeta gene polymorphisms (rs2987983, rs1271572, rs944459, rs1256049, and rs1255998) were determined by polymerase chain reaction, followed by restriction fragment length polymorphism analysis. Haplotyping analysis was used to determine the relationship among five polymorphisms in the ERbeta gene and POP. RESULTS: There was no significant difference between women with and those without POP in the distribution of any of the genotypes evaluated. In haplotype frequency estimation analysis, haplotype CGCGC was more prevalent in women with POP (16.7%) than in women without POP (8.9%) (p=0.011). Using multivariable logistic regression, age, parity and haplotype CGCGC were significantly associated with POP. CONCLUSION: Although the sample size of women with POP studied is small, the present study shows that ERbeta gene haplotype may be associated with POP.
Keywords:Pelvic organ prolapse  Estrogen receptor β gene polymorphism  Haplotype
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