A model for predicting age at menopause in white women
Objective
To develop a model to predict the age at natural menopause and the risk for premenopausal hysterectomy.
Design
Cross-sectional study.
Setting
Multicenter study.
Patient(s)
A total of 1,345 white women.
Intervention(s)
Ten single nucleotide polymorphisms (SNPs) of seven estrogen (E)-metabolizing genes (i.e., catechol-O-methyltransferase, 17-β-hydroxysteroid dehydrogenase type 1, cytochrome P-450 [CYP] 17, CYP1A1, CYP1B1, CYP19, and E receptor [ER] α) were analyzed by sequencing-on-chip-technology.
Main Outcome Measure(s)
Patients’ reproductive and medical histories were ascertained and correlated to genotypes.
Result(s)
The model incorporates the number of full term pregnancies, the body mass index (BMI), a history of breast surgery, and the presence of CYP17 and CYP1B1-4 polymorphisms as well as the BMI to predict age at natural menopause and the risk for undergoing premenopausal hysterectomy.
Conclusion(s)
We present the first model to date, which can predict age at natural menopause and the risk for undergoing premenopausal hysterectomy based on genotype information and personal history.
Key Words: Menopause , hysterectomy , gene , polymorphism , age , timing , estrogen
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Supported in part by the Ludwig Boltzmann Foundation, Institute for Gynecology and Gynecologic Oncology, Vienna, Austria.
PII: S0015-0282(05)03680-0
doi:10.1016/j.fertnstert.2005.07.1300
© 2006 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.

