Age-Related Analysis of Inhibin A, Inhibin B, and Activin A Relative to the Intercycle Monotropic Follicle-Stimulating Hormone Rise in Normal Ovulatory Women
Nancy A. Klein,
Brenda S. Houmard,
Karl R. Hansen,
Teresa K. Woodruff,
Patrick M. Sluss,
William J. Bremner and
Michael R. Soules
Departments of Obstetrics and Gynecology (N.A.K., B.S.H., K.R.H., M.R.S.) and Medicine (W.J.B.), University of Washington, Seattle, Washington 98105; Departments of Neurobiology and Physiology (T.K.W.), Northwestern University, Evanston, Illinois 60208; and Reproductive Endocrine Unit Department of Medicine (P.M.S.), Massachusetts General Hospital, Boston, Massachusetts 02114
Address all correspondence and requests for reprints to: Nancy A. Klein, M.D., Division of Reproductive Endocrinology, 4225 Roosevelt Way NE, Suite 305, Seattle, Washington 98105. E-mail: nklein{at}u.washington.edu.
Previous studies have reported that the monotropic rise in FSHin older women is associated with decreased inhibin B and/orA levels and increased levels of activin A. Whereas most investigatorshave found decreased follicular-phase inhibin B, the roles ofinhibin A and activin A as modulators of the FSH rise are unclear.The objectives of this study were to determine whether deficienciesin circulating levels of inhibin A, inhibin B, and/or activinA exist during the intercycle interval in ovulatory older (age,4045 yr; n = 16), compared with younger women (age, 2025yr; n = 13). Blood samples were obtained daily throughout onemenstrual cycle and the follicular phase of the subsequent cycleand were analyzed for LH, FSH, estradiol, inhibin A and B, andactivin A. Despite significant FSH elevation, no deficienciesin inhibin A, activin A, or estradiol were detected in oldersubjects. In fact, inhibin A was significantly higher in olderparticipants during the intercycle phase (P = 0.01), whereasinhibin B was significantly lower. Thus, the monotropic risein FSH does not appear to result from changes in inhibin A oractivin A, supporting the concept that inhibin B plays a criticalrole in mediating the FSH rise in older women.
This work was supported by grants from the National Instituteon Aging (Grant RO1-AG14579) and the National Institute of ChildHealth and Human Development (Grant U54-HD29164).
Abbreviation: CV, Coefficient(s) of variation.
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