Richard S Legro1, Robert G Brzyski2, Michael P Diamond3, Christos Coutifaris4, William D Schlaff5, Ruben Alvero5, Peter Casson6, Gregory M Christman7, Hao Huang8, Qingshang Yan8, Daniel J Haisenleder9, Kurt T Barnhart4, G Wright Bates10, Rebecca Usadi11, Richard Lucidi12, Valerie Baker13, J C Trussell14, Stephen A Krawetz3, Peter Snyder4, Dana Ohl7, Nanette Santoro5, Esther Eisenberg15, Heping Zhang8. 1. Department of Obstetrics and Gynecology, Pennsylvania State University, Hershey, Pennsylvania. Electronic address: RSL1@PSU.EDU. 2. Department of Obstetrics and Gynecology, University of Texas Health Science Center at San Antonio, Texas. 3. Department of Obstetrics and Gynecology, Wayne State University, Detroit, Michigan. 4. Department of Obstetrics and Gynecology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania. 5. Department of Obstetrics and Gynecology, University of Colorado, Denver, Colorado. 6. Department of Obstetrics and Gynecology, University of Vermont, Burlington, Vermont. 7. Department of Obstetrics and Gynecology, University of Michigan, Ann Arbor, Michigan. 8. Department of Biostatistics, Yale University School of Medicine, New Haven, Connecticut. 9. Ligand Core Laboratory University of Virginia Center for Research in Reproduction, Charlottesville, Virginia. 10. Department of Obstetrics and Gynecology, University of Alabama, Birmingham, Alabama. 11. Department of Obstetrics and Gynecology, Carolinas HealthCare Center for Reproductive Medicine, Charlotte, North Carolina. 12. Department of Obstetrics and Gynecology, Virginia Commonwealth University, Richmond, Virginia. 13. Department of Obstetrics and Gynecology, Stanford Hospital, Palo Alto, California. 14. Urology, SUNY Upstate Medical University, Syracuse, New York. 15. Fertility and Infertility Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), Rockville, Maryland.
Abstract
OBJECTIVE: To summarize baseline characteristics from a large multicenter infertility clinical trial. DESIGN: Cross-sectional baseline data from a double-blind randomized trial of two treatment regimens (letrozole vs. clomiphene). SETTING: Academic Health Centers throughout the United States. PATIENT(S): Seven hundred fifty women with polycystic ovary syndrome (PCOS) and their male partners took part in the study. INTERVENTION(S): None. MAIN OUTCOME MEASURE(S): Historic, biometric, biochemical, and questionnaire parameters. RESULT(S): Females averaged 30 years and were obese (body mass index [BMI] 35) with ∼20% from a racial/ethnic minority. Most (87%) were hirsute and nulligravid (63%). Most of the women had an elevated antral follicle count and enlarged ovarian volume on ultrasound. Women had elevated mean circulating androgens, LH-to-FSH ratio (∼2), and antimüllerian hormone levels (8.0 ng/mL). In addition, women had evidence for metabolic dysfunction with elevated mean fasting insulin and dyslipidemia. Increasing obesity was associated with decreased LH-to-FSH levels, antimüllerian hormone levels, and antral follicle counts but increasing cardiovascular risk factors, including prevalence of the metabolic syndrome. Men were obese (BMI 30) and had normal mean semen parameters. CONCLUSION(S): The treatment groups were well matched at baseline. Obesity exacerbates select female reproductive and most metabolic parameters. We have also established a database and sample repository that will eventually be accessible to investigators. CLINICAL TRIAL REGISTRATION NUMBER: NCT00719186.
RCT Entities:
OBJECTIVE: To summarize baseline characteristics from a large multicenter infertility clinical trial. DESIGN: Cross-sectional baseline data from a double-blind randomized trial of two treatment regimens (letrozole vs. clomiphene). SETTING: Academic Health Centers throughout the United States. PATIENT(S): Seven hundred fifty women with polycystic ovary syndrome (PCOS) and their male partners took part in the study. INTERVENTION(S): None. MAIN OUTCOME MEASURE(S): Historic, biometric, biochemical, and questionnaire parameters. RESULT(S): Females averaged 30 years and were obese (body mass index [BMI] 35) with ∼20% from a racial/ethnic minority. Most (87%) were hirsute and nulligravid (63%). Most of the women had an elevated antral follicle count and enlarged ovarian volume on ultrasound. Women had elevated mean circulating androgens, LH-to-FSH ratio (∼2), and antimüllerian hormone levels (8.0 ng/mL). In addition, women had evidence for metabolic dysfunction with elevated mean fasting insulin and dyslipidemia. Increasing obesity was associated with decreased LH-to-FSH levels, antimüllerian hormone levels, and antral follicle counts but increasing cardiovascular risk factors, including prevalence of the metabolic syndrome. Men were obese (BMI 30) and had normal mean semen parameters. CONCLUSION(S): The treatment groups were well matched at baseline. Obesity exacerbates select female reproductive and most metabolic parameters. We have also established a database and sample repository that will eventually be accessible to investigators. CLINICAL TRIAL REGISTRATION NUMBER: NCT00719186.
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