TY - JOUR
T1 - Impact of menopausal hormone formulations on pituitary-ovarian regulatory feedback
AU - Kling, Juliana M.
AU - Dowling, N. Maritza
AU - Bimonte-Nelson, Heather A.
AU - Gleason, Carey E.
AU - Kantarci, Kejal
AU - Manson, Joann E.
AU - Taylor, Hugh S.
AU - Brinton, Eliot A.
AU - Lobo, Rogerio A.
AU - Cedars, Marcelle I.
AU - Pal, Lubna
AU - Neal-Perry, Genevieve
AU - Naftolin, Frederick
AU - Harman, S. Mitchell
AU - Miller, Virginia M.
N1 - Funding Information:
The content of this article is solely the responsibility of the authors and does not necessarily represent the official view of the NCATS or NIH. Study medications were supplied in part by Bayer Health Care and by Abbott Pharmaceuticals. Funding for FSH/LH assays was made available through support offered by the Department of Obstetrics, Gynecology, and Reproductive Sciences at Yale and the Benneck-Polan Family Foundation.
Funding Information:
This work was supported in part by a Mayo Clinic Mentored Research Award as well as Grant National Institute on Aging (NIA) RF1 AG057547 to K. Kantarci, C. E. Gleason, and V. M. Miller; NIA AG-028084, ADHS14-052688, and the National Institutes of Health (NIH) Alzheimer’s Disease Centers P30-AG-019610 to H. A. Bimonte-Nelson; P50-AG-033514 to C. E. Gleason; and the Mayo Clinic Foundation for Research and Education. KEEPS was funded by grants from the Aurora Foundation to the Kronos Longevity Research Institute, from National Heart, Lung, and Blood Institute Grant HL-90639 to V. M. Miller, Mayo Clinic CTSA 1 UL1 RR024150, the Mayo Foundation, Brigham and Women’s Hospital/Harvard Medical School CTSA, CTSA UL1 RR024139 and UCSF CTSA UL1 RR024131 from the National Center for Advancing Translational Sciences (NCATS), a component of the NIH and NIH Roadmap for Medical Research.
Funding Information:
Kejal Kantarci serves on the data safety monitoring board for Takeda Global Research and Development Center, Inc., and receives research support from Avid Radiopharmaceuticals and Eli Lilly and funding from NIH and the Alzheimer’s Drug Discovery Foundation. Other authors have nothing additional to disclose.
Funding Information:
This work was supported in part by a Mayo Clinic Mentored Research Award as well as Grant National Institute on Aging (NIA) RF1 AG057547 to K. Kantarci, C. E. Gleason, and V. M. Miller; NIA AG-028084, ADHS14- 052688, and the National Institutes of Health (NIH) Alzheimer's Disease Centers P30-AG-019610 to H. A. Bimonte-Nelson; P50-AG-033514 to C. E. Gleason; and the Mayo Clinic Foundation for Research and Education. KEEPS was funded by grants from the Aurora Foundation to the Kronos Longevity Research Institute, from National Heart, Lung, and Blood Institute Grant HL-90639 to V. M. Miller, Mayo Clinic CTSA 1 UL1 RR024150, the Mayo Foundation, Brigham and Women's Hospital/Harvard Medical School CTSA, CTSA UL1 RR024139 and UCSF CTSA UL1 RR024131 from the National Center for Advancing Translational Sciences (NCATS), a component of the NIH and NIH Roadmap for Medical Research.
Publisher Copyright:
© 2019 American Physiological Society. All rights reserved.
PY - 2019
Y1 - 2019
N2 - Changes in pituitary-ovarian hormones across the menopausal transition have multiple physiological consequences. However, little is known about how the major types of postmenopausal hormone therapy (HT) affect pituitary-ovarian hormonal relationships. This study evaluated these relationships in recently menopausal women (52.45 ± 2.49 yr of age) in the Kronos Early Estrogen Prevention Study (KEEPS) who were compliant to randomized, double- blinded treatment with oral conjugated equine estrogen (o-CEE; n = 109), transdermal 17_abs-estradiol (t-E2; n = 107), or placebo (n = 146). Androstenedione, testosterone, 17β-estradiol, estrone, folliclestimulating hormone (FSH), and luteinizing hormone (LH) were measured in serum before (baseline) and 48 mo after randomization to treatment. Descriptive summaries of hormone levels were performed, and multiple regression analyses were used to examine the effects of o-CEE, t-E2, and placebo on these hormone levels at 48 mo, adjusting for baseline levels. A network analysis examined the covariance of changes in hormone levels over the 48 mo within treatment groups. As expected, at 48 mo of treatment, hormone levels differed between women in the two active treatment groups compared with placebo, and network analysis indicated stronger relationships among hormone levels in the t-E2 and o-CEE groups compared with placebo. Associations among testosterone, 17β-estradiol, FSH, and LH differed between the o-CEE group compared with t-E2 and placebo groups. Thus, two common HT regimens differentially alter pituitary-ovarian hormone levels, altering feedback cycles and interhormonal associations in recently menopausal women. These interactions provide the basis for future studies investigating the impact of hormonal modulation of aging, including cognitive decline in women.
AB - Changes in pituitary-ovarian hormones across the menopausal transition have multiple physiological consequences. However, little is known about how the major types of postmenopausal hormone therapy (HT) affect pituitary-ovarian hormonal relationships. This study evaluated these relationships in recently menopausal women (52.45 ± 2.49 yr of age) in the Kronos Early Estrogen Prevention Study (KEEPS) who were compliant to randomized, double- blinded treatment with oral conjugated equine estrogen (o-CEE; n = 109), transdermal 17_abs-estradiol (t-E2; n = 107), or placebo (n = 146). Androstenedione, testosterone, 17β-estradiol, estrone, folliclestimulating hormone (FSH), and luteinizing hormone (LH) were measured in serum before (baseline) and 48 mo after randomization to treatment. Descriptive summaries of hormone levels were performed, and multiple regression analyses were used to examine the effects of o-CEE, t-E2, and placebo on these hormone levels at 48 mo, adjusting for baseline levels. A network analysis examined the covariance of changes in hormone levels over the 48 mo within treatment groups. As expected, at 48 mo of treatment, hormone levels differed between women in the two active treatment groups compared with placebo, and network analysis indicated stronger relationships among hormone levels in the t-E2 and o-CEE groups compared with placebo. Associations among testosterone, 17β-estradiol, FSH, and LH differed between the o-CEE group compared with t-E2 and placebo groups. Thus, two common HT regimens differentially alter pituitary-ovarian hormone levels, altering feedback cycles and interhormonal associations in recently menopausal women. These interactions provide the basis for future studies investigating the impact of hormonal modulation of aging, including cognitive decline in women.
KW - Androgen
KW - Estrogen
KW - Follicle-stimulating hormone
KW - Hormone therapy
KW - Menopause
KW - Pituitary-ovarian hormones
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UR - http://www.scopus.com/inward/citedby.url?scp=85076330788&partnerID=8YFLogxK
U2 - 10.1152/ajpregu.00234.2019
DO - 10.1152/ajpregu.00234.2019
M3 - Article
C2 - 31663769
AN - SCOPUS:85076330788
SN - 0363-6119
VL - 317
SP - R912-R920
JO - American Journal of Physiology
JF - American Journal of Physiology
IS - 6
ER -